IP-10 and Mig facilitate accumulation of T cells in the virus-infected liver

被引:66
作者
Arai, K
Liu, ZX
Lane, T
Dennert, G [1 ]
机构
[1] Univ So Calif, Norris Comprehens Canc Ctr, Dept Mol Microbiol & Immunol, Keck Sch Med, Los Angeles, CA 90089 USA
[2] Univ Calif Irvine, Dept Biochem & Mol Biol, Irvine, CA 92697 USA
关键词
D O I
10.1016/S0008-8749(02)00584-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Viral infection of the liver causes accumulation of T cells in the infected organ, raising the question as to the signals that mediate this response. Employing an adenovirus induced hepatitis model in mice, we show that IP-10 and Mig are essential for T cell recruitment and that induction of the two chemokines occurs concomitant to production of IFNgamma. It is shown that while IFNgamma induces IP-10 and Mig in hepatocytes, for optimal chemokine induction, a co-stimulatory signal mediated by cross-linking of Fas on hepatocytes is required. Moreover, cross-linking of Fas by injection of anti-Fas antibody into mice triggers induction of IP-10 and Mig in the liver. The cells providing the two signals are shown to express NK1.1 and AsGM1; elimination of these cells leads to inhibition of IFNy and chemokine transcript induction. The conclusion is drawn that both NK cells and T cells provide the two signals for induction of IP-10 and Mig in the liver. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:48 / 56
页数:9
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