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外泌体在神经退行性疾病中的透视见解:批判性评估

Perspective Insights of Exosomes in Neurodegenerative Diseases: A Critical Appraisal.

作者信息

Jan Arif Tasleem, Malik Mudasir A, Rahman Safikur, Yeo Hye R, Lee Eun J, Abdullah Tasduq S, Choi Inho

机构信息

Department of Medical Biotechnology, Yeungnam University, Gyeongsan, South Korea.

CSIR-Indian Institute of Integrative Medicine, Jammu, India.

出版信息

Front Aging Neurosci. 2017 Sep 29;9:317. doi: 10.3389/fnagi.2017.00317. eCollection 2017.

Abstract

Exosomes are small membranous entities of endocytic origin. Their production by a wide variety of cells in eukaryotes implicates their roles in the execution of essential processes, especially cellular communication. Exosomes are secreted under both physiological and pathophysiological conditions, and their actions on neighboring and distant cells lead to the modulations of cellular behaviors. They also assist in the delivery of disease causing entities, such as prions, α-syn, and tau, and thus, facilitate spread to non-effected regions and accelerate the progressions of neurodegenerative diseases. The characterization of exosomes, provides information on aberrant processes, and thus, exosome analysis has many clinical applications. Because they are associated with the transport of different cellular entities across the blood-brain barrier (BBB), exosomes might be useful for delivering drugs and other therapeutic molecules to brain. Herein, we review roles played by exosomes in different neurodegenerative diseases, and the possibilities of using them as diagnostic biomarkers of disease progression, drug delivery vehicles and in gene therapy.

摘要

外泌体是源自内吞作用的小膜性囊泡。真核生物中多种细胞均可产生外泌体,这表明它们在执行基本过程,尤其是细胞通讯中发挥作用。外泌体在生理和病理生理条件下均会分泌,它们对邻近细胞和远处细胞的作用会导致细胞行为的调节。它们还协助传递致病因子,如朊病毒、α-突触核蛋白和tau蛋白,从而促进疾病传播至未受影响的区域并加速神经退行性疾病的进展。外泌体的特征分析可提供有关异常过程的信息,因此,外泌体分析具有许多临床应用。由于它们与不同细胞成分跨越血脑屏障(BBB)的运输有关,外泌体可能有助于将药物和其他治疗分子递送至大脑。在此,我们综述外泌体在不同神经退行性疾病中所起的作用,以及将它们用作疾病进展的诊断生物标志物、药物递送载体和基因治疗的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dad0/5626860/ffc8fff5bb1a/fnagi-09-00317-g0001.jpg

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