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人类 CD95 突变对细胞死亡和自身免疫的影响:一种模型。

Impact of human CD95 mutations on cell death and autoimmunity: a model.

机构信息

Translational Inflammation Research, Medical Faculty, Otto von Guericke University Magdeburg, 39106 Magdeburg, Germany.

Translational Inflammation Research, Medical Faculty, Otto von Guericke University Magdeburg, 39106 Magdeburg, Germany; The Federal Research Center Institute of Cytology and Genetics SB RAS, Novosibirsk, Russia; Artificial Intelligence Research Institute, Moscow, Russia.

出版信息

Trends Immunol. 2022 Jan;43(1):22-40. doi: 10.1016/j.it.2021.11.006. Epub 2021 Dec 3.

Abstract

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.

摘要

CD95/Fas/APO-1 可在免疫细胞中触发凋亡和非凋亡途径。人类的 CD95 信号可以通过几种机制来抑制,包括编码 CD95 的基因突变。CD95 突变导致自身免疫性疾病,如自身免疫性淋巴增生综合征 (ALPS)。进一步了解报告的 CD95 突变及其信号网络的改变,可能有助于进一步了解它们在某些自身免疫性疾病中的假定作用。为了说明问题,并更好地理解 CD95 突变的潜在后果,我们将其位置分配到最近确定的人 CD95 的 3D 结构中。基于此,我们对 CD95 突变缺陷在某些自身免疫性疾病中 CD95 介导的信号转导中的作用做出某些预测和推测。

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