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2014 ALS Ice Bucket Challenge – Tom Varner – Video

Posted: August 29, 2014 at 1:42 am


2014 ALS Ice Bucket Challenge - Tom Varner
I was challenged to do the 2014 ALS (Lou Gehrig #39;s Disease) Ice Bucket Challenge. I did not donate to the ALS Association because of their support of embryonic stem cell research. Instead, I...

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New Reprogramming Factor Cocktail Produces Therapy-Grade Induced Pluripotent Stem Cells

Posted: August 29, 2014 at 12:45 am

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Newswise CAMBRIDGE, Mass. (September 4, 2014) Induced pluripotent stem cells (iPSCs)adult cells reprogrammed back to an embryonic stem cell-like statemay hold the potential to cure damaged nerves, regrow limbs and organs, and perfectly model a patients particular disease. Yet through the reprogramming process, these cells can acquire serious genetic and epigenetic abnormalities that lower the cells quality and limit their therapeutic usefulness.

When the generation of iPSCs was first reported in 2006, efficiency was paramount because only a fraction of a percentage of reprogrammed cells successfully became cell lines. Accordingly, the stem cell field focused on reprogramming efficiency to boost the pool of cells that could be studied. However, as scientists gained an increased understanding of the reprogramming process, they realized that myriad variables, including the ratio of reprogramming factors and the reprogramming environment, can also greatly affect cell quality.

Now researchers working in the lab of Whitehead Institute Founding Member Rudolf Jaenisch together with scientists from the Hebrew University have determined that the reprogramming factors themselves impact the reprogramming efficiency and the quality of the resulting cells. Their work is described in the current issue of the journal Cell Stem Cell.

Postdoctoral researcher Yosef Buganim and Research Scientist Styliani Markoulaki show that a different combination of reprogramming factors may be less efficient than the original, but can produce much higher quality iPSCs, says Jaenisch, who is also a professor of biology at MIT. And quality is a really important issue. At this point, it doesnt matter if we get one colony out of 10,000 or one out of 100,000 cells, as long as it is of high quality.

To make iPSCs, scientists expose adult cells to a cocktail of genes that are active in embryonic stem cells. iPSCs can then be pushed to differentiate into almost any other cell type, such as nerve, liver, or muscle cells. Although the original combination of Oct4, Sox2, Klf4, and Myc (OSKM) efficiently reprograms cells, a relatively high percentage of the resulting cells have serious genomic aberrations, including aneuploidy, and trisomy 8, which make them unsuitable for use in clinical research.

Using bioinformatic analysis of a network of 48 genes key to the reprogramming process, Buganim and Markoulaki designed a new combination of genes, Sall4, Nanog, Esrrb, and Lin28 (SNEL). Roughly 80% of SNEL colonies made from mouse cells were of high quality and passed the most stringent pluripotency test currently available, the tetraploid complementation assay. By comparison, only 20-30% of high quality OSKM passed the same test. Buganim hypothesizes that SNEL reprograms cells better because, unlike OSKM, the cocktail does not rely on a potent oncogene like Myc, which may be causing some of the genetic problems. More importantly, the cocktail does not rely on the potent key master regulators Oct4 and Sox2 that might abnormally activate some regions in the adult cell genome.

To better understand why some reprogrammed cells are of high quality while others fall short, Buganim and Markoulaki analyzed SNEL colonies down to the genetic and epigenetic level. On their DNA, SNEL cells have deposits of the histone protein H2AX in locations very similar to those in ESCs, and the position of H2AX seems to predict the quality of the cell. The researchers believe this characteristic could be used to quickly screen for high quality colonies.

But for all of its promise, the current version of SNEL seems unable to reprogram human cells, which are generally more difficult to manipulate than mouse cells.

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2 Cases Suggest Stem Cell Transplant Might Ease 'Stiff Person' Syndrome

Posted: August 28, 2014 at 5:55 am

TUESDAY, Aug. 26, 2014 (HealthDay News) -- Two women with a rare disorder called stiff person syndrome recovered after receiving transplants of their own stem cells, a study shows.

Stiff person syndrome is rare neurological disease that causes stiffness of the skeletal muscles and painful muscle spasms. In severe cases, the disorder makes it difficult to move or walk.

Both of the women were treated in Canada by a team led by Dr. Sheilagh Sanders of the University of Ottawa.

Stem cell transplantation using a patient's own cells has been used successfully in patients with autoimmune diseases such as multiple sclerosis and scleroderma, the team noted. The treatment involves eliminating diseased immune cells and then regenerating the immune system with a person's own stem cells.

One of the women described in the new report began developing stiff person syndrome in 2005 when she was 48, the researchers said. She began suffering from progressively stiffer legs, overactive reflexes and frequent falling. The woman also, "walked with an abnormal 'tin soldier' gait," the team said.

Despite the use of medication, her condition got so bad that by late 2008 she was forced to quit work and had become "socially withdrawn."

Hoping to help, Sanders and her colleagues treated the woman in 2009 with transplanted stem cells taken from the patient's own body.

One month after the procedure, the patient no longer had symptoms and six months after the transplant she had returned to work and was playing sports.

Nearly five years later, the woman is still symptom-free, the team said.

The other woman was diagnosed with stiff person syndrome in 2008 at age 30, and had frequent spasms triggered by cold weather or stress. In the year prior to her stem cell transplant, she "made 47 emergency medical services calls with subsequent hospital visits and had required intensive care unit admission," Sanders' team said.

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Pfizer buys into Cambridge life science innovation

Posted: August 28, 2014 at 5:55 am

Stem cell technology pioneer,DefiniGEN Ltdhas joined the Pfizer-inspired European Bank for induced pluripotent stem cells (EBiSC) consortium.

The consortium comprises 26 partners, and has been newly-formed with support from the Innovative Medicines Initiative (IMI) and the European Federation of Pharmaceutical Industries and Associations (EFPIA).

DefiniGen, a Cambridge University spin-out that has raised millions, represents one of the first commercial opportunities to arise from the universitys expertise in stem cells and is based on the research of Dr Ludovic Vallier, Dr Tamir Rashid and Professor Roger Pedersen of the universitys Anne McLaren Laboratory of Regenerative Medicine.

The EBiSC iPS cell bank will act as a central storage and distribution facility for human iPS cells, to be used by researchers across academia and industry in the study of disease and the development of new therapeutics. DefiniGENs role will be to validate EBiSC iPS cell lines by generating liver hepatocyte cells for toxicology, disease modelling, and regenerative medicine applications.

Dr Marcus Yeo, CEO of DefiniGEN, said: We are delighted to be a part of this ground-breaking consortium which will provide a crucial platform resource to enable the realisation of the full potential of iPS technology.

Conceptualised and coordinated by Pfizer Ltd in Cambridge, UK and managed by Roslin Cells Ltd in Edinburgh, the EBiSC bank aims to become the European go to resource for high quality research grade human iPS cells.

Today, iPS cells are being created in an increasing number of research programmes underway in Europe, but are not being systematically catalogued and distributed at the necessary scale to keep pace with their generation, nor to meet future demand.

The 35 million project will support the initial build of a robust, reliable supply chain from the generation of customised cell lines, the specification to internationally accepted quality criteria and their distribution to any global qualified user, ensuring accessibility to consistent, high quality tools for new medicines development.

Ruth McKernan, CSO of Pfizers Neusentis research unit in Cambridge, said: We are excited to be a part of this precompetitive collaboration to build a sustainable repository of high quality human iPS cell lines.

For many areas of research in academia and in industry, understanding the biological basis of disease heterogeneity is the next horizon. A bank of well-characterised iPS lines with strong relevance to the entire research community will help us all in our mission to bring therapies to patients.

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biotechnology — Encyclopedia Britannica

Posted: August 28, 2014 at 5:49 am

biotechnology,the use of biology to solve problems and make useful products. The most prominent area of biotechnology is the production of therapeutic proteins and other drugs through genetic engineering.

People have been harnessing biological processes to improve their quality of life for some 10,000 years, beginning with the first agricultural communities. Approximately 6,000 years ago, humans began to tap the biological processes of microorganisms in order to make bread, alcoholic beverages, and cheese and to preserve dairy products. But such processes are not what is meant today by biotechnology, a term first widely applied to the molecular and cellular technologies that began to emerge in the 1960s and 70s. A fledgling biotech industry began to coalesce in the mid- to late 1970s, led by Genentech, a pharmaceutical company established in 1976 by Robert A. Swanson and Herbert W. Boyer to commercialize the recombinant DNA technology pioneered by Boyer and Stanley N. Cohen. Early companies such as Genentech, Amgen, Biogen, Cetus, and Genex began by manufacturing genetically engineered substances primarily for medical and environmental uses.

For more than a decade, the biotechnology industry was dominated by recombinant DNA technology, or genetic engineering. This technique consists of splicing the gene for a useful protein (often a human protein) into production cellssuch as yeast, bacteria, or mammalian cells in culturewhich then begin to produce the protein in volume. In the process of splicing a gene into a production cell, a new organism is created. At first, biotechnology investors and researchers were uncertain about whether the courts would permit them to acquire patents on organisms; after all, patents were not allowed on new organisms that happened to be discovered and identified in nature. But, in 1980, the U.S. Supreme Court, in the case of Diamond v. Chakrabarty, resolved the matter by ruling that a live human-made microorganism is patentable subject matter. This decision spawned a wave of new biotechnology firms and the infant industrys first investment boom. In 1982 recombinant insulin became the first product made through genetic engineering to secure approval from the U.S. Food and Drug Administration (FDA). Since then, dozens of genetically engineered protein medications have been commercialized around the world, including recombinant versions of growth hormone, clotting factors, proteins for stimulating the production of red and white blood cells, interferons, and clot-dissolving agents.

In the early years, the main achievement of biotechnology was the ability to produce naturally occurring therapeutic molecules in larger quantities than could be derived from conventional sources such as plasma, animal organs, and human cadavers. Recombinant proteins are also less likely to be contaminated with pathogens or to provoke allergic reactions. Today, biotechnology researchers seek to discover the root molecular causes of disease and to intervene precisely at that level. Sometimes this means producing therapeutic proteins that augment the bodys own supplies or that make up for genetic deficiencies, as in the first generation of biotech medications. (Gene therapyinsertion of genes encoding a needed protein into a patients body or cellsis a related approach.) But the biotechnology industry has also expanded its research into the development of traditional pharmaceuticals and monoclonal antibodies that stop the progress of a disease. Such steps are uncovered through painstaking study of genes (genomics), the proteins that they encode (proteomics), and the larger biological pathways in which they act.

In addition to the tools mentioned above, biotechnology also involves merging biological information with computer technology (bioinformatics), exploring the use of microscopic equipment that can enter the human body (nanotechnology), and possibly applying techniques of stem cell research and cloning to replace dead or defective cells and tissues (regenerative medicine). Companies and academic laboratories integrate these disparate technologies in an effort to analyze downward into molecules and also to synthesize upward from molecular biology toward chemical pathways, tissues, and organs.

In addition to being used in health care, biotechnology has proved helpful in refining industrial processes through the discovery and production of biological enzymes that spark chemical reactions (catalysts); for environmental cleanup, with enzymes that digest contaminants into harmless chemicals and then die after consuming the available food supply; and in agricultural production through genetic engineering.

Agricultural applications of biotechnology have proved the most controversial. Some activists and consumer groups have called for bans on genetically modified organisms (GMOs) or for labeling laws to inform consumers of the growing presence of GMOs in the food supply. In the United States, the introduction of GMOs into agriculture began in 1993, when the FDA approved bovine somatotropin (BST), a growth hormone that boosts milk production in dairy cows. The next year, the FDA approved the first genetically modified whole food, a tomato engineered for a longer shelf life. Since then, regulatory approval in the United States, Europe, and elsewhere has been won by dozens of agricultural GMOs, including crops that produce their own pesticides and crops that survive the application of specific herbicides used to kill weeds. Studies by the United Nations, the U.S. National Academy of Sciences, the European Union, the American Medical Association, U.S. regulatory agencies, and other organizations have found GMO foods to be safe, but skeptics contend that it is still too early to judge the long-term health and ecological effects of such crops. In the late 20th and early 21st centuries, the land area planted in genetically modified crops increased dramatically, from 1.7 million hectares (4.2 million acres) in 1996 to 160 million hectares (395 million acres) by 2011.

Overall, the revenues of U.S. and European biotechnology industries roughly doubled over the five-year period from 1996 through 2000. Rapid growth continued into the 21st century, fueled by the introduction of new products, particularly in health care.

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Stem Cell Therapy as a Treatment Option for Osteoarthritis – Video

Posted: August 28, 2014 at 5:47 am


Stem Cell Therapy as a Treatment Option for Osteoarthritis
Dr. Frank Garcia, board certified orthopedic surgeon with The San Antonio Orthopaedic Group, discusses the use of stem cell therapy in the treatment of osteo...

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STEM CELL THERAPY: with DR ANDREW J. ROCHMAN – Video

Posted: August 28, 2014 at 5:47 am


STEM CELL THERAPY: with DR ANDREW J. ROCHMAN
Dr. Andrew J Rochman is a leader in advanced surgical techniques, a native New Yorker and a Board-Certified Surgeon. His current undertaking involves promoting an educational advocacy in MODERN...

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Faith based organizations critical of ALS Association's research

Posted: August 27, 2014 at 8:57 pm

BIRMINGHAM, AL (WBRC) -

The concern that's being voiced by some individuals and groups, including some faith based organizations, is that the group receiving most of the donations, the ALS Association, conducts research using immoral methods.

But officials with the ALS Association say get all the facts before you make that decision.

Through the ice bucket challenge, close to $90 million has now been raised for ALS research.

"It's unprecedented, nothing we planned and more than we could have ever hoped for," said Cassie Barnes, Executive Director of the ALS Association's Alabama Chapter.

The majority of the money raised has gone to the ALS Association. But now some groups, including the Catholic Diocese of Birmingham, are urging people not to give to that group saying they conc duct research using embryonic stem cells.

"We have to be mindful of how they do their research. Not all medical research will respect life and the catholic church teaches we should respect life from the moment of conception to natural death. Father Doug Vu said, Spokesperson for the Catholic Diocese of Birmingham.

Father Vu stresses the Catholic Church is not against the challenges or finding a cure for any disease

"But we can never destroy life in hopes of finding a cure for sickness and or illness society might have," Father Vu said.

Cassie Barnes is head of the ALS Association's Alabama chapter and says yes, there is one single research project funded by the national chapter that uses embryonic stem cells.

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Catholic Church warns against ALS Association donations

Posted: August 27, 2014 at 8:55 pm

The Cincinnati Archdiocese in Ohio is warning Catholic school principals against donations to the Amyotrophic Lateral Sclerosis (ALS) Association.

This warning comes after the ALS's Ice Bucket Challenge went global bringing in more than $80 millionin a campaign to raise awareness for the condition.

ALS, also known as Motor Neurone Disease, is a neurodegenerative disease affecting nerve cells in both the brain and the spinal cord. The Ice Bucket Challenge, supporting the campaign, has become a pop culture and social media phenomenon.

Social networking sites like Facebook and Instagram are riddled with videos of people dumping buckets of ice water on their heads.They then challenge others to follow suit within the next 24 hours, and those who reject the challenge are encouraged to donate $100 to an ALS charity.

However, the Catholic Church has its concerns about the destination of these donations.

The Cincinatti Archdiocese has warned the pro-life community and Ohio Catholic schools to be wary when participating in the challenge as there is a chance donations made to the ALSA may end up contributing to embryonic stem cell research.

TheALSA has confirmed it supports research involving the destruction of embryos to find cures for the disease, according to Life News. Specifically, Life News reports that the ALSA supportsthe Northeast ALS Consortium, a clinical researcher.

Carrie Munk, a spokeswoman for the ALSA, confirmed in an email to Religion News Service, that the ALSA primarily funds stem cell research.

Munk stated: "Currently, The Association is funding one study using embryonic stem cells (ESC), and the stem cell line was established many years ago under ethical guidelines set by the National Institute of Neurological Disorders and Stroke (NINDS); this research is funded by one specific donor, who is committed to this area of research. The project is in its final phase and will come to an end very soon."

Catholic Church officials are encouraging pro-lifers to select a "pro-life-friendly" alternative when participating in the challenge.

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Seven days: 2228 August 2014

Posted: August 27, 2014 at 8:54 pm

Policy | Research | Events | People | Business | Trend watch | Coming up

Science adviser The post of chief scientific adviser to the European Commission came under attack again on 19August when nearly two dozen non-governmental organizations called on the incoming president of the commission to scrap the job. In an open letter to Jean-Claude Juncker, groups including Friends of the Earth Europe added their weight to an existing campaign to abolish the science role. The letter argues that the position concentrates too much influence in one person. The mandate of the commissions current chief scientific adviser, Anne Glover, is scheduled to end later this year.

Trial enrolment The US Food and Drug Administration published a plan on 20August to ensure that women and racial and ethnic minority groups are adequately included in clinical trials. The action plan aims to collect data on population subgroups in trials, to encourage and enable more women and minority groups to enrol, and to make the demographic make-up of trials more transparent. It will be implemented in stages over the next five years. The agency also published guidance on evaluating how medical devices might function differently in men and women.

Helm et al./The Cryosphere

Satellites pinpoint ice loss The massive ice sheets in Antarctica (pictured) and Greenland are together shrinking at a rate of 500 cubickilometres per year the fastest pace since satellite altimetry began 20 years ago. The European Space Agencys CryoSat-2 probe collected precise elevation data for both ice sheets (Antarcticas shown on right). The greatest ice loss (shown on left in red) between 2011 and 2014 occurred at Pine Island glacier in western Antarctica and at Jakobshavn glacier in Greenland. The findings were reported on 20August by researchers from the Alfred Wegener Institute in Potsdam, Germany (V.Helm et al.Cryosphere 8, 15391559; 2014).

MERS model Marmosets are the best animal model for Middle Eastern Respiratory Syndrome (MERS). Research on the MERS coronavirus was hindered by the lack of an animal model that showed the same respiratory symptoms as humans when infected with the virus. In two studies published on 21 August, researchers from the US National Institute of Allergy and Infectious Diseases showed that the virus could infect marmosets, and that the animals symptoms mimic the severe pneumonia seen in humans (D.Falzarano etal. PLoS Pathog. 10, e1004250 (2014); N. van Doremalen et al. J. Virol. 88, 92209232 (2014)).

African farming The Alliance for a Green Revolution in Africa (AGRA), a science-based non-governmental organization in Nairobi has helped 1.7million African farmers to rejuvenate 1.6million hectares of land, and to double, or even triple, crop yields over the past five years through its Soil Health Programme. AGRA reported the results on 22 August. The programme tests and teaches techniques to improve soil fertility and makes chemical fertilizers more affordable for poor farmers. Depleted soils cost African farmers US$4billion a year in lost productivity.

Stem-cell go-ahead Regulators in the United States have cleared the way for a clinical trial of a prospective stem-cell-derived treatment for type 1 diabetes. On 19August, ViaCyte of San Diego, California, said that the Food and Drug Administration has given it permission for a phase I/II clinical trial of a product that consists of pancreatic precursor cells packaged in a mesh pouch. ViaCytes treatment could become one of only a handful of human embryonic-stem-cell-derived products to be trialled in people, and will be an important test for the effectiveness of Californias state stem-cell institute, which provided funding to develop the product.

Icelandic volcano After a reported eruption on 23August turned out to be a false alarm, Icelands Brarbunga volcano continued to rumble deep underground. Since seismic activity began on 16August, thousands of earthquakes have shaken the ground north and east of the volcano. They show where magma is squirting up from below and forming a freshly cooled sheet of rock, or dyke, a few kilometres deep. As of 25August, the dyke was thought to be nearly 35kilometres long and to contain 300million cubic metres of magma. Aviation authorities remained on alert in case an eruption spewed ash into the air. See go.nature.com/iidaau for more.

Ebola in fifth nation The Democratic Republic of Congo became the fifth African nation to confirm cases of Ebola, on 24August. On the same day, a Senegalese epidemiologist was reported as the first person working for the World Health Organization (WHO) to contract the disease. On 22August, the WHO said that the official count of 2,615cases and 1,427deaths probably underestimates the true size of the epidemic. It blamed community resistance to reporting cases and a lack of adequate treatment facilities. The agency thinks that the epidemic could last for another 9months. See page355 for more.

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