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Tremendous progress in the development of skin stem cell treatments for butterfly children

Posted: November 27, 2014 at 2:44 pm

27.11.2014 - (idw) IMBA - Institut fr Molekulare Biotechnologie der sterreichischen Akademie der Wissenschaften GmbH

Scientists at IMBA Institute of Molecular Biotechnology of the Austrian Academy of Sciences in Vienna have made a major advancement towards a future therapy for butterfly children. A treatment with fibroblasts generated from induced pluripotent stem cells has been highly successful in mice. The next step is to establish this method in humans. Butterfly children suffer from Epidermolysis Bullosa (EB), a debilitating skin disease. It is caused by a genetic defect that leads to a deficiency or complete lack of various structural proteins. In one particularly severe form, the protein collagen 7 is either missing or present only in insufficient amounts. If that bond is missing, the skin forms blisters or tears at the slightest mechanical pressure, leading to wounds and inflammation that require extensive treatment with creams and bandages. Often these constant lesions also lead to aggressive forms of skin cancer.

Presently there is no cure for this disease. But there are promising approaches that could lead to successful treatments in the future. One of them is a method called fibroblast injection. In this procedure, fibroblasts are injected between the layers of the skin, where they can produce the necessary collagen 7.

Researchers at IMBA under the leadership of Arabella Meixner have now been successful in developing this method to treat mice affected by EB. The individual steps of this treatment have been worked out and carefully tested in many years of laboratory work, and the results have now been published in the scientific journal Science Translational Medicine.

First the scientists returned skin cells of the diseased mice to the stem cell stage and then repaired the genetic defect, the root cause of the disease. Then the researchers transformed stem cells back into fibroblasts.

Before the repaired fibroblasts could be reintroduced into the organism, measures to prevent inflammation or rejection were necessary. In this study the researchers conducted a type of toxicity test, and the results were very promising. After several months of observation, no adverse immune reactions occurred, and the risk of skin cancer did not increase. That is an important consideration because butterfly children already have a greatly increased risk of skin cancer.

The next step is to establish this skin stem cell treatment in humans. To achieve that, the IMBA scientists intend to look for partners with clinical experience. For severe forms of Epidermolysis Bullosa, a systemic application needs to be developed to spread the cells throughout the entire body via the bloodstream to reach epithelial tissues that are more difficult to access, for example the mucous membranes in the mouth or bowels. Often in butterfly children with milder forms of the disease, only certain areas of the skin are affected. The skin stem cell therapy with local injections successfully tested on mice could lead to a valuable treatment method in the very near future.

The project conducted by IMBA scientists was initiated by the patient organization DEBRA Austria, and has had the financial support of the association and of other generous supporters since 2009. DEBRA's mission is to ensure that butterfly children receive competent specialized medical care and to promote research into options to relieve and cure EB. Further thanks also go to our funding and cooperation partners sterreichische Lotterien and FK Austria Wien.

Original publication: Wenzel et. al., iPSC-based cell therapy for Recessive Dystrophic Epidermolysis Bullosa. Science Translational Medicine. 2014.

Scientific Contact: Dr. Arabella Meixner, Research Lead Tel. +43 664 2018084 arabella.meixner@imba.oeaw.ac.at Weitere Informationen:http://www.imba.oeaw.ac.at

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Tremendous progress in the development of skin stem cell treatments for butterfly children

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Leah Still prepares for stem-cell procedure – Video

Posted: November 27, 2014 at 12:47 am


Leah Still prepares for stem-cell procedure
CINCINNATI (Perry Schaible) -- Devon Still has shared his story with the world. He uses social media to keep well-wishers up to date on Leah #39;s progress. The most recent post was Leah at...

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The Project A.L.S./Jenifer Estess Laboratory for Stem cell Research – Video

Posted: November 27, 2014 at 12:46 am


The Project A.L.S./Jenifer Estess Laboratory for Stem cell Research
Founded in 2006, the Project A.L.S./Jenifer Estess Laboratory for Stem Cell Research has been responsible for many of the most striking breakthroughs in adul...

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Muscle relaxant may treat rare form of diabetes, scientists find

Posted: November 26, 2014 at 1:43 pm

Published November 25, 2014

A commonly prescribed muscle relaxant may help treat a rare form of diabetes, researchers at Washington University in St. Louis have found.

According to a news release, the drug dantrolene halts the destruction of insulin-producing beta cells in animal models of the disease and in cell models drawn from people who have the illness.

Patients who have the disease, called Wolfram syndrome, usually develop Type 1 diabetes at a young age and must receive multiple daily insulin injections. Diabetes disables the body from producing and properly using insulin, a hormone that helps convert sugar into energy for normal body function, according to the Centers for Disease Control and Prevention (CDC). This effect causes sugar to build up in the blood, which can lead to heart disease, kidney failure and other serious health problems.

In addition to Type 1 diabetes, patients with Wolfram syndrome also have difficulty with balance and hearing and vision loss. One in 500,000 people have Wolfram syndrome, and many patients die by age 40.

During their study, researchers discovered that high levels of the enzyme calpain 2 were the main cause of death in brain cells and insulin-producing cells. Dantrolene, the muscle relaxant, blocked that enzyme and prevented brain cell death in the animals and human-derived models.

Researchers studied the effects of dantrolene on stem cells from Wolfram syndrome patients and their close relatives. The stem cells were grown from skin cells, rather than gathered from cord blood or stem cells developed from embryos. According to the news release, the study authors treated the stem cells in growth factors so they would differentiate into specific cell types, such as neurons and insulin-producing cells. They found that dantrolene wasnt toxic to cells grown from the skin samples of patients relatives.

The drug interfered with cell death in cells from Wolfram patients but did not harm cells that came from parents and siblings, senior investigator Fumihiko Urano, a medicine professor at Washington University, said in the news release.

Dantrolene is often prescribed to patients with multiple sclerosis as a treatment for muscle spasticity. The drug has already been approved by the Food and Drug Administration (FDA), so researchers hope to begin clinical trials quickly.

Wed like to test the drug first in adult patients with Wolfram syndrome, and if we get positive results, we could extend the trial to children, Urano said.

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UCLA Researchers Identify Protein Key To The Development Of Blood Stem Cells

Posted: November 26, 2014 at 1:41 pm

November 25, 2014

Provided by Peter Bracke, UCLA

Understanding the self-replication mechanisms is critical for improving stem cell therapies for blood-related diseases and cancers

Led by Dr. Hanna Mikkola, a member of the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, UCLA scientists have discovered a protein that is integral to the self-replication of hematopoietic stem cells during human development.

The discovery lays the groundwork for researchers to generate hematopoietic stem cells in the lab that better mirror those that develop in their natural environment. This could in turn lead to improved therapies for blood-related diseases and cancers by enabling the creation of patient-specific blood stem cells for transplantation.

The findings are reported online ahead of print in the journal Cell Stem Cell.

Researchers have long been stymied in their efforts to make cell-based therapies for blood and immune diseases more broadly available, because of an inability to generate and expand human hematopoietic stem cells (HSCs) in lab cultures. They have sought to harness the promise of pluripotent stem cells (PSCs), which can transform into almost any cell in the human body, to overcome this roadblock. HSCs are the blood-forming cells that serve as the critical link between PSCs and fully differentiated cells of the blood system. The ability of HSCs to self-renew (replicate themselves) and differentiate to all blood cell types, is determined in part by the environment that the stem cell came from, called the niche.

In the five-year study, Mikkola, Dr. Sacha Prashad and Dr. Vincenzo Calvanese, members of Mikkolas lab and lead authors of the study, investigated a HSC surface protein called GPI-80. They found that it was produced by a specific subpopulation of human fetal hematopoietic cells that were the only group that could self-renew and differentiate into various blood cell types. They also found that this subpopulation of hematopoietic cells was the sole population able to permanently integrate into and thrive within the blood system of a recipient mouse.

Mikkola and colleagues further discovered that GPI-80 identifies HSCs during multiple phases of human HSC development and migration. These include the early first trimester of fetal development when newly generated human hematopoietic stem cells can be found in the placenta, and the second trimester when HSCs are actively replicating in the fetal liver and the fetal bone marrow.

We found that whatever HSC niche we investigated, we could use GPI-80 as the best determinant to find the stem cell as it was being generated or colonized different hematopoietic tissues, said Mikkola, associate professor of molecular, cell and development biology at UCLA and also a member of the Jonsson Comprehensive Cancer Center. Moreover, loss of GPI-80 caused the stem cells to differentiate into mature blood cells rather than HSCs. This essentially tells us that GPI-80 must be present to make HSCs. We now have a very unique marker for investigating how human hematopoietic cells develop, migrate and function.

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UCLA Researchers Identify Protein Key To The Development Of Blood Stem Cells

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Stem Cell Therapy at EmCell clinic: Dr. Khalil Fadel story – Video

Posted: November 26, 2014 at 1:40 pm


Stem Cell Therapy at EmCell clinic: Dr. Khalil Fadel story

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Clinical Trials for MS and Rheumatoid Arthritis with Umbilical Cord Mesenchymal Stem Cells – Video

Posted: November 26, 2014 at 10:48 am


Clinical Trials for MS and Rheumatoid Arthritis with Umbilical Cord Mesenchymal Stem Cells
Stem Cell Institute and Medistem Panama founder, Neil Riordan, PhD discusses clinical trials for multiple sclerosis and rheumatoid arthritis using umbilical cord tissue-derived mesenchymal...

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Stem Cell Research Alexandra Valle – Video

Posted: November 26, 2014 at 10:48 am


Stem Cell Research Alexandra Valle
This video is about PhotoStory Project 1.

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Stem Cell Research Poll Results – iSideWith

Posted: November 26, 2014 at 10:09 am

This is an obsolete question. Stem cell research has been going on, with cells that are non-fetal for several years now. I think the scientific community figured out how to do research (e.g. using nasal passage cells) when the ban on fetal cells was enacted and I don't see why the govt has to get involved at all at this point in history. 10monsago from a Republican in Newtown, PA.

Yes, as long as they are non-fetal stem cells, as long as all developments are available for public review, and as long as the developments are not used as weapons or in the creation of weapons. 10monsago from a Republican in Pfafftown, NC.

No, leave funding and research to the private sector Fetal stem cell research should be illegal. 10monsago from a Republican in Lorain, OH.

Using non-fetal stem cells only AND leave funding and research to the private sector. 10monsago from a Republican in Diberville, MS.

I agree with stem cell research but feel that strong restrictions must be placed against using cells from voluntarily aborted fetuses out of concern that fetuses could develop a "market value". Mothers should be allowed to donate their cord cells or those of miscarried babies. 10monsago from a Democrat in Glen Carbon, IL.

They are already funding adult stem cell research, they should not fund embryonic stem cell research. 10monsago from a Republican in Alameda, CA.

Yes, but not without restrictions... Regarding fetal cells, mothers need to sign legal papers stating that if there's a complication, and the baby is still born, or suffers an event that creates a mortality while giving birth or soon after, do they agree to the donation of their organs, including stem cells for research. 10monsago from a Republican in Kennedale, TX.

Yes, provided that future findings will benefit those who cannot afford to pay for stem cell treatment. 10monsago from a Democrat in Dallas, TX.

No, funding for such research should be from companies that believe they can make a profit. 10monsago from a Republican in Potwin, KS.

I CONSIDER MYSELF TOO UNFAMILIAR WITH THIS TO SAY, BUT AM AGAINST ANYTHING THAT COULD BE CONSIDERED IMMORAL. 10monsago from a Republican in Casa Grande, AZ.

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Chattanoogan.com – Chattanooga's source for breaking local news

Posted: November 26, 2014 at 10:09 am

Dr. Mary Headrick has repeatedly asserted that Congressman Fleischmann does not adequately represent the constituents of District 3, but I respectfully disagree. Chucks consistent stand for the life of the unborn, prudent government spending, the incubation and protection of small businesses, and reliable, quality healthcare resonates with my core values and concerns, as I know it does for my neighbors and a vast majority of the district.

While I dont doubt Dr. Headrick is well-meaning, I do not believe her agenda and care values line up with my own or those of many in District 3, and ultimately that is most important to me any credentials she has are outweighed by the absence of common values.

I trust Congressman Fleischmann to best represent the beliefs and interests of my family and my community, and I encourage others to closely examine their core values against each candidate to decide for yourselves who best represents your voice, your beliefs, and your needs.

Early voting starts Wednesday. As for me, Chuck Fleischmann has my vote for Congress.

Amanda Russell Chattanooga

* * *

Unfortunately, I do not share this writer's trust in Fleischmann. I find his positions extreme and not in line with my values or those of so many others here in the Tennessee 3rd.

I agree that his stand for the life of the unborn is consistent: he voted twice for the "Life Begins at Conception" bill. In doing so, he defines a fertilized egg as a person. This puts an end to abortion for any reason, would outlaw many forms of birth control, would put an end to stem cell research, and would put an end to in vitro fertilization, something many couples rely upon to help them have children.

And what has he done for poor children who are already here? Voted to take money from food stamp programs they and their parents rely upon. I worry more about a child going hungry and doing poorly in school because of that than I do about the rights of the two cells that make up a fertilized egg.

Prudent government spending? No, Fleischmann voted to shut down the government, costing the federal government many millions and costing millions to the local economy as well.

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Chattanoogan.com - Chattanooga's source for breaking local news

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