| Literature DB >> 19520754 |
Yuqing Chen1, Manjula Mahata, Fangwen Rao, Srikrishna Khandrika, Maite Courel, Maple M Fung, Kuixing Zhang, Mats Stridsberg, Michael G Ziegler, Bruce A Hamilton, Michael S Lipkowitz, Laurent Taupenot, Caroline Nievergelt, Sushil K Mahata, Daniel T O'Connor.
Abstract
Chromogranin A (CHGA), a protein released from secretory granules of chromaffin cells and sympathetic nerves, triggers endothelin-1 release from endothelial cells. CHGA polymorphisms associate with an increased risk for ESRD, but whether altered CHGA-endothelium interactions may explain this association is unknown. Here, CHGA led to the release of endothelin-1 and Weibel-Palade body exocytosis in cultured human umbilical vein endothelial cells. In addition, CHGA triggered secretion of endothelin-1 from glomerular endothelial cells and TGF-beta1 from mesangial cells cocultured with glomerular endothelial cells. In humans, plasma CHGA correlated positively with endothelin-1 and negatively with GFR. GFR was highly heritable in twin pairs, and common promoter haplotypes of CHGA predicted GFR. In patients with progressive hypertensive renal disease, a CHGA haplotype predicted rate of GFR decline. In conclusion, these data suggest that CHGA acts through the glomerular endothelium to regulate renal function.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19520754 PMCID: PMC2709688 DOI: 10.1681/ASN.2008111148
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121