ANTIGEN-INDEPENDENT MATURATION OF CD2, CD11A CD18, CD44, AND CD58 EXPRESSION ON THYMIC EMIGRANTS IN FETAL AND POSTNATAL SHEEP/

Citation
Da. Witherden et al., ANTIGEN-INDEPENDENT MATURATION OF CD2, CD11A CD18, CD44, AND CD58 EXPRESSION ON THYMIC EMIGRANTS IN FETAL AND POSTNATAL SHEEP/, Developmental immunology, 4(3), 1995, pp. 199-209
Citations number
55
Categorie Soggetti
Immunology
Journal title
ISSN journal
10446672
Volume
4
Issue
3
Year of publication
1995
Pages
199 - 209
Database
ISI
SICI code
1044-6672(1995)4:3<199:AMOCCC>2.0.ZU;2-Z
Abstract
We have compared the expression of CD2, CD11a/CD18, CD44, and CD58 on alpha beta and gamma delta T cells emigrating from the fetal and postn atal thymus. We report that both gamma delta and the CD4(+)CD8(-) and CD4(-)CD8(+) subsets of alpha beta T cells express mature levels of th e adhesion molecules CD11a/CD18, CD44, and CD58 upon emigration from t he thymus. Whereas CD44 is up-regulated on gamma delta(+) thymocytes p rior to export, down-regulation of both CD11a/CD18 and CD58 occurs pri or to emigration from the thymus, suggesting that down-regulation of t hese molecules may be a final maturational step taken by developing ga mma delta T cells before their export from the thymus. In contrast, th ere is continued up-regulation of CD2 on gamma delta and alpha beta T cells upon emigration from the thymus and as they move into the mature peripheral T-cell pool. There was also a marked reduction in the numb er of CD2(+) gamma delta T cells exported during fetal development tha t was associated with a marked reduction in the percentage of CD2+ gam ma delta thymocytes exported. The postthymic maturation of CD2 and the other changes in adhesion-molecule expression appear to be independen t of extrinsic antigen, as the same changes were observed in the antig en-free environment of the fetus as in the postnatal lamb, which has b een exposed to extrinsic antigen. It thus appears that these changes i n adhesion-molecule expression are as a result of the normal maturatio n pathway from a developing thymocyte to a mature peripheral T cell.