Suppr超能文献

γ-分泌酶复合物的生理和病理作用。

Physiological and pathological roles of the γ-secretase complex.

作者信息

Carroll Courtney M, Li Yue-Ming

机构信息

Chemical Biology Program, Memorial Sloan Kettering Cancer Center, NY, United States; Program of Neuroscience, Weill Graduate School of Medical Sciences of Cornell University, NY, United States.

Chemical Biology Program, Memorial Sloan Kettering Cancer Center, NY, United States; Program of Neuroscience, Weill Graduate School of Medical Sciences of Cornell University, NY, United States; Program of Pharmacology, Weill Graduate School of Medical Sciences of Cornell University, NY, United States.

出版信息

Brain Res Bull. 2016 Sep;126(Pt 2):199-206. doi: 10.1016/j.brainresbull.2016.04.019. Epub 2016 Apr 28.

Abstract

Gamma-secretase (GS) is an enzyme complex that cleaves numerous substrates, and it is best known for cleaving amyloid precursor protein (APP) to form amyloid-beta (Aβ) peptides. Aberrant cleavage of APP can lead to Alzheimer's disease, so much research has been done to better understand GS structure and function in hopes of developing therapeutics for Alzheimer's. Therefore, most of the attention in this field has been focused on developing modulators that reduce pathogenic forms of Aβ while leaving Notch and other GS substrates intact, but GS provides multiple avenues of modulation that could improve AD pathology. GS has complex regulation, through its essential subunits and other associated proteins, providing other targets for AD drugs. Therapeutics can also alter GS trafficking and thereby improve cognition, or move beyond Aβ entirely, effecting Notch and neural stem cells. GS also cleaves substrates that affect synaptic morphology and function, presenting another window by which GS modulation could improve AD pathology. Taken together, GS presents a unique cross road for neural processes and an ideal target for AD therapeutics.

摘要

γ-分泌酶(GS)是一种能切割多种底物的酶复合物,它因切割淀粉样前体蛋白(APP)以形成β-淀粉样蛋白(Aβ)肽而最为人所知。APP的异常切割会导致阿尔茨海默病,因此人们开展了大量研究以更好地了解GS的结构和功能,希望开发出针对阿尔茨海默病的治疗方法。因此,该领域的大部分注意力都集中在开发调节剂上,这些调节剂可减少Aβ的致病形式,同时使Notch和其他GS底物保持完整,但GS提供了多种调节途径,可改善阿尔茨海默病的病理状况。GS具有复杂的调控机制,通过其必需亚基和其他相关蛋白发挥作用,这为治疗阿尔茨海默病的药物提供了其他靶点。治疗药物还可改变GS的运输,从而改善认知,或者完全超越Aβ的范畴,影响Notch和神经干细胞。GS还能切割影响突触形态和功能的底物,这为GS调节改善阿尔茨海默病病理状况提供了另一个切入点。综上所述,GS为神经过程提供了一个独特的交叉点,是治疗阿尔茨海默病的理想靶点。

相似文献

1
Physiological and pathological roles of the γ-secretase complex.
Brain Res Bull. 2016 Sep;126(Pt 2):199-206. doi: 10.1016/j.brainresbull.2016.04.019. Epub 2016 Apr 28.
5
Gamma Secretase as an Important Drug Target for Management of Alzheimer's Disease: A Comprehensive Review.
Curr Top Med Chem. 2024;24(2):109-127. doi: 10.2174/0115680266259174231006070637.
7
Secretase inhibitors and modulators for Alzheimer's disease treatment.
Expert Rev Neurother. 2009 May;9(5):661-79. doi: 10.1586/ern.09.24.
9
gamma-Secretase modulators.
Curr Alzheimer Res. 2007 Dec;4(5):571-3. doi: 10.2174/156720507783018299.
10
Advances in gamma-secretase modulation.
Curr Opin Drug Discov Devel. 2007 Jul;10(4):392-402.

引用本文的文献

1
Evidence that cholinergic mechanisms contribute to hyperexcitability at early stages in Alzheimer's disease.
Front Dement. 2025 Jun 17;4:1513144. doi: 10.3389/frdem.2025.1513144. eCollection 2025.
5
The Intricate Notch Signaling Dynamics in Therapeutic Realms of Cancer.
ACS Pharmacol Transl Sci. 2023 May 3;6(5):651-670. doi: 10.1021/acsptsci.2c00239. eCollection 2023 May 12.
6
Gamma secretase activity modulates BMP-7-induced dendritic growth in primary rat sympathetic neurons.
Auton Neurosci. 2023 Jul;247:103085. doi: 10.1016/j.autneu.2023.103085. Epub 2023 Apr 6.
7
The human RAP1 and GFAPɛ proteins increase γ-secretase activity in a yeast model system.
G3 (Bethesda). 2023 Aug 9;13(8). doi: 10.1093/g3journal/jkad057.
9
CRISPR and iPSCs: Recent Developments and Future Perspectives in Neurodegenerative Disease Modelling, Research, and Therapeutics.
Neurotox Res. 2022 Oct;40(5):1597-1623. doi: 10.1007/s12640-022-00564-w. Epub 2022 Aug 31.
10
Distributions of Aβ42 and Aβ42/40 in the Cerebrospinal Fluid in View of the Probability Theory.
Diagnostics (Basel). 2021 Dec 16;11(12):2372. doi: 10.3390/diagnostics11122372.

本文引用的文献

1
Effect of Presenilin Mutations on APP Cleavage; Insights into the Pathogenesis of FAD.
Front Aging Neurosci. 2016 Mar 11;8:51. doi: 10.3389/fnagi.2016.00051. eCollection 2016.
2
Lingo-1 shRNA and Notch signaling inhibitor DAPT promote differentiation of neural stem/progenitor cells into neurons.
Brain Res. 2016 Mar 1;1634:34-44. doi: 10.1016/j.brainres.2015.11.029. Epub 2015 Nov 24.
3
Antagonistic Effects of BACE1 and APH1B-γ-Secretase Control Axonal Guidance by Regulating Growth Cone Collapse.
Cell Rep. 2015 Sep 1;12(9):1367-76. doi: 10.1016/j.celrep.2015.07.059. Epub 2015 Aug 20.
5
An atomic structure of human γ-secretase.
Nature. 2015 Sep 10;525(7568):212-217. doi: 10.1038/nature14892. Epub 2015 Aug 17.
6
NEUROSCIENCE. Alzheimer's amyloid theory gets modest boost.
Science. 2015 Jul 31;349(6247):464. doi: 10.1126/science.349.6247.464.
7
Presenilin-1 Dependent Neurogenesis Regulates Hippocampal Learning and Memory.
PLoS One. 2015 Jun 22;10(6):e0131266. doi: 10.1371/journal.pone.0131266. eCollection 2015.
8
Three dimensions of the amyloid hypothesis: time, space and 'wingmen'.
Nat Neurosci. 2015 Jun;18(6):800-6. doi: 10.1038/nn.4018.
9
Presenilin-1 knockin mice reveal loss-of-function mechanism for familial Alzheimer's disease.
Neuron. 2015 Mar 4;85(5):967-81. doi: 10.1016/j.neuron.2015.02.010.
10
The dynamic conformational landscape of gamma-secretase.
J Cell Sci. 2015 Feb 1;128(3):589-98. doi: 10.1242/jcs.164384.

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