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Am J Physiol Renal Physiol 288: F48-F57, 2005. First published August 31, 2004; doi:10.1152/ajprenal.00146.2004
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Vascular endothelial growth factor and nephrin interact and reduce apoptosis in human podocytes

Rebecca R. Foster,1,* Moin A. Saleem,2,* Peter W. Mathieson,3 David O. Bates,1 and Steven J. Harper1

1Microvascular Research Laboratories, Department of Physiology, University of Bristol, Preclinical Veterinary School, Bristol; and 2Children's and 3Academic Renal Unit, University of Bristol, Southmead Hospital, Bristol, United Kingdom

Submitted 22 April 2004 ; accepted in final form 18 August 2004

Vascular endothelial growth factor (VEGF) is anti-cytotoxic in podocytes. Moreover, it has been suggested that nephrin, a cell adhesion molecule of the podocyte slit diaphragm, can contribute to antiapoptotic mechanisms in these cells. We therefore investigated whether VEGF signals to reduce apoptosis and the role of nephrin in this survival mechanism. Flow cytometry showed that podocytes with nephrin mutations had a significantly greater proportion of apoptosis. Although VEGF reduced apoptosis in human conditionally immortalized podocytes [wild-type (WT)] by 18.1% of control (P < 0.001), it was unable to do so in nephrin-deficient human conditionally immortalized podocytes. Moreover, Western blotting and immunodetection with an anti-nephrin antibody showed that the phosphorylation of nephrin, compared with serum-starved WTs, was significantly increased (ratio of 3.36 ± 1.2 to control, P < 0.05) by VEGF treatment and significantly reduced by treatment with a neutralizing VEGF monoclonal antibody (mAb) (ratio of 0.2 ± 0.09 to control, P < 0.05). The AKT signaling pathway has been implicated in nephrin-mediated inhibition of apoptosis in transfected cells, but the role of this pathway has not previously been shown in podocytes. Surprisingly, exogenous VEGF decreased AKT/PKB phosphorylation in normal podocytes but increased it in nephrin-deficient podocytes. We suggest therefore that both exogenous and endogenous (podocyte derived) VEGF can stimulate the phosphorylation of nephrin and through this action may prevent podocyte apoptosis. However, the involvement of AKT in this survival response in normal human podocytes is not clear.

glomerular filtration rate; nephritis; VEGF; filtration; foot process



Address for reprint requests and other correspondence: D. O. Bates, Microvascular Research Laboratories, Dept. of Physiology, Univ. of Bristol, Preclinical Veterinary School, Southwell St., Bristol BS2 8EJ, UK (E-mail: Dave.Bates{at}bristol.ac.uk)




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