Journal article

EGFR-PLCγ1 signaling mediates high glucose-induced PKCβ1-Akt activation and collagen I upregulation in mesangial cells

D Wu, F Peng, B Zhang, AJ Ingram, DJ Kelly, RE Gilbert, B Gao, S Kumar, JC Krepinsky

American Journal of Physiology Renal Physiology | Published : 2009

Abstract

Glomerular matrix accumulation is a hallmark of diabetic nephropathy. We have recently shown that epidermal growth factor receptor (EGFR) transactivation mediates high glucose (HG)-induced collagen I upregulation through PI3K-PKCβ1-Akt signaling in mesangial cells (MC). Phospholipase Cγ1 (PLCγ1) interacts with activated growth factor receptors and activates classic PKC isoforms. We thus studied its role in HG-induced collagen I upregulation in MC. Primary rat MC were treated with HG (30 mM) or mannitol as osmotic control. Protein kinase activation was assessed by Western blotting and collagen I upregulation by Northern blotting. Diabetes was induced in rats by streptozotocin. HG treatment fo..

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University of Melbourne Researchers

Grants

Funding Acknowledgements

J. Krepinsky is supported by the Canadian Diabetes Association (CDA) and Canadian Institutes of Health Research (CIHR). D. Wu is a recipient of the Krescent Fellowship sponsored by the Kidney Foundation of Canada and CIHR. F. Peng is a recipient of the Father Sean O'Sullivan Research Center Fellowship, St. Joseph's Hospital, Hamilton, Ontario, Canada.