Caveolin-1 in the Pathogenesis of Diabetic Nephropathy: Potential Therapeutic Target?

Abstract:

PURPOSE OF REVIEW:Diabetic nephropathy, a major microvascular complication of diabetes and the most common cause of end-stage renal disease, is characterized by prominent accumulation of extracellular matrix. The membrane microdomains caveolae, and their integral protein caveolin-1, play critical roles in the regulation of signal transduction. In this review we discuss current knowledge of the contribution of caveolin-1/caveolae to profibrotic signaling and the pathogenesis of diabetic kidney disease, and assess its potential as a therapeutic target. RECENT FINDINGS:Caveolin (cav)-1 is key to facilitating profibrotic signal transduction induced by several stimuli known to be pathogenic in diabetic nephropathy, including the most prominent factors hyperglycemia and angiotensin II. Phosphorylation of cav-1 on Y14 is an important regulator of these responses. In vivo studies support a pathogenic role for caveolae in the progression of diabetic nephropathy. Targeting caveolin-1/caveolae would enable inhibition of multiple profibrotic pathways, representing a novel and potentially potent therapeutic option for diabetic nephropathy.

journal_name

Curr Diab Rep

journal_title

Current diabetes reports

authors

Van Krieken R,Krepinsky JC

doi

10.1007/s11892-017-0844-9

subject

Has Abstract

pub_date

2017-03-01 00:00:00

pages

19

issue

3

eissn

1534-4827

issn

1539-0829

pii

10.1007/s11892-017-0844-9

journal_volume

17

pub_type

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