Destruction of microfilament bundles in mouse embryo fibroblasts treated with inhibitors of energy metabolism

A. D. Bershadsky, V. I. Gelfand*, T. M. Svitkina, I. S. Tint

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

73 Scopus citations

Abstract

Immunofluorescence with an antiactin antibody and electron microscopy were used to study the distribution of actin in cultured mouse fibroblasts during treatment with inhibitors of energy metabolism. The inhibitors induce gradual disorganization of actin-containing microfilament bundles. At the first stage of the process the bundles degrade into separate fragments; later only small patches of actin can be found in the inhibitor-treated cells. This transformation takes about 90 min and is fully reversible as microfilament bundles are recovered after incubation of the cells in the inhibitor-free growth medium. The inhibitors do not alter actin distribution in the presence of glucose. This shows that their action is due to a reduction of the ATP level in the cells. A 90 min incubation with the inhibitors does not markedly alter either the cell shape or the microtubule system. Inhibitors of the energy metabolism prevent cytochalasin action on cells. Cytochalasin B (CB) or cytochalasin D (CD) rapidly disorganize the microfilament bundles and cause cell arborization. However, microfilament bundle destruction in the cells incubated in the mixture of cytochalasin and any of the inhibitors requires 90 min and is not accompanied by dramatic changes in the cell morphology, so the process is indistinguishable from microfilament bundle destruction in the presence of the inhibitors alone.

Original languageEnglish (US)
Pages (from-to)421-429
Number of pages9
JournalExperimental Cell Research
Volume127
Issue number2
DOIs
StatePublished - Jun 1980

ASJC Scopus subject areas

  • Cell Biology

Fingerprint

Dive into the research topics of 'Destruction of microfilament bundles in mouse embryo fibroblasts treated with inhibitors of energy metabolism'. Together they form a unique fingerprint.

Cite this