Government cash injection for University spin-out company's stem cell researchJanuary 24, 2005A spin-out company from the University of Nottingham has been awarded around £250,000 of Government funding to develop innovative stem cell therapies that could one day provide new treatments for patients suffering from illnesses including Parkinson's disease and stroke. RegenTec, a company at the cutting-edge of regenerative medicine that specialises in the development of stem cell and tissue engineering technology, is a partner in two projects that have attracted a total of £3.7 million from the Department of Trade and Industry's Technology Programme. The first award, made to a five-partner consortium led by the company ReNeuron, will bring together science and industry experts to develop new stem cell products for commercial use in treating neurodegenerative diseases such as stroke, Huntington's disease and Parkinson's disease, as well as other illnesses including diabetes, blindness and cardiac disease. RegenTec will be working on the development of delivery systems that provide a supportive environment for stem cells. Once administered, the stem cells either encourage the growth of tissue by triggering the body's own repair processes or themselves begin to grow and form new tissue. The second project, led by the company NovaThera, will aim to develop our understanding of the way in which cells grow and develop into specific cells for different functions. The research, which will initially focus on cells to repair bone, lung and liver tissue, will look at ways in which this growth can be effectively controlled or manipulated. RegenTec specialises in the development of a range of materials that can be injected to deliver cells directly to the area of the body where they are needed. The materials are designed to solidify upon injection to create templates for tissue repair known as scaffolds. The scaffolds aim to enhance the survival and function of the stem cells and provide a controlled environment that encourages the cells to grow. Research will also be carried out into ways of taking scarce stem cells and growing a larger supply for use in treating a range of patients and diseases. RegenTec, which is based at BioCity, Nottingham's groundbreaking new healthcare and bioscience innovation centre, was set up four years ago by The University of Nottingham's Professor Kevin Shakesheff. Welcoming the DTI grant funding, Professor Shakesheff said: "Stem cell technology could revolutionise the treatment of life-threatening or long-term diseases. These awards confirm RegenTec's position as a key partner in advancing regenerative medicine from The University of Nottingham's world-class research labs through to patient treatments. "I'm delighted that the partnership between the University and RegenTec is again generating biotech jobs at BioCity Nottingham." Nottingham, University of |
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| Related Stem Cells Current Events and Stem Cells News Articles First reconstitution of an epidermis from human embryonic stem cells Stem cell research is making great strides. This is yet again illustrated by a study carried out by the I-STEM* Institute (I-STEM/ Inserm UEVE U861/AFM), published in the Lancet on 21 November 2009. The I-STEM team, directed by Marc Peschanski has just succeeded in recreating a whole epidermis from human embryonic stem cells. Bone Implant Offers Hope for Skull Deformities A synthetic bone matrix offers hope for babies born with craniosynostosis, a condition that causes the plates in the skull to fuse too soon. Your Own Stem Cells Can Treat Heart Disease The largest national stem cell study for heart disease showed the first evidence that transplanting a potent form of adult stem cells into the heart muscle of subjects with severe angina results in less pain and an improved ability to walk. The transplant subjects also experienced fewer deaths than those who didn't receive stem cells. Is hepatic differentiation of embryonic stem cells induced by valproic acid and cytokines? Embryonic stem (ES) cells, known for their capacity to proliferate indefinitely and differentiate into almost all types of cells including hepatocytes, have raised the hope of cellular replacement therapy for liver failure. Paradoxical protein might prevent cancer One difficulty with fighting cancer cells is that they are similar in many respects to the body's stem cells. By focusing on the differences, researchers at Karolinska Institutet have found a new way of tackling colon cancer. The study is presented in the prestigious journal Cell. U of M researchers find 2 units of umbilical cord blood reduce risk of leukemia recurrence A new study from the Masonic Cancer Center, University of Minnesota shows that patients who have acute leukemia and are transplanted with two units of umbilical cord blood (UCB) have significantly reduced risk of the disease returning. The use of stem cells in regenerative medicine may also be detrimental for health The use of stem cells in regenerative medicine is not always beneficial for human health, it may even be harmful according to a work done by the University of Granada and University of León. Scientists have demonstrated that transplantation of human mononuclear cells isolated from umbilical cord blood exerted a deleterious effect in rats with liver cirrhosis. Penn Study Provides First Clear Idea of How Rare Bone Disease Progresses An international team of scientists, led by researchers at the University of Pennsylvania School of Medicine, is taking the first step in developing a treatment for a rare genetic disorder called fibrodysplasia ossificans progressiva (FOP), in which the body's skeletal muscles and soft connective tissue turns to bone, immobilizing patients over a lifetime with a second skeleton. Iowa State University researcher discovers key to vital DNA, protein interaction A researcher at Iowa State University has discovered how a group of proteins from plant pathogenic bacteria interact with DNA in the plant cell, opening up the possibility for what the scientist calls a "cascade of advances." Scientists successfully reprogram blood cells Researchers have transplanted genetically modified hematopoietic stem cells into mice so that their developing red blood cells produce a critical lysosomal enzyme -preventing or reducing organ and central nervous system damage from the often-fatal genetic disorder Hurler's syndrome. More Stem Cells Current Events and Stem Cells News Articles |
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