IMR Press / FBL / Volume 13 / Issue 12 / DOI: 10.2741/3035

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article
Bone morphogenetic protein-7 (BMP7) in chronic kidney disease
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1 Los Angeles Biomedical Research Institute (LABioMed) at Harbor-UCLA Medical Center and UCLA, Torrance, CA 90502

*Author to whom correspondence should be addressed.

 

Front. Biosci. (Landmark Ed) 2008, 13(12), 4726–4739; https://doi.org/10.2741/3035
Published: 1 May 2008
Abstract

Bone morphogenetic protein-7 (BMP7) is a member of the BMP-subfamily of perhaps a dozen proteins within the TGFβ – superfamily of cysteine-knot fold cytokine – growth factors. BMP7 has pivotal functions during renal and eye development. In adult organisms, BMP7 is heavily expressed in kidney, specifically in podocytes, distal tubules and collecting ducts. The activity of BMP7 is reduced by inhibitors including some members of the dan – cerberus group and CTGF but can be enhanced by endoglin and KCP. Renal BMP7 disappears early in fibrogenic renal diseases which may facilitate progression. Exogenous administration of rhBMP7 or transgenic overexpression reduces renal fibrogenesis and apoptosis as well as transdifferentiation of epithelial cells. BMP7 improves maintenance of nephron function and structural integrity. These antifibrogenic activities result from inhibition of the nuclear translocation of TGFβ-activated smad3 by smad6 downstream of BMP7-activated smad5. Although at present the beneficial effects of BMP7 have only been studied in rodent models of chronic renal diseases, there is promise for therapeutic utility of rhBMP7 or small molecule BMP7 agonists in patients.

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