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

Am J Physiol Renal Physiol. 2000 Jun;278(6):F886-93. doi: 10.1152/ajprenal.2000.278.6.F886.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Actins / ultrastructure*
  • Adenosine Triphosphate / metabolism
  • Animals
  • Cell Compartmentation
  • Cell Hypoxia / physiology
  • Cytoskeleton / metabolism
  • Cytoskeleton / ultrastructure
  • Female
  • In Vitro Techniques
  • Kidney Tubules, Proximal / metabolism*
  • Kidney Tubules, Proximal / ultrastructure*
  • Microscopy, Video
  • Microvilli / metabolism
  • Microvilli / ultrastructure
  • Rabbits
  • Solubility

Substances

  • Actins
  • Adenosine Triphosphate