Upadhya Raghavendra, Zingg Winston, Shetty Siddhant, Shetty Ashok K
Institute for Regenerative Medicine, Department of Molecular and Cellular Medicine, Texas A&M University College of Medicine, College Station, TX, USA.
Institute for Regenerative Medicine, Department of Molecular and Cellular Medicine, Texas A&M University College of Medicine, College Station, TX, USA.
J Control Release. 2020 Jul 10;323:225-239. doi: 10.1016/j.jconrel.2020.04.017. Epub 2020 Apr 11.
Extracellular vesicles (EVs) released by neural cells play an essential role in brain homeostasis and the crosstalk between neural cells and the periphery. EVs are diverse, nano-sized vesicles, which transport proteins, nucleic acids, and lipids between cells over short and long expanses and hence are proficient for modulating the target cells. EVs released from neural cells are implicated in synaptic plasticity, neuron-glia interface, neuroprotection, neuroregeneration, and the dissemination of neuropathological molecules. This review confers the various properties of EVs secreted by astrocytes and their potential role in health and disease with a focus on evolving concepts. Naïve astrocytes shed EVs containing a host of neuroprotective compounds, which include fibroblast growth factor-2, vascular endothelial growth factor, and apolipoprotein-D. Stimulated astrocytes secrete EVs with neuroprotective molecules including heat shock proteins, synapsin 1, unique microRNAs, and glutamate transporters. Well-characterized astrocyte-derived EVs (ADEVs) generated in specific culture conditions and ADEVs that are engineered to carry the desired miRNAs or proteins are likely useful for treating brain injury and neurogenerative diseases. On the other hand, in conditions such as Alzheimer's disease (AD), stroke, Parkinson's disease, Amyotrophic lateral sclerosis (ALS), and other neuroinflammatory conditions, EVs released by activated astrocytes appear to mediate or exacerbate the pathological processes. The examples include ADEVs spreading the dysregulated complement system in AD, mediating motoneuron toxicity in ALS, and stimulating peripheral leukocyte migration into the brain in inflammatory conditions. Strategies restraining the release of EVs by activated astrocytes or modulating the composition of ADEVs are likely beneficial for treating neurodegenerative diseases. Also, periodic analyses of ADEVs in the blood is useful for detecting astrocyte-specific biomarkers in different neurological conditions and for monitoring disease progression and remission with distinct therapeutic approaches.
神经细胞释放的细胞外囊泡(EVs)在脑内稳态以及神经细胞与外周之间的相互作用中起着至关重要的作用。EVs是多种多样的纳米级囊泡,可在细胞间短距离和长距离运输蛋白质、核酸和脂质,因此能够有效调节靶细胞。神经细胞释放的EVs与突触可塑性、神经元-胶质细胞界面、神经保护、神经再生以及神经病理分子的传播有关。本综述阐述了星形胶质细胞分泌的EVs的各种特性及其在健康和疾病中的潜在作用,并重点关注不断发展的概念。未受刺激的星形胶质细胞释放含有多种神经保护化合物的EVs,这些化合物包括成纤维细胞生长因子-2、血管内皮生长因子和载脂蛋白-D。受刺激的星形胶质细胞分泌含有神经保护分子的EVs,包括热休克蛋白、突触素1、独特的微小RNA和谷氨酸转运体。在特定培养条件下产生的、特征明确的星形胶质细胞衍生的EVs(ADEVs)以及经过工程改造以携带所需微小RNA或蛋白质的ADEVs可能对治疗脑损伤和神经退行性疾病有用。另一方面,在阿尔茨海默病(AD)、中风、帕金森病、肌萎缩侧索硬化症(ALS)等疾病以及其他神经炎症状态下,活化的星形胶质细胞释放的EVs似乎介导或加剧了病理过程。例如,ADEVs在AD中传播失调的补体系统,在ALS中介导运动神经元毒性,并在炎症状态下刺激外周白细胞迁移到脑内。抑制活化的星形胶质细胞释放EVs或调节ADEVs组成的策略可能对治疗神经退行性疾病有益。此外,定期分析血液中的ADEVs有助于检测不同神经疾病中星形胶质细胞特异性生物标志物,并通过不同的治疗方法监测疾病进展和缓解情况。