豁免特权
Fas配体
炎症
免疫系统
细胞凋亡
免疫学
配体(生物化学)
医学
移植
生物
癌症研究
受体
程序性细胞死亡
内科学
遗传学
作者
Yoichiro Sano,Chie Sotozono
出处
期刊:Cornea
[Lippincott Williams & Wilkins]
日期:2002-03-01
卷期号:21: S30-S32
被引量:7
标识
DOI:10.1097/00003226-200203001-00007
摘要
The expression of Fas ligand (FasL) in the eye is an important factor in the maintenance of immune privilege. Although FasL expression in donor corneas contributes to prolonged survival of orthotopic corneal allografts in solid organ transplantation, FasL gene-transfected tissues reportedly lead to graft destruction through neutrophil recruitment. Differences in the effects of FasL have been attributed to different roles of soluble FasL (sFasL) and membrane FasL (mFasL). This is based on the presumption that the signals through sFasL and mFasL differ, with one causing apoptosis and the other activating inflammation. It was recently reported that inflammation caused by FasL was inhibited at an immune-privileged site, and therefore the effects of FasL may depend on differences in the anatomic sites where FasL-expressing cells are located. In this article, we discuss the role of sFasL and mFasL in ocular immune privilege.
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