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揭示驱动蛋白-1、tau蛋白和微管在阿尔茨海默病相关神经退行性变中的相互作用。

Unraveling the interplay of kinesin-1, tau, and microtubules in neurodegeneration associated with Alzheimer's disease.

作者信息

Durairajan Siva Sundara Kumar, Selvarasu Karthikeyan, Singh Abhay Kumar, Patnaik Supriti, Iyaswamy Ashok, Jaiswal Yogini, Williams Leonard L, Huang Jian-Dong

机构信息

Molecular Mycology and Neurodegenerative Disease Research Laboratory, Department of Microbiology, Central University of Tamil Nadu, Thiruvarur, India.

Li Ka Shing Faculty of Medicine, School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

出版信息

Front Cell Neurosci. 2024 Oct 23;18:1432002. doi: 10.3389/fncel.2024.1432002. eCollection 2024.

Abstract

Alzheimer's disease (AD) is marked by the gradual and age-related deterioration of nerve cells in the central nervous system. The histopathological features observed in the brain affected by AD are the aberrant buildup of extracellular and intracellular amyloid-β and the formation of neurofibrillary tangles consisting of hyperphosphorylated tau protein. Axonal transport is a fundamental process for cargo movement along axons and relies on molecular motors like kinesins and dyneins. Kinesin's responsibility for transporting crucial cargo within neurons implicates its dysfunction in the impaired axonal transport observed in AD. Impaired axonal transport and dysfunction of molecular motor proteins, along with dysregulated signaling pathways, contribute significantly to synaptic impairment and cognitive decline in AD. Dysregulation in tau, a microtubule-associated protein, emerges as a central player, destabilizing microtubules and disrupting the transport of kinesin-1. Kinesin-1 superfamily members, including kinesin family members 5A, 5B, and 5C, and the kinesin light chain, are intricately linked to AD pathology. However, inconsistencies in the abundance of kinesin family members in AD patients underline the necessity for further exploration into the mechanistic impact of these motor proteins on neurodegeneration and axonal transport disruptions across a spectrum of neurological conditions. This review underscores the significance of kinesin-1's anterograde transport in AD. It emphasizes the need for investigations into the underlying mechanisms of the impact of motor protein across various neurological conditions. Despite current limitations in scientific literature, our study advocates for targeting kinesin and autophagy dysfunctions as promising avenues for novel therapeutic interventions and diagnostics in AD.

摘要

阿尔茨海默病(AD)的特征是中枢神经系统中神经细胞随年龄逐渐退化。在受AD影响的大脑中观察到的组织病理学特征是细胞外和细胞内β淀粉样蛋白的异常堆积以及由过度磷酸化的tau蛋白组成的神经原纤维缠结的形成。轴突运输是货物沿轴突移动的基本过程,依赖于驱动蛋白和动力蛋白等分子马达。驱动蛋白在神经元内运输关键货物的作用表明其功能障碍与AD中观察到的轴突运输受损有关。轴突运输受损和分子运动蛋白功能障碍,以及信号通路失调,对AD中的突触损伤和认知衰退有显著影响。tau蛋白(一种微管相关蛋白)的失调成为核心因素,破坏微管稳定性并干扰驱动蛋白-1的运输。驱动蛋白-1超家族成员,包括驱动蛋白家族成员5A、5B和5C,以及驱动蛋白轻链,与AD病理学密切相关。然而,AD患者中驱动蛋白家族成员丰度的不一致凸显了进一步探索这些运动蛋白对一系列神经疾病中神经退行性变和轴突运输破坏的机制影响的必要性。本综述强调了驱动蛋白-1在AD中的顺行运输的重要性。它强调需要研究运动蛋白在各种神经疾病中的影响的潜在机制。尽管目前科学文献存在局限性,但我们的研究主张将驱动蛋白和自噬功能障碍作为AD新型治疗干预和诊断的有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/506e/11537874/3090a3601cc0/fncel-18-1432002-g001.jpg

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