By Holly Ober
Creating a model of atrial fibrillation with live human heart cells on a chip is the goal of a new $6 million, five-year grant to Professor Steven George at the UC Davis Department of Biomedical Engineering and colleagues at Washington University in St. Louis.
UC Davis biomedical engineer Steven George will grow heart cells on a chip to study atrial fibrillation.
Atrial fibrillation is an irregular heartbeat caused when the heart’s upper chambers beat chaotically and out of sync with the lower chambers, leading to a variety of health problems including stroke and death. Nearly one in ten people over the age of 65 suffer from atrial fibrillation at a cost of around $6 billion.
By Dawn Rowe
The UC Davis Mouse Biology Program (MBP) has received an award of $414,000 from the National Institutes of Health to move towards sustainable, environment-friendly technology for its high-containment vivarium for mutant mice. The grant will also improve animal health and welfare, ergonomics for vivarium staff, and operational efficiencies.
Prof. Kent Lloyd, director of the UC Davis Mouse Biology Program, in the lab. Gene-edited and “knockout” mice have become a vital tool in biomedical research. (Karin Higgins/UC Davis photo)
Going ‘green” is a multi-step process that will take place over the next 12 months, and led by Kristin Grimsrud, associate director of vivaria and veterinary care for the program.
By Carlos Villatoro
Imagine a world where maladies such as cystic fibrosis, Huntington’s Disease, or sickle cell anemia no longer exist. While the U.S. is far from achieving this lofty goal, it recently came a step closer at the California National Primate Research Center (CNPRC), where scientists have efficiently used CRISPR/Cas9 technology to modify the genes of rhesus macaque embryos.
The research, recently published in the latest edition of Human Molecular Genetics, paves the way for future studies where the possibility of birthing gene-edited monkeys that can serve as models for new therapies is greatly increased.
Event Includes Horse Therapies For First Time
By Pat Bailey
Four UC Davis researchers with expertise in the application of stem cell science for therapies in human or veterinary medicine are slated to speak during the World Stem Cell Summit in Palm Beach, Florida, Dec. 6-9.
UC Davis researchers are exploring stem cell technology to treat both horses and humans. Photo by Karin Higgins/UC Davis.
This will be the 12th consecutive year that the summit has brought together scientists, physicians and veterinarians, industry representatives and patient advocates from around the world to share medical breakthroughs in stem cell research, also known as regenerative medicine.
[Contributed by Holly Ober, Biomedical Engineering]
Transplanted liver cells could repair livers damaged by toxins or infections. Stem cells hold tremendous promise for liver-related therapies because they can grow in a Petri dish to become any cell type, including liver cells. However, scientists have yet to identify the best reagents to add into the Petri dish to push stem cells to become liver cells. An expensive and time-consuming process of trial and error guides the discovery of reagents and signals for stem cell differentiation. Now, a team of biomedical engineers led by Prof. Alexander Revzin at UC Davis has found a way to grow liver cells from stem cells more cheaply and effectively than current methods.
Full post: Printed spots for growing liver stem cells
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The most complete version to date of the mouse genome was published yesterday in the journal PLoS Biology. “Build 36,” from the C57 inbred strain of black mice, has 175,000 fewer gaps, 139 megabytes of new sequences and realigns genes that were incorrectly described in an earlier version of the mouse genome.
The new genome map predicts just over 20,000 protein-coding genes in the mouse. About 75 percent of these are 1:1 “orthologs” or counterparts of human genes. The authors note that about 5,000 of these genes can be studied in “knockout” mice.
Full post: Final mouse genome published
(290 words, estimated 1:10 mins reading time)
Therapy restores blood flow in mice, forms the basis for upcoming clinical trials in humans
(SACRAMENTO, Calif.) — Researchers have successfully induced the formation of new blood vessels in mice with reduced blood flow (ischemia) to their limbs using adult human stem cells. The breakthrough treatment resulted in fully functioning limbs that showed both increased blood flow to previously damaged areas and an increase in the number of blood vessels. The study, published in this week’s print edition of the journal Blood, paves the way for the stem cell-based treatment of peripheral arterial disease (PAD) in humans, a painful condition common in diabetic patients that can lead to amputation.
Four UC Davis stem cell experts will give brief presentations on stem cell research followed by question-and-answer sessions during a community forum on Tuesday, May 12 from 5:30 to 7:30 p.m. at the UC Davis Cancer Center auditorium, 4501 X Street, in Sacramento.
The event, which is free and open to the public, is the first in a series of three discussions entitled “Stem Cell Dialogues,” which offer opportunities for the public to learn about the stem cell therapies UC Davis is developing to potentially treat and cure a wide array of disease and injury. With limited seating, those interested in attending this first session should reserve seats by contacting Michele Steiner at firstname.lastname@example.org or calling her at 916-734-9116.
Paul Knoepfler, an assistant professor of cell biology and human anatomy at the UC Davis School of Medicine, has been awarded a grant of $2 million over five years to support his work on how embryonic stem cells are programmed.
Embryonic stem cells and induced pluripotent stem cells are promising for medical purposes because they can develop into a wide range of tissues. But they can also give rise to tumors in mice. Knoepfler is studying the genetic mechanisms that control whether a stem cell develops properly, or forms a tumor.
Full post: Grant for stem cell researcher
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