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阿尔茨海默病中的TMP21:分子机制与潜在靶点

TMP21 in Alzheimer's Disease: Molecular Mechanisms and a Potential Target.

作者信息

Qiu Kaixin, Zhang Xiaojie, Wang Shuai, Li Chunyan, Wang Xin, Li Xuezhi, Wu Yili

机构信息

Cheeloo College of Medicine, Shandong University, Jinan, China.

Shandong Collaborative Innovation Center for Diagnosis, Treatment and Behavioral Interventions, Institute of Mental Health, Jining Medical University, Jining, China.

出版信息

Front Cell Neurosci. 2019 Jul 17;13:328. doi: 10.3389/fncel.2019.00328. eCollection 2019.

DOI:10.3389/fncel.2019.00328
PMID:31379512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6651510/
Abstract

Alzheimer's disease (AD) is the most common form of dementia in the elderly, which is characterized by progressive cognitive impairment. Neuritic plaques, neurofibrillary tangles and neuronal loss are the major neuropathological hallmarks in AD brains. TMP21 is a key molecule for protein trafficking in cells. Growing evidence indicates that TMP21 is dysregulated in AD, which plays a pivotal role in neuritic plaque formation. Therefore, we aim to review the dysregulation of TMP21 in AD, the role of TMP21 in neuritic plaque formation and underlying mechanisms. Moreover, the potential role of TMP21 in neurofibrillary tangle formation, synaptic impairment and neuronal loss is discussed. It will provide an outlook into the potential of regulating TMP21 as a therapeutic approach for AD treatment.

摘要

阿尔茨海默病(AD)是老年人中最常见的痴呆形式,其特征为进行性认知障碍。神经炎性斑块、神经原纤维缠结和神经元丢失是AD大脑中的主要神经病理学特征。TMP21是细胞内蛋白质运输的关键分子。越来越多的证据表明,TMP21在AD中表达失调,在神经炎性斑块形成中起关键作用。因此,我们旨在综述TMP21在AD中的失调情况、TMP21在神经炎性斑块形成中的作用及其潜在机制。此外,还讨论了TMP21在神经原纤维缠结形成、突触损伤和神经元丢失中的潜在作用。这将为将调节TMP21作为AD治疗的一种治疗方法的潜力提供展望。

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2
Abnormal ER quality control of neural GPI-anchored proteins via dysfunction in ER export processing in the frontal cortex of elderly subjects with schizophrenia.异常的内质网质量控制通过神经 GPI-锚定蛋白在老年精神分裂症患者额皮质中的内质网输出加工功能障碍。
Transl Psychiatry. 2019 Jan 16;9(1):6. doi: 10.1038/s41398-018-0359-4.
3
BACE2, a conditional β-secretase, contributes to Alzheimer's disease pathogenesis.
全基因组上位性分析在阿尔茨海默病中的作用及其对遗传风险预测的影响。
Alzheimers Res Ther. 2021 Mar 4;13(1):55. doi: 10.1186/s13195-021-00794-8.
4
RCAN1 Inhibits BACE2 Turnover by Attenuating Proteasome-Mediated BACE2 Degradation.RCAN1 通过抑制蛋白酶体介导的 BACE2 降解来抑制 BACE2 的周转。
Biomed Res Int. 2020 Jun 5;2020:1920789. doi: 10.1155/2020/1920789. eCollection 2020.
5
Diagnostic and Therapeutic Potential of TSPO Studies Regarding Neurodegenerative Diseases, Psychiatric Disorders, Alcohol Use Disorders, Traumatic Brain Injury, and Stroke: An Update.TSPO 研究在神经退行性疾病、精神障碍、酒精使用障碍、创伤性脑损伤和中风中的诊断和治疗潜力:更新。
Cells. 2020 Apr 2;9(4):870. doi: 10.3390/cells9040870.
6
The Dual Role of Kinin/Kinin Receptors System in Alzheimer's Disease.激肽/激肽受体系统在阿尔茨海默病中的双重作用
Front Mol Neurosci. 2019 Oct 1;12:234. doi: 10.3389/fnmol.2019.00234. eCollection 2019.
β位点淀粉样前体蛋白裂解酶2(BACE2)作为一种条件性β分泌酶,参与阿尔茨海默病的发病机制。
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4
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