alexa
Reach Us +44-1522-440391
A Novel Intrinsic System For Endothelial Stress Resistance | 4348
ISSN: 2161-0959

Journal of Nephrology & Therapeutics
Open Access

Like us on:

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

A novel intrinsic system for endothelial stress resistance

International Conference and Exhibition on Nephrology & Therapeutics

Yasufumi Sato

Accepted Abstracts: J Nephrol Therapeut

DOI: 10.4172/2161-0959.S1.007

Abstract
B lood vessels distribute entire body, supplying oxygen and nutrient. Endothelial cells (ECs) cover the entire inner lumen of the vessels and form interface between blood and vasculature; therefore receive continuous mechanical and/or chemical stresses. Accumulation of damages to ECs is thought to be the primary cause of various vascular diseases including atherosclerosis, diabetic vascular complication and so forth. We recently isolated vasohibin-1 (VASH1) as a novel angiogenesis inhibitor produced by ECs, and its homologue vasohibin-2 (VASH2). Human VASH1 gene is encoded in 14q24.3 while human VASH2 gene is encoded in 1q32.3, and these 2 molecules are highly conserved between species. Angiogenesis is controlled by the local balance between its stimulators and inhibitors. In general, angiogenesis stimulators promote EC survival, whereas angiogenesis inhibitors induce EC death and vascular regression. Since VASH1 is synthesized by ECs and inhibits angiogenesis, VASH1 can be a suicidal molecule. We therefore characterized the role of VASH1 in EC survival/ death. To our surprise, overexpression of VASH1 in ECs increased stress resistance and prevented cell death induced by cellular stresses including H2O2 or serum starvation, whereas the knockdown of VASH1 induced premature senescence of ECs, and those ECs were easily killed by cellular stresses. These results indicate that VASH1 plays important role not only in angiogenesis inhibition but also in vascular maintenance. The molecular mechanism of VASH1-mediated stress resistance and possible relation to glomerular function will be discussed in the meeting
Biography

Dr. Sato is a full Professor of the Department of Vascular Biology, Institute of Development, Aging and Cancer, Tohoku University. He received his M.D. from Kobe University in 1978 and his Ph.D. from Kyushu University in 1987. He was a postdoctoral fellow at New York University Medical Center from 1987 to 1989. He returned to Oita Medical University as an assistant Professor in 1989, and promoted to the present position in 1994. He published more than 150 peer-reviewed original papers, and is now appointed as the president of the Japanese Vascular Biology and Medicine Organization

Top