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首页> 外文期刊>Journal of Anatomy >Astrocyte-endothelial interactions and blood-brain barrier permeability.
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Astrocyte-endothelial interactions and blood-brain barrier permeability.

机译:星形胶质细胞-内皮相互作用和血脑屏障通透性。

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The blood-brain barrier (BBB) is formed by brain endothelial cells lining the cerebral microvasculature, and is an important mechanism for protecting the brain from fluctuations in plasma composition, and from circulating agents such as neurotransmitters and xenobiotics capable of disturbing neural function. The barrier also plays an important role in the homeostatic regulation of the brain microenvironment necessary for the stable and co-ordinated activity of neurones. The BBB phenotype develops under the influence of associated brain cells, especially astrocytic glia, and consists of more complex tight junctions than in other capillary endothelia, and a number of specific transport and enzyme systems which regulate molecular traffic across the endothelial cells. Transporters characteristic of the BBB phenotype include both uptake mechanisms (e.g. GLUT-1 glucose carrier, L1 amino acid transporter) and efflux transporters (e.g. P-glycoprotein). In addition to a role in long-term barrier induction and maintenance, astrocytes and other cells can release chemical factors that modulate endothelial permeability over a time-scale of seconds to minutes. Cell culture models, both primary and cell lines, have been used to investigate aspects of barrier induction and modulation. Conditioned medium taken from growing glial cells can reproduce some of the inductive effects, evidence for involvement of diffusible factors. However, for some features of endothelial differentiation and induction, the extracellular matrix plays an important role. Several candidate molecules have been identified, capable of mimicking aspects of glial-mediated barrier induction of brain endothelium; these include TGFbeta, GDNF, bFGF, IL-6 and steroids. In addition, factors secreted by brain endothelial cells including leukaemia inhibitory factor (LIF) have been shown to induce astrocytic differentiation. Thus endothelium and astrocytes are involved in two-way induction. Short-term modulation of brain endothelial permeability has been shown for a number of small chemical mediators produced by astrocytes and other nearby cell types. It is clear that endothelial cells are involved in both long- and short-term chemical communication with neighbouring cells, with the perivascular end feet of astrocytes being of particular importance. The role of barrier induction and modulation in normal physiology and in pathology is discussed.
机译:血脑屏障(BBB)是由位于脑微血管内的脑内皮细胞形成的,是保护脑部免受血浆成分波动以及免受循环介质(如神经递质和能干扰神经功能的异生物)的重要机制。该屏障在稳定和协调神经元活动所必需的大脑微环境的稳态调节中也起着重要作用。 BBB表型在相关脑细胞(尤其是星形胶质细胞)的影响下发展,并且比其他毛细管内皮细胞具有更复杂的紧密连接,以及调节跨内皮细胞分子运输的许多特定转运和酶系统。 BBB表型的特征性转运蛋白包括摄取机制(例如GLUT-1葡萄糖载体,L1氨基酸转运蛋白)和外排转运蛋白(例如P-糖蛋白)。除了在长期的屏障诱导和维持中发挥作用外,星形胶质细胞和其他细胞还可以释放化学因子,从而在数秒至数分钟的时间范围内调节内皮的通透性。原代和细胞系的细胞培养模型已用于研究屏障诱导和调节的各个方面。从生长中的神经胶质细胞中提取的条件培养基可以再现某些诱导作用,这是扩散因子参与的证据。但是,对于内皮细胞分化和诱导的某些特征,细胞外基质起着重要的作用。已经鉴定出几种候选分子,它们能够模拟神经胶质介导的对脑内皮屏障的诱导。这些包括TGFbeta,GDNF,bFGF,IL-6和类固醇。此外,脑内皮细胞分泌的因子,包括白血病抑制因子(LIF)已显示出诱导星形胶质细胞分化的作用。因此内皮和星形胶质细胞参与双向诱导。星形胶质细胞和其他附近细胞类型产生的许多小化学介体已显示出大脑内皮通透性的短期调节。显然,内皮细胞参与了与相邻细胞的长期和短期化学通讯,星形胶质细胞的血管周端足特别重要。讨论了屏障诱导和调节在正常生理学和病理学中的作用。

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