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Am J Pathol. 2014 Jun;184(6):1727-39. doi: 10.1016/j.ajpath.2014.03.002. Epub 2014 Apr 13.

Ezrin is down-regulated in diabetic kidney glomeruli and regulates actin reorganization and glucose uptake via GLUT1 in cultured podocytes.

Author information

1
Department of Pathology, Haartman Institute, University of Helsinki, Helsinki, Finland.
2
Department of Pathology, Haartman Institute, University of Helsinki, Helsinki, Finland; Children's Hospital, University of Helsinki, Helsinki, Finland.
3
Department of Pathology, Haartman Institute, University of Helsinki, Helsinki, Finland; Laboratory Animal Centre, University of Helsinki, Helsinki, Finland.
4
Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
5
Department of Pathology, HUSLAB, Helsinki University Central Hospital, Helsinki and Hyvinkää, Finland.
6
Department of Virology, Haartman Institute, University of Helsinki, Helsinki, Finland.
7
Clinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.
8
Institute of Pathophysiology, Semmelweis University, Budapest, Hungary.
9
Department of Food and Environmental Sciences, University of Helsinki, Helsinki, Finland.
10
Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
11
Department of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Helsinki, Finland.
12
Department of Pathology, Haartman Institute, University of Helsinki, Helsinki, Finland. Electronic address: sanna.h.lehtonen@helsinki.fi.

Abstract

Diabetic nephropathy is a complication of diabetes and a major cause of end-stage renal disease. To characterize the early pathophysiological mechanisms leading to glomerular podocyte injury in diabetic nephropathy, we performed quantitative proteomic profiling of glomeruli isolated from rats with streptozotocin-induced diabetes and controls. Fluorescence-based two-dimensional difference gel electrophoresis, coupled with mass spectrometry, identified 29 differentially expressed spots, including actin-binding protein ezrin and its interaction partner, NHERF2, which were down-regulated in the streptozotocin group. Knockdown of ezrin by siRNA in cultured podocytes increased glucose uptake compared with control siRNA-transfected cells, apparently by increasing translocation of glucose transporter GLUT1 to the plasma membrane. Knockdown of ezrin also induced actin remodeling under basal conditions, but reduced insulin-stimulated actin reorganization. Ezrin-dependent actin remodeling involved cofilin-1 that is essential for the turnover and reorganization of actin filaments. Phosphorylated, inactive cofilin-1 was up-regulated in diabetic glomeruli, suggesting altered actin dynamics. Furthermore, IHC analysis revealed reduced expression of ezrin in the podocytes of patients with diabetes. Our findings suggest that ezrin may play a role in the development of the renal complication in diabetes by regulating transport of glucose and organization of the actin cytoskeleton in podocytes.

PMID:
24726496
DOI:
10.1016/j.ajpath.2014.03.002
[Indexed for MEDLINE]

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