Monthly Archives: March 2014

New Method Makes Muscle Cells From Human Stem Cells

Posted: March 24, 2014 at 10:47 am

March 24, 2014

Image Caption: Muscle cells are stained green in this micrograph of cells grown from embryonic stem cells in the lab of Masatoshi Suzuki at the University of Wisconsin -- Madison. Cell nuclei are stained blue; the muscle fibers contain multiple nuclei. Nuclei outside the green fibers are from non-muscle cells. Suzuki has developed a new method of growing stem cells into muscle cells that could be more suitable for treating disease. Suzuki hopes to experiment next with animals that model muscular dystrophy and amyotrophic lateral sclerosis. Credit: Masatoshi Suzuki

David Tenenbaum, University of Wisconsin-Madison

As stem cells continue their gradual transition from the lab to the clinic, a research group at the University of Wisconsin-Madison has discovered a new way to make large concentrations of skeletal muscle cells and muscle progenitors from human stem cells.

The new method, described in the journal Stem Cells Translational Medicine, could be used to generate large numbers of muscle cells and muscle progenitors directly from human pluripotent stem cells. These stem cells, such as embryonic (ES) or induced pluripotent stem (iPS) cells, can be made into virtually any adult cell in the body.

Adapting a method previously used to make brain cells, Masatoshi Suzuki, an assistant professor of comparative biosciences in the School of Veterinary Medicine, has directed those universal stem cells to become both adult muscle cells and muscle progenitors.

Importantly, the new technique grows the pluripotent stem cells as floating spheres in high concentrations of two growth factors, fibroblast growth factor-2 and epidermal growth factor. These growth factors urge the stem cells to become muscle cells.

Researchers have been looking for an easy way to efficiently differentiate stem cells into muscle cells that would be allowable in the clinic, says Suzuki. The novelty of this technique is that it generates a larger number of muscle stem cells without using genetic modification, which is required by existing methods for making muscle cells.

Many other protocols have been used to enhance the number of cells that go to a muscle fate, says co-author Jonathan Van Dyke, a post-doctoral fellow in Suzukis laboratory. But whats exciting about the new protocol is that we avoid some techniques that would prohibit clinical applications. We think this new method has great promise for alleviating human suffering.

Last year, Suzuki demonstrated that transplants of another type of human stem cells somewhat improved survival and muscle function in rats that model amyotrophic lateral sclerosis (ALS). Also known as Lou Gehrigs disease, ALS destroys nerves and causes a loss of muscle control. The muscle progenitors generated with Suzukis new method could potentially play a similar role but with enhanced effect.

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New Method Makes Muscle Cells From Human Stem Cells

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New way to make muscle cells from human stem cells

Posted: March 24, 2014 at 10:47 am

As stem cells continue their gradual transition from the lab to the clinic, a research group at the University of Wisconsin-Madison has discovered a new way to make large concentrations of skeletal muscle cells and muscle progenitors from human stem cells.

The new method, described in the journal Stem Cells Translational Medicine, could be used to generate large numbers of muscle cells and muscle progenitors directly from human pluripotent stem cells. These stem cells, such as embryonic (ES) or induced pluripotent stem (iPS) cells, can be made into virtually any adult cell in the body.

Adapting a method previously used to make brain cells, Masatoshi Suzuki, an assistant professor of comparative biosciences in the School of Veterinary Medicine, has directed those universal stem cells to become both adult muscle cells and muscle progenitors.

Importantly, the new technique grows the pluripotent stem cells as floating spheres in high concentrations of two growth factors, fibroblast growth factor-2 and epidermal growth factor. These growth factors "urge" the stem cells to become muscle cells.

"Researchers have been looking for an easy way to efficiently differentiate stem cells into muscle cells that would be allowable in the clinic," says Suzuki. The novelty of this technique is that it generates a larger number of muscle stem cells without using genetic modification, which is required by existing methods for making muscle cells.

"Many other protocols have been used to enhance the number of cells that go to a muscle fate," says co-author Jonathan Van Dyke, a post-doctoral fellow in Suzukis laboratory. "But what's exciting about the new protocol is that we avoid some techniques that would prohibit clinical applications. We think this new method has great promise for alleviating human suffering."

Last year, Suzuki demonstrated that transplants of another type of human stem cells somewhat improved survival and muscle function in rats that model amyotrophic lateral sclerosis (ALS). Also known as Lou Gehrig's disease, ALS destroys nerves and causes a loss of muscle control. The muscle progenitors generated with Suzukis new method could potentially play a similar role but with enhanced effect.

The new technique can also be used to grow muscle cells from iPS cells from patients with neuromuscular diseases like ALS, spinal muscular atrophy and muscular dystrophy. Thus, the technique could produce adult muscle cells in a dish that carry genetic diseases. These cells could then be used as a tool for studying these diseases and screening potential drug compounds, says Suzuki. "Our protocol can work in multiple ways and so we hope to provide a resource for people who are exploring specific neuromuscular diseases in the laboratory."

The new protocol incorporates a number of advantages. First, the cells are grown in defined supplements without animal products such as bovine serum, enhancing the clinical safety for the muscle stem cells. Second, when grown as spheres, the cells grow faster than with previous techniques. Third, 40 to 60 percent of the cells grown using the process are either muscle cells or muscle progenitors, a high proportion compared to traditional non-genetic techniques of generating muscle cells from human ES and iPS cells.

Suzuki and his group hope that by further manipulating the chemical environment of the spheres of stem cells, they may increase that number, further easing the path toward human treatment.

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UW-Madison researchers discover new way to turn stem cells into muscle cells

Posted: March 24, 2014 at 10:47 am

Researchers at the University of Wisconsin-Madison discovered a new method for generating muscle cells from stem cells, according to a Friday news release.

The new procedure is unique in its ability to yield large quantities of muscle cells, as well as muscle progenitors, directly from pluripotent stem cells without the use of genetic modification, according to the release. Pluripotent stem cells have yet to undergo differentiation and can develop effectively into any adult cell in the body.

Masatoshi Suzuki, UW-Madison assistant professor of comparative biosciences and co-author of the research project, pioneered the discovery. His method calls for the placement of stem cells in high concentrations of growth factors that influence growth and cell differentiation.

Last year, Suzuki showed that transplanting another type of human stem cell to rats suffering from Lou Gehrigs disease improved longevity and muscle function. He said in the release muscle progenitors, which serve as prototype for the formation of muscles, could have a similar but heightened effect.

While various methods have been used to increase the number of stem cells that become muscles, Suzukis co-author Jonathan Van Dyke explained in the release these often cannot be worked within a clinical setting.

What's exciting about the new protocol is that we avoid some techniques that would prohibit clinical applications, Van Dyke said in the release. We think this new method has great promise for alleviating human suffering.

Additionally, the new technique could advance disease and drug research by allowing cells infected with certain genetic diseases to be grown in a dish.

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Pioneer Award recipients Marina Cavazzana and Adrian Thrasher recognized for advancing gene therapy to the clinic for …

Posted: March 24, 2014 at 10:45 am

PUBLIC RELEASE DATE:

24-Mar-2014

Contact: Vicki Cohn vcohn@liebertpub.com 914-740-2100 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, March 24, 2014Marina Cavazzana, MD, PhD, Paris Descartes University, France and Adrian J. Thrasher, MD, PhD, University College London Institute of Child Health, UK, have been honored with the Pioneer Award for basic and clinical gene therapy for immunodeficiency disorders. Human Gene Therapy, a peer-reviewed journal from Mary Ann Liebert, Inc., publishers, is commemorating its 25th anniversary by bestowing this honor on the leading 12 Pioneers in the field of cell and gene therapy selected by a blue ribbon panel* and publishing a Pioneer Perspective by the award recipients

Dr. Cavazzana has been at the forefront of advances in treating life-threatening inherited diseases of the immune system with gene therapy, using a patient's own modified stem cells. She describes the translation of this work to the clinic and its ongoing advances and novel applications in the article "Hematopoetic Stem Cell Gene Therapy: Progress on the Clinical Front." The article by Dr. Cavazzana is available free on the Human Gene Therapy website at http://online.liebertpub.com/doi/full/10.1089/hum.2014.2504.

A pioneer of gene therapy in the UK, Dr. Thrasher has been at the leading edge of basic science research on the function of therapeutic genes for inherited disorders and the development of viral vectors to deliver them to affected patients. He has collaborated on gene therapy clinical trials targeting immunodeficiency disorders with groups in Europe and the USA.

"Cell therapy and gene therapy are advancing together to improve patient care," says Dr. Cavazzana. "We can expect to be able to rebuild a new immune system not only in primary immunodeficiencies but also in severe acquired clinical conditions (such as those in HIV-1-infected patients)."

"I've seen some very exciting times in the field, from the first evidence that biochemical defects can be corrected in vitro, to some remarkable clinical successes in patients with devastating diseases. I look forward with huge enthusiasm to the exciting developments on the horizon, which are likely to impact on more patients with an even wider range of disorders," says Dr. Thrasher.

"These pioneers contributed to the first real clinical successes of gene therapy through their work in inherited immune deficiency disorders," says James M. Wilson, MD, PhD, Editor-in-Chief of Human Gene Therapy, and Director of the Gene Therapy Program, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia.

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Heart Stem cell therapy – Video

Posted: March 24, 2014 at 10:41 am


Heart Stem cell therapy
Clara answers some questions regarding the stem-cell therapy she received for congenital heart disease. For more info visit: http://www.stemaid.com.

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Heart Stem cell therapy - Video

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Wounded Pa. soldier seeks Chinese stem cell cure

Posted: March 24, 2014 at 10:41 am

YORK, Pa. (AP) - A York County soldier left partially paralyzed when he was shot in Afghanistan nearly two years ago is banking on stem cells to help him regain movement.

Matthew Hanes, 22, of Manchester Township will head to China in April to undergo surgery to repair part of his damaged spinal cord.

Doctors essentially will use minor surgery and stem cell therapy to build a bridge over two vertebrae that were shattered when Hanes was shot.

At the minimum Ill get at least some feeling back where I dont have it in certain places, but I could get everything back if it goes well, Hanes said.

U.S. Army Cpl. Hanes was shot while on patrol in Afghanistan in June 2012. He was left with limited use of his upper body and no use of his lower extremities.

RESEARCH: Soon after he returned to the U.S., Hanes began researching stem cell therapy as possible treatment.

Thats how he found Puhua International Hospital in Beijing, where he will fly on April 1 for the treatment. Hes slated to return stateside later that month.

Its coming up slowly now that I know its on, Hanes said.

During his research, Hanes said he found the U.S. is so far behind on stem cell research compared to some countries in Asia, such as China, and Europe.

For years, the federal government imposed tight restrictions on stem cell research until it was loosened in 2009 by President Barrack Obama.

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Forever Young Peter Nygard- Stem Cell Research – Video

Posted: March 24, 2014 at 5:40 am


Forever Young Peter Nygard- Stem Cell Research
Interview with fashion mogul Peter Nygard about his research with stem cells, ..he tells how he #39;s working with the medical community to develop a virtual fou...

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Forever Young Peter Nygard- Stem Cell Research - Video

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Arthritic shoulders; Len discusses his results 9 months after stem cell therapy by Dr Harry Adelson – Video

Posted: March 23, 2014 at 8:44 pm


Arthritic shoulders; Len discusses his results 9 months after stem cell therapy by Dr Harry Adelson
Arthritic shoulders; Len discusses his results 9 months after stem cell therapy by Dr Harry Adelson http://www.docereclinics.com.

By: Harry Adelson, N.D.

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Arthritic shoulders; Len discusses his results 9 months after stem cell therapy by Dr Harry Adelson - Video

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Kula veterinarian offering in-house stem cell therapy

Posted: March 23, 2014 at 8:44 pm

Before undergoing regenerative stem cell therapy in November, a 5-year-old Newfoundland named Bella had been on medication for most of her life.

A congenital issue that affects about 25 percent of her breed left 138-pound Bella walking with a limp and unable to keep up with her brother, Ollie, on their twice-daily walks at Polipoli Spring State Recreation Area, said her owner, Art Terry of Kula.

"We were at the point of being hopeless," he said. "She'd been progressing to where she couldn't walk anymore. I couldn't take her to the park. She used to hobble around the house."

Bella, a 138-pound Newfoundland, and her owner, Art Terry, wait outside the Animal Care Hospital and Wellness Center in Kula just before she underwent stem cell therapy in November.

Animal Care Hospital and Wellness Center photo

Veterinary head technician Michelle James processes fat cells for stem cell activation with veterinarian Dennis Brown at the Animal Care Hospital and Wellness Center in Kula.

Animal Care Hospital and Wellness Center photo

Veterinary technician Samara Phillips (left) monitors anesthesia with veterinary head technician Michelle James and Dr. Dennis Brown during Bellas stem cell therapy procedure.

Animal Care Hospital and Wellness Center photo

Since the stem cell therapy, "you can't believe it's the same dog," Terry said. "I had to stop her chasing cars a couple of times at Polipoli park."

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Kula veterinarian offering in-house stem cell therapy

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Should stem cell therapy be used in DLBCL? – Video

Posted: March 23, 2014 at 8:44 am


Should stem cell therapy be used in DLBCL?

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Should stem cell therapy be used in DLBCL? - Video

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