Mehal W Z, Juedes A E, Crispe I N
Section of Immunobiology, Yale School of Medicine, New Haven, CT 06520, USA.
J Immunol. 1999 Sep 15;163(6):3202-10.
Activation-induced cell death resulting in peripheral deletion of CD8+ T cells is associated with the accumulation of large numbers of apoptotic T cells in the liver. The hypothesis that this accumulation results from the intrahepatic trapping of T cells from the circulating pool predicts that the liver should retain T cells, which subsequently undergo apoptosis. Here we test this prediction. Perfusion of the liver with lymphocyte mixtures showed retention of activated, but neither resting nor apoptosing, T cells. This trapping was selective for CD8+ cells and was mediated primarily by ICAM-1 constitutively expressed on sinusoidal endothelial cells and Kupffer cells. T cells trapped in the liver became apoptotic. The normal liver is therefore a "sink" for activated T cells.
导致CD8+ T细胞外周缺失的活化诱导细胞死亡与肝脏中大量凋亡T细胞的积累有关。这种积累是由于循环池中T细胞在肝内滞留的假说预测,肝脏应该保留随后发生凋亡的T细胞。在此我们验证这一预测。用淋巴细胞混合物灌注肝脏显示,活化的T细胞会滞留,但静止或凋亡的T细胞则不会。这种滞留对CD8+细胞具有选择性,主要由窦状内皮细胞和库普弗细胞组成性表达的细胞间黏附分子-1(ICAM-1)介导。滞留在肝脏中的T细胞会发生凋亡。因此,正常肝脏是活化T细胞的一个“汇集处”。