A Month in the Life of a Stem Cell Lab – Undark Magazine

Yi Yu, a research assistant in the Melton lab, holds flasks containing human embryonic stem cells. Researchers have developed a recipe to turn them into beta cells, which secrete insulin in the pancreas. In what they call the Foundry, they hope to produce 200 flasks of beta cells this year. (All images by Chlo Hecketsweiler)

Pluripotent stem cells have the potential to generate any human cell type and researchers have shown that they may be used to repair damaged tissues and organs in the body. But what looks good in the lab doesnt always translate to the clinic. In laboratories around the world, thousands of scientists are trying to close the gap between promise and real-world therapies.

For a month and a half, starting in January, I was embedded in the daily life of one such group of scientists Douglas A. Meltons laboratory at the Harvard Stem Cell Institute. I watched their experiments, learned about the complex science of stem cells, and talked with the researchers about their work and hopes. I was allowed to take pictures, and for this photo essay I tried to pick out moments and details that I found revealing, although scientists may see them as business as usual.

Meltons lab focuses on diabetes, a disease that affects almost one in 10 Americans. In the lifelong form of the disease (known as type 1), the bodys immune system attacks and destroys the beta cells that produce insulin in the pancreas. Diabetic patients must rely on daily injections of insulin to control the level of sugar in their blood.

Meltons team has invented aprotocolto turn embryonic stem cells into beta cellsand has shown that they effectively secrete insulin when transplanted into diabetic mice. To push the research forward, Melton has co-founded a biotech company, Semma Therapeutics, and hopes to start a clinical trial in the next three or four years.

He is not alone in the race. Timothy Kieffers lab, in Vancouver, British Columbia, has developedanother protocolto turn stem cells into beta cells that reverse diabetes in mice, and theapproach is being tested by California biotech company ViaCyte. Big pharmaceutical companies are on the lookout too. AstraZeneca collaborates with Meltons lab, and the Danish company Novo Nordisk, the worldwide leader in diabetes drugs, is working on its own project.

All have major challenges to overcome before any stem cell therapy hits the market. How results in mice translate into humans is not clear, and finding ways to trick the bodys defense system will be a huge step. New tools such as the gene-editing technology CRISPR-Cas 9 and the ability to handle huge sets of data will help, but they also raise many new questions. The idea that we can have some mastery and control of the cells is a fantastic thing, Melton told me, adding that while in the 20th century humans gained control over much of their physical environment, we are now entering a century when we are going to get control over the human body.

Chlo Hecketsweiler, a 2016-17 Knight Science Journalism fellow, is a Paris-based journalist with Le Monde, specializing in the pharmaceutical and life sciences industries.

You Have to Keep the Cells Happy Precision is critical in the lab, lest cells become damaged or experiments rendered uncertain.

Elise Engquist, a research assistant, looks at the sizes and shapes of stem cell clusters. They have to be monitored closely, as they multiply quickly and take about one month to turn into beta cells. The differentiation is done in six steps and is guided by a cocktail of growth factors added according to precise timing. Scientists always follow the same recipe, but there are still some differences between batches.

Maria Keramari, a postdoc from Greece, delicately handles a dish with human embryonic stem cells. She uses the gene-editing tool CRISPR-Cas9 to create a line of cells that will be fluorescent when they express insulin. Scientists must feed the cells at regular intervals and be careful not to hurt them during the experiment. You have to keep the cells happy before you keep yourself happy, Keramari says.

Jos Rivera-Feliciano, a postdoc from Puerto Rico, prepares samples for DNA analysis. Rivera-Feliciano works on a new family of proteins that play important roles in the development of the pancreas, and he hopes to have his own lab in the future. Its very competitive, he says. For every faculty position you have 100 to 300 candidates.

Here, Rivera-Feliciano prepares the gel for electrophoresis, a technique for separating DNA fragments based on their size. If the result is positive, he can turn to more sophisticated and expensive DNA sequencing techniques to get more information.

They Are Like Our Babies Sophisticated experiments still require some day-to-day innovation inside the lab.

Nadav Sharon, a postdoc from Israel, adds small segments of DNA, called plasmids, into petri dishes containing E. coli bacteria. Some of these bacteria will take up the foreign DNA and clone it as they replicate. Researchers routinely use these bacterial factories to build genetic tools that will be used to modify stem cells or create transgenic animal models. To design their experiments, scientists can dig into huge databases of bacteria, enzymes, and genes with well-known properties. Most of them can be ordered online from specialized companies and are delivered by mail.

Sharon handles vials of bacteria and puts them on ice. The heat shock causes some of them to take up the plasmids that have just been added to the vial. Sophisticated experiments often start with this kind of handmade biological tool. The recipes are well known, but there is always a measure of uncertainty in the results. Researchers can lose weeks of work without knowing what exactly went wrong.

Ornella Barrandon, a postdoc, tests 3,000 compounds to find out which ones boost the replication of beta cells in the pancreas. Beta cells derived from human embryonic stem cells could accelerate the discovery of new drugs, as research is hindered by the limited supply of beta cells extracted from cadavers. We spend so much time on our projects, they are like our babies, she says.

Biology Has Taken a Turn But even with sophisticated genome editing tools such as CRISPR-Cas 9, this is not an exact science.

Adrian Veres, a graduate student from Canada, prepares samples for single-cell analysis, a cutting-edge technique that allows scientists to look at all the cells that constitute an organ and better understand which genes are expressed in each of them. It requires them to deal with unprecedented quantities of data: Biology has taken a turn, and biologists must learn to deal with statistics, Veres says. You cant just give the data to a statistician and look at the results.

Chi Yang Chen, a research assistant, with a lab notebook. Each scientist has one, and must record every step of every experiment. Its the memory and the legacy of the research done in the lab. Its also a legal document that will be closely scrutinized in case the lab applies for a patent or is ever sued for fraud.

Jennifer Kenty, a research assistant, feeds mice with pellets. The Melton labs mouse house hosts about 1,200 mice. Beta cells derived from human stem cells are transplanted into mice that are both immunodeficient and diabetic. The goal is to determine how much insulin they secrete in response to glucose injections. Genetically modified mice are also used to test the role of different genes in the development of the pancreas and endocrine cells.

Pancreases of mouse embryos float in vials. Many questions regarding pancreas development are still open. By analyzing the type of cells that compose it at different stages of fetal development, scientists hope to create a kind of movie that will help them understand what may go wrong along the way. In other experiments, transgenic mice models are used to study the role of specific genes. Even with sophisticated genome editing tools such as CRISPR-Cas 9, this is not an exact science. I tried once to create a CRISPR mouse, says Nadav Sharon. When you read the papers, it looks like magic but that is not that simple.

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A Month in the Life of a Stem Cell Lab - Undark Magazine

Science | UM researchers develop new technology for stem cell storage – Macau Daily Times

Home | Macau | Science | UM researchers develop new technology for stem cell storage

UM researchers have developed a new technology for cell storage and transport

The University of Macau (UM) Faculty of Health Sciences (FHS) has developed a technology that enables the storage of stem cells at room temperature for at least seven days without the loss of viability or biological activities. According to a statement issued by UM, this new technology does not rely on the traditional cryopreservation method which requires costly equipment and tedious cryopreservation procedures, thus enabling cell storage and transport under ambient conditions.

Under professor Ren-He Xus supervision, doctoral student Jiang Bin and postdoctoral researcher Yan Li, both from the FHS, engaged in the research study titled Spheroidal Formation Preserves Human Stem Cells for Prolonged Environment under Ambient Conditions for Facile Storage and Transportation. Together with the participation of Chris Wong Koon Ho, an assistant professor at the FHS, they successfully developed the new technology. The related paper has been published in Biomaterials, a renowned international journal in the field of biological materials.

The study found that preparing human mesenchymal stem cells (hMSC) to form spheroids with the hanging-drop or other methods, can reduce the cell metabolism and increase cell viability. Stored in a sealed vessel filled with regular culture medium, under ambient conditions without oxygen supply, the viability of hMSC in spheroids remained over 90 percent even after 11 days. This method is also applicable to higher pluripotent human embryonic stem cells.

Stem cells are found in various locations of the body such as bone marrow, blood, brain, spinal cord, skin, and corneal limbus. They are responsible for regenerating and repairing damaged tissues and organs in the body. Transplantation of stem cells can restore damaged tissues and organs to their original functions. For this reason, stem cells have significant clinical value. However, they require strict culturing and storage conditions. Extended exposure (over 24 to 48 hours) to unfavorable temperature, humidity, or levels of oxygen and carbon dioxide will cause the cells to gradually lose their functions and viability.

Currently, long-distance cell transport mainly relies on the costly method of cryopreservation. For short-distance transport, cells can be prepared in suspension or adherent culture, but the number of cells that can be transported via this method is limited. Moreover, cell viability decreases dramatically after transport for 48 hours under ambient conditions.

The UM claims that the new technology developed by its researchers can overcome the above limitations. With this technology, a sufficient dose of stem cells that are being transported can be used in patients without the need to freeze stem cells before transport and to thaw, revive, and proliferate the transported stem cells, a statement from the institution reads.

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Science | UM researchers develop new technology for stem cell storage - Macau Daily Times

Two Day FDA’s Regulation of Regenerative Medicine Seminar … – Business Wire (press release)

DUBLIN--(BUSINESS WIRE)--Research and Markets has announced the addition of the "FDA's Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering & Gene Therapies: 2-Day In-person Seminar" conference to their offering.

Stem cells harness the power to differentiate into numerous cells upon stimulation. This has led to their wide exploration across all of medicine, including high risk diseases. Of course, significant scientific breakthroughs in the use of stem cells to prevent, diagnose, and treat numerous diseases has caused numerous start-up companies to form. Despite, such promise, the FDA has yet to approve stem cell therapies for a wide range of diseases, except cord blood-derived hematopoietic progenitor cells for certain indications.

This tutorial will provide an historical context for the use of stem cells in medicine, where the field has been and where it is going. It will also provide the few examples of FDA approved use of stem cells in medicine and what is needed for the field to progress. For example, in 2006, the U.S. FDA implemented regulations governing the use of human cells, tissues, and cellular and tissue-based products in humans including bone, ligament, skin, dura mater, stem cells, cartilage cells, and various other cellular and tissue-based products. Currently, there is an ongoing debate in industry on how such therapies should be regulated, in particular by the FDA or under the practice of medicine, under federal law or state law, and as drugs or simply biologics.

Learning Objectives:

Fundamentals of stem cells

- What is all the excitement about

- How to control stem cell differentiation

- Sources of stem cells

- Incorporating stem cells into biomaterials

- Avoiding immune system clearance of stem cells

FDA regulatory approvals for the use of stem cells in medicine

- Currently approved use of stem cells in medicine

- FDA guidance documents for stem cell technologies

- Global approval of stem cell technologies

- How the FDA regulates regenerative treatments and therapies

- The use of human cells, tissues, and cellular and tissue-based product criteria and Minimal Manipulation Standard

- The drug and biological approval process

- Regenerative products as medical devices

- How to design appropriate clinical trials

- Applicable good manufacturing and good laboratory practices

- Product labeling, marketing and advertising

- FDA and other federal agency enforcement action

Future thoughts on approaches for regulatory approval of stem cell technologies

- Remaining hurdles

- Outlook for new technologies

For more information about this conference visit http://www.researchandmarkets.com/research/ljt255/fdas_regulation

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Two Day FDA's Regulation of Regenerative Medicine Seminar ... - Business Wire (press release)

Scientists find skin cells at the root of balding, gray hair – Medical Xpress

May 8, 2017 by Carol Marie Cropper Strand of human hair at 200x magnification. Credit: Jan Homann/Wikipedia

UT Southwestern Medical Center researchers have identified the cells that directly give rise to hair as well as the mechanism that causes hair to turn gray findings that could one day help identify possible treatments for balding and hair graying.

"Although this project was started in an effort to understand how certain kinds of tumors form, we ended up learning why hair turns gray and discovering the identity of the cell that directly gives rise to hair," said Dr. Lu Le, Associate Professor of Dermatology with the Harold C. Simmons Comprehensive Cancer Center at UT Southwestern. "With this knowledge, we hope in the future to create a topical compound or to safely deliver the necessary gene to hair follicles to correct these cosmetic problems."

The researchers found that a protein called KROX20, more commonly associated with nerve development, in this case turns on in skin cells that become the hair shaft. These hair precursor, or progenitor, cells then produce a protein called stem cell factor (SCF) that the researchers showed is essential for hair pigmentation.

When they deleted the SCF gene in the hair progenitor cells in mouse models, the animal's hair turned white. When they deleted the KROX20-producing cells, no hair grew and the mice became bald, according to the study.

The findings are published online in Genes & Development.

Dr. Le, who holds the Thomas L. Shields, M.D. Professorship in Dermatology, said he and his researchers serendipitously uncovered this explanation for balding and hair graying while studying a disorder called Neurofibromatosis Type 1, a rare genetic disease that causes tumors to grow on nerves.

Scientists already knew that stem cells contained in a bulge area of hair follicles are involved in making hair and that SCF is important for pigmented cells, said Dr. Le, a member of the Hamon Center for Regenerative Science and Medicine.

What they did not know in detail is what happens after those stem cells move down to the base, or bulb, of hair follicles and which cells in the hair follicles produce SCF or that cells involved in hair shaft creation make the KROX20 protein, he said.

If cells with functioning KROX20 and SCF are present, they move up from the bulb, interact with pigment-producing melanocyte cells, and grow into pigmented hairs.

But without SCF, the hair in mouse models was gray, and then turned white with age, according to the study. Without KROX20-producing cells, no hair grew, the study said.

UT Southwestern researchers will now try to find out if the KROX20 in cells and the SCF gene stop working properly as people age, leading to the graying and hair thinning seen in older people as well as in male pattern baldness, Dr. Le said.

The research also could provide answers about why we age in general as hair graying and hair loss are among the first signs of aging.

Explore further: New research provides clues on why hair turns gray

More information: Chung-Ping Liao et al. Identification of hair shaft progenitors that create a niche for hair pigmentation, Genes & Development (2017). DOI: 10.1101/gad.298703.117

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Scientists find skin cells at the root of balding, gray hair - Medical Xpress

Reprogrammed Cells Improve Heart Function After a Heart Attack – Medical News Bulletin

In a recent study published in Circulation, researchers managed to convert de-differentiated human fibroblasts, support cells key in healing, to red blood cells or cells that line the interiors of blood vessels via manipulation of the SOX17 transcription factor. The de-differentiated fibroblasts can improve heart function after a heart attack and provide patient-specific cells that do not suffer from premature aging.

Fibroblasts, a support cell key in healing, are commonly used for de-differentiation. De-differentiated cells are similar to stem cells; depending on the environment they are in and what genes are active, they become different cells. De-differentiated cells have many medical uses; as many as the number of cells that they can become. In a recent study published in Circulation, researchers from the University of Illinois College of Medicine and the Indiana University School of Medicine managed to convert de-differentiated human fibroblasts to endothelial cells and erythroblasts. Endothelial cells are the cells that make up the lining of the interior of blood vessels. Erythroblasts are commonly known as red blood cells.

The researchers first de-differentiated the fibroblasts by overexpression of the proteins that transcribe DNA into RNA, specifically, pluripotency transcription factors. The de-differentiated cells were then placed into different media to transform them into endothelial cells and erythroblasts. The researchers observed that a specific transcriptional regulator, SOX17, and its respective activity corresponded to which cell the de-differentiated fibroblasts became. The researchers also experimented on rats that had suffered heart attacks. They implanted the de-differentiated fibroblasts into the rats and found that they improved heart function after a heart attack. Finally, the researchers observed that the cells generated from the de-differentiated fibroblast had increased production of telomerase. Telomerase is a transcription factor that produces telomeres, which are at the ends of chromosomes. The length of telomeres corresponds to the age of a cell, with longer being younger.

All this research shows the power of de-differentiated cells. De-differentiated fibroblasts can make patient-specific cells. These cells may avoid premature aging because of the increased production of telomerase: Helpful for enabling older patients to have personalized cells. Though only shown in mice, the de-differentiated fibroblasts did improve cardiac function after their heart attacks and may benefit humans as well. Pinpointing SOX17 as the switch for making endothelial cells or erythroblasts will optimize their generation, which will prove valuable for tissue regeneration and disease modeling.

Written By:Brian Jones

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Reprogrammed Cells Improve Heart Function After a Heart Attack - Medical News Bulletin

Researchers use modified insulin and red blood cells to regulate blood sugar – Medical Xpress

May 8, 2017 by Matt Shipman Credit: North Carolina State University

Researchers from North Carolina State University and the University of North Carolina at Chapel Hill have developed a new technique that uses modified insulin and red blood cells to create a glucose-responsive "smart" insulin delivery system. In an animal model study, the new technique effectively reduced blood sugar levels for 48 hours in a strain of mice that had Type 1 diabetes.

The researchers modified insulin by chemically binding it to a glucose derivative called glucosamine. The glucosamine could then bind to glucose transporters on the surface of a red blood cell, effectively attaching the insulin to the blood cell. The end result is a red blood cell studded with insulin molecules.

The idea is that these insulin-loaded blood cells could then be injected into a diabetic patient. In this study, the work was done in Type 1 diabetic mice.

Once in the bloodstream, the blood cells carrying insulin interact with their environment. If glucose levels are high, glucose molecules effectively displace the glucosamine in the blood cells' glucose transporters. And when the glucosamine is set free from the blood cell, so is the insulin.

The insulin can then bind to insulin receptors in the liver, muscles and fatty tissues, triggering a process that reduces glucose levels in the blood.

"In short, this is a fully biocompatible smart system that responds, when needed, to normalize glucose levels in the blood," says Zhen Gu, co-corresponding author of a paper on the work and an associate professor in the joint biomedical engineering program at NC State and UNC.

In the study, researchers compared mice receiving the modified insulin and blood cell system to three other groups: a group that received saline solution; a group that got only modified insulin; and a group that got a mixture of unmodified insulin and red blood cells.

The researchers found that the Type I diabetic mice that received the modified insulin and blood cell system were able to significantly reduce blood glucose levels for more than two days. The best performance among the other groups saw an initial dip in blood sugar levels, but returned to high glucose levels within 12 hours.

The researchers also tested each of the drug combinations in a group of healthy mice, and found that the modified insulin and blood cell system reduced the risk of hypoglycemia compared to the other drug combinations.

In addition, the researchers conducted an experiment in the Type I diabetic mice using modified insulin and nanoparticles that had been coated with red blood cell membranes. The modified insulin and nanoparticle system achieved comparable results to those found using modified insulin and red blood cells.

"This is a positive result, because it bodes well for developing a standardized means of delivering this glucose regulation system," Gu says.

"The team will further evaluate the long-term biocompatibility of the modified insulin system in an animal model before determining whether to move to clinical trials," says co-author Dr. John Buse, professor of medicine at the UNC School of Medicine and director of the UNC Diabetes Care Center and the NC Translational and Clinical Sciences Institute. "The vision, if realized, would be one of the most exciting advances in diabetes care."

"We are also exploring the use of painless microneedles to deliver this system, rather than relying on the conventional injections which were used in this study," Gu says. "The possibility of using a different drug delivery system makes it difficult to assess cost, but we're optimistic that the cost of the potential formulation would be comparable to existing treatments."

The paper, "Red Blood Cells for Glucose-Responsive Insulin Delivery," is published in the journal Advanced Materials. Lead author of the paper is Chao Wang, a postdoctoral researcher in Gu's research group. The paper was co-authored by Yanqi Ye, Wujin Sun and Jicheng Yu, Ph.D. students in Gu's group; Jingqiang Wang, a postdoctoral researcher in Gu's group; and David Lawrence of UNC.

Explore further: Post-biotics may help shield obese from diabetes

More information: Chao Wang et al, Red Blood Cells for Glucose-Responsive Insulin Delivery, Advanced Materials (2017). DOI: 10.1002/adma.201606617

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Researchers use modified insulin and red blood cells to regulate blood sugar - Medical Xpress

Aspirin Prevents Platelets from Suppressing Anticancer T Cells – Genetic Engineering & Biotechnology News (blog)

Platelets do more than promote clotting. They weaken one of the bodys immune defenses against cancer. Unfortunately, platelets tend to work against the immuno-oncology treatments that try to strengthen T-cell attacks on cancer.

Platelets, new research indicates, suppress T-cell immunity against cancer by expressing a transmembrane protein, the glycoprotein A repetitions predominant (GARP) receptor. Platelet GARP can snag a growth factor, transforming growth factor- (TGF), and thereby promote cancer. When GARP binds with TGF, the latter can become activated and then convert effector T cells, which normally attack cancer with an inflammatory reaction, into regulatory (suppressor) T cells, which turn off the inflammatory reaction.

The new findings appeared May 5 in the journal Science Immunology, in an article entitled Platelets Subvert T Cell Immunity against Cancer via GARP-TGF Axis. This study expands on earlier findings that indicated platelets, in cancer-associated thrombocytosis, might make cancer worse.

An unbiased biochemical and structural biology approach established TGF and lactate as major platelet-derived soluble factors to obliterate CD4+ and CD8+ T cell functions, wrote the articles authors. Moreover, we found that platelets are the dominant source of functional TGF systemically as well as in the tumor microenvironment through constitutive expression of the TGF-docking receptor GARP rather than secretion of TGF per se.

Scientists have known for several years that certain cancers suppress T cells to avoid the immune system. That is why adoptive T-cell therapy is one of the most promising advances in modern cancer treatment. It is a type of immunotherapy that awakens the immune system by retraining a patient's T cells to recognize their cancer. T cells are isolated from a patient's blood and retrained, or "primed," to recognize tumor cells. They are then injected back into the patient's bloodstream where they can now hunt and fight cancer.

In the current study, scientists have shown that genetic targeting of platelets enhances adoptive T-cell therapy of cancer. Platelet-specific deletion of the GARP-encoding gene Lrrc32, the authors of the Science Immunology article indicated, blunted TGF activity at the tumor site and potentiated protective immunity against both melanoma and colon cancer.

This work, which was carried out by scientists based at the Medical University of South Carolina, revealed the mechanism behind platelets activation of TGF. The scientists showed that in genetically modified mice without GARP, the molecular hook on the surface of platelets, adoptive T-cell therapy was more successful at controlling melanoma. This meant that platelets without the ability to grab and activate TGF were not able to suppress cancer-fighting T cells. Similar experiments confirmed this result in mice with colon carcinoma.

Finally, mice with normal platelets that were given melanoma and then adoptive T-cell therapy survived longer and relapsed less when aspirin and clopidogrel, two antiplatelet drugs, were added. The researchers noted that antiplatelet drugs by themselves were not successful in combating melanoma in their experiments.

This study could inform future treatment of melanoma and other cancers and offers a sound reason to test antiplatelet drugs in clinical trials of adoptive T-cell therapy. In patients with melanoma or other cancers, adoptive T-cell therapy may be successful if highly available platelet-blocking drugs such as aspirin are added to the treatment. However, the current standard of care for melanoma is not adoptive T-cell therapy, but rather so-called checkpoint inhibitors.

The team at the Medical University of South Carolina, which was led by Zihai Li, M.D., Ph.D., want to know if combination therapy with antiplatelet drugs could improve existing cancer treatment. They are waiting for approval to begin a clinical trial that will test certain checkpoint inhibitors in combination with aspirin and clopidogrel for the treatment of patients with advanced cancers. Dr. Li's trial will complement clinical trials that are already testing adoptive T-cell therapy as a single treatment for cancer.

"I'm very excited about this," said Dr. Li. "We can test simple, over-the-counter antiplatelet agents to really improve immunity and make a difference in how to treat people with cancer."

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Aspirin Prevents Platelets from Suppressing Anticancer T Cells - Genetic Engineering & Biotechnology News (blog)

Presidential Symposium at the American Society of Gene and Cell Therapy (ASGCT) 20th Annual Meeting Will Feature … – Yahoo Finance

FREMONT, Calif., May 3, 2017 /PRNewswire/ --Asterias Biotherapeutics, Inc. (NYSE MKT: AST), a biotechnology company pioneering the field of regenerative medicine, today announced that data from its AST-OPC1 clinical program for severe cervical spinal cord injury will be presented during the Presidential Symposium at the American Society of Gene and Cell Therapy (ASGCT) 20th Annual Meeting, being held in Washington, D.C. during May 10-13, 2017.

"The ASGCT decision to include a presentation on AST-OPC1 in its Presidential Symposium signifies the ground-breaking nature of our program, and reflects the encouraging efficacy and safety data we have seen to date in patients with severe spinal cord injuries that have been treated with AST-OPC1," said Steve Cartt, President and Chief Executive Officer of Asterias. "Data will be presented from our SCiStar study demonstrating the potential of AST-OPC1 to help patients with complete paralysis regain increased arm, hand and finger function, and thus greater ability to live independently."

Jane S. Lebkowski, Ph.D., Asterias' President of R&D and Chief Scientific Officer, will be one of the presenters during the Presidential Symposium session scheduled on Friday, May 12, 2017 at 1:00pm Eastern Time. Dr. Lebkowski's presentation, titled "498 - Safety and Efficacy of Human Embryonic Stem Cell Derived Oligodendrocyte Progenitor Cells (AST-OPC1) in Patients with Subacute Cervical Spinal Cord Injury," is expected to begin at 2:15pm Eastern Time. The abstract for Dr. Lebkowski's presentation at the ASGCT meeting is available online at: http://www.abstractsonline.com/pp8/#!/4399/presentation/1996.

ASGCT is the primary professional membership organization for gene and cell therapy. The Society's members are scientists, physicians, patient advocates, and other professionals. Its members work in a wide range of settings including universities, hospitals, government agencies, foundations, biotechnology and pharmaceutical companies. Its mission is to advance knowledge, awareness, and education leading to the discovery and clinical application of gene and cell therapies to alleviate human disease.

About the SCiStar Trial

The SCiStar trial is an open-label, single-arm trial testing three sequential escalating doses of AST-OPC1 administered at up to 20 million AST-OPC1 cells in as many as 35 patients with sub-acute, C-5 to C-7, motor complete (AIS-A or AIS-B) cervical SCI. These individuals have essentially lost all movement below their injury site and experience severe paralysis of the upper and lower limbs. AIS-A patients have lost all motor and sensory function below their injury site, while AIS-B patients have lost all motor function but may retain some minimal sensory function below their injury site. AST-OPC1 is being administered 14 to 30 days post-injury. Patients will be followed by neurological exams and imaging procedures to assess the safety and activity of the product.

The study is being conducted at six centers in the U.S. and the company plans to increase this to up to 12 sites to accommodate the expanded patient enrollment. Clinical sites involved in the study include the Medical College of Wisconsin in Milwaukee, Shepherd Medical Center in Atlanta, University of Southern California (USC) jointly with Rancho Los Amigos National Rehabilitation Center in Los Angeles, Indiana University, Rush University Medical Center in Chicago and Santa Clara Valley Medical Center in San Jose jointly with Stanford University.

Asterias has received a Strategic Partnerships Award grant from the California Institute for Regenerative Medicine, which provides $14.3 million of non-dilutive funding for the Phase 1/2a clinical trial and other product development activities for AST-OPC1.

Additional information on the Phase 1/2a trial, including trial sites, can be found at http://www.clinicaltrials.gov, using Identifier NCT02302157, and at the SCiStar Study Website (www.SCiStar-study.com).

About AST-OPC1

AST-OPC1, an oligodendrocyte progenitor population derived from human embryonic stem cells, has been shown in animals and in vitro to have three potentially reparative functions that address the complex pathologies observed at the injury site of a spinal cord injury. These activities of AST-OPC1 include production of neurotrophic factors, stimulation of vascularization, and induction of remyelination of denuded axons, all of which are critical for survival, regrowth and conduction of nerve impulses through axons at the injury site. In preclinical animal testing, AST-OPC1 administration led to remyelination of axons, improved hindlimb and forelimb locomotor function, dramatic reductions in injury-related cavitation and significant preservation of myelinated axons traversing the injury site.

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In a previous Phase 1 clinical trial, five patients with neurologically complete, thoracic spinal cord injury were administered two million AST-OPC1 cells at the spinal cord injury site 7-14 days post-injury. They also received low levels of immunosuppression for the next 60 days. Delivery of AST-OPC1 was successful in all five subjects with no serious adverse events associated with AST-OPC1. No evidence of rejection of AST-OPC1 was observed in detailed immune response monitoring of all patients. In four of the five patients, serial MRI scans indicated that reduced spinal cord cavitation may have occurred. Based on the results of this study, Asterias received clearance from FDA to progress testing of AST-OPC1 to patients with cervical spine injuries, which represents the first targeted population for registration trials.

About Asterias Biotherapeutics

Asterias Biotherapeutics, Inc. is a biotechnology company pioneering the field of regenerative medicine. The company's proprietary cell therapy programs are based on its pluripotent stem cell and immunotherapy platform technologies. Asterias is presently focused on advancing three clinical-stage programs which have the potential to address areas of very high unmet medical need in the fields of neurology and oncology. AST-OPC1 (oligodendrocyte progenitor cells) is currently in a Phase 1/2a dose escalation clinical trial in spinal cord injury. AST-VAC1 (antigen-presenting autologous dendritic cells) is undergoing continuing development by Asterias based on promising efficacy and safety data from a Phase 2 study in Acute Myeloid Leukemia (AML), with current efforts focused on streamlining and modernizing the manufacturing process. AST-VAC2 (antigen-presenting allogeneic dendritic cells) represents a second generation, allogeneic cancer immunotherapy. The company's research partner, Cancer Research UK, plans to begin a Phase 1/2a clinical trial of AST-VAC2 in non-small cell lung cancer in 2017. Additional information about Asterias can be found at http://www.asteriasbiotherapeutics.com.

FORWARD-LOOKING STATEMENTS

Statements pertaining to future financial and/or operating and/or clinical research results, future growth in research, technology, clinical development, and potential opportunities for Asterias, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to statements that contain words such as "will," "believes," "plans," "anticipates," "expects," "estimates") should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products, uncertainty in the results of clinical trials or regulatory approvals, need and ability to obtain future capital, and maintenance of intellectual property rights. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the businesses of Asterias, particularly those mentioned in the cautionary statements found in Asterias' filings with the Securities and Exchange Commission. Asterias disclaims any intent or obligation to update these forward-looking statements.

To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/presidential-symposium-at-the-american-society-of-gene-and-cell-therapy-asgct-20th-annual-meeting-will-feature-presentation-on-asterias-ast-opc1-for-spinal-cord-injury-300450272.html

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Presidential Symposium at the American Society of Gene and Cell Therapy (ASGCT) 20th Annual Meeting Will Feature ... - Yahoo Finance

Dr. Nathan Newman’s Stem Cell Lift Helps Women Get Their Sex Life Back! – Business Wire (press release)

BEVERLY HILLS, Calif.--(BUSINESS WIRE)--Stem cell therapy is revolutionizing medicine and now has come to the rescue once again, this time, to help those who suffer from a debilitating, auto-immune skin disease called Lichen Sclerosus (LS). For most patients, this condition attacks the genitalia causing unbearable burning and itching, as well as making sexual intercourse very painful and impossible for some. Severe symptoms can interfere with activities such as exercising, sitting for extended periods of time, or even wearing tight clothing. Previously reported that LS only occurs in post-menopausal women, recent reports, however, state that as many as one in 30 people may suffer from LS and yet, the information on this disease is sparse and relief is hard to find. To date, there is no known cure for this painful disease, which can also affect men and children.

The tragedy of Lichen Sclerosus, says Board Certified Dermatologist, Nathan Newman, M.D. of Beverly Hills, CA is that it often goes unrecognized for years and is frequently misdiagnosed as a post-menopausal change, a yeast infection, urinary tract infection or even a venereal disease, such as herpes. Until now, the main treatment for LS has been topical potent steroids to alleviate the symptoms. However, many patients report no symptomatic relief from conventional treatments and some even experience an exacerbation of symptoms.

Now, with the Stem Cell Lift developed by Dr. Newman, there is hope for these patients for not only relief of their symptoms, but also to help prevent disease progression. Dr. Newman, a well-known pioneer in stem cell therapy, developed his proprietary Stem Cell Lift over 16 years ago for post-cancer reconstruction, wound healing and the innovative, natural, scar-free, knife-free rejuvenating face lift. During this procedure, fat is removed from your own body and the stem cells found in this fat are concentrated and injected back into the treatment area. Stem cells are specialized cells that are genetically programmed to help repair, restore and replenish damaged cells and tissues in our body. Through my experience and knowledge of stem cell therapy, explains Dr. Newman, I knew that stem cells have been able to positively affect the immune response and put other auto-immune diseases in remission.

He applied his knowledge of stem cell therapy to treating patients suffering from LS with the Stem Cell Lift and is finding success in helping to alleviate the symptoms of Lichen Sclerosus. In fact, the first patient he treated for LS with the Stem Cell Lift has been in remission for almost four years.

Anna, a 56-year-old woman diagnosed two years ago with LS says, The fusing, burning and tearing were so painful, I couldnt sit down. Topical steroids were not providing her relief from her painful symptoms. After her first Stem Cell Lift treatment, Anna is thrilled to report she is experiencing 91-100% relief from her debilitating symptoms. ANNA VIDEO

To date, I have treated more than 150 patients with Lichen Sclerosus with the Stem Cell Lift, states Dr. Newman. Remarkably, 25% of these patients are in complete remission; meaning they have no symptoms and no disease progression. Most describe significant improvement in symptoms, are no longer using any topical steroids and do not have any anatomical changes. Patients report they can resume their normal activities, such as exercising, wearing jeans or underwear and are able to have intercourse without discomfort.

He adds, My staff and I are in constant contact with our Lichen Sclerosus patients to monitor their progress and to study the effectiveness of the Stem Cell Lift. Although all of his patients have reported significant overall improvement in their symptoms, most patients require 2-3 treatments to achieve optimal benefits. Dr. Newman continues, The Stem Cell Lift is showing very promising results in bringing relief to Lichen Sclerosus sufferers. Our hope is it will continue to result in remission of LS.

After discovering how little information is available to those who suffer from LS, Dr. Newman is dedicated to raising more awareness about it and is determined to help those suffering from this horrible disease. To achieve this personal mission, he is launching a campaign called #LS HOPE: Helping Open Peoples Eyes to Lichen Sclerosus in May 2017. His dream is to create an annual LS HOPE month every May.

For more information on Dr. Nathan Newman and his treatment of Lichen Sclerosus, please visit his website http://stem-cell-lift.com/ and LS link http://stem-cell-lift.com/lichen-sclerosus/ that includes videos of patient testimonials. Dr. Newman is located at 9301 Wilshire Boulevard, Beverly Hills, CA and can be reached at 310-273-3344.

Links to patient testimonials TRACI VIDEO LAURIE VIDEO

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Dr. Nathan Newman's Stem Cell Lift Helps Women Get Their Sex Life Back! - Business Wire (press release)