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Am J Physiol Renal Physiol 292: F76-F81, 2007. First published August 8, 2006; doi:10.1152/ajprenal.00128.2006
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Rapamycin at subimmunosuppressive levels inhibits mesangial cell proliferation and extracellular matrix production

Helen R. Lock, Steven H. Sacks, and Michael G. Robson

Department of Nephrology and Transplantation, King's College London School of Medicine, London, United Kingdom

Submitted 16 April 2006 ; accepted in final form 31 July 2006

In view of its proven antiproliferative effects, rapamycin offers potential in the treatment of mesangioproliferative disease. Previous data have shown an effect of rapamycin on mesangial cell proliferation at high doses and have not explored the mechanism of action. Therefore, we explored the effects and mechanism of action of low levels of rapamycin on mesangial cell proliferation. Primary cultures of mouse mesangial cells were grown in medium containing serum with differing concentrations of rapamycin. A rapamycin concentration of 0.1 ng/ml caused a decrease in cell number and DNA synthesis with no effect on apoptosis. Type IV collagen protein production was inhibited at 0.01 ng/ml rapamycin, although gene expression was unaffected. P70S6K phosphorylation was inhibited in parallel with the effects on cell number and DNA synthesis in a dose-dependent manner, but no effect was seen at 0.01 ng/ml rapamycin. These data show an effect on mesangial cell proliferation and p70S6 kinase phosphorylation of 0.1 ng/ml rapamycin and an effect on collagen IV production of 0.01 ng/ml rapamycin. We suggest that further in vivo studies should explore the potential for low-dose rapamycin in the treatment of mesangioproliferative glomerulonephritis.

glomerulus; kidney; collagen



Address for reprint requests and other correspondence: M. Robson, Dept. of Nephrology and Transplantation, King's College London, Guys Hospital, London SE1 9RT, UK (e-mail: michael.robson{at}kcl.ac.uk)




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Differential Effects of Rapamycin in Anti-GBM Glomerulonephritis
J. Am. Soc. Nephrol., August 1, 2008; 19(8): 1520 - 1529.
[Abstract] [Full Text] [PDF]




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