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The Journal of Biophysical and Biochemical Cytology logoLink to The Journal of Biophysical and Biochemical Cytology
. 1958 May 25;4(3):243–250. doi: 10.1083/jcb.4.3.243

Surface Responses in Cultured Fibroblasts Elicited by Ethylenediaminetetraacetic Acid

Ernst J Dornfeld 1, Alfred Owczarzak 1
PMCID: PMC2224478  PMID: 13549494

Abstract

Cultures of chick heart fibroblasts were perfused with the chelating agent ethylenediaminetetraacetic acid (EDTA). Cellular responses were observed under phase optics and recorded by time-lapse cinemicrography. In interphasic fibroblasts, EDTA induces cellular contraction followed by continuous protrusion and retraction of ectoplasmic blebs ("surface bubbling"), formation of motile vermiform processes, and production of rotatory ectoplasmic swellings. The contraction and surface bubbling closely resemble the metaphase contraction and "anaphase bubbling" normally displayed by cultured fibroblasts. In dividing cells, EDTA does not affect metaphases, but anaphase bubbling appears and persists; telophasic expansion and migration of daughter cells are prevented. Initiation of new mitoses occurs during and after exposure to EDTA. No cellular responses are induced by calcium, magnesium, or ferrous chelates of EDTA. The EDTA elects are completely reversible on removal of the chelating agent, resulting in the restoration of the normal interphasic cell form and the normal expansion and migration of mitotic products. The EDTA effects are interpreted to result from the chelation and removal of divalent cations from the cell surface. Possible relations to surface activities observed in normal mitosis are considered, and an hypothesis is presented regarding the role of the developing spindle in cation transfer.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BOSS J. Mitosis in cultures of newt tissues. IV. The cell surface in late anaphase and the movements of ribonucleoprotein. Exp Cell Res. 1955 Feb;8(1):181–187. doi: 10.1016/0014-4827(55)90055-0. [DOI] [PubMed] [Google Scholar]
  2. COMAN D. R. Cellular adhesiveness in relation to the invasiveness of cancer; electron microscopy of liver perfused with a chelating agent. Cancer Res. 1954 Aug;14(7):519–521. [PubMed] [Google Scholar]
  3. Eversole R. A., Tatum E. L. CHEMICAL ALTERATION OF CROSSING-OVER FREQUENCY IN CHLAMYDOMONAS. Proc Natl Acad Sci U S A. 1956 Feb;42(2):68–73. doi: 10.1073/pnas.42.2.68. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. NISHIMURA E. T., DIPAOLO J. A., HILL W. T. Studies on the viscosity of the cytoplasm of mouse Ehrlich ascites tumor cells. AMA Arch Pathol. 1955 Apr;59(4):487–494. [PubMed] [Google Scholar]
  5. ROSE G. A separable and multipurpose tissue culture chamber. Tex Rep Biol Med. 1954;12(4):1074–1083. [PubMed] [Google Scholar]

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