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

被引:30
作者
White, P
Doctor, RB
Dahl, RH
Chen, J [1 ]
机构
[1] Indiana State Univ, Dept Life Sci, Terre Haute, IN 47809 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80262 USA
关键词
ischemia; ATP depletion; cytoskeleton; kidney; villin;
D O I
10.1152/ajprenal.2000.278.6.F886
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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.
引用
收藏
页码:F886 / F893
页数:8
相关论文
共 22 条
  • [1] BACALLAO R, 1994, J CELL SCI, V107, P3301
  • [2] VILLIN IS A MAJOR PROTEIN OF THE MICROVILLUS CYTOSKELETON WHICH BINDS BOTH G-ACTIN AND F-ACTIN IN A CALCIUM-DEPENDENT MANNER
    BRETSCHER, A
    WEBER, K
    [J]. CELL, 1980, 20 (03) : 839 - 847
  • [3] Loss of cytoskeletal support is not sufficient for anoxic plasma membrane disruption in renal cells
    Chen, J
    Dai, JW
    Grant, RL
    Doctor, RB
    Sheetz, MP
    Mandel, LJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (04): : C1319 - C1328
  • [4] CYTOSKELETAL DISSOCIATION OF EZRIN DURING RENAL ANOXIA - ROLE IN MICROVILLAR INJURY
    CHEN, J
    DOCTOR, RB
    MANDEL, LJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (03): : C784 - C795
  • [5] Unopposed phosphatase action initiates ezrin dysfunction: a potential mechanism for anoxic injury
    Chen, J
    Mandel, LJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 273 (02): : C710 - C716
  • [6] DEPHOSPHORYLATION OF EZRIN AS AN EARLY EVENT IN RENAL MICROVILLAR BREAKDOWN AND ANOXIC INJURY
    CHEN, J
    COHN, JA
    MANDEL, LJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7495 - 7499
  • [7] GLYCOLYTIC AND OXIDATIVE-METABOLISM IN PRIMARY RENAL PROXIMAL TUBULE CULTURES
    DICKMAN, KG
    MANDEL, LJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (02): : C333 - C340
  • [8] Reorganization of cholangiocyte membrane domains represents an early event in rat liver ischemia
    Doctor, RB
    Dahl, RH
    Salter, KD
    Fitz, JG
    [J]. HEPATOLOGY, 1999, 29 (05) : 1364 - 1374
  • [9] Loss of plasma membrane structural support in ATP-depleted renal epithelia
    Doctor, RB
    Zhelev, DV
    Mandel, LJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (02): : C439 - C449
  • [10] GLAUMANN B, 1975, VIRCHOWS ARCH B, V19, P281