• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

阿尔茨海默病内吞风险基因的细胞类型特异性功能。

Cell type-specific functions of Alzheimer's disease endocytic risk genes.

机构信息

Cardiff University, Dementia Research Institute, Cardiff University¸ Cardiff, CF24 4HQ, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2024 Apr 8;379(1899):20220378. doi: 10.1098/rstb.2022.0378. Epub 2024 Feb 19.

DOI:10.1098/rstb.2022.0378
PMID:38368934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10874703/
Abstract

Endocytosis is a key cellular pathway required for the internalization of cellular nutrients, lipids and receptor-bound cargoes. It is also critical for the recycling of cellular components, cellular trafficking and membrane dynamics. The endocytic pathway has been consistently implicated in Alzheimer's disease (AD) through repeated genome-wide association studies and the existence of rare coding mutations in endocytic genes. and are two of the most significant late-onset AD risk genes after and are both key to clathrin-mediated endocytic biology. Pathological studies also demonstrate that endocytic dysfunction is an early characteristic of late-onset AD, being seen in the prodromal phase of the disease. Different cell types of the brain have specific requirements of the endocytic pathway. Neurons require efficient recycling of synaptic vesicles and microglia use the specialized form of endocytosis-phagocytosis-for their normal function. Therefore, disease-associated changes in endocytic genes will have varied impacts across different cell types, which remains to be fully explored. Given the genetic and pathological evidence for endocytic dysfunction in AD, understanding how such changes and the related cell type-specific vulnerabilities impact normal cellular function and contribute to disease is vital and could present novel therapeutic opportunities. This article is part of a discussion meeting issue 'Understanding the endo-lysosomal network in neurodegeneration'.

摘要

内吞作用是细胞内化细胞营养物质、脂质和受体结合货物所必需的关键细胞途径。它对于细胞成分的再循环、细胞运输和膜动力学也至关重要。通过反复的全基因组关联研究和内吞作用基因中罕见编码突变的存在,内吞作用途径一直与阿尔茨海默病(AD)有关。 和 是除 之外最重要的两种晚发性 AD 风险基因,它们都是网格蛋白介导的内吞生物学的关键。病理研究还表明,内吞作用功能障碍是晚发性 AD 的早期特征,在疾病的前驱期就可见到。大脑的不同细胞类型对内吞作用途径有特定的要求。神经元需要有效地回收突触囊泡,而小胶质细胞则利用内吞作用的特殊形式——吞噬作用——来发挥其正常功能。因此,与疾病相关的内吞作用基因的变化将对不同的细胞类型产生不同的影响,这仍有待充分探索。鉴于 AD 中内吞作用功能障碍的遗传和病理证据,了解这些变化以及相关的细胞类型特异性脆弱性如何影响正常细胞功能并导致疾病是至关重要的,并且可能提供新的治疗机会。本文是关于“理解神经退行性疾病中的内体-溶酶体网络”的讨论会议的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c39/10874703/22d46ccde1fb/rstb20220378f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c39/10874703/025386f24998/rstb20220378f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c39/10874703/22d46ccde1fb/rstb20220378f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c39/10874703/025386f24998/rstb20220378f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c39/10874703/22d46ccde1fb/rstb20220378f02.jpg

相似文献

1
Cell type-specific functions of Alzheimer's disease endocytic risk genes.阿尔茨海默病内吞风险基因的细胞类型特异性功能。
Philos Trans R Soc Lond B Biol Sci. 2024 Apr 8;379(1899):20220378. doi: 10.1098/rstb.2022.0378. Epub 2024 Feb 19.
2
The role of Alzheimer's disease risk genes in endolysosomal pathways.阿尔茨海默病风险基因在溶酶体途径中的作用。
Neurobiol Dis. 2022 Jan;162:105576. doi: 10.1016/j.nbd.2021.105576. Epub 2021 Dec 3.
3
Impact of late-onset Alzheimer's genetic risk factors on beta-amyloid endocytic production.晚期阿尔茨海默病遗传风险因素对β-淀粉样蛋白内吞生成的影响。
Cell Mol Life Sci. 2018 Jul;75(14):2577-2589. doi: 10.1007/s00018-018-2825-9. Epub 2018 Apr 27.
4
Endocytic pathway abnormalities precede amyloid beta deposition in sporadic Alzheimer's disease and Down syndrome: differential effects of APOE genotype and presenilin mutations.内吞途径异常先于散发性阿尔茨海默病和唐氏综合征中的β淀粉样蛋白沉积:APOE基因型和早老素突变的不同影响。
Am J Pathol. 2000 Jul;157(1):277-86. doi: 10.1016/s0002-9440(10)64538-5.
5
Traffic jam hypothesis: Relationship between endocytic dysfunction and Alzheimer's disease.交通堵塞假说:内吞作用功能障碍与阿尔茨海默病的关系。
Neurochem Int. 2018 Oct;119:35-41. doi: 10.1016/j.neuint.2017.07.002. Epub 2017 Jul 8.
6
Differential effects of deficiency on the endo-lysosomal network in human neurons and microglia.缺乏症对人类神经元和小神经胶质细胞内溶酶体网络的差异影响。
Philos Trans R Soc Lond B Biol Sci. 2024 Apr 8;379(1899):20220389. doi: 10.1098/rstb.2022.0389. Epub 2024 Feb 19.
7
Down syndrome fibroblast model of Alzheimer-related endosome pathology: accelerated endocytosis promotes late endocytic defects.唐氏综合征成纤维细胞模型中与阿尔茨海默病相关的内体病理:加速内吞作用会加剧晚期内吞缺陷。
Am J Pathol. 2008 Aug;173(2):370-84. doi: 10.2353/ajpath.2008.071053. Epub 2008 Jun 5.
8
PICALM Rescues Endocytic Defects Caused by the Alzheimer's Disease Risk Factor APOE4.载脂蛋白 E4 所致阿尔茨海默病风险因子导致的内吞缺陷被 PICALM 挽救。
Cell Rep. 2020 Oct 6;33(1):108224. doi: 10.1016/j.celrep.2020.108224.
9
Bin1 and CD2AP polarise the endocytic generation of beta-amyloid.Bin1和CD2AP使β-淀粉样蛋白的内吞生成极化。
EMBO Rep. 2017 Jan;18(1):102-122. doi: 10.15252/embr.201642738. Epub 2016 Nov 28.
10
Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences.内吞途径中的罕见变异与阿尔茨海默病及其相关表型和功能后果有关。
PLoS Genet. 2021 Sep 13;17(9):e1009772. doi: 10.1371/journal.pgen.1009772. eCollection 2021 Sep.

引用本文的文献

1
Neuronal Deletion of () Causes Rapid Apoptotic Loss of Hippocampal CA3 Neurons.()的神经元缺失导致海马CA3神经元迅速发生凋亡性丢失。
Biomolecules. 2025 May 28;15(6):786. doi: 10.3390/biom15060786.
2
Endosomal protein DENND10 promotes developmental competence of neurite extension.内涵体蛋白DENND10促进神经突延伸的发育能力。
iScience. 2025 Apr 8;28(5):112385. doi: 10.1016/j.isci.2025.112385. eCollection 2025 May 16.
3
The Alzheimer's Disease Gene SORL1 Regulates Lysosome Function in Human Microglia.阿尔茨海默病基因SORL1调节人类小胶质细胞中的溶酶体功能。

本文引用的文献

1
Anti-malaria drug artesunate prevents development of amyloid-β pathology in mice by upregulating PICALM at the blood-brain barrier.抗疟药青蒿琥酯通过在血脑屏障上调 PICALM 来预防小鼠淀粉样β病理的发展。
Mol Neurodegener. 2023 Jan 27;18(1):7. doi: 10.1186/s13024-023-00597-5.
2
Cell type-specific histone acetylation profiling of Alzheimer's disease subjects and integration with genetics.阿尔茨海默病受试者的细胞类型特异性组蛋白乙酰化谱分析及其与遗传学的整合。
Front Mol Neurosci. 2023 Jan 6;15:948456. doi: 10.3389/fnmol.2022.948456. eCollection 2022.
3
PICALM and Alzheimer's Disease: An Update and Perspectives.
Glia. 2025 Jul;73(7):1329-1348. doi: 10.1002/glia.70009. Epub 2025 Apr 4.
4
Regulatory Mechanisms and Therapeutic Implications of Lysosomal Dysfunction in Alzheimer's Disease.阿尔茨海默病中溶酶体功能障碍的调节机制及治疗意义
Int J Biol Sci. 2025 Jan 13;21(3):1014-1031. doi: 10.7150/ijbs.103028. eCollection 2025.
5
Microglial CD2AP deficiency exerts protection in an Alzheimer's disease model of amyloidosis.小胶质细胞CD2AP缺乏在淀粉样变性的阿尔茨海默病模型中发挥保护作用。
Mol Neurodegener. 2024 Dec 18;19(1):95. doi: 10.1186/s13024-024-00789-7.
6
Amyloid-β but not tau accumulation is strongly associated with longitudinal cognitive decline.淀粉样蛋白-β而非 tau 积聚与纵向认知能力下降密切相关。
CNS Neurosci Ther. 2024 Jul;30(7):e14860. doi: 10.1111/cns.14860.
7
The Alzheimer's disease gene regulates lysosome function in human microglia.阿尔茨海默病基因调节人类小胶质细胞中的溶酶体功能。
bioRxiv. 2025 Jan 7:2024.06.25.600648. doi: 10.1101/2024.06.25.600648.
8
Clathrin mediated endocytosis in Alzheimer's disease: cell type specific involvement in amyloid beta pathology.网格蛋白介导的内吞作用在阿尔茨海默病中的作用:细胞类型特异性参与淀粉样β病理过程。
Front Aging Neurosci. 2024 Apr 17;16:1378576. doi: 10.3389/fnagi.2024.1378576. eCollection 2024.
载脂蛋白 E 与阿尔茨海默病:研究进展与展望
Cells. 2022 Dec 10;11(24):3994. doi: 10.3390/cells11243994.
4
Assaying Microglia Functions In Vitro.体外分析小胶质细胞功能。
Cells. 2022 Oct 28;11(21):3414. doi: 10.3390/cells11213414.
5
ApoE3 vs. ApoE4 Astrocytes: A Detailed Analysis Provides New Insights into Differences in Cholesterol Homeostasis.载脂蛋白E3与载脂蛋白E4星形胶质细胞:详细分析为胆固醇稳态差异提供新见解。
Antioxidants (Basel). 2022 Nov 1;11(11):2168. doi: 10.3390/antiox11112168.
6
Genetic polymorphism in BIN1 rather than APOE is associated with poor recognition memory among men without dementia.在没有痴呆的男性中,BIN1 的遗传多态性而非 APOE 与较差的识别记忆有关。
Sci Rep. 2022 Oct 24;12(1):17802. doi: 10.1038/s41598-022-20587-9.
7
Loss of forebrain BIN1 attenuates hippocampal pathology and neuroinflammation in a tauopathy model.大脑前 BIN1 的缺失减轻了神经tau 病模型中的海马病理学和神经炎症。
Brain. 2023 Apr 19;146(4):1561-1579. doi: 10.1093/brain/awac318.
8
Lipid accumulation induced by APOE4 impairs microglial surveillance of neuronal-network activity.载脂蛋白 E4 引起的脂质积累会损害小胶质细胞对神经元网络活动的监测。
Cell Stem Cell. 2022 Aug 4;29(8):1197-1212.e8. doi: 10.1016/j.stem.2022.07.005.
9
BIN1 is a key regulator of proinflammatory and neurodegeneration-related activation in microglia.BIN1 是小胶质细胞中促炎和神经退行性变相关激活的关键调节因子。
Mol Neurodegener. 2022 May 7;17(1):33. doi: 10.1186/s13024-022-00535-x.
10
Allele-specific analysis reveals exon- and cell-type-specific regulatory effects of Alzheimer's disease-associated genetic variants.等位基因特异性分析揭示了阿尔茨海默病相关遗传变异的外显子和细胞类型特异性调节作用。
Transl Psychiatry. 2022 Apr 18;12(1):163. doi: 10.1038/s41398-022-01913-1.