Press Release - Feb 1, 2011Researchers Unlock the Potential for Exploring Kidney Regeneration
Boston, MA - It is estimated that up to 10 percent of the U.S. population may have some form of renal disease, with 450,000 patients with end stage renal disease (ESRD) requiring hemodialysis. Researchers at Brigham and Women’s Hospital, Massachusetts General Hospital and the University of Pittsburgh have identified a cell in zebrafish that can be transplanted from one fish to another to regenerate nephrons, providing the potential to improve kidney function. These findings are published in the February 3 edition of Nature.
Currently, the five-year survival rate for patients on dialysis is 33 percent, worse than the survival rate for many forms of cancer. This epidemic of renal failure is projected to grow as obesity, poor nutrition and lack of exercise increase the incidence of diabetes and hypertension. There is also evidence that intra-uterine growth retardation and low birth weight/prematurity reduce the number of nephrons in each kidney thereby increasing the risk of hypertension and renal failure when these premature infants become adults. The cost of treating end stage renal disease is currently 32 billion dollars annually and is likely to double in the next decade.
In a collaborative effort including two groups that are part of the Harvard Stem Cell Institute, the laboratory of Dr. Alan Davidson, at the Center for Regenerative Medicine at the Massachusetts General Hospital and the laboratory of Dr. Robert Handin, in the Hematology Division in the Department of Medicine at the Brigham and Woman’s Hospital, together with Dr. Neil Hukriede’s team at the University of Pittsburgh, have identified and characterized, for the first time, a progenitor cell in adult zebrafish kidneys that can be transplanted from one fish to another and generate new nephrons. Now that this cell has been identified it may be possible to better understand how to increase its number and capacity to generate nephrons.
Lead author, Dr. Alan Davidson, said “We hope to eventually be able to cross species barriers and understand why similar cells, present in mouse and human kidneys during embryonic life, disappear around the time of birth”. The groups plan to continue studies on zebrafish and apply their data to mouse models and eventually humans.
In addition to support from the National Institutes of Health and the American Society of Nephrology (ASN), we wish to acknowledge the support of HSCI in the form of pilot and program grants. HSCI and ASN funding helped with the initial phases of the work. In addition, the HSCI has provided the ideal inter-disciplinary milieu within which this work could be undertaken.
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