Early T cell development can be traced in rat fetal liver

Abstract

The degree of T cell commitment reached by cell precursors present in the fetal liver is a controversial issue. In the present work, the occurrence of fully T cell-committed progenitors among CD45+Thy-1+CD44+ 13-day-old rat fetal liver cells was demonstrated when limiting numbers of these cells in vitro reconstituted SCID mouse fetal thymic lobes providing single lineage-containing lobes for T, natural killer or dendritic cells. In addition, expression of rat pre-TCRalpha chain mRNA was detected in the CD45+ but not in the CD45- fetal liver cells and fully rearranged TCR VBeta8-Cbeta mRNA transcripts were specifically detected in the former population, demonstrating early transcription of some rearranged TCRVBeta genes in the rat fetal liver of 13 days of gestation. Finally, fetal liver organ cultures provided low numbers of TCR gamma delta T cells and CD2+CD8+NKR-P1A- intracytoplasmic CD3+ immature T cells, which intracellularly reacted with a mAb specific to the TCRalpha Beta molecule. These results prove T, NK and DC cell lineage determination at a prethymic stage in the fetal liver.

Ontogeny of the immune system of fish

“…On the other hand, it is difficult to understand the expression of both Rag and/or Ig chains before the appearance of thymus and pronephros. Some authors have remarked the high frequency of sterile and aberrant transcripts that occur in teleosts [19] but, on the other hand, evidence of TcR/BcR gene rearrangements before lymphoid progenitors colonize the primary lymphoid organs has been found in mammals [38,39]. The expression of Hox-11 transcripts in a small region on the left anterior gut marks the appearance of the zebrafish splenic primordium by day 4 postfertilization [40].…”