Emerging roles of the actin cytoskeleton in cholangiocyte function and disease

被引:16
作者
Doctor, RB
Fouassier, L
机构
[1] Univ Colorado, Hlth Sci Ctr, Div Gastroenterol & Hepatol, Denver, CO 80202 USA
[2] Univ Paris 06, U402, INSERM, Paris, France
关键词
intrahepatic bile duct; CFTR; ischemia; ATP depletion; vesicle trafficking; Cl secretion;
D O I
10.1055/s-2002-34504
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Actin is a ubiquitous, abundant protein whose monomers polymerize into polarized actin filament;. Within epithelial cells, filamentous actin is concentrated at the plasma membrane where a wide variety of actin-associated proteins harness the potential and structure of actin filaments to moderate functions at the plasma membrane. These functions include structural support of the plasma membrane, establishing and maintaining cell polarity, regulation of membrane protein distribution and activity and enhancing membrane vesicle trafficking. Consequently, the actin cytoskeleton contributes significantly to the cellular pathogenesis in a number of disease states. In recent years, the actin cytoskeleton has been found to contribute significantly to cholangiocyte function and disease. This includes directing cyclic adenosine monophosphate (cAMP)-mediated Cl secretion, modulating vesicular trafficking at the apical membrane and initiating structural and functional alterations in ischemic bile ducts. Although much remains to be discovered, this article will highlight observations that indicate that the actin cytoskeleton plays a central role in the physiology and diseases of the intrahepatic bile duct.
引用
收藏
页码:263 / 276
页数:14
相关论文
共 88 条
  • [81] ATP depletion alters myosin I beta cellular location in LLC-PK1 cells
    Wagner, MC
    Molitoris, BA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (05): : C1680 - C1690
  • [82] Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity
    Wang, SS
    Yue, HW
    Derin, RB
    Guggino, WB
    Lit, M
    [J]. CELL, 2000, 103 (01) : 169 - 179
  • [83] WEINMAN E, 2001, AM J PHYSIOL, V281, pF372
  • [84] CHARACTERIZATION OF A PROTEIN COFACTOR THAT MEDIATES PROTEIN-KINASE-A REGULATION OF THE RENAL BRUSH-BORDER MEMBRANE NA+-H+ EXCHANGER
    WEINMAN, EJ
    STEPLOCK, D
    WANG, YP
    SHENOLIKAR, S
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) : 2143 - 2149
  • [85] Coincident microvillar actin bundle disruption and perinuclear actin sequestration in anoxic proximal tubule
    White, P
    Doctor, RB
    Dahl, RH
    Chen, J
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (06) : F886 - F893
  • [86] Ezrin/radixin/moesin (ERM) proteins bind to a positively charged amino acid cluster in the juxta-membrane cytoplasmic domain of CD44, CD43, and ICAM-2
    Yonemura, S
    Hirao, M
    Doi, Y
    Takahashi, N
    Kondo, T
    Tsukita, S
    Tsukita, S
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 140 (04) : 885 - 895
  • [87] NHE3 kinase A regulatory protein E3KARP binds the epithelial brush border Na+/H+ exchanger NHE3 and the cytoskeletal protein ezrin
    Yun, CHC
    Lamprecht, G
    Forster, DV
    Sider, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) : 25856 - 25863
  • [88] Tyrosine phosphorylation of villin regulates the organization of the actin cytoskeleton
    Zhai, LW
    Zhao, PL
    Panebra, A
    Guerrerio, AL
    Khurana, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) : 36163 - 36167