THYMIC AND EXTRATHYMIC ORIGINS OF GUT INTRAEPITHELIAL LYMPHOCYTE POPULATIONS IN MICE

We have investigated the origin of intraepithelial lymphocytes (IEL) populations in the murine gut, using reconstitution experiments in which the presence of thymus-derived cells of host or donor origin is rigorously controlled: RAG(-/-) mutant mice which have no T cells, were injected either with the bone marrow (BM) cells of nude mice or with selected peripheral lymph node (LN) T cells of euthymic mice. In thymectomized RAG(-/-) mice, injection of BM cells from nude mice led, after 2 mo, to the development of a peripheral B cell compartment and to the appearance, in the gut, of IEL bearing homodimeric CD8 alpha chains and either gamma/delta or alpha/beta TCR. In RAG(-/-) mice with a thymus, a similar injection led to complete lymphoid reconstitution, with the additional appearance in the gut of CD4(+), CD8 alpha/beta(+) or CD4(+)CD8 alpha/alpha(+) IEL, all bearing alpha/beta TCR. In contrast, injection of LN T cells into these mice reconstituted a gut IEL population made of CD4(+), CD8 alpha/beta(+), or CD4(+) CD8 alpha/alpha(+) cells, all bearing alpha/beta TCR; CD8 alpha/alpha(+) TCR-gamma/delta(+) or alpha/beta(+) IEL were not observed. These results demonstrate that the thymus and/or thymic-derived peripheral T cells are absolutely required for the generation of CD4(+), CD8 alpha/beta(+), and CD4(+)CD8 alpha/alpha(+) IEL, which are thus thymus dependent. In contrast, TCR(+) CD8 alpha/alpha(+) IEL appear in the absence of the thymus, and thus are thymus independent.