Arf1 and Arf6 Promote Ventral Actin Structures Formed by Acute Activation of Protein Kinase C and Src

被引:12
作者
Caviston, Juliane P. [1 ]
Cohen, Lee Ann [1 ]
Donaldson, Julie G. [1 ]
机构
[1] NHLBI, Cell Biol & Physiol Ctr, NIH, Bethesda, MD 20892 USA
关键词
Arf1; PKC; Src; cortical actin; ventral surface; ADP-RIBOSYLATION FACTOR; CLATHRIN-INDEPENDENT ENDOCYTOSIS; NUCLEOTIDE EXCHANGE FACTORS; EPITHELIAL-CELL MIGRATION; PHOSPHOLIPASE-D ACTIVITY; BREAST-CANCER CELLS; PLASMA-MEMBRANE; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; DOWNSTREAM ACTIVATION; F-ACTIN;
D O I
10.1002/cm.21181
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Arf proteins regulate membrane traffic and organelle structure. Although Arf6 is known to initiate actin-based changes in cell surface architecture, Arf1 may also function at the plasma membrane. Here we show that acute activation of protein kinase C (PKC) induced by the phorbol ester PMA led to the formation of motile actin structures on the ventral surface of Beas-2b cells, a lung bronchial epithelial cell line. Ventral actin structures also formed in PMA-treated HeLa cells that had elevated levels of Arf activation. For both cell types, formation of the ventral actin structures was enhanced by expression of active forms of either Arf1 or Arf6 and by the expression of guanine nucleotide exchange factors that activate these Arfs. By contrast, formation of these structures was blocked by inhibitors of PKC and Src and required phosphatidylinositol 4, 5-bisphosphate, Rac, Arf6, and Arf1. Furthermore, expression of ASAP1, an Arf1 GTPase activating protein (GAP) was more effective at inhibiting the ventral actin structures than was ACAP1, an Arf6 GAP. This study adds to the expanding role for Arf1 in the periphery and identifies a requirement for Arf1, a "Golgi Arf," in the reorganization of the cortical actin cytoskeleton on ventral surfaces, against the substratum. Published 2014. This article is a U. S. Government work and is in the public domain in the USA
引用
收藏
页码:380 / 394
页数:15
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