Suppr超能文献

恢复可溶性淀粉样前体蛋白α的功能作为阿尔茨海默病的一种潜在治疗方法。

Restoring Soluble Amyloid Precursor Protein α Functions as a Potential Treatment for Alzheimer's Disease.

作者信息

Habib Ahsan, Sawmiller Darrell, Tan Jun

机构信息

Rashid Laboratory for Developmental Neurobiology, Silver Child Development Center, Department of Psychiatry and Behavioral Neurosciences, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.

出版信息

J Neurosci Res. 2017 Apr;95(4):973-991. doi: 10.1002/jnr.23823. Epub 2016 Aug 17.

Abstract

Soluble amyloid precursor protein α (sAPPα), a secreted proteolytic fragment of nonamyloidogenic amyloid precursor protein (APP) processing, is known for numerous neuroprotective functions. These functions include but are not limited to proliferation, neuroprotection, synaptic plasticity, memory formation, neurogenesis, and neuritogenesis in cell culture and animal models. In addition, sAPPα influences amyloid-β (Aβ) production by direct modulation of APP β-secretase proteolysis as well as Aβ-related or unrelated tau pathology, hallmark pathologies of Alzheimer's disease (AD). Thus, the restoration of sAPPα levels and functions in the brain by increasing nonamyloidogenic APP processing and/or manipulation of its signaling could reduce AD pathology and cognitive impairment. It is likely that identification and characterization of sAPPα receptors in the brain, downstream effectors, and signaling pathways will pave the way for an attractive therapeutic target for AD prevention or intervention. © 2016 Wiley Periodicals, Inc.

摘要

可溶性淀粉样前体蛋白α(sAPPα)是淀粉样前体蛋白(APP)非淀粉样生成性加工过程中分泌的蛋白水解片段,因其众多神经保护功能而闻名。这些功能包括但不限于细胞培养和动物模型中的增殖、神经保护、突触可塑性、记忆形成、神经发生和神经突形成。此外,sAPPα通过直接调节APPβ-分泌酶蛋白水解以及阿尔茨海默病(AD)的标志性病理——与淀粉样β(Aβ)相关或不相关的tau病理,来影响Aβ的产生。因此,通过增加非淀粉样生成性APP加工和/或操纵其信号传导来恢复大脑中sAPPα的水平和功能,可能会减少AD病理和认知障碍。大脑中sAPPα受体、下游效应器和信号通路的鉴定与表征,很可能为AD预防或干预提供一个有吸引力的治疗靶点。©2016威利期刊公司。

相似文献

1
Restoring Soluble Amyloid Precursor Protein α Functions as a Potential Treatment for Alzheimer's Disease.
J Neurosci Res. 2017 Apr;95(4):973-991. doi: 10.1002/jnr.23823. Epub 2016 Aug 17.
2
APP/Go protein Gβγ-complex signaling mediates Aβ degeneration and cognitive impairment in Alzheimer's disease models.
Neurobiol Aging. 2018 Apr;64:44-57. doi: 10.1016/j.neurobiolaging.2017.12.013. Epub 2017 Dec 20.
3
The roles of amyloid precursor protein (APP) in neurogenesis: Implications to pathogenesis and therapy of Alzheimer disease.
Cell Adh Migr. 2011 Jul-Aug;5(4):280-92. doi: 10.4161/cam.5.4.16986. Epub 2011 Jul 1.
4
Amyloid precursor protein glycosylation is altered in the brain of patients with Alzheimer's disease.
Alzheimers Res Ther. 2020 Aug 12;12(1):96. doi: 10.1186/s13195-020-00664-9.
7
Deciphering the neuroprotective and neurogenic potential of soluble amyloid precursor protein alpha (sAPPα).
Cell Mol Life Sci. 2020 Jun;77(12):2315-2330. doi: 10.1007/s00018-019-03404-x. Epub 2020 Jan 20.
8
Human Umbilical Cord Blood Serum-derived α-Secretase: Functional Testing in Alzheimer's Disease Mouse Models.
Cell Transplant. 2018 Mar;27(3):438-455. doi: 10.1177/0963689718759473. Epub 2018 Mar 21.
9
Alzheimer's disease.
Subcell Biochem. 2012;65:329-52. doi: 10.1007/978-94-007-5416-4_14.
10
The Absence of Myelin Basic Protein Reduces Non-Amyloidogenic Processing of Amyloid Precursor Protein.
Curr Alzheimer Res. 2021;18(4):326-334. doi: 10.2174/1567205018666210701162851.

引用本文的文献

1
The potential link between the development of Alzheimer's disease and osteoporosis.
Biogerontology. 2025 Jan 20;26(1):43. doi: 10.1007/s10522-024-10181-z.
3
Therapeutic effects of a novel synthetic α-secretase.
Front Aging Neurosci. 2024 Jun 7;16:1383905. doi: 10.3389/fnagi.2024.1383905. eCollection 2024.
4
Blood-based therapies to combat neurodegenerative diseases.
Metab Brain Dis. 2024 Jun;39(5):985-1004. doi: 10.1007/s11011-024-01368-x. Epub 2024 Jun 6.
5
Investigation of the Iron Oxide Nanoparticle Effects on Amyloid Precursor Protein Processing in Hippocampal Cells.
Basic Clin Neurosci. 2023 Mar-Apr;14(2):203-212. doi: 10.32598/bcn.2021.2005.1. Epub 2023 Mar 1.
7
SIRT2 as a potential new therapeutic target for Alzheimer's disease.
Neural Regen Res. 2024 Jan;19(1):124-131. doi: 10.4103/1673-5374.375315.
9
Upregulation of endocytic protein expression in the Alzheimer's disease male human brain.
Aging Brain. 2023 Jun 21;4:100084. doi: 10.1016/j.nbas.2023.100084. eCollection 2023.
10
Amyloid precursor protein and its interacting proteins in neurodevelopment.
Biochem Soc Trans. 2023 Aug 31;51(4):1647-1659. doi: 10.1042/BST20221527.

本文引用的文献

2
Endothelial LRP1 transports amyloid-β(1-42) across the blood-brain barrier.
J Clin Invest. 2016 Jan;126(1):123-36. doi: 10.1172/JCI81108. Epub 2015 Nov 30.
3
Viral gene transfer of APPsα rescues synaptic failure in an Alzheimer's disease mouse model.
Acta Neuropathol. 2016 Feb;131(2):247-266. doi: 10.1007/s00401-015-1498-9. Epub 2015 Nov 4.
4
5
sAβPPα is a Potent Endogenous Inhibitor of BACE1.
J Alzheimers Dis. 2015;47(3):545-55. doi: 10.3233/JAD-150282.
6
7
Human umbilical cord blood-derived monocytes improve cognitive deficits and reduce amyloid-β pathology in PSAPP mice.
Cell Transplant. 2015;24(11):2237-50. doi: 10.3727/096368915X688894. Epub 2015 Jul 30.
10
Interaction of the amyloid precursor protein-like protein 1 (APLP1) E2 domain with heparan sulfate involves two distinct binding modes.
Acta Crystallogr D Biol Crystallogr. 2015 Mar;71(Pt 3):494-504. doi: 10.1107/S1399004714027114. Epub 2015 Feb 26.

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