Monthly Archives: February 2017

Biotechnology | University of Wisconsin River Falls

Posted: February 10, 2017 at 11:44 am

Mission Statement

The mission of the Biotechnology Program at the University of Wisconsin-River Falls is to provide its students with an education that establishes a strong foundation and appreciation for understanding developments in the rapidly advancing field of biotechnology, to develop the technical and critical thinking skills necessary for success in the field, to foster ethical behavior, and to promote outreach.

The field of modern biotechnology was born of molecular biology and biochemistry. Modern Biotechnology provides a set of tools that allow scientists to modify and harness the genetic capabilities of organisms. This has led to rapid advances in many areas including pharmaceutical development, agriculture, food microbiology, medical devices and environmental sciences.

Some examples of the products of biotechnology include herbicide, drought and insect resistant crops, drugs targeted specifically to disease processes resulting in fewer side effects, and bioremediation capable of removing greater amounts of environmental toxins at reduced cost.

The Biotechnology major at UWRF is an interdepartmental program with an emphasis on the molecular basis of life and the techniques utilized to study and control these processes under in vivo, in vitro, and commercial production conditions. UWRF LogoThe Biotechnology curriculum is an integrated sequence of courses selected from the curricula of the departments of Biology, Chemistry, Physics, Animal and Food Science, and Plant and Earth Science. It includes both traditional offerings of the departments involved and courses that reflect advances in biochemistry, biophysics, and molecular biology. The Biotechnology major is designed to provide students interested in pursuing careers in this rapidly expanding field with the academic background required to either secure entry level positions in industry or to continue their education in graduate or professional schools. A student may complete a B.S. degree in Biotechnology in the College of Arts and Sciences or the College of Agriculture, Food and Environmental Sciences.

Current curriculum check list (2008-2009)

Planning sheets

A scholarship has been established that is awarded to an outstanding junior or senior biotechnology major that either has worked on a research project, or will be participating in a research project during the year of the scholarship award. Follow the link above for information regarding scholarship criteria, recipients of the scholarship, and contributing to the scholarship fund.

Assessment of student learning is important to the University, the Colleges and the Biotechnology Program. Through appropriate assessment practices, we maintain a strong, current degree program and improve the quality of the education our students receive.

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Biotechnology | University of Wisconsin River Falls

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Revolutionizing Biotechnology with Artificial Restriction Enzymes … – Genetic Engineering & Biotechnology News (press release)

Posted: February 10, 2017 at 11:44 am

Scientists at the University of Illinois say they have developed a new technique of genetic engineering for basic and applied biological research and medicine. Their work ("Programmable DNA-Guided Artificial Restriction Enzymes"), reported inACS Synthetic Biology,could open new doors in genomic research by improving the precision and adherence of sliced DNA, according to the investigators.

"Using our technology, we can create highly active artificial restriction enzymes with virtually any sequence specificity and defined sticky ends of varying length," said Huimin Zhao, Ph.,D., professor of chemical and biomolecular engineering, who leads a synthetic biology research group at the Carl R. Woese Institute for Genomic Biology at Illinois. "This is a rare example in biotechnology where a desired biological function or reagent can be readily and precisely designed in a rational manner."

Restriction enzymes cut DNA at a specific site and create a space wherein foreign DNA can be introduced for gene-editing purposes. This process is not achieved only by naturally occurring restriction enzymes; artificial restriction enzymes, or AREs, have risen to prominence in recent years. CRISPR/Cas9, a bacterial immune system used for "cut-and-paste" gene editing, and TALENs, or transcription activator-like effector nucleases, which are modified restriction enzymes, are two popular examples of such techniques.

Though useful in genetic engineering, no AREs generate defined "sticky ends"an uneven break in the DNA ladder structure that leaves complementary overhangs, improving adhesion when introducing new DNA. "If you can cleave two different DNA samples with the same restriction enzyme, the sticky ends that are generated are complementary," explained graduate student Behnam Enghiad. "They will hybridize with each other, and if you use a ligase, you can stick them together."

However, restriction enzymes themselves have a critical drawback: the recognition sequence that prompts them to cut is very short, usually only four to eight base pairs. Because the enzymes will cut anywhere that sequence appears, researchers rely on finding a restriction enzyme whose cut site appears only once in the genome of their organism or plasmid, an often difficult proposition when the DNA at hand might be thousands of base pairs long.

This problem has been partially solved simply by the sheer number of restriction enzymes discovered: more than 3600 have been characterized, and over 250 are commercially available. "Just in our freezer, for our other research, we have probably over 100 different restriction enzymes," said Enghiad. "We look through them all whenever we want to assemble something. The chance of finding the unique restriction site is so low."

"Our new technology unifies all of those restriction enzymes into a single system consisting of one protein and two DNA guides. Not only have you replaced them, but you can now target sites that no available restriction enzymes can."

The new method creates AREs through the use of an Argonaute protein (PfAgo) taken fromPyrococcus furiosus, an archeal species. Led by a DNA guide, PfAgo is able to recognize much longer sequences when finding its cut site, increasing specificity and removing much of the obstacles posed by restriction enzymes. Furthermore, PfAgo can create longer sticky ends than even restriction enzymes, a substantial benefit as compared to other AREs.

"When we started, I was inspired by a paper about a related proteinTtAgo. It could use a DNA guide to cleave DNA, but only up to 70 degrees," continued Enghiad. "DNA strands start to separate over 75 degrees, which could allow a protein to create sticky ends. If there were a protein that was active at higher temperatures, I reasoned, that protein could be used as an artificial restriction enzyme. SoI started looking for that, and what I found was PfAgo."

In addition to replacing restriction enzymes in genetic engineering processes, Enghiad and Dr. Zhao believe their technology will have broad applications in the biological research. By creating arbitrary sticky ends, PfAgo could make assembly of large DNA molecules easier and would enable cloning of large DNA molecules, such as biochemical pathways and large genes.

The application of these techniques is broad-reaching, they say, ranging from discovery of new small-molecule drugs to engineering of microbial cell factories for synthesis of fuels and chemicals to molecular diagnostics of genetic diseases and pathogens, which are the areas Dr. Zhao and Enghiad are currently exploring.

"Due to its unprecedented simplicity and programmability (a single protein plus DNA guides for targeting), as well as accessibility...we expect PfAgo-based AREs will become a powerful and indispensable tool in all restriction enzyme or nuclease-enabled biotechnological applications and fundamental biological research," predicts Dr. Zhao. "It is to molecular biology as the CRISPR technology is to cell biology."

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Harry Boxer’s stocks to watch: biotechnology and technology … – MarketWatch

Posted: February 10, 2017 at 11:44 am

Biotechnology and technology stocks are dominating our charts to watch this week, because they are displaying strong technical momentum.

Esperion Therapeutics Inc. ESPR, +0.54% is absolutely rocketing. The clinical-stage biopharma, which is focused on developing drugs that treat cardiovascular disease, popped 29% on Friday in response to good clinical news from Amgen AMGN, -0.10% regarding its own cardiovascular drug. The stock followed through on Monday and then again Tuesday, up $2.48, or 14%, to $20.14 on nearly 3.4 million shares traded. The stock pulled back toward the close, testing the bottom of its rising channel and resting in a tight wedge formation. This formation looks poised to break to the upside, with the next target at the channel top near $22.

Exelixis Inc. EXEL, -1.69% also had a strong session on Tuesday, up 54 cents, or 2.7%, to $20.57, on nearly 6.7 million shares traded. The cancer-drug companys stock needs to get through the rising trendline, near $21, connecting the most recent tops from September, December and January. The challenge beyond that would be the mid-channel line at around $22.75, a break through that could accelerate the stock into the high $20s.

Finisar Corp. FNSR, +2.37% edged above resistance on Tuesday, though closed slightly below it, up 76 cents, or 2.5%, to $30.89, on 2.7 million shares. The provider of optical subsystems for data communications recently traversed from the top of its price channel at around $37 in December to the bottom just above $27 on January 23, before rallying in the last two weeks. The stock did close above its 50-day moving average at $30.77 on Tuesday, and a break above current levels could get it to $33.25 next, followed by $35.50.

KEMET Corp. KEM, +3.40% has been in a steady rising channel since its breakout in November. The stock last week bounced off the channel bottom and rallied after the electronic-capacitor maker beat Wall Streets third-quarter earnings and revenue forecasts. The stock popped on Thursday and Friday, had an inside day on Monday (remaining inside the price range from Friday), and on Tuesday it had another solid day, up 17 cents, or 2.2%, to 7.81, on 652,900 shares traded. The stock looks like its about to take out the $7.90 area, and run up toward the channel top in the $9-$9.75 area.

See Harrys video chart analysis on these and other stocks.

The writer has no investments in the stocks mentioned in this column.

Harry Boxer is the founder of TheTechTrader.com, a live trading room featuring his stock picks, technical market analysis and live chart presentations.

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Harry Boxer's stocks to watch: biotechnology and technology ... - MarketWatch

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Biotechnology Considerations for the Unitary Patent System in Light of Brexit and Other Current Developments – JD Supra (press release)

Posted: February 10, 2017 at 11:44 am

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‘Economical stem cell treatment will revolutionise medicine’ – The Hindu

Posted: February 10, 2017 at 11:42 am

Cost-effective stem cell treatment has to be the next revolution to transform personalised treatment of patients, said Hunterian Professorship Awardee A.A.Shetty. Speaking at a felicitation function, Dr. Shetty said there is a need to create awareness about stem cells and patient-specific treatment specifically designed for individuals.

It is going to be simple, with minimal complications. Our role is to make it cost effective. Once it happens, it will revolutionise treatment, said Dr. Shetty.

Surgery using stem cell technology is developing at a rapid pace and the role of stem cell therapy in Orthopaedics is gaining importance, said Trauma and Orthopaedic Speciality Hospital (TOSH) Managing Director S.H. Jaheer Hussain. The ability of stem cells to transform into bone and cartilage has given a new dimension in the treatment of osteoarthritis, fracture non union, ligament tears. Stem cells have shown significant clinical results in osteoarthritis and cartilage defects. Recent advances in stem cells centrifuging techniques have lead to the introduction of the new concept of single- stage knee cartilage regeneration.

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'Economical stem cell treatment will revolutionise medicine' - The Hindu

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Hopkins researchers discover newborn rats hold secret to … – Baltimore Sun

Posted: February 10, 2017 at 11:42 am

Human heart muscle cells can be created in the lab, but researchers have been unable to grow the immature cells to the point where they could be useful.

It's a conundrum that's stumped researchers in regenerative medicine.

"You cannot really use them for regeneration. You cannot even use them for disease models," said Chulan Kwon, a professor at the Johns Hopkins School of Medicine.

But Kwon said he's discovered a solution for the problem in an unlikely place newborn rats and he published a study about his reasearch last month in the journal Cell Reports.

When immature human heart cells are injected into baby rats, they match the rodents' rapid growth cycle and develop fully. These rats act as living incubators, said Dr. David Kass, a Hopkins professor and cardiologist who co-authored the study.

"The biological environment gives you whatever the magic juice is," Kass said. "There were a lot of people looking for this magic juice."

Researchers at the University of Washington, Harvard and Stanford universities and beyond have been working to solve this puzzle fundamental to regenerative medicine.

"Laboratories throughout the world are working on this," said Dr. Richard Lee, a Harvard professor of stem cell and regenerative biology. "We are all very excited that we can make heart cells, but they're heart cells like an infant's heart cells. We want to make heart cells like our patients, who are mostly adults."

Lee said his research team is working to unravel the conditions that stimulate cells to mature inside the body. He praised the Hopkins discovery.

"It's a very nice step forward," Lee said.

Dr. Charles Murry at the University of Washington also has tried to grow the cells to maturity.

"We tried a whole lot of things that didn't work," he said. "Sort of like Edison and the light bulb."

Murry has seen some positive signs when feeding the cells fat instead of sugar.

"But we haven't seen anything that works as well as putting them back into their natural environment, which is back into a heart," he said.

Soon after the late 1990s when researchers isolated embryonic stem cells, people in the field wondered if the process could be used to grow heart muscles in the lab and someday repair the lasting damage from heart attacks and disease. Researchers in 2007 developed methods to modify skin cells to behave as stem cells, and, about five years later, Murry's research team at the University of Washington developed techniques to activate these modified skin cells into early forms of heart muscle cells.

From there researchers have worked to fully develop them into heart cells, a feat that has proven elusive.

Kass, the Hopkins researcher, compares the cell to a car engine. In an undeveloped state, the engine parts are present but scrambled, so the engine doesn't function.

"When you look at a normal heart muscle cell, it's an exquisitely complicated and well organized engine. Every little protein has to be positioned precisely," Kass said. "This doesn't work if they're willy-nilly, oriented randomly and loosely around the cell."

These undeveloped cells have about 1 percent of the pumping force of an adult heart cell, Kwon said.

"The frustrating thing is even if you culture the dish for more than a year," he said, "they're just kind of stuck in embryonic stages."

Around the summer of 2013, he began experimenting with rats. He uses newborn rats engineered to have no immune system. This ensures the pups don't reject the foreign cells. Mouse hearts were too small.

He injects the rat hearts with as many as 200,000 human cells. These human cells are tagged with a protein that glows green or red under fluorescent light. After about a week, the cells remained immature. But after a month, they appeared developed. The researchers tested these cells and found they could contract or beat precisely like an adult heart cell.

The researchers suspect two forces at play: The rats faster life cycle quickens the cells' development. And the rats' biological cues cause the cells to leap the threshold into maturity.

"So the million dollar question would be: What are those cues?" Kwon said.

Their work was published Jan. 10 in Cell Reports, an open-access journal, and they're still trying to pinpoint the cues.

Further discoveries might allow them to replicate the cues in a petri dish and expedite cell growth by avoiding the delicate injections into rat hearts. While promising, their methods remain too small in scale to offer much help to patients. At least, not yet.

"It has to be a bit more practical," Kass said. "If you're injecting things into rat neonates, they're small. So how many cells can you really get in there, and how many can you actually find?"

The abillity to culture larger quantities would allow doctors to test heart medicines on a patients' own cells, furthering the emerging trend of precision medicine.

In 2015, President Barack Obama announced a $215 million precision medicine initiative aimed at developing treatments that consider someone's genes, environment and lifestyle. The grant money funds efforts at the National Institutes of Health and the National Cancer Institute to advance such treatments.

Dr. Roberto Bolli at the University of Louisville School of Medicine sees potential in the rat method for screening patients with different medicines. Doctors could swab the cheek of a particular patient, modify the cheek cells to behave as stem cells, activate them into early heart cells, and inject them into the rats.

Once grown, the cells could be tested with various treatments.

"This would help tremendously to understand the mechanism or these hereditary diseases and also screen for drugs," Bolli said.

The Hopkins researchers are taking steps to produce more mature cells. Kwon said they will try the method with pig hearts, which are larger and can hold more implanted cells.

"If we can really scale this up," he said, "it has a lot of utilities."

tprudente@baltsun.com

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IFT20 protein’s role in helping cancer cells to invade – Science Daily

Posted: February 10, 2017 at 11:42 am

IFT20 protein's role in helping cancer cells to invade
Science Daily
This research was carried out by an international team including Associate Professor NISHITA Michiru (Kobe University Graduate School of Medicine Department of Physiology and Cell Biology), Professor MINAMI Yasuhiro (Kobe University Graduate School ...

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I believe that this will be the next generation of medicine. Area … – WTHITV.com

Posted: February 10, 2017 at 11:42 am

VINCENNES, Ind. (WTHI) In the past, new moms would be asked if they wanted to save their umbilical cord blood for future, personal use.

But at one area hospital, a new partnership is taking that concept and making it public.

Amelia Nance and her fianc just welcomed their second child on Monday, a baby boy named Finn.

The new mom says, Its neat to be a part of something thats growing in a positive way.

Nance just donated the umbilical cord, cord blood, placenta, and amniotic fluid from Finns birth to Life Line Stem Cell.

Its a partnership at Good Samaritan Hospital thats just weeks old.

However, officials say around 90% of patients take part in the program.

Margaret Suozzi, MSN/RN is the Director of Women & Children Services at Good Samaritan.

She says, Like any program we havent been up and running long enough to have monthly stats yet, but we anticipate that we will be pretty close to that even from the very beginning. And any time you start a new program, its always one of those things where theyre like, What does this mean? What do I do?'

One of the first questions asked is, Does this cost anything? The answer is no. It is a free service.

Since being a new or expecting mom is hard enough, Life Line has narrowed the donation process down to a questionnaire.

Nance says, The form is actually really simple its pretty laid out, open questions, it asks you about your history, your parents history.

If the tissues werent donated they would be properly disposed of by the hospital.

Suozzi says that could mean missing out on countless possibilities to change someone elses life.

Suozzi says, I believe that this will be the next generation of medicine. We are already finding a million things that stem cells can do for our existing patients in other areas: diabetics, wound care, Chrons disease, and many other things. And I think it is the tip of the ice berg. So for our patients to be able to donate to the cause and to be able to help others, is just one sign of Indiana hospitality.

Life Line Stem Cell allows the family that provides the tissue first dibs if a family member could benefit from the blood.

But after that, its donated to a registry for public use.

Thats part of the reason Nance decided she wanted to take part.

The new mom says, I would say its excellent. The fact that, again, it was absolutely no cost to me, it didnt hurt our child, and we could donate it and it could possibly help him out again or you know, one of my family members. Ive had family members thats died of cancer or different diseases. And its nice to know that there can possibly be research done with this blood that would help progress you know, a cure or even just something that would help prolong a positive future for somebody. Whether it be a kid or a child with a disease that might otherwise be painful or negative in their life.

A rep for Life Line Stem Cell says one placenta can be used to heal as many as 100 eyes.

He says amniotic fluid is showing great results in the healing process for burn victims too.

Tricia Crowe is a Life Line Stem Cell Training Manager. She says, It is important that families understand that we are only using hematopoietic blood cells that are found in the umbilical cord and are blood forming. They give rise to red blood cells, white blood cells and platelets.

Suozzi says Good Samaritan is the only hospital in the Southwest region that is offering this program.

For more information on stem cell donation, contact Good Samaritans Women and Infants Center at 812-885-3369 or click here.

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I believe that this will be the next generation of medicine. Area ... - WTHITV.com

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Why does type 1 diabetes kill some cells but not others? – Medical News Today

Posted: February 10, 2017 at 11:40 am

Diabetes is a serious disease affecting millions of people in the United States, adults and children alike. While there is yet no cure for diabetes, researchers are gradually learning more about the mechanism behind the illness. New research identifies how insulin-producing cells can change to avoid the autoimmune attack present in type 1 diabetes.

The Centers for Disease Control and Prevention (CDC) report that more than 29 million people (or over 9 percent of the population) currently have diabetes in the U.S.

Although type 1 diabetes is the least prevalent - accounting for only 5 percent of diabetes cases - it is not yet known how to prevent the illness.

Type 1 diabetes is an autoimmune disease. The body does not recognize its own insulin-producing beta cells, so the immune system attacks and destroys them as if they were invaders. The body needs insulin to metabolize sugar and turn it into energy.

However, of these beta cells, some manage to survive. In fact, some of the cells persist and proliferate for years after the disease has started.

New research, led by professor of immunobiology Dr. Kevan Herold of Yale University in New Haven, CT, identifies the mechanism that explains how these beta cells survive the immune attack. The study was a collaboration with the Broad Institute of Massachusetts Institute of Technology and Harvard.

The findings were published in the journal Cell Metabolism.

The scientists investigated the adaptive changes in beta cells that take place during the immune attack in both mouse models and in human cell culture. They used cyclophosphamide to accelerate the diabetes onset.

Herold and colleagues identified a resistant subpopulation of beta cells in 9-week-old, non-obese diabetic mice. The new subpopulation seems to develop from normal beta cells when they detect infiltration into the islet.

These new cells have a lower granularity, and they develop during the progression of type 1 diabetes.

"During the development of diabetes, there are changes in beta cells so you end up with two populations of beta cells. One population is killed by the immune response. The other population seems to acquire features that render it less susceptible to killing."

Dr. Kevan Herold

The new subpopulation is also less differentiated and displays stem-like properties. Much like stem cells, they have the ability to revert to a previous stage of development that enables them to survive and continue to replicate despite the immune attack.

As the study's senior author explains, these cells "duck and cover" as they develop molecules that inhibit the immune response. Human beta cells were revealed to go through similar changes when the researchers cultured them together with immune cells.

Although the cells do eventually die, the authors explain, the mechanism they uncovered might account for the long-term development of type 1 diabetes.

"Eventually, in [non-obese diabetic] mice as in humans, the majority of - if not all - [beta] cells are destroyed by immune effectors and products. However, the process is protracted. We have identified mechanisms that [beta] cells use to survive. Future studies that can recover mature [beta] cells from the pool of modified cells may identify ways of restoring normal metabolic function together with immune therapy," the authors conclude.

As Herold notes: "The next question is, can we recover these cells so that there is insulin production in someone [with] type 1 diabetes?"

Herold and team intend to conduct clinical trials to test drugs that might have the potential to change this subpopulation of beta cells, and transform it into insulin-producing cells.

Learn how interspecies transplantation may be a viable treatment for type 1 diabetes.

Written by Ana Sandoiu

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Why does type 1 diabetes kill some cells but not others? - Medical News Today

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Hackers are sparking a do-it-yourself revolution in diabetes care – WCSH6.com

Posted: February 10, 2017 at 11:40 am

Breaking through technology to help diabetes

WATERVILLE, Maine (NEWS CENTER) --More than one million people in the U.S. have type 1 diabetes, a disease where patients don't produce insulin to manage blood sugars. Left unchecked it can lead to blindness, damage to vital organs and even death.

Diabetics have to monitor their blood sugars all day, every day. With no cure in sight, a group of parents tired of waiting for technology to better manage their children's diabetes are hacking into medical devices and creating systems that work with their smart phones.

It all started with a Facebook group of tech-savvy parents who took matters in their own hands, tinkering with medical devices to track their children's blood sugar levels remotely. Other patients also transformed their insulin pumps and monitors into 'artificial pancreas systems'.

Now families in Maine are using the software to build devices not approved by the FDA but they say keeping their children safe outweighs the risks.

Leo Koch was diagnosed with Type 1 diabetes when he was two years old. When he sleeps at night extremely high and low sugar levels could put him in a potential fatal diabetic coma.

'It's a very real fear at night time, when they're asleep because he wouldn't necessarily say I don't feel well, I feel sick and their blood sugar plummets and you wouldn't have any kind of warning," said Koch.

The 5th grader wears a continuous glucose monitor with a hair-thin sensor placed under his skin on his arm. It records precise readings every five minutes. He also wears a pump so he can inject insulin when he needs it. Desperate to keep better track of her son's unpredictable blood sugars Koch joined a Facebook group of parents called 'WeAreNotWaiting'.

'We are absolutely not waiting, we're done waiting. It's taken too long we know there is technology out there that makes his life better,' said Koch.

Dubbed "Nightscout', the parents designed a system that hacks into continuous glucose monitor and uploads the data to a cloud via smartphone or smartwatch connected to the device.

Hilary down loaded the free software and built a website that displays Leo's data. It also sends alerts if his sugars are too low or too high. Leo's phone and texts from his Mom remind him to take insulin or eat something. With Leo participating in a variety of sports his mother needed better way to control his blood sugar levels but there wasn't anything available approved by the FDA.

Following instructions shared online, which hacked an old insulin pump so it could automatically dose insulin in response to blood sugar levels, Koch built an 'artificial pancreas'. Also called a closed loop, she had to buy a special transmitter that allows Leo's glucose sensor and insulin pump to communicate with each other for the first time.

Dr. Mick Davidson is an endocrinologist at Wentworth Health Partners in Dover, New Hampshire. A specialty that treats diabetics. Diagnosed with Type 1 at a young age, he joined the do-it-yourself revolution to help manage his disease.

Dr. Davidson uses both Nightscout and the closed loop system which he controls with this app on his iphone. Dr. Davidson says since using the device his blood sugar levels have become more stable. His finger stick blood sugars have gone from as much as 15 a day to less than four.

He feels the system helps patients better control their blood sugar especially while sleeping. Because the system is not FDA approved, he nor his practice can help a patient in building a system but.

'If someone is interested and willing to build it on their own and again trouble shoot it using the help of all the members of this huge online community, I have no hesitation recommending it," said Dr. Davidson.

Koch and other volunteers are helping families in Maine build Nightscout websites and closed loop systems. Ashley Thomass husband Ross and 5 year-old son Liam have Type 1 diabetes. Liam went online with his artificial pancreas a couple of months ago.

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