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PMID: 8095954 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Exogenous IL-7 promotes the growth of CD3-CD4-CD8-CD44+CD25+/- precursor cells and blocks the differentiation pathway of TCR-alpha beta cells in fetal thymus organ culture.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 150 ·No. 7 ·1993-04-01 ·Pages 2706-16

Plum J, De Smedt M, Leclercq G

Abstract

Addition of human rIL-7 to fetal thymic organ culture started at day 13, 14, or 15 did not influence the number of cells generated during a 12-day culture period. However, the IL-7 treatment resulted in a preferential expansion of cells with a phenotype characteristic for cells at an early step of differentiation. The cells were CD4-CD8-CD3-CD2- and SCA-1+. Analysis of the coordinate expression of CD44 and CD25 on these cells showed that the majority of the cells were either CD44+CD25- or CD44+CD25intermediate. TCR-alpha beta cells were present but in a significantly lower number as compared to the control cultures. The cell number of TCR-gamma delta cells was increased. All these effects were moderate after 6 days, but unequivocal after 12 days of culture. Treatment of the fetal organ culture with mAb-neutralizing murine IL-7 resulted in an inhibition of the proliferation of the fetal thymocytes. No particular subset studied was preferentially inhibited. By using a model of reconstitution of 14-day embryonic thymuses depleted of thymocytes by deoxyguanosine and reconstituted with fetal day 13 liver cells and set up in organ culture with or without IL-7, it was shown in a clear cut way that IL-7 indeed promotes expansion of the early precursor cells and TCR-gamma delta cells, but prevents the generation of TCR-alpha beta cells. In addition, reconstitution experiments were set up in the presence of mAb-neutralizing murine IL-7. This treatment resulted in the inhibition of the growth of the fetal thymocytes without inhibiting preferentially a particular subset. These data indicate that IL-7 acts at an early step of T cell differentiation and plays a role to expand precursor cells, but prevents this population from additional differentiation towards the TCR-alpha beta pathways, whereas the differentiation towards TCR-gamma delta cells is not influenced or even enhanced.

MeSH Terms
Animals Antigens, CD/analysis Antigens, Differentiation, T-Lymphocyte/metabolism Antigens, Ly/metabolism CD2 Antigens CD3 Complex CD4 Antigens CD8 Antigens Cell Differentiation/drug effects,immunology Cell Division/drug effects,immunology Cell Size/immunology Fetus Hematopoietic Stem Cells/cytology,drug effects,immunology Interleukin-7/pharmacology Leukocyte Count/drug effects Membrane Proteins/metabolism Mice Mice, Inbred BALB C Organ Culture Techniques Phenotype Receptors, Antigen, T-Cell, alpha-beta/immunology Receptors, Antigen, T-Cell, gamma-delta/metabolism Receptors, Immunologic/metabolism Receptors, Interleukin-2 Receptors, Lymphocyte Homing T-Lymphocytes/cytology,drug effects,immunology Thymus Gland/cytology
Chemicals
Antigens, CD Antigens, Differentiation, T-Lymphocyte Antigens, Ly CD2 Antigens CD3 Complex CD4 Antigens CD8 Antigens Interleukin-7 Ly6a protein, mouse Membrane Proteins Receptors, Antigen, T-Cell, alpha-beta Receptors, Antigen, T-Cell, gamma-delta Receptors, Immunologic Receptors, Interleukin-2 Receptors, Lymphocyte Homing
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Plum J
Department of Bacteriology, Virology and Immunology, University Hospital Gent, Belgium.
De Smedt M
Leclercq G
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1993-04-01
Pages
2706-16
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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