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星形胶质细胞对纹状体多巴胺能去神经支配的反应。

The astrocytic response to the dopaminergic denervation of the striatum.

作者信息

Morales Ingrid, Sanchez Alberto, Rodriguez-Sabate Clara, Rodriguez Manuel

机构信息

Laboratory of Neurobiology and Experimental Neurology, Department of Physiology, Faculty of Medicine, University of La Laguna, La Laguna, Tenerife, Canary Islands, Spain.

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

出版信息

J Neurochem. 2016 Oct;139(1):81-95. doi: 10.1111/jnc.13684. Epub 2016 Jun 18.

Abstract

Increasing evidence suggests that the dopaminergic degeneration which characterizes Parkinson's disease starts in the striatal dopamine terminals and progresses retrogradely to the body of dopamine cells in the substantia nigra. The role of striatal astrocytes in the striatal initiation of the dopaminergic degeneration is little known. This work was aimed at studying the astrocytic response to the dopaminergic denervation of the striatum. The injection of 6-hydroxydopamine (25 μg) in the lateral ventricle of adult Sprague-Dawley rats induced a fast (4 h) and selective (unaccompanied by unspecific lesions of striatal tissue or microgliosis) degeneration of the dopaminergic innervation of the striatum which was followed by a selective astrocytosis unaccompanied by microgliosis. This astrocytosis was severe and had a specific profile which included some (e.g. up-regulation of glial fibrillary acidic protein, GS, S100β, NDRG2, vimentin) but not all (e.g. astrocytic proliferation or differentiation from NG2 cells, astrocytic scars, microgliosis) the characteristics observed after the non-selective lesion of the striatum. This astrocytosis is similar to those observed in the parkinsonian striatum and, because it is was unaccompanied by changes in other striatal cells (e.g. by microgliosis), it may be suitable to study the role of striatal astrocytes during the dopaminergic denervation which characterizes the first stages of Parkinson's disease. The dopaminergic denervation of the striatum induced a severe astrogliosis with a specific profile which included some (e.g. up-regulation of GFAP, GS, S100β, NDRG2, vimentin) but not all (e.g. astrocytic proliferation or differentiation from NG2 cells, astrocytic scars, microgliosis) the characteristics observed after the non-selective striatal lesions. This response may help to understand the role of striatal astrocytes during the dopaminergic denervation which characterizes the first stages of PD. Cover Image for this issue: doi: 10.1111/jnc.13336.

摘要

越来越多的证据表明,帕金森病所特有的多巴胺能神经元变性始于纹状体多巴胺能终末,并逆向发展至黑质中多巴胺能细胞体。纹状体星形胶质细胞在多巴胺能神经元变性的纹状体起始过程中的作用鲜为人知。这项研究旨在探讨纹状体星形胶质细胞对多巴胺能去神经支配的反应。向成年Sprague-Dawley大鼠侧脑室内注射6-羟基多巴胺(25μg)可诱导纹状体多巴胺能神经支配快速(4小时)且选择性地变性(不伴有纹状体组织的非特异性损伤或小胶质细胞增生),随后出现选择性星形胶质细胞增生且无小胶质细胞增生。这种星形胶质细胞增生较为严重,具有特定特征,包括一些(如胶质纤维酸性蛋白、谷氨酰胺合成酶、S100β、NDRG2、波形蛋白上调)但并非所有(如星形胶质细胞增殖或从NG2细胞分化、星形胶质细胞瘢痕、小胶质细胞增生)在纹状体非选择性损伤后观察到的特征。这种星形胶质细胞增生与帕金森病纹状体中观察到的相似,并且由于其未伴随其他纹状体细胞的变化(如小胶质细胞增生),可能适合用于研究在帕金森病早期特征性的多巴胺能去神经支配过程中纹状体星形胶质细胞的作用。纹状体多巴胺能去神经支配诱导了严重的星形胶质细胞增生,具有特定特征,包括一些(如GFAP、GS、S100β、NDRG2、波形蛋白上调)但并非所有(如星形胶质细胞增殖或从NG2细胞分化、星形胶质细胞瘢痕、小胶质细胞增生)在纹状体非选择性损伤后观察到的特征。这种反应可能有助于理解在帕金森病早期特征性的多巴胺能去神经支配过程中纹状体星形胶质细胞的作用。本期封面图片:doi: 10.1111/jnc.13336 。

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