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Am J Physiol Renal Physiol 278: F886-F893, 2000;
0363-6127/00 $5.00
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Vol. 278, Issue 6, F886-F893, June 2000

Coincident microvillar actin bundle disruption and perinuclear actin sequestration in anoxic proximal tubule

Peter White1, R. Brian Doctor2, Rolf H. Dahl2, and Jing Chen1

1 Department of Life Sciences, Indiana State University, Terre Haute, Indiana 47809; and 2 Department of Medicine, University of Colorado, Health Sciences Center, Denver, Colorado 80262

The present studies investigated acute disruption of microvillar actin cytoskeleton and actin association with other cytoskeletal components in ATP-depleted rabbit proximal tubular cells. Video-enhanced differential-interference contrast microscopy and confocal microscopy were used to follow the fate of F-actin during the disruption of microvilli. Within individual cells, all microvilli collapsed simultaneously. Microvillar actin filaments underwent a parallel decrease in length. Using a sequential cytoskeletal extraction protocol and electron microscopy, we revealed in the present studies the coincident sequestration of a distinct, perinuclear pool of actin that was primarily absent in control cells. Actin sequestration progressed in a duration-dependent manner, occurring as early as 15 min of anoxia when cellular ATP dropped to <5% of control level. Phalloidin staining and depolymerization treatment showed the majority (>90%) of this sequestered actin to be F-actin. A microvillar actin bundling protein villin was also sequestered in the same perinuclear complex of anoxic proximal tubules. In conclusion, the present results demonstrate a coincident microvillar actin bundle disruption and the perinuclear sequestration of F-actin in ATP-depleted proximal tubular cells.

ischemia; ATP depletion; cytoskeleton; kidney; villin


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