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. 1973 Aug 1;138(2):452–460. doi: 10.1084/jem.138.2.452

THE LIFE SPAN OF IgA PLASMA CELLS FROM THE MOUSE INTESTINE

Carlos A Mattioli 1, Thomas B Tomasi Jr 1
PMCID: PMC2139405  PMID: 4578299

Abstract

Tritiated thymidine was injected during the neonatal period into conventional CBA mice. The disappearance rate of tritium-labeled IgA plasma cells was followed by a technique combining immunofluorescence with autoradiography which permitted the identification of the immunoglobulin class of plasma cells with labeled nuclei. In this way, it was possible to calculate that the major population of intestinal IgA plasma cells have a half-life of 4.7 days under physiological conditions of stimulation. It was also found that the maximum life span of both intestinal IgA plasma cells and the IgA, IgG, and IgM plasma cells from the spleen is of the order of 7–8 wk.

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Selected References

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

  1. Bazin H., Levi G., Doria G. Predominant contribution of IgA antibody-forming cells to an immune response detected in extraintestinal lymphoid tissues of germ-free mice exposed to antigen by the oral route. J Immunol. 1970 Oct;105(4):1049–1051. [PubMed] [Google Scholar]
  2. Claflin A. J., Smithies O. Antibody-producing cells in division. Science. 1967 Sep 29;157(3796):1561–1562. [PubMed] [Google Scholar]
  3. Crabbé P. A., Bazin H., Eyssen H., Heremans J. F. The normal microbial flora as a major stimulus for proliferation of plasma cells synthesizing IgA in the gut. The germ-free intestinal tract. Int Arch Allergy Appl Immunol. 1968;34(4):362–375. doi: 10.1159/000230130. [DOI] [PubMed] [Google Scholar]
  4. Crabbé P. A., Nash D. R., Bazin H., Eyssen H., Heremans J. F. Immunohistochemical observations on lymphoid tissues from conventional and germ-free mice. Lab Invest. 1970 May;22(5):448–457. [PubMed] [Google Scholar]
  5. LESHER S., WALBURG H. E., Jr, SACHER G. A., Jr GENERATION CYCLE IN THE DUODENAL CRYPT CELLS OF GERM-FREE AND CONVENTIONAL MICE. Nature. 1964 May 30;202:884–886. doi: 10.1038/202884a0. [DOI] [PubMed] [Google Scholar]
  6. La Via M. F., Vatter A. E. A morphologic study of the terminal events of primary antibody response. J Reticuloendothel Soc. 1969 Jun;6(3):221–231. [PubMed] [Google Scholar]
  7. MILLER J. J., 3rd AN AUTORADIOGRAPHIC STUDY OF PLASMA CELL AND LYMPHOCYTE SURVIVAL IN RAT POPLITEAL LYMPH NODES. J Immunol. 1964 May;92:673–681. [PubMed] [Google Scholar]
  8. Mandel M. A., Asofsky R. Studies of thoracic duct lymphocytes of mice. I. Immunoglobulin synthesis in vitro. J Immunol. 1968 Feb;100(2):363–370. [PubMed] [Google Scholar]
  9. NOSSAL G. J., MAKELA O. Autoradiographic studies on the immune response.I. The kinetics of plasma cell proliferation. J Exp Med. 1962 Jan 1;115:209–230. doi: 10.1084/jem.115.1.209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. SCHOOLEY J. C. Autoradiographic observations of plasma cell formation. J Immunol. 1961 Mar;86:331–337. [PubMed] [Google Scholar]

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