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大鼠脑炎性、自身免疫性和退行性病变中微胶质细胞白细胞介素-16的表达。

Expression of interleukin-16 by microglial cells in inflammatory, autoimmune, and degenerative lesions of the rat brain.

作者信息

Guo Liang-Hao, Mittelbronn Michel, Brabeck Christine, Mueller Christian A, Schluesener Hermann J

机构信息

Institute of Brain Research, University of Tuebingen, Calwer Str. 3, Tuebingen D-72076, Germany.

出版信息

J Neuroimmunol. 2004 Jan;146(1-2):39-45. doi: 10.1016/j.jneuroim.2003.09.017.

Abstract

Here we report a comparative analysis of interleukin-16 (IL-16) expression by microglial cells of the normal rat brain in trimethyltin (TMT) neurotoxicity, experimental autoimmune uveitis (EAU), encephalomyelitis (EAE), and viral infection (Borna disease, Borna disease virus) by immunohistochemistry. Striking differences were observed. In contrast to the human brain, IL-16 was not expressed constitutively in the rat brain. Remote activation of microglial cells of the optic tract in EAU did not result into IL-16 expression. TMT intoxication induced expression in microglial cells of the hippocampus. In EAE and BDV, massive IL-16(+) microglial cells could be seen. Thus, IL-16 is a descriptor of microglial cell activation that discriminates between different disease models, and might be a valuable marker for the detection of microglia activation in human and rat central nervous system (CNS) diseases.

摘要

在此,我们通过免疫组织化学方法报告了对正常大鼠脑内小胶质细胞在三甲基锡(TMT)神经毒性、实验性自身免疫性葡萄膜炎(EAU)、脑脊髓炎(EAE)和病毒感染(博尔纳病、博尔纳病病毒)中白细胞介素-16(IL-16)表达的比较分析。观察到显著差异。与人类大脑不同,IL-16在大鼠大脑中不是组成性表达。EAU中视束小胶质细胞的远程激活未导致IL-16表达。TMT中毒诱导海马小胶质细胞表达。在EAE和BDV中,可以看到大量IL-16(+)小胶质细胞。因此,IL-16是小胶质细胞激活的一个描述符,可区分不同疾病模型,并且可能是检测人类和大鼠中枢神经系统(CNS)疾病中小胶质细胞激活的有价值标志物。

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