Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1975 May 1;141(5):1147–1162. doi: 10.1084/jem.141.5.1147

Cell cycle-associated changes in receptors for IgE during growth and differentiation of a rat basophilic leukemia cell line

PMCID: PMC2189775  PMID: 1168692

Abstract

The rat basophilic leukemia cell line (RBL-1) showed an inverse relationship between growth rate and expression of receptor activity for IgE. After prolonged exponential growth, the number of receptors per cell stabilized at 4-6 times 10-5. Cells in stationary cultures, which are arrested in the G1 phase of the cell cycle, continued to accumulate up to 0.9-1.7 times 10-6 receptors/cell with no increase in volume. Upon resuspension in fresh medium at low density, these cells were shown to lose up to 70% of the receptor activity within 4 h. Assessment of cultures synchronized by double thymidine block and cells fractionated by centrifugation of a Ficoll gradient indicated that the RBL-1 cells acquire receptors in the G1 phase of the cell cycle. No accumulation of active receptors occurred during the S and G2 phases, though the average cell volume increased. Cell division resulted in a drop in number of receptors per cell while the number of cell-bound receptors in the culture remained unchanged. This indicates that during mitosis receptors were simply distributed to daughter cells.

Full Text

The Full Text of this article is available as a PDF (927.7 KB).

Selected References

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

  1. BASERGA R. THE RELATIONSHIP OF THE CELL CYCLE TO TUMOR GROWTH AND CONTROL OF CELL DIVISION: A REVIEW. Cancer Res. 1965 Jun;25:581–595. [PubMed] [Google Scholar]
  2. Bazin H., Querinjean P., Beckers A., Heremans J. F., Dessy F. Transplantable immunoglobulin-secreting tumours in rats. IV. Sixty-three IgE-secreting immunocytoma tumours. Immunology. 1974 Apr;26(4):713–723. [PMC free article] [PubMed] [Google Scholar]
  3. Carson D. A., Metzger H. Interaction of IgE with rat basophilic leukemia cells. IV. Antibody-induced redistribution of IgE receptors. J Immunol. 1974 Oct;113(4):1271–1277. [PubMed] [Google Scholar]
  4. Churchill J. R., Studzinski G. P. Thymidine as synchronizing agent. 3. Persistence of cell cycle patterns of phosphatase activities and elevation of nuclease activity during inhibition of DNA synthesis. J Cell Physiol. 1970 Jun;75(3):297–303. doi: 10.1002/jcp.1040750306. [DOI] [PubMed] [Google Scholar]
  5. Cikes M., Friberg S., Jr Expression of H-2 and Moloney leukemia virus-determined cell-surface antigens in synchronized cultures of a mouse cell line. Proc Natl Acad Sci U S A. 1971 Mar;68(3):566–569. doi: 10.1073/pnas.68.3.566. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cikes M., Friberg S., Jr, Klein G. Quantitative studies of antigen expression in cultured murine lymphoma cells. II. Cell-surface antigens in synchronized cultures. J Natl Cancer Inst. 1972 Dec;49(6):1607–1611. doi: 10.1093/jnci/49.6.1607. [DOI] [PubMed] [Google Scholar]
  7. Cikes M., Klein G. Quantitative studies of antigen expression in cultured murine lymphoma cells. I. Cell-surface antigens in "Asynchronous" cultures. J Natl Cancer Inst. 1972 Dec;49(6):1599–1606. doi: 10.1093/jnci/49.6.1599. [DOI] [PubMed] [Google Scholar]
  8. Crissman H. A., Tobey R. A. Cell-cycle analysis in 20 minutes. Science. 1974 Jun 21;184(4143):1297–1298. doi: 10.1126/science.184.4143.1297. [DOI] [PubMed] [Google Scholar]
  9. Everson L. K., Buell D. N., Rogentine G. N., Jr Separation of human lymphoid cells into G 1 , S, and G 2 cell cycle populations by use of a velocity sedimentation technique. J Exp Med. 1973 Feb 1;137(2):343–358. doi: 10.1084/jem.137.2.343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Everson L. K., Plocinik B. A., Rogentine G. N., Jr HL-A expression on the G1, S, and G2 cell-cycle stages of human lymphoid cells. J Natl Cancer Inst. 1974 Oct;53(4):913–920. doi: 10.1093/jnci/53.4.913. [DOI] [PubMed] [Google Scholar]
  11. Ferrone S., Cooper N. R., Pellegrino M. A., Reisfeld R. A. Interaction of histocompatibility (HL-A) antibodies and complement with synchronized human lymphoid cells in continuous culture. J Exp Med. 1973 Jan 1;137(1):55–68. doi: 10.1084/jem.137.1.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Galavazi G., Schenk H., Bootsma D. Synchronization of mammalian cells in vitro by inhibition of the DNA synthesis. I. Optimal conditions. Exp Cell Res. 1966 Feb;41(2):428–437. doi: 10.1016/s0014-4827(66)80149-0. [DOI] [PubMed] [Google Scholar]
  13. Gerner E. W., Glick M. C., Warren L. Membranes of animal cells. V. Biosynthesis of the surface membrane during the cell cycle. J Cell Physiol. 1970 Jun;75(3):275–279. doi: 10.1002/jcp.1040750303. [DOI] [PubMed] [Google Scholar]
  14. Glick M. C., Comstock C., Warren L. Membranes of animal cells. VII. Carbohydrates of surface membranes and whole cells. Biochim Biophys Acta. 1970 Dec 1;219(2):290–300. doi: 10.1016/0005-2736(70)90208-7. [DOI] [PubMed] [Google Scholar]
  15. Graham J. M., Sumner M. C., Curtis D. H., Pasternak C. A. Sequence of events in plasma membrane assembly during the cell cycle. Nature. 1973 Nov 30;246(5431):291–295. doi: 10.1038/246291a0. [DOI] [PubMed] [Google Scholar]
  16. Kuhns W. J., Bramson S. Variable behaviour of blood group H on HeLa cell populations synchronized with thymidine. Nature. 1968 Aug 31;219(5157):938–939. doi: 10.1038/219938a0. [DOI] [PubMed] [Google Scholar]
  17. Kulczycki A., Jr, Isersky C., Metzger H. The interaction of IgE with rat basophilic leukemia cells. I. Evidence for specific binding of IgE. J Exp Med. 1974 Mar 1;139(3):600–616. doi: 10.1084/jem.139.3.600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kulczycki A., Jr, Metzger H. The interaction of IgE with rat basophilic leukemia cells. II. Quantitative aspects of the binding reaction. J Exp Med. 1974 Dec 1;140(6):1676–1695. doi: 10.1084/jem.140.6.1676. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Lambert W. C., Studzinski G. P. Thymidine as a synchronizing agent. II. Partial recovery of HeLa cells from unbalanced growth. J Cell Physiol. 1969 Jun;73(3):261–266. doi: 10.1002/jcp.1040730310. [DOI] [PubMed] [Google Scholar]
  20. Melchers F., Andersson J. IgM in bone marrow-derived lymphocytes. Changes in synthesis, turnover and secretion, and in numbers of molecules on the surface of B cells after mitogenic stimulation. Eur J Immunol. 1974 Mar;4(3):181–188. doi: 10.1002/eji.1830040306. [DOI] [PubMed] [Google Scholar]
  21. Moore M. A., Williams N., Metcalf D. In vitro colony formation by normal and leukemic human hematopoietic cells: characterization of the colony-forming cells. J Natl Cancer Inst. 1973 Mar;50(3):603–623. doi: 10.1093/jnci/50.3.603. [DOI] [PubMed] [Google Scholar]
  22. Nameroff M., Holtzer H. The loss of phenotypic traits by differentiated cells. IV. Changes in polysaccharides produced by dividing chondrocytes. Dev Biol. 1967 Sep;16(3):250–281. doi: 10.1016/0012-1606(67)90026-7. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Onodera K., Sheinin R. Macromolecular glucosamine-containing component of the surface of cultivated mouse cells. J Cell Sci. 1970 Sep;7(2):337–355. doi: 10.1242/jcs.7.2.337. [DOI] [PubMed] [Google Scholar]
  25. Osborne D. P., Jr, Katz D. H. The allogeneic effect in inbred mice. IV. Regulatory influences of graft-vs.-host reactions on host T lymphocyte functions. J Exp Med. 1973 Oct 1;138(4):825–838. doi: 10.1084/jem.138.4.825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Pellegrino M. A., Ferrone S., Natali P. G., Pellegrino A., Reisfeld R. A. Expression of HL-A antigens in synchronized cultures of human lymphocytes. J Immunol. 1972 Feb;108(2):573–576. [PubMed] [Google Scholar]
  27. Pfeiffer S. E., Herschman H. R., Lightbody J., Sato G. Synthesis by a clonal line of rat glial cells of a protein unique to the nervous system. J Cell Physiol. 1970 Jun;75(3):329–339. doi: 10.1002/jcp.1040750309. [DOI] [PubMed] [Google Scholar]
  28. Porter K., Prescott D., Frye J. Changes in surface morphology of Chinese hamster ovary cells during the cell cycle. J Cell Biol. 1973 Jun;57(3):815–836. doi: 10.1083/jcb.57.3.815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Rubin R. W., Everhart L. P. The effect of cell-to-cell contact on the surface morphology of Chinese hamster ovary cells. J Cell Biol. 1973 Jun;57(3):837–844. doi: 10.1083/jcb.57.3.837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Simantov R., Sachs L. Regulation of acetylcholine receptors in relation to acetylcholinesterase in neuroblastoma cells. Proc Natl Acad Sci U S A. 1973 Oct;70(10):2902–2905. doi: 10.1073/pnas.70.10.2902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Steinkamp J. A., Fulwyler M. J., Coulter J. R., Hiebert R. D., Horney J. L., Mullancy P. F. A new multiparameter separator for microscopic particles and biological cells. Rev Sci Instrum. 1973 Sep;44(9):1301–1310. doi: 10.1063/1.1686375. [DOI] [PubMed] [Google Scholar]
  32. Studzinski G. P., Lambert W. C. Thymidine as a synchronizing agent. I. Nucleic acid and protein formation in synchronous HeLa cultures treated with excess thymidine. J Cell Physiol. 1969 Apr;73(2):109–117. doi: 10.1002/jcp.1040730204. [DOI] [PubMed] [Google Scholar]
  33. Van Dilla M. A., Trujillo T. T., Mullaney P. F., Coulter J. R. Cell microfluorometry: a method for rapid fluorescence measurement. Science. 1969 Mar 14;163(3872):1213–1214. doi: 10.1126/science.163.3872.1213. [DOI] [PubMed] [Google Scholar]
  34. Warren L., Glick M. C. Membranes of animal cells. II. The metabolism and turnover of the surface membrane. J Cell Biol. 1968 Jun;37(3):729–746. doi: 10.1083/jcb.37.3.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. 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]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES