Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1972 Jan;69(1):253–257. doi: 10.1073/pnas.69.1.253

Cytochalasin B: Effects on Cell Morphology, Cell Adhesion, and Mucopolysaccharide Synthesis

J W Sanger 1, H Holtzer 1
PMCID: PMC427586  PMID: 4257818

Abstract

Cytochalasin B reversibly causes extensive branching of myoblasts, fibroblasts, and nonencapsulated chondroblasts; it does not induce the formation of similar processes in myotubes, erythrocytes, amnion cells, encapsulated chondroblasts, or HeLa cells. The drug has no effect on the spontaneous contractions of isolated skeletal, cardiac, or smooth-muscle cells. Within 60 min, it depresses the incorporation of [14C]glucosamine into total mucopolysaccharide and glycoproteins by over 50%. The drug interferes with adhesion and sorting-out of dissociated embryonic cells. Cytochalasin B is likely to produce changes in components of the cell surface whose function is not readily or solely related to a system of “primitive contractile microfilaments.”

Keywords: cultured cells, contractile microfilaments, glycoproteins, embryonic cells, sorting-out

Full text

PDF
253

Images in this article

Selected References

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

  1. Abbott J., Holtzer H. The loss of phenotypic traits by differentiated cells, V. The effect of 5-bromodeoxyuridine on cloned chondrocytes. Proc Natl Acad Sci U S A. 1968 Apr;59(4):1144–1151. doi: 10.1073/pnas.59.4.1144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bischoff R. Acid mucopolysaccharide synthesis by chick amnion cell cultures. Inhibition by 5-bromodeoxyuridine. Exp Cell Res. 1971 May;66(1):224–236. doi: 10.1016/s0014-4827(71)80032-0. [DOI] [PubMed] [Google Scholar]
  3. Bischoff R., Holtzer H. Inhibition of myoblast fusion after one round of DNA synthesis in 5-bromodeoxyuridine. J Cell Biol. 1970 Jan;44(1):134–150. doi: 10.1083/jcb.44.1.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bischoff R., Holtzer H. Mitosis and the processes of differentiation of myogenic cells in vitro. J Cell Biol. 1969 Apr;41(1):188–200. doi: 10.1083/jcb.41.1.188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Carter S. B. Effects of cytochalasins on mammalian cells. Nature. 1967 Jan 21;213(5073):261–264. doi: 10.1038/213261a0. [DOI] [PubMed] [Google Scholar]
  6. Chacko S., Abbott J., Holtzer S., Holtzer H. The loss of phenotypic traits by differentiated cells. VI. Behavior of the progeny of a single chondrocyte. J Exp Med. 1969 Aug 1;130(2):417–442. doi: 10.1084/jem.130.2.417. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chacko S., Holtzer S., Holtzer H. Suppression of chondrogenic expression in mixtures of normal chondrocytes and BUDR-altered chondrocytes grown in vitro. Biochem Biophys Res Commun. 1969 Jan 27;34(2):183–189. doi: 10.1016/0006-291x(69)90629-9. [DOI] [PubMed] [Google Scholar]
  8. Cloney R. A. Cytoplasmic filaments and morphogenesis: the role of the notochord in ascidian metamorphosis. Z Zellforsch Mikrosk Anat. 1969;100(1):31–53. doi: 10.1007/BF00343819. [DOI] [PubMed] [Google Scholar]
  9. Estensen R. D., Rosenberg M., Sheridan J. D., Wessells N. K., Spooner B. S., Ash J. F., Ludueña M. A., Wrenn J. T. Cytochalasin B: microfilaments and "contractile" processes. Science. 1971 Jul 23;173(3994):356–359. doi: 10.1126/science.173.3994.356. [DOI] [PubMed] [Google Scholar]
  10. Estensen R. D., Rosenberg M., Sheridan J. D., Wessells N. K., Spooner B. S., Ash J. F., Ludueña M. A., Wrenn J. T. Cytochalasin B: microfilaments and "contractile" processes. Science. 1971 Jul 23;173(3994):356–359. doi: 10.1126/science.173.3994.356. [DOI] [PubMed] [Google Scholar]
  11. Ishikawa H., Bischoff R., Holtzer H. Formation of arrowhead complexes with heavy meromyosin in a variety of cell types. J Cell Biol. 1969 Nov;43(2):312–328. [PMC free article] [PubMed] [Google Scholar]
  12. Krishan A. Fine structure of cytochalasin-induced multinucleated cells. J Ultrastruct Res. 1971 Jul;36(1):191–204. doi: 10.1016/s0022-5320(71)80097-7. [DOI] [PubMed] [Google Scholar]
  13. Krishan A., Ray-Chaudhuri R. Asynchrony of nuclear development in cytochalasin-induced multinucleate cells. J Cell Biol. 1969 Dec;43(3):618–621. doi: 10.1083/jcb.43.3.618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Marchesi V. T., Steers E., Jr Selective solubilization of a protein component of the red cell membrane. Science. 1968 Jan 12;159(3811):203–204. doi: 10.1126/science.159.3811.203. [DOI] [PubMed] [Google Scholar]
  15. Mayne R., Sanger J. W., Holtzer H. Inhibition of mucopolysaccharide synthesis by 5-bromodeoxyuridine in cultures of chick amnion cells. Dev Biol. 1971 Aug;25(4):547–567. doi: 10.1016/0012-1606(71)90005-4. [DOI] [PubMed] [Google Scholar]
  16. Mazia D., Ruby A. Dissolution of erythrocyte membranes in water and comparison of the membrane protein with other structural proteins. Proc Natl Acad Sci U S A. 1968 Nov;61(3):1005–1012. doi: 10.1073/pnas.61.3.1005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Nachmias V. T., Huxley H. E. Electron microscope observations on actomyosin and actin preparations from Physarum polycephalum, and on their interaction with heavy meromyosin subfragment I from muscle myosin. J Mol Biol. 1970 May 28;50(1):83–90. doi: 10.1016/0022-2836(70)90105-1. [DOI] [PubMed] [Google Scholar]
  18. Okazaki K., Holtzer H. An analysis of myogenesis in vitro using fluorescein-labeled antimyosin. J Histochem Cytochem. 1965 Nov-Dec;13(8):726–739. doi: 10.1177/13.8.726. [DOI] [PubMed] [Google Scholar]
  19. Okazaki K., Holtzer H. Myogenesis: fusion, myosin synthesis, and the mitotic cycle. Proc Natl Acad Sci U S A. 1966 Nov;56(5):1484–1490. doi: 10.1073/pnas.56.5.1484. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pollard T. D., Shelton E., Weihing R. R., Korn E. D. Ultrastructural characterization of F-actin isolated from Acanthamoeba castellanii and identification of cytoplasmic filaments as F-actin by reaction with rabbit heavy meromyosin. J Mol Biol. 1970 May 28;50(1):91–97. doi: 10.1016/0022-2836(70)90106-3. [DOI] [PubMed] [Google Scholar]
  21. Ridler M. A., Smith G. F. The response of human cultured lymphocytes to cytochalasin B. J Cell Sci. 1968 Dec;3(4):595–602. doi: 10.1242/jcs.3.4.595. [DOI] [PubMed] [Google Scholar]
  22. STOCKDALE F., OKAZAKI K., NAMEROFF M., HOLTZER H. 5-BROMODEOXYURIDINE: EFFECT ON MYOGENESIS IN VITRO. Science. 1964 Oct 23;146(3643):533–535. doi: 10.1126/science.146.3643.533. [DOI] [PubMed] [Google Scholar]
  23. Sanger J. W., Holtzer S., Holtzer H. Effects of cytochalasin B on muscle cells in tissue culture. Nat New Biol. 1971 Jan 27;229(4):121–123. doi: 10.1038/newbio229121a0. [DOI] [PubMed] [Google Scholar]
  24. Schroeder T. E. The contractile ring. I. Fine structure of dividing mammalian (HeLa) cells and the effects of cytochalasin B. Z Zellforsch Mikrosk Anat. 1970;109(4):431–449. [PubMed] [Google Scholar]
  25. Spooner B. S., Yamada K. M., Wessells N. K. Microfilaments and cell locomotion. J Cell Biol. 1971 Jun;49(3):595–613. doi: 10.1083/jcb.49.3.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Weintraub H., Campbell G. le M., Holtzer H. Primitive erythropoiesis in early chick embryogenesis. I. Cell cycle kinetics and the control of cell division. J Cell Biol. 1971 Sep;50(3):652–668. doi: 10.1083/jcb.50.3.652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Wessells N. K., Spooner B. S., Ash J. F., Bradley M. O., Luduena M. A., Taylor E. L., Wrenn J. T., Yamada K. Microfilaments in cellular and developmental processes. Science. 1971 Jan 15;171(3967):135–143. doi: 10.1126/science.171.3967.135. [DOI] [PubMed] [Google Scholar]
  28. Yamada K. M., Spooner B. S., Wessells N. K. Ultrastructure and function of growth cones and axons of cultured nerve cells. J Cell Biol. 1971 Jun;49(3):614–635. doi: 10.1083/jcb.49.3.614. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES