自身免疫性淋巴增生综合征
自身免疫
突变
基因
免疫学
生物
细胞凋亡
免疫系统
Fas受体
遗传学
程序性细胞死亡
作者
Kamil Seyrek,Nikita V. Ivanisenko,Fabian Wohlfromm,Johannes Espe,Inna N. Lavrik
标识
DOI:10.1016/j.it.2021.11.006
摘要
CD95/Fas/APO-1 can trigger apoptotic as well as nonapoptotic pathways in immune cells. CD95 signaling in humans can be inhibited by several mechanisms, including mutations in the gene encoding CD95. CD95 mutations lead to autoimmune disorders, such as autoimmune lymphoproliferative syndrome (ALPS). Gaining further insight into the reported mutations of CD95 and resulting alterations of its signaling networks may provide further understanding of their presumed role in certain autoimmune diseases. For illustrative purposes and to better understand the potential outcomes of CD95 mutations, here we assign their positions to the recently determined 3D structures of human CD95. Based on this, we make certain predictions and speculate on the putative role of CD95 mutation defects in CD95-mediated signaling for certain autoimmune diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI