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Induction of retinol dehydrogenase 9 expression in podocytes attenuates kidney injury.

Abstract
The intracellular concentration of retinoic acid is determined by two sequential oxidation reactions that convert retinol to retinoic acid. We recently demonstrated that retinoic acid synthesis is significantly impaired in glomeruli of HIV-1 transgenic mice (Tg26), a murine model of HIV-associated nephropathy. This impaired retinoic acid synthesis correlates with reduced renal expression of retinol dehydrogenase 9, which catalyzes the rate-limiting step of retinoic acid synthesis by converting retinol to retinal. Because retinoic acid has renal protective effects and can induce podocyte differentiation, we hypothesized that restoration of retinoic acid synthesis could slow the progression of renal disease. Herein, we demonstrate that overexpression of retinol dehydrogenase 9 in cultured podocytes induces the expression of podocyte differentiation markers. Furthermore, we confirm that podocyte-specific overexpression of retinol dehydrogenase 9 in mice with established kidney disease due to either HIV-associated nephropathy or adriamycin-induced nephropathy decreases proteinuria, attenuates kidney injury, and restores podocyte differentiation markers. Our data suggest that restoration of retinoic acid synthesis could be a new approach to treat kidney disease.
AuthorsXuezhu Li, Yan Dai, Peter Y Chuang, John Cijiang He
JournalJournal of the American Society of Nephrology : JASN (J Am Soc Nephrol) Vol. 25 Issue 9 Pg. 1933-41 (Sep 2014) ISSN: 1533-3450 [Electronic] United States
PMID24652806 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 by the American Society of Nephrology.
Chemical References
  • Biomarkers
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Tretinoin
  • Alcohol Oxidoreductases
  • cis-retinol - androgen dehydrogenase
Topics
  • Alcohol Oxidoreductases (biosynthesis, genetics)
  • Animals
  • Biomarkers (metabolism)
  • Cell Differentiation
  • Cells, Cultured
  • Disease Models, Animal
  • Gene Expression
  • Kidney (enzymology, injuries, physiopathology)
  • Mice
  • Mice, Transgenic
  • Podocytes (enzymology, pathology)
  • Proteinuria (enzymology, genetics, prevention & control)
  • RNA, Messenger (genetics, metabolism)
  • Recombinant Fusion Proteins (biosynthesis, genetics)
  • Tretinoin (metabolism)
  • Up-Regulation

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