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早老素蛋白的生物学功能及其在 AD 发病机制中的作用。

Biological function of Presenilin and its role in AD pathogenesis.

机构信息

Townsend Family Laboratories, Department of Psychiatry, Brain Research Center, Graduate Program in Neuroscience, The University of British Columbia, 2255 Wesbrook Mall, Vancouver, BC V6T 1Z3, Canada.

出版信息

Transl Neurodegener. 2013 Jul 17;2(1):15. doi: 10.1186/2047-9158-2-15.

Abstract

Presenilins (PSs) are the catalytic core of γ-secretase complex. However, the mechanism of FAD-associated PS mutations in AD pathogenesis still remains elusive. Here we review the general biology and mechanism of γ-secretase and focus on the catalytic components - presenilins and their biological functions and contributions to the AD pathogenesis. The functions of presenilins are divided into γ-secretase dependent and γ-secretase independent ones. The γ-secretase dependent functions of presenilins are exemplified by the sequential cleavages in the processing of APP and Notch; the γ-secretase independent functions of presenilins include stabilizing β-catenin in Wnt signaling pathway, regulating calcium homeostasis and their interaction with synaptic transmission.

摘要

早老素蛋白(PSs)是γ-分泌酶复合物的催化核心。然而,FAD 相关 PS 突变在 AD 发病机制中的作用机制仍不清楚。在这里,我们回顾了 γ-分泌酶的一般生物学和机制,并重点介绍了催化成分——早老素及其生物学功能及其对 AD 发病机制的贡献。早老素的功能分为 γ-分泌酶依赖性和 γ-分泌酶非依赖性。早老素的 γ-分泌酶依赖性功能的例子有 APP 和 Notch 加工中的顺序切割;早老素的 γ-分泌酶非依赖性功能包括稳定 Wnt 信号通路中的β-连环蛋白、调节钙稳态及其与突触传递的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80ae/3718700/7f4945f8825c/2047-9158-2-15-1.jpg

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