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PMID: 7859295 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Effect of protein kinase inhibitor H-7 on the contractility, integrity, and membrane anchorage of the microfilament system.

Cell motility and the cytoskeleton ·Vol. 29 ·No. 4 ·1994-00-00 ·Pages 321-38

Volberg T, Geiger B, Citi S, Bershadsky AD

Abstract

Addition of protein kinase inhibitor H-7 leads to major changes in cell structure and dynamics. In previous studies [Citi, 1992: J. Cell Biol. 117:169-178] it was demonstrated that intercellular junctions in H-7-treated epithelial cells become calcium independent. To elucidate the mechanism responsible for this effect we have examined the morphology, dynamics, and cytoskeletal organization of various cultured cells following H-7-treatment. We show here that drug treated cells display an enhanced protrusive activity. Focal contact-attached stress fibers and the associated myosin, vinculin, and talin deteriorated in such cells while actin, vinculin, and N-cadherin associated with cell-cell junctions were retained. Furthermore, we demonstrate that even before these cytoskeletal changes become apparent, H-7 suppresses cellular contractility. Thus, short pretreatment with H-7 leads to strong inhibition of the ATP-induced contraction of saponin permeabilized cells. Comparison of H-7 effects with those of other kinase inhibitors revealed that H-7-induced changes in cell shape, protrusional activity, and actin cytoskeleton structure are very similar to those induced by selective inhibitor of myosin light chain kinase, KT5926. Specific inhibitors of protein kinase C (Ro31-8220 and GF109203X), on the other hand, did not induce similar alterations. These results suggest that the primary effect of H-7 on cell morphology, motility, and junctional interactions may be attributed to the inhibition of actomyosin contraction. This effect may have multiple effects on cell behavior, including general reduction in cellular contractility, destruction of stress fibers, and an increase in lamellipodial activity. It is proposed that this reduction in tension also leads to the apparent stability of cell-cell junctions in low-calcium medium.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Actin Cytoskeleton/chemistry,drug effects,physiology Actins/analysis Alkaloids/pharmacology Animals Cadherins/analysis Calcium/physiology Carbazoles Cell Adhesion/drug effects Cell Movement/drug effects Cell Size/drug effects Cells, Cultured Cytoskeletal Proteins/physiology Indoles/pharmacology Intercellular Junctions/drug effects Isoquinolines/pharmacology Microfilament Proteins/physiology Myosin Subfragments/drug effects Piperazines/pharmacology Protein Kinase C/antagonists & inhibitors Talin/analysis Vinculin/analysis
Chemicals
Actins Alkaloids Cadherins Carbazoles Cytoskeletal Proteins Indoles Isoquinolines Microfilament Proteins Myosin Subfragments Piperazines Talin Vinculin KT 5926 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Protein Kinase C Calcium Ro 31-8220
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Volberg T
Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
Geiger B
Citi S
Bershadsky A D
Article Info
Journal
Cell motility and the cytoskeleton
Abbr.
Cell Motil Cytoskeleton
ISSN
0886-1544
Published
1994-00-00
Pages
321-38
Language
English
Region
United States
NLM ID
8605339
Subset
IM
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