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血脑屏障中跨细胞转运多种因素间的串扰概述

Overview of Crosstalk Between Multiple Factor of Transcytosis in Blood Brain Barrier.

作者信息

Tjakra Marco, Wang Yeqi, Vania Vicki, Hou Zhengjun, Durkan Colm, Wang Nan, Wang Guixue

机构信息

Key Laboratory for Biorheological Science and Technology, Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing, China.

The Nanoscience Centre, University of Cambridge, Cambridge, United Kingdom.

出版信息

Front Neurosci. 2020 Jan 21;13:1436. doi: 10.3389/fnins.2019.01436. eCollection 2019.

Abstract

Blood brain barrier (BBB) conserves unique regulatory system to maintain barrier tightness while allowing adequate transport between neurovascular units. This mechanism possess a challenge for drug delivery, while abnormality may result in pathogenesis. Communication between vascular and neural system is mediated through paracellular and transcellular (transcytosis) pathway. Transcytosis itself showed dependency with various components, focusing on caveolae-mediated. Among several factors, intense communication between endothelial cells, pericytes, and astrocytes is the key for a normal development. Regulatory signaling pathway such as VEGF, Notch, S1P, PDGFβ, Ang/Tie, and TGF-β showed interaction with the transcytosis steps. Recent discoveries showed exploration of various factors which has been proven to interact with one of the process of transcytosis, either endocytosis, endosomal rearrangement, or exocytosis. As well as providing a hypothetical regulatory pathway between each factors, specifically miRNA, mechanical stress, various cytokines, physicochemical, basement membrane and junctions remodeling, and crosstalk between developmental regulatory pathways. Finally, various hypotheses and probable crosstalk between each factors will be expressed, to point out relevant research application (Drug therapy design and BBB-on-a-chip) and unexplored terrain.

摘要

血脑屏障(BBB)具有独特的调节系统,可维持屏障的紧密性,同时允许神经血管单元之间进行充分的物质运输。这种机制给药物递送带来了挑战,而其异常可能导致发病机制。血管系统与神经系统之间的通讯是通过细胞旁和跨细胞(转胞吞作用)途径介导的。转胞吞作用本身显示出对各种成分的依赖性,主要集中在小窝介导的过程。在几个因素中,内皮细胞、周细胞和星形胶质细胞之间的紧密通讯是正常发育的关键。诸如血管内皮生长因子(VEGF)、Notch、鞘氨醇-1-磷酸(S1P)、血小板衍生生长因子β(PDGFβ)、血管生成素/酪氨酸激酶(Ang/Tie)和转化生长因子-β(TGF-β)等调节信号通路与转胞吞作用步骤相互作用。最近的发现表明,对各种已被证明与转胞吞作用的内吞、内体重排或外排过程之一相互作用的因素进行了探索。此外,还提供了各因素之间的假设调节途径,特别是微小RNA(miRNA)、机械应力、各种细胞因子、物理化学因素、基底膜和连接重塑,以及发育调节途径之间的串扰。最后,将阐述各因素之间的各种假设和可能的串扰,以指出相关的研究应用(药物治疗设计和芯片上的血脑屏障)以及未探索的领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e43b/6990130/5974b5d9907e/fnins-13-01436-g001.jpg

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