TY - JOUR
T1 - T cells with γ/δ T cell receptors (TCR) of intestinal type are preferentially expanded in TCR-α-deficient lpr mice
AU - Hughes, Dennis P.M.
AU - Hayday, Adrian
AU - Craft, Joseph E.
AU - Owen, Michael J.
AU - Crispe, I. Nicholas
PY - 1995/7/1
Y1 - 1995/7/1
N2 - Fas-mediated apoptosis is essential for activation-induced cell death of α/β T cells, but it is not clear what role, if any, it plays in regulating other components of the immune system. To study the role of Fas in γ/δ T cell development, Fas-deficient lpr mice were bred with T cell receptor α gene-ablated (TCR-α-/-) mice to generate mice deficient in one or both genes. The TCR-α-/-, lpr/lpr mice had a nearly 10-fold increase in total lymph node cell (LNC) number compared with Fas-intact TCR-α-/- mice, because of expansion of TCR-γ/δ+ and TCR-β+ cells. In Fas-intact TCR-α-/- mice, approximately one third of the LNCs expressed TCR-γ/δ. These were evenly divided between the CD4-, CD8-α+ and the CD4-, CD8- subsets, and rarely expressed the B220 epitope of CD45. In contrast, in TCR-α-/-, lpr/lpr mice, TCR-γ/δ+ cells comprised half of the LNCs and were primarily CD4-, CD8- , and B220+. Moreover, Fas deficiency in TCR-α-/- mice caused a preferential expansion of γ/δ T cells expressing variable region genes characteristic of intestinal intraepithelial lymphocytes. These results demonstrate a role for Fas in regulating the γ/δ T cell contribution to peripheral lymph nodes. This mechanism may be most important in limiting the access of activated intestinal intraepithelial lymphocytes to the peripheral lymphoid system.
AB - Fas-mediated apoptosis is essential for activation-induced cell death of α/β T cells, but it is not clear what role, if any, it plays in regulating other components of the immune system. To study the role of Fas in γ/δ T cell development, Fas-deficient lpr mice were bred with T cell receptor α gene-ablated (TCR-α-/-) mice to generate mice deficient in one or both genes. The TCR-α-/-, lpr/lpr mice had a nearly 10-fold increase in total lymph node cell (LNC) number compared with Fas-intact TCR-α-/- mice, because of expansion of TCR-γ/δ+ and TCR-β+ cells. In Fas-intact TCR-α-/- mice, approximately one third of the LNCs expressed TCR-γ/δ. These were evenly divided between the CD4-, CD8-α+ and the CD4-, CD8- subsets, and rarely expressed the B220 epitope of CD45. In contrast, in TCR-α-/-, lpr/lpr mice, TCR-γ/δ+ cells comprised half of the LNCs and were primarily CD4-, CD8- , and B220+. Moreover, Fas deficiency in TCR-α-/- mice caused a preferential expansion of γ/δ T cells expressing variable region genes characteristic of intestinal intraepithelial lymphocytes. These results demonstrate a role for Fas in regulating the γ/δ T cell contribution to peripheral lymph nodes. This mechanism may be most important in limiting the access of activated intestinal intraepithelial lymphocytes to the peripheral lymphoid system.
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U2 - 10.1084/jem.182.1.233
DO - 10.1084/jem.182.1.233
M3 - Article
C2 - 7540652
AN - SCOPUS:0029057835
SN - 0022-1007
VL - 182
SP - 233
EP - 241
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 1
ER -