ONTOGENY OF FETAL CD8(LO)4(LO)THYMOCYTES - EXPRESSION OF CD44, CD25 AND EARLY EXPRESSION OF TCR-ALPHA MESSENGER-RNA

Citation
S. Andjelic et al., ONTOGENY OF FETAL CD8(LO)4(LO)THYMOCYTES - EXPRESSION OF CD44, CD25 AND EARLY EXPRESSION OF TCR-ALPHA MESSENGER-RNA, European Journal of Immunology, 23(9), 1993, pp. 2109-2115
Citations number
27
Categorie Soggetti
Immunology
ISSN journal
00142980
Volume
23
Issue
9
Year of publication
1993
Pages
2109 - 2115
Database
ISI
SICI code
0014-2980(1993)23:9<2109:OOFC-E>2.0.ZU;2-V
Abstract
CD8lo4lo cells are the immediate precursors of immature CD8hi4(lo)TcR( lo), CD8lo4(hi)TcR(lo) and CD8hi4(hi)TcR(lo) double-positive (DP) thym ocytes in the adult murine thymus. These cells are the first subset in the adult thymus to express accessory CD8 and CD4 molecules, to rearr ange the T cell receptor (TcR) alpha chain genes and to express the Tc R alphabeta heterodimer at low levels at the surface. Here, we investi gate the fetal ontogeny of CD8lo4lo cells. We detect these cells on da y 15 of fetal development. They dominate the thymus on day 15.5, to be come progressively less prominent thereafter. An important characteris tic of fetal CD8lo4lo cells is the early expression of TcR alpha mRNA (on fetal day 15, 36-48 h earlier than reported previously). Our resul ts also suggest, but do not prove, that the receptor may be expressed on the surface as early as day 15.5. Fetal CD8lo4lo cells, like their adult counterparts, become DP in vitro. However, early fetal CD8lo4lo thymocytes express both CD44 and CD25 - unlike the adult subset - and that links them to their putative precursors, fetal CD44+CD25+ double- negative cells. This finding underscores the difference between adult and fetal thymocytes in turnover of membrane molecules and/or the kine tics of progression through phenotypic stages.