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Israel Welcomes British Minister For Discussions About Stem Cell Research Collaboration

Posted: March 26, 2014 at 1:43 pm

By Liisa Vexler

The UK and Israel join forces during a two-day conference at the Technion-Israel Institute of Technology in Haifa, Israel this week that will focus on continued joint stem-cell therapy research. This conference is part of the second BIRAX Regenerative Medicine event, which is a project initiated by the British Council in Israel and the British Embassy.

The United Kingdoms minister of state for universities and science, David Willetts, is on the list of conference attendees. This list also includes approximately 300 of Israels most prominent research scientists and 80 attendees from Britain who are involved in the research on stem cell therapies to treat chronic and degenerative diseases such as type 1 (juvenile) diabetes, heart disease, Parkinsons and Alzheimers. It will also be attended by 300 leading Israeli scientists and 80 British scientists, whose research is advancing the fight against devastating illnesses, such as type 1 diabetes, heart diseases, Parkinsons and Alzheimers. The conference co-chairs are Chris Mason, University Colleges chairman of regenerative medicine bioprocessing at University College, and former chief scientist of Israel, Ehud Gazit.

The UK and Israel have committed 10 million to stem cell research to be invested over the course of five years. To date, BIRAX has provided funding for seven British and Israeli large research projects looking at stem cell therapies for multiple sclerosis, liver disease and Parkinsons.

Britains Minister Willets will officially open the second call for proposals during the conference, with Prime Minister David Cameron having launched the initiative during his recent Israeli visit. This call for proposals will provide funding for innovative research in stem cell therapies for cardiovascular disease, type 1 diabetes, Parkinsons and Alzheimers.

British ambassador to Israel Matthew Gould said, This conference will bring together British and Israeli scientists working with stem cells. Our goal is that they will form collaborations to develop cures for some of the worlds most common diseases. Israel and Britain are both at the forefront of stem cell research. Building a stronger partnership between the two countries will be to the benefit of both and has the potential to transform lives around the world. The first conference was hugely successful, and led to some amazing joint research. We have high hopes for this one.

On behalf of the Israeli research community, Technion president Peretz Lavie said his institution is thrilled to play host to the second BIRAX Regenerative Medicine conference.

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Stem Cells Shed Light on Bipolar Disorder

Posted: March 25, 2014 at 10:55 pm

Researchers have grown embryonic-like stem cells from patients with bipolar disorder and transformed them into brain cells that are already answering questions about the condition.

The cells, which carry the precisely tailored genetic instructions from the patients own cells, behave differently than cells taken from people without the disorder, the researchers report.

Already, we see that cells from people with bipolar disorder are different in how often they express certain genes, how they differentiate into neurons, how they communicate, and how they respond to lithium," Sue O'Shea, a stem cell specialist at the University of Michigan who led the study, said in a statement.

The work, described in the journal Translational Psychiatry, helps fulfill one of the big promises of stem cells research using a patients own cells to study his or her disease.

Mental illness is especially hard to study. Getting into a living persons brain is almost impossible, and scientists cant deliberately cause it in people in order to study it.

Creating animals such as mice with what looks like human mental illness is imprecise at best.

The University of Michigan team turned instead to what are called induced pluripotent stem cells, or iPS cells. These are ordinary skin cells taken from a patient and tricked into turning back into the state of a just-conceived embryo.

These cells, grown from skin cells taken from people with bipolar disorder, arose from stem cells and were coaxed to become neural progenitor cells -- the kind that can become any sort of nervous system cell. The research showed differences in cell behavior compared with cells grown from people without bipolar disorder.

They are pluripotent, meaning they can become any type of cell there is. In this case, the Michigan team redirected the cells to become neurons the cells that make up much of the brain. "This gives us a model that we can use to examine how cells behave as they develop into neurons, OShea said.

Bipolar disorder, once called manic-depression, is very common, affecting an estimated 3 percent of the population globally. It runs in families, suggesting a strong genetic cause, and is marked by mood swings from depression to feelings of euphoria and creativity thats considered the manic phase.

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Stem Cells Shed Light On Bipolar Disease

Posted: March 25, 2014 at 10:55 pm

Researchers have grown embryonic-like stem cells from patients with bipolar disorder and transformed them into brain cells that are already answering questions about the condition.

The cells, which carry the precisely tailored genetic instructions from the patients own cells, behave differently than cells taken from people without the disorder, the researchers report.

Already, we see that cells from people with bipolar disorder are different in how often they express certain genes, how they differentiate into neurons, how they communicate, and how they respond to lithium," Sue O'Shea, a stem cell specialist at the University of Michigan who led the study, said in a statement.

The work, described in the journal Translational Psychiatry, helps fulfill one of the big promises of stem cells research using a patients own cells to study his or her disease.

Mental illness is especially hard to study. Getting into a living persons brain is almost impossible, and scientists cant deliberately cause it in people in order to study it.

Creating animals such as mice with what looks like human mental illness is imprecise at best.

The University of Michigan team turned instead to what are called induced pluripotent stem cells, or iPS cells. These are ordinary skin cells taken from a patient and tricked into turning back into the state of a just-conceived embryo.

These cells, grown from skin cells taken from people with bipolar disorder, arose from stem cells and were coaxed to become neural progenitor cells -- the kind that can become any sort of nervous system cell. The research showed differences in cell behavior compared with cells grown from people without bipolar disorder.

They are pluripotent, meaning they can become any type of cell there is. In this case, the Michigan team redirected the cells to become neurons the cells that make up much of the brain. "This gives us a model that we can use to examine how cells behave as they develop into neurons, OShea said.

Bipolar disorder, once called manic-depression, is very common, affecting an estimated 3 percent of the population globally. It runs in families, suggesting a strong genetic cause, and is marked by mood swings from depression to feelings of euphoria and creativity thats considered the manic phase.

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Stem Cells Shed Light On Bipolar Disease

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Stem cells offer clue to bipolar disorder treatment

Posted: March 25, 2014 at 10:55 pm

What a nerve! Skin cells taken from people with bipolar disorder have been turned into brain cells. These in turn are offering up clues about the changes in the brain that drive the disorder, and may also provide a way to test new treatments.

About three in every 100 people develop bipolar disorder a mental illness characterised by episodes of depression and euphoria. But the condition remains poorly understood.

That's because it would be too invasive to obtain and study viable nerve cells from the brains of people with the condition.

There are also no good animal models, because bipolar disorder although highly heritable has, for the most part, not been linked to any specific genes that can be studied using animals.

"People say the condition is probably the result of a lot of small contributions by multiple genes," says Sue O'Shea at the University of Michigan in Ann Arbor.

Now O'Shea and her colleagues may have found an ethical way to make a genetic model of the condition. First, they took skin samples from 22 people with bipolar disorder and 10 healthy volunteers. They induced these adult skin cells to return to a stem-cell-like state, creating what are called induced pluripotent stem cells (iPSCs) and then encouraged these cells to mature into neurons.

O'Shea was surprised to find that neurons derived from people with bipolar disorder grew differently from those from people without the condition. "I was expecting it would take decades of careful science before we would find any real differences," she says.

The "bipolar" neurons expressed more genes involved in calcium signalling between cells. Interfering with this cellular communication can disrupt healthy brain activity, and calcium signalling has already been implicated as a likely factor in diseases like bipolar disorder. Treating the cells with lithium a common treatment for bipolar disorder reduced the abnormal signalling to normal levels.

Some of the genes which influenced activity of neurons were not previously known to be involved in bipolar disorder. "Some of the genes misdirect neurons to the wrong area in the brain," says O'Shea.

This could cause some neurons programmed to become part of one brain region the cortex, for example to express genes typical of a different brain region entirely. Such a genetic difference might provide clues as to why certain people are predisposed to developing bipolar disorder in later life, she says. What might trigger the condition is still unclear.

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New method yields potent, renewable human stem cells with promising therapeutic properties

Posted: March 25, 2014 at 10:52 pm

PUBLIC RELEASE DATE:

25-Mar-2014

Contact: Vicki Cohn vcohn@liebertpub.com 914-740-2100 x2156 Mary Ann Liebert, Inc./Genetic Engineering News

New Rochelle, NY, March 24, 2014The curative and therapeutic potential of mesenchymal stem cells (MSCs) offers much promise, as these multipotent cells are currently being tested in more than 300 clinical trials in a range of diseases. A new, easier, and more reliable way to make large quantities of highly potent MSCs could accelerate progress toward their use in regenerative medicine, as described in an article in Stem Cells and Development, a peer-reviewed journal from Mary Ann Liebert, Inc., publishers. The article is available on the Stem Cells and Development website.

Robert Lanza, MD and colleagues from Advanced Cell Technology (Marlborough, MA) and the David Geffen School of Medicine, UCLA (Los Angeles, CA), developed an innovative method for deriving MSCs from human embryonic stem cells (hESCs) through the use of a developmental precursor called the hemangioblast. They describe the technique and evidence of therapeutic efficacy using the hESC-MSCs to treat mouse models of lupus erythematosus and uveitis in the article "Mesenchymal Stem Cell Population Derived from Human Pluripotent Stem Cells Displays Potent Immunomodulatory and Therapeutic Properties."

"This new population of hESC-derived MSCs has a 30,000-fold greater proliferative capacity than bone marrow-derived MSCs," says Dr. Lanza, Chief Scientific Officer, Advanced Cell Technology. "In addition to being easy to derive in very large numbers, they are more youthful and live much longer." Dr. Lanza is Editor-in-Chief of BioResearch Open Access, a peer-reviewed open access journal from Mary Ann Liebert, Inc., publishers that provides a rapid-publication forum for a broad range of scientific topics.

###

About the Journal

Stem Cells and Development is an authoritative peer-reviewed journal published 24 times per year online with Open Access options and in print. Led by Editor-in-Chief Graham C. Parker, PhD, the Journal is dedicated to communication and objective analysis of developments in the biology, characteristics, and therapeutic utility of stem cells, especially those of the hematopoietic system. Complete tables of content and a sample issue may be viewed on the Stem Cells and Development website.

About the Publisher

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New method yields potent, renewable human stem cells with promising therapeutic properties

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A/Professor Dr Chin on Stem Cell Therapy – Video

Posted: March 25, 2014 at 10:48 pm


A/Professor Dr Chin on Stem Cell Therapy
Interview on Bernama TV - Dr Chin Sze Piaw, Consultant Physician Cardiologist SUBSCRIBE: http://www.youtube.com/BeverlyWilshir... FACEBOOK: http://face...

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Stem cell trials on tackling osteoarthritis may lead to treatment in five years

Posted: March 25, 2014 at 10:48 pm

The trials involve injecting adult stem cells derived from adipose tissue or fat into cartilage to stimulate its regeneration

Researchers in Galway predict that stem cells could be used to treat osteoarthritis within five years, following successful initial clinical trials.

The trials involve injecting adult stem cells derived from adipose tissue or fat into cartilage to stimulate its regeneration.

Osteoarthritis affects some 70 million people across the EU, and current treatment is limited to surgery or pain management.

Some 400,000 people in Ireland are affected by this most common form of human arthritis, which is characterised by the often very painful degeneration of cartilage in joints.

Successful trial NUI Galway (NUIG) scientists, who are part of a 9 million EU-funded project, have just finished the successful phase one clinical trial.

Prof Frank Barry, scientific director of NUIGs Regenerative Medicine Institute (Remedi), yesterday said the positive early results indicate a treatment was in sight.

From the clinical trials conducted so far, we have seen the first signs of finding a cure for this truly incapacitating disease which affects so many, Prof Barry said. Using the patients own stem cells we have been able to treat their diseased joints, and relieve their suffering and burden of pain.

Whilst we are still in the early stages of clinical trials, the results so far are extremely positive such that the use of stem cell therapy for osteoarthritis could become a reality for patients within the next five years, he said.

Adipose stem cells Stem cells can be harvested in large quantities from adipose tissue or fat, with minimally invasive surgery. These cells have emerged in recent years as a good alternative to stem cells derived from bone marrow, Prof Barry notes.

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Stem Cell-Derived Beta Cells Under Skin Replace Insulin

Posted: March 25, 2014 at 10:48 pm

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Newswise Scientists at University of California, San Diego School of Medicine and Sanford-Burnham Medical Research Institute have shown that by encapsulating immature pancreatic cells derived from human embryonic stem cells (hESC), and implanting them under the skin of diabetic mouse models, sufficient insulin is produced to maintain glucose levels without unwanted potential trade-offs of the technology.

The research, published online in Stem Cell Research, suggests that encapsulated hESC-derived insulin-producing cells may be an effective and safe cell replacement therapy for insulin dependent-diabetes.

Our study critically evaluates some of the potential pitfalls of using stem cells to treat insulin dependent-diabetes, said Pamela Itkin-Ansari, PhD, assistant project scientist in the UC San Diego Department of Pediatrics and adjunct assistant professor in Development, Aging and Regenerative program at Sanford-Burnham.

We have shown that encapsulated hESC-derived insulin-producing cells are able to produce insulin in response to elevated glucose without an increase in the mass or their escape from the capsule, said Itkin-Ansari. These results are important because it means that the encapsulated cells are both fully functional and retrievable.

Previous attempts to replace insulin producing cells, called beta cells, have met with significant challenges. For example, researchers have tried treating diabetics with mature beta cells, but because these cells are fragile and scarce, the method is fraught with problems. Moreover, since the cells come from organ donors, they may be recognized as foreign by the recipients immune system requiring patients to take immunosuppressive drugs to prevent their immune system from attacking the donors cells, ultimately leaving patients vulnerable to infections, tumors and other adverse events.

Encapsulation technology was developed to protect donor cells from exposure to the immune system and has proven extremely successful in preclinical studies.

Itkin-Ansari and her research team previously made an important contribution to the encapsulation approach by showing that pancreatic islet progenitor cells are an optimal cell type for encapsulation. They found that progenitor cells were more robust than mature beta cells to encapsulate, and while encapsulated, they matured into insulin-producing cells that secreted insulin only when needed.

In the study, Itkin-Ansari and her team used bioluminescent imaging to determine if encapsulated cells stay in the capsule after implantation.

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Stem Cell-Derived Beta Cells Under Skin Replace Insulin

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Replacing insulin through stem cell-derived pancreatic cells under the skin

Posted: March 25, 2014 at 10:47 pm

PUBLIC RELEASE DATE:

24-Mar-2014

Contact: Susan Gammon Ph.D. sgammon@sanfordburnham.org 858-795-5012 Sanford-Burnham Medical Research Institute

LA JOLLA, Calif., March 25, 2014 Sanford-Burnham Medical Research Institute (Sanford-Burnham) and UC San Diego School of Medicine scientists have shown that by encapsulating immature pancreatic cells derived from human embryonic stem cells (hESC), and implanting them under the skin in animal models of diabetes, sufficient insulin is produced to maintain glucose levels without unwanted potential trade-offs of the technology. The research suggests that encapsulated hESC-derived insulin-producing cells hold great promise as an effective and safe cell-replacement therapy for insulin-dependent diabetes.

"Our study critically evaluates some of the potential pitfalls of using stem cells to treat insulin-dependent diabetes," said Pamela Itkin-Ansari, Ph.D., adjunct assistant professor in the Development, Aging, and Regenerative Program at Sanford-Burnham, with a joint appointment at UC San Diego.

"We have shown that encapsulated hESC-derived pancreatic cells are able to produce insulin in response to elevated glucose without an increase in the mass or their escape from the capsule. These results are important because it means that the encapsulated cells are both fully functional and retrievable," said Itkin-Ansari.

In the study, published online in Stem Cell Research, Itkin-Ansari and her team used bioluminescent imaging to see if encapsulated cells stay in the capsule after implantation.

Previous attempts to replace insulin-producing cells, called beta cells, have met with significant challenges. For example, researchers have tried treating diabetics with mature beta cells, but because mature cells are fragile and scarce, the method is fraught with problems. Moreover, since the cells come from organ donors, they may be recognized as foreign by the recipient's immune systemrequiring patients to take immunosuppressive drugs to prevent their immune system from attacking the donor's cells, ultimately leaving patients vulnerable to infections, tumors, and other adverse events.

Encapsulation technology was developed to protect donor cells from exposure to the immune systemand has proven extremely successful in preclinical studies.

Itkin-Ansari and her research team previously made an important contribution to the encapsulation approach by showing that pancreatic islet progenitor cells are an optimal cell type for encapsulation. They found that progenitor cells were more robust than mature beta cells to encapsulate, and while encapsulated, they matured into insulin-producing cells, which secreted insulin only when needed.

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Replacing insulin through stem cell-derived pancreatic cells under the skin

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Differentiated stem cells into cardiac cells! – Video

Posted: March 25, 2014 at 5:43 am


Differentiated stem cells into cardiac cells!
This video was uploaded from an Android phone.

By: Brandon dale

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