Suppr超能文献

SIVA-1 通过调节 XIAP 与死亡受体拮抗剂 FAIM-L 的相互作用来调节细胞凋亡和突触功能。

SIVA-1 regulates apoptosis and synaptic function by modulating XIAP interaction with the death receptor antagonist FAIM-L.

机构信息

Cell Signaling and Apoptosis Group, Vall d'Hebron Research Institute (VHIR), 08035, Barcelona, Spain.

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), ISCIII, 28031, Madrid, Spain.

出版信息

Cell Death Dis. 2020 Feb 3;11(2):82. doi: 10.1038/s41419-020-2282-x.

Abstract

The long isoform of Fas apoptosis inhibitory molecule (FAIM-L) is a neuron-specific death receptor antagonist that modulates apoptotic cell death and mechanisms of neuronal plasticity. FAIM-L exerts its antiapoptotic action by binding to X-linked inhibitor of apoptosis protein (XIAP), an inhibitor of caspases, which are the main effectors of apoptosis. XIAP levels are regulated by the ubiquitin-proteasome pathway. FAIM-L interaction with XIAP prevents the ubiquitination and degradation of the latter, thereby allowing it to inhibit caspase activation. This interaction also modulates non-apoptotic functions of caspases, such as the endocytosis of AMPA receptor (AMPAR) in hippocampal long-term depression (LTD). The molecular mechanism of action exerted by FAIM-L is unclear since the consensus binding motifs are still unknown. Here, we performed a two-hybrid screening to discover novel FAIM-L-interacting proteins. We found a functional interaction of SIVA-1 with FAIM-L. SIVA-1 is a proapoptotic protein that has the capacity to interact with XIAP. We describe how SIVA-1 regulates FAIM-L function by disrupting the interaction of FAIM-L with XIAP, thereby promoting XIAP ubiquitination, caspase-3 activation and neuronal death. Furthermore, we report that SIVA-1 plays a role in receptor internalization in synapses. SIVA-1 is upregulated upon chemical LTD induction, and it modulates AMPAR internalization via non-apoptotic activation of caspases. In summary, our findings uncover SIVA-1 as new functional partner of FAIM-L and demonstrate its role as a regulator of caspase activity in synaptic function.

摘要

Fas 凋亡抑制分子(FAIM-L)的长异构体是一种神经元特异性死亡受体拮抗剂,可调节细胞凋亡和神经元可塑性的机制。FAIM-L 通过与 X 连锁凋亡抑制蛋白(XIAP)结合发挥其抗凋亡作用,XIAP 是细胞凋亡的主要效应物半胱天冬酶的抑制剂。XIAP 水平受泛素-蛋白酶体途径调节。FAIM-L 与 XIAP 的相互作用阻止了后者的泛素化和降解,从而使其能够抑制半胱天冬酶的激活。这种相互作用还调节了半胱天冬酶的非凋亡功能,如海马长时程抑制(LTD)中 AMPA 受体(AMPAR)的内吞作用。FAIM-L 发挥作用的分子机制尚不清楚,因为共识结合基序仍不清楚。在这里,我们进行了双杂交筛选以发现新的 FAIM-L 相互作用蛋白。我们发现 SIVA-1 与 FAIM-L 之间存在功能相互作用。SIVA-1 是一种促凋亡蛋白,能够与 XIAP 相互作用。我们描述了 SIVA-1 如何通过破坏 FAIM-L 与 XIAP 的相互作用来调节 FAIM-L 功能,从而促进 XIAP 的泛素化、半胱天冬酶-3 的激活和神经元死亡。此外,我们报告 SIVA-1 在突触中参与受体内化。化学 LTD 诱导后 SIVA-1 上调,并通过非凋亡激活半胱天冬酶调节 AMPAR 内化。总之,我们的发现揭示了 SIVA-1 是 FAIM-L 的新功能伙伴,并证明了它作为调节突触功能中半胱天冬酶活性的调节剂的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2378/6997380/3a445b4b2f4d/41419_2020_2282_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验