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Changes in cell surface antigen expression during murine bone marrow cell regeneration in vivo and proliferation in vitro.

Authors :
Bertoncello, I.
Bartelmez, S.H.
Bradley, T.R.
Hodgson, G.S.
Source :
Immunology & Cell Biology; Apr1989, Vol. 67 Issue 2, p127-133, 7p
Publication Year :
1989

Abstract

Modulations in surface antigen expression during marrow regeneration in vivo, and proliferation in vitro in response to haemopoietic growth factors, were studied using a panel of monoclonal antibodies recognizing antigenic determinants expressed by primitive multipotential progenitor cells (Thy-1, Qa-m7), or lineage antigens restricted to committed progenitors and differentiated cells of the neutrophil/macrophage (7/4) and B lymphocyte (B220) lineages. These two categories of antigen exhibited differing responses to marrow perturbation and proliferation. Following administration of a cytotoxic dose of 5-fluorouracil, or lethal irradiation and transplantation of normal donor marrow, the levels of Thy-1 and Qa-m7 antigen expression rapidly increase, reaching a peak at the onset of regeneration: the nadir of marrow cellularity. Expression of these antigens returns to normal as regeneration proceeds and marrow is reconstituted. 7/4 and B220 antigen expression reflect the presence or absence of maturing cells bearing these markers: antigen expression declining following perturbation, and re-emerging during the course of regeneration. In vitro, when marrow cells taken from mice 8 days following treatment with 5-FU are grown in liquid culture in the presence of colony-stimulating factor-1 plus bladder cell carcinoma cell line 5637 conditioned medium, marrow cells are stimulated to proliferate and differentiate along the neutrophil/macrophage lineage. 7/4 antigen expression increases throughout the culture period, and B220 antigen is undetectable after the fifth day of culture. Thy-1 antigen expression also rises and remains elevated, and Qa-m7 antigen expression remains stable. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08189641
Volume :
67
Issue :
2
Database :
Complementary Index
Journal :
Immunology & Cell Biology
Publication Type :
Academic Journal
Accession number :
17308807
Full Text :
https://doi.org/10.1038/icb.1989.18