THE CONTRIBUTIONS OF MICROTUBULES AND F-ACTIN TO THE INVITRO MIGRATORY MECHANISMS OF HYDRA NEMATOCYTES AS DETERMINED BY DRUG INTERFERENCE EXPERIMENTS

被引:15
作者
AGOSTI, CG [1 ]
STIDWILL, RP [1 ]
机构
[1] UNIV ZURICH,DEPT ZOOL,WINTERTHURERSTR 190,CH-8057 ZURICH,SWITZERLAND
关键词
D O I
10.1016/S0014-4827(05)80088-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In order to investigate the contributions of microtubules and of F-actin to the in vitro migration mechanisms of Hydra nematocytes we have studied the effects of agents directed against cytoskeletal structures. Disassembly of microtubules by treatment with the drug nocodazole in moving nematocytes resulted in the loss of all locomotory activity within 20 min after the onset of treatment and in the detachment from the substratum after about 30 min. Depolymerization of microtubules by exposure to low temperatures had the same effect but was reversible in this case. Locomoting cells treated with cytochalasin D, which disrupts the actin filaments, stopped movement 2 min after drug administration and detached from the substratum after 15 min. The pattern of F-actin, α-tubulin, and tyrosinated tubulin in drug- or cold-treated cells was determined by immunocytochemical techniques and confocal laser scanning microscopy. These patterns and the reactions of the cells to the various drug treatments suggest that both actin filaments and microtubules play a crucial role in nematocyte locomotion. Analysis of the cytoskeletal pattern in drug-treated cells shows that the microtubules which are involved in locomotion are mostly tyrosinated. Furthermore it is suggested that microtubules and actin filaments interact with each other during the locomotion of nematocytes. © 1992 Academic Press, Inc.
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页码:196 / 204
页数:9
相关论文
共 40 条
[1]   CALMODULIN AND THE REGULATION OF THE ACTIN MYOSIN INTERACTION IN SMOOTH-MUSCLE AND NON-MUSCLE CELLS [J].
ADELSTEIN, RS .
CELL, 1982, 30 (02) :349-350
[2]   INVITRO MIGRATION OF HYDRA NEMATOCYTES - THE INFLUENCE OF THE NATURAL EXTRACELLULAR-MATRIX (THE MESOGLEA), OF COLLAGEN TYPE-IV AND TYPE-I, LAMININ, AND FIBRONECTIN ON CELL ATTACHMENT, MIGRATION PARAMETERS, AND ON PATTERNS OF CYTOSKELETAL PROTEINS [J].
AGOSTI, CG ;
STIDWILL, RP .
CELL MOTILITY AND THE CYTOSKELETON, 1991, 20 (03) :215-227
[3]   HYDRA MESOGLEA - SIMILARITY OF ITS AMINO-ACID AND NEUTRAL SUGAR COMPOSITION TO THAT OF VERTEBRATE BASAL LAMINA [J].
BARZANSKY, B ;
LENHOFF, HM ;
BODE, H .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1975, 50 (NB3) :419-&
[4]   PSEUDOPODIAL ACTIVITY AT THE ACTIVE EDGE OF MIGRATING FIBROBLAST IS DECREASED AFTER DRUG-INDUCED MICROTUBULE DEPOLYMERIZATION [J].
BERSHADSKY, AD ;
VAISBERG, EA ;
VASILIEV, JM .
CELL MOTILITY AND THE CYTOSKELETON, 1991, 19 (03) :152-158
[5]   LAMININ-INDUCED CAPPING AND RECEPTOR EXPRESSION AT CELL-SURFACE IN A RAT RHABDOMYOSARCOMA CELL-LINE - INVOLVEMENT IN CELL-ADHESION AND MIGRATION ON LAMININ SUBSTRATES [J].
BOUZON, M ;
LISSITZKY, JC ;
KOPP, F ;
MARTIN, PM .
EXPERIMENTAL CELL RESEARCH, 1989, 185 (02) :482-495
[6]   TAXONOMY OF THE EUROPEAN HYDRA (CNIDARIA, HYDROZOA) - A RE-EXAMINATION OF ITS HISTORY WITH EMPHASIS ON THE SPECIES HYDRA-VULGARIS PALLAS, HYDRA-ATTENUATA PALLAS AND HYDRA-CIRCUMCINCTA SCHULZE [J].
CAMPBELL, RD .
ZOOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, 1989, 95 (03) :219-244
[7]   CORRELATED DISTRIBUTION OF ACTIN, MYOSIN, AND MICROTUBULES AT THE LEADING-EDGE OF MIGRATING SWISS 3T3 FIBROBLASTS [J].
CONRAD, PA ;
NEDERLOF, MA ;
HERMAN, IM ;
TAYLOR, DL .
CELL MOTILITY AND THE CYTOSKELETON, 1989, 14 (04) :527-543
[8]   EFFECTS OF CYTOCHALASIN AND PHALLOIDIN ON ACTIN [J].
COOPER, JA .
JOURNAL OF CELL BIOLOGY, 1987, 105 (04) :1473-1478
[9]   IMMUNOCYTOCHEMICAL DEMONSTRATION OF ALPHA-TUBULIN MODIFICATION DURING AXONAL MATURATION IN THE CEREBELLAR CORTEX [J].
CUMMING, R ;
BURGOYNE, RD ;
LYTTON, NA .
JOURNAL OF CELL BIOLOGY, 1984, 98 (01) :347-351
[10]   POST-TRANSLATIONAL MODIFICATIONS OF TUBULIN AND THE DYNAMICS OF MICROTUBULES IN MOUSE OOCYTES AND ZYGOTES [J].
DEPENNART, H ;
HOULISTON, E ;
MARO, B .
BIOLOGY OF THE CELL, 1988, 64 (03) :375-378