| Abstract: |
CD8lo 4lo cells are the immediate precursors of immature CD8hi4lcTcRlo, CD8hi 4hiTcRlo and CD8hi4hiTcRlo double‐positive (DP) thymocytes in the adult murine thymus. These cells are the first subset in the adult thymus to express accessory CD8 and CD4 molecules, to rearrange the T cell receptor (TcR) a chain genes and to express the TcR αβ heterodimer at low levels at the surface. Here, we investigate the fetal ontogeny of CD8lo 4lo cells. We detect these cells on day 15 of fetal development. They dominate the thymus on day 15.5, to become progressively less prominent thereafter. An important characteristic of fetal CD8lo 4lo cells is the early expression of TcR α mRNA (on fetal day 15, 36–48 h earlier than reported previously). Our results also suggest, but do not prove, that the receptor may be expressed on the surface as early as day 15.5. Fetal CD8lo 4lo cells, like their adult counterparts, become DP in vitro. However, early fetal CD8lo 4lo 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 kinetics of progression through phenotypic stages. Copyright © 1993 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim |
| Keywords: |
genetics; nonhuman; molecular genetics; cd8 antigen; antigen expression; t lymphocyte; t-lymphocytes; animal cell; mouse; animal; metabolism; mice; cells, cultured; mice, inbred c57bl; lymphocyte differentiation; t lymphocyte receptor beta chain; immunology; gene rearrangement; molecular sequence data; cell culture; thymus; messenger rna; rna, messenger; nucleotide sequence; base sequence; pregnancy; fetus; cd4 antigen; mouse strain; hermes antigen; thymocyte; t lymphocyte subpopulation; lymphocyte antigen receptor; receptors, antigen, t-cell, alpha-beta; fetus development; t lymphocyte receptor alpha chain; ontogeny; interleukin 2 receptor; receptors, interleukin-2; homing receptor; receptors, lymphocyte homing; prolymphocyte; t lymphocyte receptor gene; female; priority journal; article; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; receptors, antigen, t cell, alpha beta; receptors, interleukin 2; cd8 / cd4 / t cell development / cd25 / cd44 / fetal ontogeny
|
