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Meet the Founders of Cord Blood Registry – Video

February 9th, 2012 1:51 am

01-02-2012 13:37 Meet founders of Cord Blood Registry, Tom and Wendy. Hear why they started CBR -- a family business dedicated to helping people live healthier lives through cord blood stem cell medicine. Today, CBR has grown, but the attention to healthy families is the same. For more than 15 years, Cord Blood Registry has led the umbilical cord banking industry in technical innovations and provided families with peace of mind and hope. CBR's experience and dedication to quality has enabled CBR to help more clients use their cord blood stem cells in treatments than any other family bank. Our research and development efforts are focused on helping leading clinical researchers advance stem cell regenerative medicine that may help families in the future. Ultimate use of cord blood stem cells will be determined by the treating physician who will consider if they are applicable for the condition and should come from the patient or a suitable donor (like an HLA matched sibling). There is no guarantee that treatments being studied in the laboratory or in clinical trials will be available in the future. CBR is the preferred choice of OB/Gyns. © 2011 Cord Blood Registry. All rights reserved. Privacy Policy.

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Adult Stem Cell Treatments for COPD -Real patient results, USA Stem Cells- Leon B. Testimonial – Video

February 9th, 2012 1:51 am

12-01-2012 07:24 If you would like more information please call us Toll Free at 877-578-7908. Or visit our website at http://www.usastemcells.com Or click here to have a Free Phone Constultation with Dr. Matthew Burks usastemcells.com Real patient testimonials for USA Stem Cells. Adult stem cell therapy for COPD, Emphysema, and Pulmonary fibrosis.

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Healing Bones With Stem Cells – Video

February 8th, 2012 9:24 pm

08-02-2012 09:53

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Adult Stem Cell Sucess Stories – Barry Goudy – Video

February 8th, 2012 9:30 am

03-02-2012 15:53 When Barry Goudy found out he had multiple sclerosis he feared the worst. Doctors told him he might lose his eye sight and the ability to walk. As a very active husband, father and hockey coach, Barry couldn't think of anything worse than losing his ability to get around. But then he learned of a new way to treat MS with a stem cell transplant. The transplant worked and today he's living proof of the miracles that can come from Adult Stem Cell Research.

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Hormel Institute study makes key finding in stem cell self-renewal

February 8th, 2012 9:30 am

A University of Minnesota-led research team has proposed a mechanism for the control of whether embryonic stem cells continue to proliferate and stay stem cells, or differentiate into adult cells like brain, liver or skin.

The work has implications in two areas. In cancer treatment, it is desirable to inhibit cell proliferation. But to grow adult stem cells for transplantation to victims of injury or disease, it would be desirable to sustain proliferation until a sufficient number of cells have been produced to make a usable organ or tissue.

The study gives researchers a handle on how those two competing processes might be controlled. It was performed at the university's Hormel Institute in Austin, Minn., using mouse stem cells. The researchers, led by Hormel Institute Executive Director Zigang Dong and Associate Director Ann M. Bode, have published a report in the journal Nature: Structure and Molecular Biology.

"This is breakthrough research and provides the molecular basis for development of regenerative medicine," said Dong. "This research will aid in the development of the next generation of drugs that make repairs and regeneration within the body possible following damage by such factors as cancer, aging, heart disease, diabetes, or paralysis caused by traumatic injury."

The mechanism centers on a protein called Klf4, which is found in embryonic stem cells and whose activities include keeping those cells dividing and proliferating rather than differentiating. That is, Klf4 maintains the character of the stem cells; this process is called self-renewal. The researchers discovered that two enzymes, called ERK1 and ERK2, inactivate Klf; this allows the cells to begin differentiating into adult cells.

The two enzymes are part of a "bucket brigade" of signals that starts when a chemical messenger arrives from outside the embryonic stem cells. Chemical messages are passed to inside the cells, resulting in, among other things, the two enzymes swinging into action.

The researchers also discovered how the enzymes control Klf4. They attach a small molecule--phosphate, consisting of phosphorus and oxygen--to Klf4. This "tag" marks it for destruction by the cellular machinery that recycles proteins.

Further, they found that suppressing the activity of the two enzymes allows the stem cells to maintain their self-renewal and resist differentiation. Taken together, their findings paint a picture of the ERK1 and ERK2 enzymes as major players in deciding the future of embryonic stem cells--and potentially cancer cells, whose rapid growth mirrors the behavior of the stem cells.

Klf4 is one of several factors used to reprogram certain adult skin cells to become a form of stem cells called iPS (induced pluripotent stem) cells, which behave similarly to embryonic stem cells.

Also, many studies have shown that Klf4 can either activate or repress the functioning of genes and, in certain contexts, act as either an oncogene (that promotes cancer) or a tumor suppressor. Given these and their own findings reported here, the Hormel Institute researchers suggest that the self-renewal program of cancer cells might resemble that of embryonic stem cells.

"Although the functions of Klf4 in cancer are controversial, several reports suggest Klf4 is involved in human cancer development," Bode said.

Established in 1942, the Hormel Institute is a world-renowned medical research center specializing in research leading to cancer prevention and control. It is a research unit of the University of Minnesota and a collaborative cancer research partner with Mayo Clinic.

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This Week in Modern Pathology

February 8th, 2012 9:30 am

In Modern Pathology this week, researchers from the Seoul National University in South Korea report on the association between the patterns of promoter CpG island methylation of breast cancer subtypes and cancer stem cell phenotypes. The team analyzed methylation status of 15 promoter CpG island loci involved in breast cancer progression, and determined their cancer stem cell phenotypes. They found that "the number of CpG island loci methylated differed significantly between subtypes, and was highest in the luminal-HER2 subtype and lowest in the basal-like subtype. Methylation frequencies and levels in 12 of the 15 genes differed significantly between subtypes, and the basal-like subtype had significantly lower methylation frequencies and levels in nine of the genes than the other subtypes." These findings suggest that breast cancer subtypes have distinct methylation patterns and that these patterns are associated with different stem cell phenotypes, the authors add.

Also in Modern Pathology, a team of French researchers elucidates the role of the mTOR pathway in leiomyosarcomas and pleomorphic sarcomas. The team assessed PTEN level and protein expression as well as the activation of downstream pathways, in a large series of sarcomas. They observed PTEN partial genomic loss in 46 percent of the tumors and a loss of protein expression in up to 68 percent of the tumors. "PTEN mutations were rare, with only 4 point mutations in the 65 samples studied," the authors write. "Subsequent activation of AKT and mTOR pathways was only observed in 2 out of 3 of PTEN-deleted tumors. On the other hand, RICTOR, a major component of the mTOR complex 2, was significantly overexpressed in well-differentiated leiomyosarcomas." The results suggest a link between RICTOR over-expression and leiomyosarcomas oncogenesis, the researchers add.

Finally in Modern Pathology this week, Macher-Goeppinger et al. report on the molecular heterogeneity of TFE3 activation in renal cell carcinomas. The team examined TFE3 expression and underlying genetic alterations in a series of renal cell carcinomas with long-term follow-up information. They found that five out of a total 876 tumors had TFE3 translocations, but that 9 percent of all renal cell carcinoma samples showed some degree of TFE3 reactivity. "Interestingly, these cases were associated with high nuclear grade, greater tumor extent and metastatic disease as well as an unfavorable patient outcome on uni- and multivariate analysis," the authors write. "Fluorescence in situ hybridisation revealed TFE3 amplifications as an additional, novel mechanism leading to increased TFE3 expression levels."

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IndiaMART Leaders of Tomorrow AWards 2011 – Regenerative Medical Services Pvt Ltd – Video

February 8th, 2012 9:28 am

09-12-2011 00:46 Yash Sanghavi a visionary distributor in the pharmaceutical sector with his futuristic approach established Regenerative Medical Services in 2008. Regenerative Medical Services more popularly known as Regrow is one of the key players in stem cell therapy and cell banking in India. Sanghvi has done B. Com and MBA.

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3D Printer Joins Organ Replacement Revolution

February 8th, 2012 9:25 am

Creating custom organs for individual patients is an idea that's been bandied about for some time, but it's no longer just a possibility for the distant future. A woman has been fitted with a brand new jawbone built by a 3D printer. "The combination of additive manufacturing and tissue engineering can result in real organ printing," said medical engineer Jules Poukens. "In this case, bone is the organ."

They're building people out of 3D printers now -- parts, anyway. LayerWise announced Sunday that it has applied a process called "additive manufacturing" to produce a titanium total lower jaw implant for facial reconstruction. The project was developed in collaboration with partners from medical industries and academia.

This is the first complete patient-specific implant for the lower jaw. The complex implant design incorporates articulated joints and dedicated features. The implant restored a patient's facial aesthetics and allowed her to regain her speech within hours.

The printer uses a high-precision laser to selectively heat metal powder particles that fully melt to adhere to the next layer without using glue or binder liquid. The additive manufacturing prints functional implant shapes that could be very difficult to produce using standard metalworking processes.

The implant was awarded the 2012 additive manufacturing award by the Additive Manufacturing Network in Belgium due to the fact that additive manufacturing played the main role in the realization of this new technology.

Medical Field Breakthrough

This advancement in the field of implant reconstruction goes beyond facial surgery. The technology could change the way all implants are designed and produced.

"This is a real breakthrough, exhibiting the possibilities of additive manufacturing in the field of medicine," Peter Mercelis, PhD, managing director of LayerWise, told TechNewsWorld. "Not only patient-specific implants are possible, but the technology can also be applied for serial manufacturing of implants. Applications of additive manufacturing and 3D printing are not limited to facial surgery, but also orthopedic surgery and traumatology may benefit from this technology."

These methods will become more common as more people become aware of the benefits, suggested Mercelis.

"It is now very new, but when awareness grows, also the acceptance of this technology will follow," he said. "This kind of technology was originally developed as a prototyping technique, but we successfully used our additive manufacturing technology to make fully functional components instead of prototypes. "

Price Will Go Down

The medical industry will recognize the benefits of the patient-specific implant, Mercelis predicted, including reduced operation time, faster recovery, better long-term outcomes and better functionality for patients.

"Of course, a broad acceptance will also allow the technology to become cheaper," he said.

Body Parts Just for You

Implants using additive manufacturing allow new possibilities and are easier for the body to adapt to due to the detail that doctors are able to put into the individual pieces.

"We already use the technology on a large scale for patient-specific dental prostheses through our dental division, DentWise," said Mercelis. "Biocompatible implants may be designed with integrated porosities to allow the natural bone of the patient to really grow inside the implant to allow for an improved fixation of the implant. This offers many new possibilities; one can integrate drugs that promote bone formation."

In the future, combinations of titanium implants and biodegradable 3D printed structures may be used, Mercelis added.

The Future: Growing Our Own Bones

This revolutionary step in mandibular treatment was developed under the supervision of Jules Poukens, professor in medical engineering at University Hasselt Belgium and cranio-maxillofacial surgeon at Orbis Medical Center.

"The combination of additive manufacturing and tissue engineering can result in real organ printing," Poukens told TechNewsWorld. "In this case, bone is the organ."

Further research, involving the combination of 3D printing with human tissue, will be carried out in cooperation with the research institute Sirris. "3D printed resorbable scaffolds can be combined with stem cells from the patient in order to create a viable implant without the need to harvest large bone transplants from the patient," said Poukens.

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L. Grozdinski, MD [Stem Cell Therapy | CCSVI Symposium 2011 – 38 of 46] – Video

February 8th, 2012 9:24 am

02-02-2012 08:37 CCSVI Symposium 2011 - Second Annual Meeting Crowne Plaza Hotel Times Square, Manhattan New York, NY July 15-17, 2011 http://www.ccsvicare.com Stem Cell Therapy L. Grozdinski, MD Angiology Sector Chief Tokuda Hospital Sofia, Bulgaria [38 out of 46 videos]

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US begins stem cell trial for hearing loss

February 8th, 2012 9:24 am

The phase I trial follows promising studies on mice showing that such transplants were able to rebuild the structures of the inner ear, and some anecdotal evidence from humans, sparking hope of a cure for some forms of deafness.

One of those people is two-year-old Finn McGrath, who suffered brain damage after being deprived of oxygen during a prolonged and complicated delivery, according to his mother, Laura.

"His doctors told us he was at high risk for cerebral palsy, vision issues, hearing problems and mental retardation," she said in an interview with AFP.

Finn's early days were an all-out struggle to survive, so for his parents, learning that he had failed his hearing tests and had damaged hair cells -- the sensory receptors in the inner ear that pick up sounds -- was almost an afterthought.

He had organ failure, breathing problems, and his cerebral palsy left him unable to roll, crawl or walk, hold his head up, talk or eat.

As his parents searched for ways to help him, they came upon stories online that told of studies using cord blood to help children with cerebral palsy and other disorders.

Prior to his birth, the McGraths had arranged to privately bank his umbilical cord blood, a procedure that costs around $2,000 plus storage fees, and remains controversial among pediatricians.

Private companies such as the Cord Blood Registry, which is funding the Texas study on hearing loss, urge expecting parents to bank their umbilical cord blood and reserve it for personal use as a way to protect their family.

That advice runs counter to the guidelines issues by the American Academy of Pediatrics in 2007, which calls such claims "unsubstantiated" and says banking for personal or family use "should be discouraged" but is "encouraged" if it is to be stored in a bank for public use.

Since Finn's parents had already banked his, they enrolled him in cord blood trial for cerebral palsy in North Carolina and he received his first transplant in November 2009 when he was about seven weeks old.

A second transfusion followed and by May, his parents began to notice a change.

Nighttime noises, like an alarm on his food pump or the sound of ripping medical tape, would suddenly startle him awake, his mother recalled.

"He started vocalizing sounds and we could tell that he was anticipating things that we would say. Like, if he had heard a story a number of times or a song, he would smile like he recognized the song or the story."

Finn had a third infusion in September 2010, when he was one year old. Four months later, an otoacoustic emissions test (OAE), which plays a sound and picks up vibrations in the cochlea and hair cells, came back normal.

The early hearing tests that showed hearing loss were not exactly the same as the later tests that came back normal, so McGrath is cautious about comparing them directly, but she believes the cord blood transfusions may have helped.

"All I can tell you is anecdotally he was not able to hear for probably the first three or four months of his life, and then when he was about six to eight months old, he started hearing."

The hearing trial in Texas aims to take a first step in testing the safety, and later the efficacy, of transfusing cord blood in children age six weeks to 18 months who have sustained post-birth sensorineural hearing loss.

Some reasons that children lose their hearing at or after birth may include oxygen deprivation, head injury, infection, strong doses of antibiotics or loud noises.

Sensorineural hearing loss affects approximately six per 1,000 children, and there is no available medical treatment. Hearing aids or cochlear implants are typically offered to boost the ability of the damaged tissues.

"Stem cell therapy may potentially repair the damaged structures of the inner ear and restore normal hearing," lead investigator Sami Fakhri told AFP.

"We are at the initial stages of this process and the results are looking promising," Fakhri added.

Research using stem cells in cord blood, known as hematopoietic cells, is already under way on some types of brain injury, cerebral palsy, juvenile diabetes, kidney and lung disease, he said.

The new study at Memorial Hermann-Texas Medical Center is being funded by the Cord Blood Registry, a private bank, and those eligible must have already banked their own umbilical cord blood with CBR.

But to Stephen Epstein, an otolaryngologist in Maryland, that does not pose a conflict of interest, because separate medical institutions in Texas and Georgia are conducting the Food and Drug Administration-approved research.

"If both of them can reproduce the same results then I would say it has some validity to it," said Epstein, who is not involved in the study.

"This is certainly a welcome, acceptable experiment, but it should be looked at with caution and time will tell."

One patient is already enrolled and the study, which runs for one year, has room for nine more.

While Finn McGrath still faces many challenges due to his cerebral palsy, his mother is grateful for the things he can do.

"I don't know how much worse off he would have been without the stem cell transfusion," McGrath said, pointing to his normal cognition, lack of seizures, good hearing and vision.

"We remain hopeful that he will continue to improve."

(c) 2012 AFP

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American CryoStem Completes Cell Processing for Clinical Study

February 8th, 2012 3:55 am

RED BANK, NJ--(Marketwire -02/07/12)- American CryoStem Corporation (OTCQB: CRYO.OB - News) announced today that it has completed providing stem cell processing services for Personal Cell Sciences Corp., a cutting edge manufacturer of anti-aging skin care products.

The study involves researching the regenerative function of a conditioned medium obtained from each participant's adipose (fat tissue) derived mesenchymal stem cells and their ability to promote the production or secretion of collagen, elastin and fibronectin related to skin wound healing.

John Arnone, CEO of American CryoStem and Founder of Personal Cell Sciences, commented, "CRYO's patented tissue culture media and its proprietary, aseptic adipose tissue processing methodology allows, as an added benefit for PCS customers to store a clinical grade sample of their own stem cells for future use in regenerative medicine. We are pleased to provide comprehensive Bio-Insurance storage solutions at our clinical facility."

The adipose tissue samples were acquired utilizing a mini-liposuction procedure. A total of sixty milliliters (approximately 2 fluid ounces) of adipose tissue was collected in the physician's office and sent to CRYO's laboratory for processing. Once processed, the resulting stromal vascular fraction (SVF) was forwarded to the Personal Cell Sciences laboratory for proprietary formulation for patient specific products.

"We are very excited to announce our service agreement and participation in this clinical study for Personal Cell Sciences. This contractual manufacturing agreement reinforces our capabilities to provide CRYO's exceptional clinical processing for relevant adult stem cell related products," said Anthony Dudzinski, COO of American CryoStem. "We look forward to our continued business relationship with PCS and expanding these services to other developers to speed their product's time to market."

About American CryoStem: American CryoStem Corporation (OTCQB: CRYO.OB - News) markets clinical processing products and services for Adipose (fat) Tissue and Adipose Derived Adult Stem Cells. CRYO's clinical processing and preservation platform supports the science and applications being discovered globally by providing the highest quality, clinically processed cells and assuring their sterility, viability and growth cap abilities, while at the same time developing cutting edge application, therapies and laboratory products and services for consumers and physicians.

The Private Securities Litigation Reform Act of 1995 provides a "safe harbor" for forward-looking statements. Certain of the statements contained herein, which are not historical facts, are forward-looking statements with respect to events, the occurrence of which involve risks and uncertainties. These forward-looking statements may be impacted, either positively or negatively, by various factors. Information concerning potential factors that could affect the Company is detailed from time to time in the Company's reports filed with the Securities and Exchange Commission.

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IntelliCell Demonstrates at the American Sports Medicine Institute Held in Conjunction with and at the Andrews Sports …

February 8th, 2012 3:55 am

NEW YORK--(BUSINESS WIRE)--

IntelliCell BioSciences, Inc. (OTCQB: SVFC.PK) (PINKSHEETS: SVFC.PK); (“IntelliCell”) or the (“Company”), was invited to demonstrate its stromal vascular fraction technology at the recent Baseball Injuries Symposium at the Andrews Sports Medicine Institute in Alabama held and sponsored by USA Baseball. The course Chairman is Dr. James Andrews, and moderated by PT Kevin Wilk, and Dr. Jeff Dugas. One of the courses presented during the three day event was on stem cell technology presented by Dr. Joshua Hackel. Dr. Hackel presented the state of regenerative medicine technology in the role of treating sports injuries. The link is http://www.mediafire.com/?u7bfa662e3r1sdp.

Dr. Hackel compared the IntelliCell SVF technology to several other methods of regenerative medicine being considered to be used by the leading orthopedic sports medicine doctors. Dr. Steven Victor, CEO of IntelliCell stated, "We are extremely excited that IntelliCell’s technology compares very favorably to all the other technologies, for procedures common to all major sports industries. We are extremely grateful to have the opportunity to present to over 200 leading doctors and trainers looking to treat major league, collegiate and amateur baseball players with regenerative medicine. IntelliCell Biosciences believes that its technology will be utilized by such experts this year."

About IntelliCell BioSciences, Inc.

IntelliCell is a pioneering regenerative medicine company focused on the expanding regenerative medical markets using stromal vascular fraction derived from adult adipose tissue. IntelliCell intends to initially focus on selling laboratory suites and licensing its technology to doctors for use in their offices for their patients. The company is also setting up Centers of Excellence where doctors can treat their patients. In addition, IntelliCell BioSciences is exploring storing the stromal vascular fraction in cryo-storage for future uses. The company is also starting FDA IND clinical trials at major medical centers for clinical indication approval. IntelliCell intends to pursue expansion to secondary markets and beyond the U.S. through a combination of company-owned and licensed clinical facilities.

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American CryoStem Completes Cell Processing for Clinical Study

February 7th, 2012 5:03 pm

RED BANK, NJ--(Marketwire -02/07/12)- American CryoStem Corporation (OTCQB: CRYO.OB - News) announced today that it has completed providing stem cell processing services for Personal Cell Sciences Corp., a cutting edge manufacturer of anti-aging skin care products.

The study involves researching the regenerative function of a conditioned medium obtained from each participant's adipose (fat tissue) derived mesenchymal stem cells and their ability to promote the production or secretion of collagen, elastin and fibronectin related to skin wound healing.

John Arnone, CEO of American CryoStem and Founder of Personal Cell Sciences, commented, "CRYO's patented tissue culture media and its proprietary, aseptic adipose tissue processing methodology allows, as an added benefit for PCS customers to store a clinical grade sample of their own stem cells for future use in regenerative medicine. We are pleased to provide comprehensive Bio-Insurance storage solutions at our clinical facility."

The adipose tissue samples were acquired utilizing a mini-liposuction procedure. A total of sixty milliliters (approximately 2 fluid ounces) of adipose tissue was collected in the physician's office and sent to CRYO's laboratory for processing. Once processed, the resulting stromal vascular fraction (SVF) was forwarded to the Personal Cell Sciences laboratory for proprietary formulation for patient specific products.

"We are very excited to announce our service agreement and participation in this clinical study for Personal Cell Sciences. This contractual manufacturing agreement reinforces our capabilities to provide CRYO's exceptional clinical processing for relevant adult stem cell related products," said Anthony Dudzinski, COO of American CryoStem. "We look forward to our continued business relationship with PCS and expanding these services to other developers to speed their product's time to market."

About American CryoStem: American CryoStem Corporation (OTCQB: CRYO.OB - News) markets clinical processing products and services for Adipose (fat) Tissue and Adipose Derived Adult Stem Cells. CRYO's clinical processing and preservation platform supports the science and applications being discovered globally by providing the highest quality, clinically processed cells and assuring their sterility, viability and growth cap abilities, while at the same time developing cutting edge application, therapies and laboratory products and services for consumers and physicians.

The Private Securities Litigation Reform Act of 1995 provides a "safe harbor" for forward-looking statements. Certain of the statements contained herein, which are not historical facts, are forward-looking statements with respect to events, the occurrence of which involve risks and uncertainties. These forward-looking statements may be impacted, either positively or negatively, by various factors. Information concerning potential factors that could affect the Company is detailed from time to time in the Company's reports filed with the Securities and Exchange Commission.

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$30 million donation from Boris family will help McMaster turn stem cell research into therapy

February 7th, 2012 5:00 pm

McMaster University is on its way to moving stem cell research “from the bench to the bedside” thanks to a $30 million boost from a local family.

The Marta and Owen Boris Foundation made the large donation to establish a human stem cell therapy centre and a unique clinic for patients with complex health conditions.

Owen, the founder of Mountain Cablevision, was in talks with McMaster about investing in their work before he died last April. His children and wife contacted the university a month later and carried out his vision, firming up their commitment last November.

The Boris Family Centre in Human Stem Cell Therapies will be developed as part of the McMaster Stem Cell and Cancer Research Institute using $24 million of the funds.

“It’s getting over that chasm from the bench to the bedside that this (donation) is going to allow us to do,” the institute’s scientific director Dr. Mick Bhatia said.

The centre will give scientists the resources to focus on converting McMaster’s breakthroughs — such as the ability to make blood or types of neural cells with stem cells — into clinical applications through investigative trials, Bhatia said.

“In the absence of this donation, I think we would not be in the position to move our discoveries forward,” he said. “This is a huge leg-up. I’m hoping what it’s really going to do is have a ripple effect to change the way McMaster views translating basic science.”

They plan on developing human stem cell therapies targeting leukemia and possibly neural diseases such as Alzheimer’s and Parkinson’s, said Dr. John Kelton, dean and vice-president of the faculty of health sciences.

The remaining $6 million will go toward building a clinic in partnership with Hamilton Health Sciences (HHS) where patients with complex health issues can see specialists and undergo tests in one visit.

This was a result of his parents’ frustrating experiences in recent years with co-ordinating specialists and getting diagnostic testing done in Canada, said Owen’s son, Les Boris.

They ended up going to Mayo Clinic in Rochester, Minn., where they had a case manager who co-ordinated their appointments with specialists and made sure testing was done in-house, he said. “They like the idea of a one-stop shop … (My father) said: ‘This is the kind of model we need here in this country.’”

Kelton said the medical clinic, which will be built in the university’s medical centre, will look for rapid turnaround times and avoid duplications of lab tests. McMaster and HHS will also evaluate the clinic’s success and keep an electronic medical record that patients could access, he said.

Kelton and Owen met three years ago and had their last meeting about the projects three days before the philanthropist died.

Owen had worked on the Avro Arrow and was frustrated with Canada’s lost opportunity of making jet planes for the world, Kelton said.

“He said, ‘Tell me about some opportunities (that) – if we invested in it – could make Hamilton and McMaster world-class. What are some of the areas like an Avro Arrow?’”

The funds for the human stem cell therapy centre will go toward hiring a research chair in blood stem cells and a research chair in neural stems cells, setting up several fellowships and technician positions, and building the facility.

Bhatia says they hope to bring in new scientists and fellows by the early summer.

The Boris family previously donated $6 million to addiction research at St. Joseph’s Healthcare for its new mental health hospital being built on the Mountain and another $5 million for the da Vinci SI Surgical Robotic System.

“We’re very appreciative that we’re in a position to be doing something for the community,” Les said. “And it was the community that put us in the position to do this.

dawong@thespec.com

905-526-2468 | @WongatTheSpec

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Directing stem cells to boost bone formation, strength

February 7th, 2012 12:43 pm

SACRAMENTO — A research team led by UC Davis Health System scientists has developed a novel technique to enhance bone growth by using a molecule which, when injected into the bloodstream, directs the body's stem cells to travel to the surface of bones. Once these cells are guided to the bone surface by this molecule, the stem cells differentiate into bone-forming cells and synthesize proteins to enhance bone growth. The study, which was published online today in Nature Medicine, used a mouse model of osteoporosis to demonstrate a unique treatment approach that increases bone density and prevents bone loss associated with aging and estrogen deficiency.

"There are many stem cells, even in elderly people, but they do not readily migrate to bone," said Wei Yao, the principal investigator and lead author of the study. "Finding a molecule that attaches to stem cells and guides them to the targets we need is a real breakthrough."

Researchers are exploring stem cells as possible treatments for a wide variety of conditions and injuries, ranging from peripheral artery disease and macular degeneration to blood disorders, skin wounds and diseased organs. Directing stem cells to travel and adhere to the surface of bone for bone formation has been among the elusive goals in regenerative medicine.

The researchers made use of a unique hybrid molecule, LLP2A-alendronate, developed by a research team led by Kit Lam, professor and chair of the UC Davis Department of Biochemistry and Molecular Medicine. The researchers' hybrid molecule consists of two parts: the LLP2A part that attaches to mesenchymal stem cells in the bone marrow, and a second part that consists of the bone-homing drug alendronate. After the hybrid molecule was injected into the bloodstream, it picked up mesenchymal stem cells in the bone marrow and directed those cells to the surfaces of bone, where the stem cells carried out their natural bone-formation and repair functions.

"Our study confirms that stem-cell-binding molecules can be exploited to direct stem cells to therapeutic sites inside an animal," said Lam, who also is an author of the article. "It represents a very important step in making this type of stem cell therapy a reality."

Twelve weeks after the hybrid molecule was injected into mice, bone mass in the femur (thigh bone) and vertebrae (in the spine) increased and bone strength improved compared to control mice who did not receive the hybrid molecule. Treated mice that were normally of an age when bone loss would occur also had improved bone formation, as did those that were models for menopause.

Alendronate, also known by the brand name Fosamax, is commonly taken by women with osteoporosis to reduce the risk of fracture. The research team incorporated alendronate into the hybrid molecules because once in the bloodstream, it goes directly to the bone surface, where it slows the rate of bone breakdown. According to Nancy Lane, a co-investigator on the study and director of the UC Davis Musculoskeletal Diseases of Aging Research Group, the dose of alendronate in the hybrid compound was low and unlikely to have inhibited the compound's therapeutic effect.

"For the first time, we may have potentially found a way to direct a person's own stem cells to the bone surface where they can regenerate bone," said Lane, who is an Endowed Professor of Medicine and Rheumatology and an expert on osteoporosis. "This technique could become a revolutionary new therapy for osteoporosis as well as for other conditions that require new bone formation."

Osteoporosis is a major public health problem for 44 million Americans. One in two women will suffer a fracture due to osteoporosis in their lifetime. Although effective medications are available to help prevent fracture risk, including alendronate, their use is limited by potential harmful effects of long-term use.

The major causes for osteoporosis in women include estrogen deficiency, aging and steroid excess from treatment of chronic inflammatory conditions such as rheumatoid arthritis. Generally, the osteoporosis generated by these metabolic conditions results from change in the bone remodeling cycle that weakens the bone's architecture and increases fracture risk.

Mesenchymal stem cells from bone marrow induce new bone remodeling, which thicken and strengthen bone.

The authors noted that the potential use of this stem cell therapy is not limited to treating osteoporosis. They said it may prove invaluable for other disorders and conditions that could benefit from enhanced bone rebuilding, such as bone fractures, bone infections or cancer treatments.

"These results are very promising for translating into human therapy," said Jan Nolta, professor of internal medicine, an author of the study and director of the UC Davis Institute for Regenerative Cures. "We have shown this potential therapy is effective in rodents, and our goal now is to move it into clinical trials."

Funding for the study came from the Endowment on Healthy Aging and the National Institutes of Health. The California Institute for Regenerative Medicine has given the team a planning grant to develop a proposal for human clinical trials.

"This research was a collaboration of stem cell biologists, biochemists, translational scientists, a bone biologist and clinicians," said Lane. "It was a truly fruitful team effort with remarkable results."

The Nature Medicine article is titled "Directing mesenchymal stem cells to bone to augment bone formation and increase bone mass." Min Guan, who is affiliated with the UC Davis Department of Internal Medicine, was co-lead author of the paper. Other UC Davis authors were Ruiwu Liu, Junjing Jia, Liping Meng, Ping Zhou and Mohammad Shahnazari, from the departments of Internal Medicine, and Biochemistry and Molecular Medicine, as well as the UC Davis Institute for Regenerative Cures. Authors Brian Panganiban and Robert O. Ritchie are with the Department of Materials Science and Engineering at UC Berkeley.

UC Davis is playing a leading role in regenerative medicine, with nearly 150 scientists working on a variety of stem cell-related research projects at campus locations in both Davis and Sacramento. The UC Davis Institute for Regenerative Cures, a facility supported by the California Institute for Regenerative Medicine (CIRM), opened in 2010 on the Sacramento campus. This $62 million facility is the university's hub for stem cell science. It includes Northern California's largest academic Good Manufacturing Practice laboratory, with state-of-the-art equipment and manufacturing rooms for cellular and gene therapies. UC Davis also has a Translational Human Embryonic Stem Cell Shared Research Facility in Davis and a collaborative partnership with the Institute for Pediatric Regenerative Medicine at Shriners Hospital for Children Northern California. All of the programs and facilities complement the university's Clinical and Translational Science Center, and focus on turning stem cells into cures. For more information, visit http://www.ucdmc.ucdavis.edu/stemcellresearch.

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Directing stem cells to boost bone formation, strength

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Muscle Stem Cells Activated By Exercise

February 7th, 2012 12:43 pm

February 7, 2012

University of Illinois researchers determined that an adult stem cell present in muscle is responsive to exercise, a discovery that may provide a link between exercise and muscle health. The findings could lead to new therapeutic techniques using these cells to rehabilitate injured muscle and prevent or restore muscle loss with age.

Mesenchymal stem cells (MSCs) in skeletal muscle have been known to be important for muscle repair in response to non-physiological injury, predominantly in response to chemical injections that significantly damage muscle tissue and induce inflammation. The researchers, led by kinesiology and community health professor Marni Boppart, investigated whether MSCs also responded to strain during exercise, and if so, how.

“Since exercise can induce some injury as part of the remodeling process following mechanical strain, we wondered if MSC accumulation was a natural response to exercise and whether these cells contributed to the beneficial regeneration and growth process that occurs post-exercise,” said Boppart, who also is affiliated with the Beckman Institute for Advanced Science and Technology at the U. of I.

The researchers found that MSCs in muscle are very responsive to mechanical strain. They witnessed MSC accumulation in muscle of mice after vigorous exercise. Then, they determined that although MSCs don’t directly contribute to building new muscle fibers, they release growth factors that spur other cells in muscle to fuse and generate new muscle, providing the cellular basis for enhanced muscle health following exercise.

A key element to the Illinois team’s method was in exercising the mice before isolating the cells to trigger secretion of beneficial growth factors. Then, they dyed the cells with a fluorescent marker and injected them into other mice to see how MSCs coordinated with other muscle-building cells.

In addition to examining the cells in vivo, the researchers studied the cells’ response to strain on different substrates. They found that MSC response is very sensitive to the mechanical environment, indicating that conditions of muscle strain affect the cells’ activity.

“These findings are important because we’ve identified an adult stem cell in muscle that may provide the basis for muscle health with exercise and enhanced muscle healing with rehabilitation/movement therapy,” Boppart said. “The fact that MSCs in muscle have the potential to release high concentrations of growth factor into the circulatory system during exercise also makes us wonder if they provide a critical link between enhanced whole-body health and participation in routine physical activity.”

Next, the group hopes to determine whether these cells contribute to the decline in muscle mass over a person’s lifetime. Preliminary data suggest MSCs become deficient in muscle with age. The team hopes to develop a combinatorial therapy that utilizes molecular and stem-cell-based strategies to prevent age-related muscle loss.

“Although exercise is the best strategy for preserving muscle as we age, some individuals are just not able to effectively engage in physical activity,” Boppart said. “Disabilities can limit opportunities for muscle growth. We’re working hard to understand how we can best utilize these cells effectively to preserve muscle mass in the face of atrophy.”

The team published its findings in the journal PLoS One. The Illinois Regenerative Medicine Institute, the Ellison Medical Foundation and the Mary Jane Neer Foundation supported this work.

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Source: University of Illinois

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Salk News Clip – Long Lived Fruit Flies (KPBS) – Video

February 7th, 2012 12:39 pm

18-11-2011 17:40 Fruit fly intestine may hold secret to the fountain of youth Long-lived fruit flies offer Salk scientists clues to slowing human aging and fighting disease November 02, 2011 LA JOLLA, CA—One of the few reliable ways to extend an organism's lifespan, be it a fruit fly or a mouse, is to restrict calorie intake. Now, a new study in fruit flies is helping to explain why such minimal diets are linked to longevity and offering clues to the effects of aging on stem cell behavior. Scientists at the Salk Institute for Biological Studies and their collaborators found that tweaking a gene known as PGC-1, which is also found in human DNA, in the intestinal stem cells of fruit flies delayed the aging of their intestine and extended their lifespan by as much as 50 percent. "Fruit flies and humans have a lot more in common than most people think," says Leanne Jones, an associate professor in Salk's Laboratory of Genetics and a lead scientist on the project. "There is a tremendous amount of similarity between a human small intestine and the fruit fly intestine." Learn more at: salk.edu

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Stem Cells Help Heart Attack Victims – Video

February 7th, 2012 12:35 pm

29-01-2012 23:26 Fourteen patients were randomized to see if adipose-derived adult stem cells would help limit the damage from an acute heart attack. Infarct size was decreased by 50%, the perfusion defect was 17% smaller, and the left ventriclular ejection fraction was increased about 6% better than the control group. Stem cell vocabulary was reviewed and highlighted that there are embryonic stem cells and adult stem cells and that sources of stem cell are from bone marrow, adipose tissue, blood, umbilical cord blood and from cloned embryonic cell lines. Stem cells can develop into 200 different cell types.

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Stem Cells Help Heart Attack Victims - Video

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Stem Cell Treatment Helps on Blindness

February 7th, 2012 12:34 pm

Jan 23, 2012 6:35pm

The first results of human embryonic stem cell therapy are in, and they look good.

Two women, 51 and 78, who were legally blind became the first patients to receive human embryonic stem cell treatment, for their condition. The treatment, also called hESC-RPE, involved scientists injecting stem cells into each patient’s eye. One woman had a condition known as Stargardt’s macular dystrophy and the other, age-related macular degeneration. Both conditions cause severe vision loss. The surgery appeared safe after four months and both women experienced an improvement in vision.

“Our study is designed to test the safety and tolerability of hESC-RPE in patients with advanced-stage Stargardt’s macular dystrophy and dry age-related macular degeneration,” the authors wrote. “So far, the cells seem to have transplanted into both patients without abnormal proliferation … or other untoward pathological reactions or safety signals. Continued follow-up and further study is needed. The ultimate therapeutic goal will be to treat patients earlier in the disease processes, potentially increasing the likelihood of photoreceptor and central visual rescue.”

Eye experts say this is an important study because it could show a promising trend in vision improvement. According to the National Eye Institute, about 1.75 million Americans currently suffer from macular degeneration, and this number is expected to grow to 2.95 million in 2020.

“Stem cell biology has an enormous potential to correct genomically derived ocular diseases, both in correcting deficiencies and amending altered anatomy and physiology,” said Barrett Katz, Frances DeJur Chair in ophthalmology at Montefiore Medical Center in New York. “The eye is the very best organ to expect such advances to be made within, as it is relatively easily accessible and immunologically privileged.”

The research, conducted at UCLA and Advanced Cell Technology in Massachusetts and published today in the Lancet, was small in scope and population and no patients were given a placebo treatment for the sake of comparison.

For this reason, some doctors worried the report would raise hopes prematurely.

“To reach any conclusions on the safety or efficacy of two patients treated for four months without a control population for comparison is unreasonable,” said Martin Friedlander, professor of ophthalmology at Scripps Health in La Jolla, Calif. “This is why anecdotal reports like this are not published.”

“This falsely raises the hopes of millions of individuals suffering from these diseases,” he said.

The use of human embryonic stem cells has long been seen as an ethically controversial medical technology because many ague that an embryo is the earliest form of life. Extracting stem cells from that embryo almost always damages it.

But proponents of the use of human embryonic stem cells  say this argument lacks validity and detracts from the medical benefits that could be achieved.

“It has been over a decade since the discovery of human embryonic stem cells,” Dr. Robert Lanza, co-author of the study and Chief Scientific Officer at Advanced Cell Technology, said in a statement. “This is the first report of hESC-derived cells ever transplanted into patients, and the safety and engraftment data to-date looks very encouraging… Despite the progressive nature of these conditions, the vision of both patients appears to have improved after transplantation of the cells, even at the lowest dosage.

“This is particularly important, since the ultimate goal of this therapy will be to treat patients earlier in the course of the disease where more significant results might potentially be expected,” Lanza said

 

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$30m Gift to Fast Forward Stem Cell Therapies and One-Stop Patient Care

February 7th, 2012 5:44 am

Boris family gift propels stem cell therapies and one-stop patient care

Newswise — HAMILTON, ON (Feb. 6, 2012) – A Hamilton family is giving McMaster University $30 million to accelerate the university’s innovations in health research, education and care.

“McMaster University has proven its ability to fast forward discoveries from the lab bench to the patients’ bedside, it made perfect sense to make this investment in this world class university,” said Les Boris, on behalf of his parents’ Marta and Owen Boris Foundation. His sister Jackie Work added: “The Michael G. DeGroote School of Medicine is ranked among the top 20 medical schools in the world. This is the best place to commit to the future.”

The funding was announced in a ceremony at the University today.

Of the total, $24 million is designated to establish The Boris Family Centre in Human Stem Cell Therapies, which will speed the commercial development of discoveries at the McMaster Stem Cell and Cancer Research Institute. The six-year-old institute has had several major breakthroughs, including the ability to turn human skin into blood.

The funds will establish two senior research chairs, one in blood stem cells and the other in neuro stem cells; set up several fellowships and technician positions;
build the facility and provide a fund for emerging opportunities.

An additional $6 million is for a unique clinic which will allow patients with complex health problems to see several specialists and have related tests during one visit. Established in partnership with Hamilton Health Sciences, this patient-oriented clinic will be built in the McMaster University Medical Centre in Hamilton and led by a senior research chair.

The Marta and Owen Boris Foundation was established by Marta and Owen Boris who created the Hamilton cable company Mountain Cablevision and developed it over 50 years before selling it to Shaw Communications in 2009.

Owen Boris died in April, 2011.

“McMaster has been renewing its commitment to our community, and to have community members make such a significant contribution to the University is truly outstanding,” said Patrick Deane, president of McMaster. “Great research, great discoveries, and better patient care. The Boris family gift will accelerate nour ability to make great things happen.”

Dr. John Kelton, dean and vice-president of the Faculty of Health Sciences, added: “This is an innovative and action oriented family. They understand the great potential McMaster has to make medical breakthroughs, and their willingness to place their bets on McMaster is a tremendous vote of confidence in us.”

Mick Bhatia is scientific director of the McMaster Stem Cell and Cancer Research Institute. He said: “In a short time we’ve become world renowned for our human stem cell discoveries. Now is the time to move these discoveries to the patient.”

About the clinic for day patients, Dr. Akbar Panju, professor and deputy chair clinical of the Department of Medicine, said the new format is unique in Canada and will put patients first.

“Too often patients go from office to office to receive essential medical care from several specialists. This clinic will ensure they will get everything they need in one place,” he said, noting that the clinic will also be a centre of learning for
health sciences students and residents from many disciplines.

McMaster University, one of four Canadian universities listed among the Top 100 universities in the world, is renowned for its innovation in both learning and discovery. It has a student population of 23,000, and more than 150,000 alumni in 128 countries.


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