Category Archives: Stell Cell Research


Cromwell’s Biological Industries inks stem-cell training pact with Calif. Institute – Hartford Business

PHOTO | Steve Laschever

Biological Industries has a distribution-storage depot in Cromwell for its line of cell-culture media in which human and animal stem cells are grown.

Cromwell-based Biological Industries USA is partnering with a Monrovia, Calif.-based nonprofit stem cell institute to provide training for aspiring young scientists.

Biological Industries' partner, the Pathways to Stem Cell Science institute, will host early career scientists ranging from high school to college-level students and beyond and provide hands-on experience in culturing human pluripotent stem cells. Biological Industries will provide stem cell product and technology support through program scholarships for the Pathways to Stem Cell Science training programs.

The financial terms of the deal were not disclosed.

Biological Industries, which specializes in stem cell research, cellular reprogramming and regenerative medicine, is a division of Biological Industries Israel LTD. Pathways to Stem Cell Science programs provide classroom and laboratory-based courses in molecular cell biology, stem cell biology, and regenerative medicine to equip students with the skills to help them gain a competitive edge in the industry.

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Cromwell's Biological Industries inks stem-cell training pact with Calif. Institute - Hartford Business

Hundreds of new stem cell lines ready to help research – The San Diego Union-Tribune

Induced pluripotent stem cells have revolutionized stem cell science in the decade since their invention. Theyre yielding clues into the nature of diseases such as cancer and Alzheimers, and are also being tapped for therapy.

But creating these IPS cells is lengthy, complicated and tricky, and the facilities equipped to make them cant accommodate all the scientists whod like to get their hands on them.

A UK-led consortium has removed that bottleneck, by producing 711 lines of ready-to-go IPS cells from healthy individuals. These lines are meant to help scientists understand the normal variations between healthy individuals and those involved in disease, as well as to understand normal human biology and development.

The IPS lines are available for research purposes to academic scientists and industry by contacting the Human Induced Pluripotent Stem Cell Initiative (HipSci), at http://www.hipsci.org and the European Bank for induced Pluripotent Stem Cells at https://www.ebisc.org.

The accomplishment was announced in a study published in Nature. It can be found online at j.mp/711ips.

While many other efforts have generated IPS cells to address rare diseases, this study produces them from healthy volunteers to plumb common genetic variation, Fiona Watt, a lead author on the paper and co-principal investigator of HipSci, from King's College London, said in a statement.

"We were able to show similar characteristics of iPS cells from the same person, and revealed that up to 46 per cent of the differences we saw in iPS cells were due to differences between individuals, Watt said in the statement. These data will allow researchers to put disease variations in context with healthy people."

Andrs Bratt-Leal, director of the Parkinson's Cell Therapy Program at The Scripps Research Institute in La Jolla, agreed.

This kind of study is extremely important because it leads to a deeper understanding of the differences between normal genetic variation and genetic changes that could negatively impact cell behavior, said Bratt-Leal, who was not involved in the study.

This data will help scientists using induced pluripotent stem cells to model diseases as well as scientists developing cell therapies, said Bratt-Leal, who works in the lab of stem cell researcher Jeanne Loring.

Because DNA sequencing has become a routine tool in the lab, enormous amounts of data have been produced, he said. Not only have we have observed a high level of genetic diversity between different people, but also a more subtle variation exists among the cells from an individual person. The next step is a better understanding of how this diversity translates to function and behavior of stem cells and mature cells derived from stem cells.

Loring and Bratt-Leal are studying the use of induced pluripotent stem cells to relieve symptoms of Parkinsons disease. They are in the process of translating the research into a therapy, aided with a grant from the California Institute for Regenerative Medicine.

The work was the product of a large-scale collaboration of scientists from various institutions in the United Kingdom, including the European Molecular Biology Laboratory in Cambridge; Wellcome Trust Sanger Institute in Cambridge; the University of Dundee in Dundee; and the University of Cambridge. Also participating was St Vincent's Institute of Medical Research in Victoria, Australia.

bradley.fikes@sduniontribune.com

(619) 293-1020

UPDATES:

1:00 p.m.: This article was updated with additional details.

This article was originally published at 10:00 a.m.

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Hundreds of new stem cell lines ready to help research - The San Diego Union-Tribune

Growth in Stem Cell Research | Financial Tribune – Financial Tribune

Iran is expanding investment in stem cell research and its application in various therapies, particularly for hard-to-treat diseases, through the Office of the Vice- Presidency for Science and Technology. As a result of the increase in the number of companies active in the domain of stem cells in the past three years, more than 400 products are processed in the country, indicating a multifold growth compared with the eight-year tenure of previous administration when there were fewer than 50 knowledge-based firms in total.

There are over 40 knowledgebased firms in the field of stem cell and regenerative medicine alone in Iran today, said Amir Ali Hamidiyeh, secretary of the Headquarters for Development of Stem Cell Science and Technology (HDSCST). He made the statement at a press briefing for the second National Festival and International Congress on Stem Cell Sciences and Technologies and Regenerative Medicine to be held July 13- 15 in Tehran, Mehr News Agency reports. According to the conference secretariat, 1,444 people have signed up to attend the event from across the world, including from Iraq, India, Pakistan, Jordan, Russia, Australia, Germany, China, Britain and South Korea. They all are among their countrys respected figures in centers with high academic standing.

The congress is co-sponsored by the Vice-Presidency for Science and Technology and Council on Development of Stem Cell Sciences and Technology. So far, eight stem-cell therapy products for use in hospitals have been produced at the HDSCST laboratories. Manufacturinglicenses have been granted for anadditional number, while others are on thewait list.

Prior to 2014, only 25 knowledgebased companies had applied to operate in this field, of which only one was actively producing quality stem cell products, Hamidiyeh pointed out.

But since then, over 25 workgroups have been formed in cooperation with experts in the specific sciences. Stem cells are cells that have the ability to divide and develop into many different cell types in the body during early life and growth. Stem-cell therapy is the use of stem cells to treat or prevent a disease or condition. Bone marrow transplant is the most widely used stem-cell therapy, but some therapies derived from umbilical cord blood are also in use.

Future of Medicine in Stem

Cells The future of medicine is interrelated with stem cell therapy and the treatment ofrefractory and incurable diseases is in this field of medicine, according to Dr. Ahmad Vosouq Dizaj, the clinical deputy of Royan Institute. Having access to engineering sciences as well as the combination of biology and medicine can play a crucial role in redressing health problems, he said. Stem cells have the ability to replace damaged cells and treat disease. They can also be used to study diseases and provide a resource for testing new medical treatments. The use of stem cells reduces the risk of viral diseases transmission and incidence of Graft Versus Host Disease (GVHD). The ability to perform organ transplants is among the benefits ofumbilical cord blood transfusion.Using stems cells is also one of thebest ways to treat blood diseases sincethe method has a success rate of 70%worldwide.

Storage of stem cells is a valuable investment. So far, 27 cord blood banks have been launched across the country. There are two types: public and private banks for stem cell storage. The former does not charge a fee for storage. But in the latter, the cost of collection and genetictesting is about $645 and the annualcharge for storage is $33, according toISNA.Iran is a leading country in biomedicalresearch. Researchers and physicians have been successfully performing bone marrow transplants during the past fewyears.Irans stem cell research is centeredat the Royan Institute for ReproductiveBiomedicine, Stem Cell Biology andTechnology, located in northern Tehran.

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Growth in Stem Cell Research | Financial Tribune - Financial Tribune

Will Stem Cell Research Change Treatment of Heart Disease? – Health Essentials from Cleveland Clinic (blog)

Q: Ive been reading a lot about stem cells recently. Willstem cell research change the treatment of heart disease?

A: Theres some exciting early data where scientists have been able to use stem cells for regeneration of cardiac tissue, in particular certain parts of the heart or maybe even an entire heart in mice or rats.

Cleveland Clinic is a non-profit academic medical center. Advertising on our site helps support our mission. We do not endorse non-Cleveland Clinic products or services. Policy

However, its not been done yet in humans reliably and that would be the next step. If the research bears out, we may see this as an option for heart patients in perhaps five to 10 years.

The area where stem cells might first be used is in patients who have had damage to their heart because of a heart attack. These patients have scarring on the heart and that area of the heart is not beating anymore. If we can regenerate cardiac tissue to replace this scarred tissue, the hope is to get the heart fully working again.

Growing whole new hearts will likely be later down the line and will depend on the success of the research.

Preventive cardiologistHaitham Ahmed, MD, MPH

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Will Stem Cell Research Change Treatment of Heart Disease? - Health Essentials from Cleveland Clinic (blog)

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

My husband’s heart failure inspired a life-saving stem cell therapy – Telegraph.co.uk

Its our goal for this to be a normal NHS procedure, so everyone who has a heart problem [and could benefit from this] will be able to. There are few downsides because theres no rejection as theyre your own stem cells, and every patient who has successfully had this treatment ends up taking less medication.

Jenifer is overjoyed with the progress already made, and knows that Ian would be, too, had he lived to tell his story.

For Ian, the treatment gave him an extra three years of life, but in 2006 he died from heart failure, at the age of 70.

He would be so thrilled, says Jenifer. His concern would be were not doing it quick enough, because for him everything had to be done immediately. But to have achieved this much well, the medical world says weve done it all in a very short space of time.

The couple spent their final years together alternating between their family home in St Johns Wood, north London, and a holiday home in Miami.

They were both each others second spouses, having married in 1980 after a whirlwind romance in Cannes Jenifers first husband had died, while Ian had divorced his wife and did not have children together. But Ian had two children from his first marriage, as well as two young grandchildren who he was able to spend those extra three years with.

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My husband's heart failure inspired a life-saving stem cell therapy - Telegraph.co.uk

Cellaria and Biological Industries USA Partner on Stem Cell Media … – EconoTimes

Thursday, May 4, 2017 11:31 AM UTC

CAMBRIDGE, Mass. and CROMWELL, Conn., May 04, 2017 -- Cellaria, LLC, a scientific innovator that develops revolutionary new patient-specific models for challenging diseases, and Biological Industries USA (BI-USA), a subsidiary of Biological Industries (Israel), today announced a new sales and marketing agreement to promote custom stem cell services. The partnership combines BI-USAs strength in stem cell culture media and manufacturing with Cellarias comprehensive Stem Cell Services program, which includes industry leading RNA reprogramming and custom differentiation services. Together, the companies will offer one of the industrys most innovative and comprehensive stem cell service offerings available to biotechnology companies and academic institutions.

As part of the agreement, Cellaria will distribute BI-USAs stem cell media offering, including its NutriStem hPSC Medium, a cGMP xeno-free media specifically designed for human pluripotent stem cell culture. Cellaria will also incorporate the product into its stem cell services. BI-USA will market Cellaria's customized stem cell services, establishing an integrated, single source solution for iPS cell line derivation, culture maintenance, banking, characterization and differentiation services.

BI is one of the most respected names in life sciences today, said David Deems, chief executive officer at Cellaria. The companys strong market presence and innovative media products will enhance our stem cell and RNA reprogramming service offerings and significantly increase the availability and appeal of our combined offerings.

This is an important partnership for us, added Tanya Potcova, chief executive officer of BI-USA. In combination, our teams bring a wealth of stem cell experience but also share a common goal of creating higher quality, more consistent research outcomes for researchers in the life sciences field. We are pleased to be working with the team at Cellaria to put the best possible tools and support in the hands of our present and future customers.

Please visit Cellaria and BI at the International Society of Stem Cell Research Annual Meeting in Boston, MA June 14-17, 2017 at booth# 407.

About Cellaria Cellaria creates high quality, next generation in vitro disease models that reflect the unique nature of a patients biology. All models begin with tissue from a patient, capturing clinically relevant details that inform model characterization. For cancer, Cellarias cell models exhibit molecular and phenotypic characteristics that are highly concordant to the patient. For RNA-mediated iPS cell line derivation and stem cell services, Cellarias cell models enable interrogation of patient and disease-specific mechanisms of action. Cellarias innovative products and services help lead the research community to more personalized therapeutics, revolutionizing and accelerating the search for a cure. For more information, visitwww.cellariabio.com.

About Biological Industries Biological Industries (BI) is one of the worlds leading and trusted suppliers to the life sciences industry, with over 35 years experience in cell culture media development and cGMP manufacturing. BIs products range from classical cell culture media to supplements and reagents for stem cell research and potential cell therapy applications, to serum-free, xeno-free media. BI is committed to a Culture of Excellence through advanced manufacturing and quality-control systems, regulatory expertise, in-depth market knowledge, and extensive technical customer-support, training, and R&D capabilities.

Biological Industries USA (BI-USA) is the US commercialization arm of BI, with facilities in Cromwell, Connecticut. Members of the BI-USA team share a history and expertise of innovation and success in the development of leading-edge technologies in stem cell research, cellular reprogramming, and regenerative medicine. For more information, visit http://www.bioind.com or connect onLinkedIn,Twitter, andFacebook.

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Cellaria and Biological Industries USA Partner on Stem Cell Media ... - EconoTimes

California Today: Waiting on the Promise of Stem Cells – New York Times


New York Times
California Today: Waiting on the Promise of Stem Cells
New York Times
In 2004, voters approved Proposition 71, a bond measure amounting to $6 billion with interest, which created a stem cell agency to help fund research. It was in part a response to limits on federal funding for stem cell research imposed by the ...

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California Today: Waiting on the Promise of Stem Cells - New York Times

CIRM California’s stem cell research funding agency to lose … – San Francisco Business Times


Xconomy
CIRM California's stem cell research funding agency to lose ...
San Francisco Business Times
Randy Mills, who came in to right California's semi-public stem cell research funding agency, is leaving to head the National Marrow Donor Program. Mills three ...
CA Stem Cell Agency Chief Randy Mills to Leave After Three Years ...Xconomy
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CIRM California's stem cell research funding agency to lose ... - San Francisco Business Times

StemCONN Symposium Shows Connecticut is Leader in Stem Cell Research – Wesleyan Connection (blog)


Wesleyan Connection (blog)
StemCONN Symposium Shows Connecticut is Leader in Stem Cell Research
Wesleyan Connection (blog)
Stem cell research continues to be an exciting and fast-paced field with new discoveries fueling prospects for new therapies based on regenerative medicine for a range of debilitating medical conditions, and Connecticut is at the leading edge of this ...

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StemCONN Symposium Shows Connecticut is Leader in Stem Cell Research - Wesleyan Connection (blog)