Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1975 Oct 1;142(4):949–959. doi: 10.1084/jem.142.4.949

Serum albumin is essential for in vitro growth of activated human lymphocytes

PMCID: PMC2189952  PMID: 1176892

Abstract

The effect of human plasma, the plasma protein fractions of Cohn, and crystallized serum albumin on the in vitro growth of human lymphocytes activated by concanavalin A (Con A) or bacterial lipopolysaccharide was compared. It was found that fraction V or serum albumin (SA) is essential for growth of activated T and B lymphocytes. The other plasma proteins have no effect. The growth response of Con A-activated T lymphocytes to increasing concentrations of SA is similar to the response to increasing equivalent concentrations of plasma suggesting but not proving that SA is the only growth-stimulating factor in plasma when added to a protein-free culture medium. The growth-promoting effect of SA is not due to the fatty acids or hormones bound to SA but is attributed to the albumin molecule itself or to a factor tightly bound to it. SA can also effectively replace plasma to stimulate proliferation of lymphocytes activated by allogeneic lymphocytes or purified protein derivative of tuberculin.

Full Text

The Full Text of this article is available as a PDF (639.8 KB).

Selected References

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

  1. Andersson J., Sjöberg O., Möller G. Mitogens as probes for immunocyte activation and cellular cooperation. Transplant Rev. 1972;11:131–177. doi: 10.1111/j.1600-065x.1972.tb00048.x. [DOI] [PubMed] [Google Scholar]
  2. BENDER M. A., PRESCOTT D. M. DNA synthesis and mitosis in cultures of human peripheral leukocytes. Exp Cell Res. 1962 Aug;27:221–229. doi: 10.1016/0014-4827(62)90225-2. [DOI] [PubMed] [Google Scholar]
  3. DAUGHADAY W. H. Binding of corticosteroids by plasma proteins. IV. The electrophoretic demonstration of corticosteroid binding globulin. J Clin Invest. 1958 Apr;37(4):519–523. doi: 10.1172/JCI103633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. EAGLE H. Nutrition needs of mammalian cells in tissue culture. Science. 1955 Sep 16;122(3168):501–514. doi: 10.1126/science.122.3168.501. [DOI] [PubMed] [Google Scholar]
  5. Gospodarowicz D. Localisation of a fibroblast growth factor and its effect alone and with hydrocortisone on 3T3 cell growth. Nature. 1974 May 10;249(453):123–127. doi: 10.1038/249123a0. [DOI] [PubMed] [Google Scholar]
  6. Greaves M., Janossy G., Doenhoff M. Selective triggering of human T and B lymphocytes in vitro by polyclonal mitogens. J Exp Med. 1974 Jul 1;140(1):1–18. doi: 10.1084/jem.140.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Greaves M., Janossy G. Elicitation of selective T and B lymphocyte responses by cell surface binding ligands. Transplant Rev. 1972;11:87–130. doi: 10.1111/j.1600-065x.1972.tb00047.x. [DOI] [PubMed] [Google Scholar]
  8. Gunther G. R., Wang J. L., Edelman G. M. The kinetics of cellular commitment during stimulation of lymphocytes by lectins. J Cell Biol. 1974 Aug;62(2):366–377. doi: 10.1083/jcb.62.2.366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lindahl-Kiessling K. Mechanism of phytohemagglutinin (PHA) action. V. PHA compared with concanavalin A (Con A). Exp Cell Res. 1972 Jan;70(1):17–26. doi: 10.1016/0014-4827(72)90176-0. [DOI] [PubMed] [Google Scholar]
  10. Lohrmann H. P., Whang-Peng J. Human mixed leukocyte culture: identification of the proliferating lymphocyte subpopulation by sex chromosome markers. J Exp Med. 1974 Jul 1;140(1):54–60. doi: 10.1084/jem.140.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Marshall W. H., Valentine F. T., Lawrence H. S. Cellular immunity in vitro. Clonal proliferation of antigen-stimulated lymphocytes. J Exp Med. 1969 Aug 1;130(2):327–343. doi: 10.1084/jem.130.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Polet H., Geyer R. P. A quantitative human mixed lymphocyte culture using suspension cultures. Proc Soc Exp Biol Med. 1973 Nov;144(2):666–670. doi: 10.3181/00379727-144-37658. [DOI] [PubMed] [Google Scholar]
  13. Polet H. The effect of lymphokines on the growth, the metabolism, and the functions of the cellular membrane of Chang liver cells in vitro. Cell Immunol. 1974 Mar 30;11(1-3):247–256. doi: 10.1016/0008-8749(74)90025-2. [DOI] [PubMed] [Google Scholar]
  14. Polet H. The mixed lymphocyte culture as a tool for the quantitative determination of HL-A differences. Transplantation. 1972 May;13(5):472–480. doi: 10.1097/00007890-197205000-00005. [DOI] [PubMed] [Google Scholar]
  15. Stoien J. D., Wang R. J. Effect of near-ultraviolet and visible light on mammalian cells in culture II. Formation of toxic photoproducts in tissue culture medium by blacklight. Proc Natl Acad Sci U S A. 1974 Oct;71(10):3961–3965. doi: 10.1073/pnas.71.10.3961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wilson D. B., Blyth JL NOWELL P. C. Quantitative studies on the mixed lymphocyte interaction in rats. 3. Kinetics of the response. J Exp Med. 1968 Nov 1;128(5):1157–1181. doi: 10.1084/jem.128.5.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Younkin L. H. In vitro response of lymphocytes to phytohemagglutinin (PHA) as studied with antiserum to PHA. I. Initiation period, daughter-cell proliferation, and restimulation. Exp Cell Res. 1972 Nov;75(1):1–10. doi: 10.1016/0014-4827(72)90512-5. [DOI] [PubMed] [Google Scholar]

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

RESOURCES