Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012 Jul;39(7):7717-26.
doi: 10.1007/s11033-012-1608-x. Epub 2012 Feb 21.

The connection between GRKs and various signaling pathways involved in diabetic nephropathy

Affiliations
Review

The connection between GRKs and various signaling pathways involved in diabetic nephropathy

Feng-Ling Wang et al. Mol Biol Rep. 2012 Jul.

Abstract

Diabetic nephropathy (DN) is a known microvascular complication in patients with diabetes mellitus. DN has become one of the main causes of death in diabetic patients. The occurrence and development of DN results from the comprehensive action of multi-factors, though the exact mechanism is not very clear. Recently, a study found that numerous pathways are activated during the course of the disease, including the PGE2-EP-G protein system, the renin-angiotensin system, protein kinase C, MAPK and oxidative stress, and transforming growth factor-β. G protein-coupled receptor kinases (GRKs), specifically recognize and phosphorylate agonist-activated G protein-coupled receptors, which play a major role in the above-mentioned pathways. The purpose of this paper is to review current information concerning the connection between GRKs and various signaling pathways involved in DN.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Biol Chem. 1998 Nov 20;273(47):31510-8 - PubMed
    1. Hypertension. 1992 May;19(5):403-18 - PubMed
    1. Science. 1992 Aug 28;257(5074):1264-7 - PubMed
    1. Free Radic Biol Med. 2006 Jan 1;40(1):13-20 - PubMed
    1. J Am Soc Nephrol. 2004 Jan;15 Suppl 1:S55-7 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources