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在发育、衰老以及应对创伤、疾病和毒性损伤过程中,神经内膜微环境的体内平衡调节。

Homeostatic regulation of the endoneurial microenvironment during development, aging and in response to trauma, disease and toxic insult.

机构信息

Department of Pathology 0612, School of Medicine, University of California-San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0612, USA.

出版信息

Acta Neuropathol. 2011 Mar;121(3):291-312. doi: 10.1007/s00401-010-0783-x. Epub 2010 Dec 7.

Abstract

The endoneurial microenvironment, delimited by the endothelium of endoneurial vessels and a multi-layered ensheathing perineurium, is a specialized milieu intérieur within which axons, associated Schwann cells and other resident cells of peripheral nerves function. The endothelium and perineurium restricts as well as regulates exchange of material between the endoneurial microenvironment and the surrounding extracellular space and thus is more appropriately described as a blood-nerve interface (BNI) rather than a blood-nerve barrier (BNB). Input to and output from the endoneurial microenvironment occurs via blood-nerve exchange and convective endoneurial fluid flow driven by a proximo-distal hydrostatic pressure gradient. The independent regulation of the endothelial and perineurial components of the BNI during development, aging and in response to trauma is consistent with homeostatic regulation of the endoneurial microenvironment. Pathophysiological alterations of the endoneurium in experimental allergic neuritis (EAN), and diabetic and lead neuropathy are considered to be perturbations of endoneurial homeostasis. The interactions of Schwann cells, axons, macrophages, and mast cells via cell-cell and cell-matrix signaling regulate the permeability of this interface. A greater knowledge of the dynamic nature of tight junctions and the factors that induce and/or modulate these key elements of the BNI will increase our understanding of peripheral nerve disorders as well as stimulate the development of therapeutic strategies to treat these disorders.

摘要

神经内膜的微环境由神经内膜血管的内皮和多层神经束膜鞘限定,是一个特殊的内在环境,其中轴突、相关的施万细胞和周围神经的其他固有细胞发挥功能。内皮和神经束膜限制并调节神经内膜微环境与周围细胞外空间之间的物质交换,因此更准确地描述为血神经界面(BNI),而不是血神经屏障(BNB)。神经内膜微环境的输入和输出通过血神经交换和由近-远向液压梯度驱动的对流性神经内膜液流发生。内皮和神经束膜成分在发育、衰老和对创伤的反应中的独立调节与神经内膜微环境的稳态调节一致。实验性变应性神经炎(EAN)、糖尿病和铅中毒神经病中神经内膜的病理生理改变被认为是神经内膜稳态的扰动。施万细胞、轴突、巨噬细胞和肥大细胞通过细胞-细胞和细胞-基质信号的相互作用调节这个界面的通透性。对紧密连接的动态性质以及诱导和/或调节 BNI 这些关键要素的因素有更多的了解,将增加我们对周围神经疾病的理解,并刺激开发治疗这些疾病的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a05b/3038236/1b69d04d332f/401_2010_783_Fig1_HTML.jpg

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