Rossner S, Schliebs R, Härtig W, Perez-Polo J R, Bigl V
Department of Neurochemistry, Paul Flechsig Institute for Brain Research, University of Leipzig, Medical Faculty, Germany.
Neuroreport. 1997 Jul 7;8(9-10):2199-202. doi: 10.1097/00001756-199707070-00022.
Cholinergic basal forebrain neurons are the major source of cortical cholinergic innervation. The number of these neurons is regulated by the availability of nerve growth factor (NGF) during development while in adulthood their cholinergic activity is modulated by NGF. In previous studies we have shown that cholinergic immunolesions of basal forebrain neurons increase local immediate early gene expression and NGF synthesis in the regions of degeneration. In this study we identify the cellular source of c-Jun and NGF expression using dual immunolabeling of c-Jun and NGF in combination with neuronal and glial markers. We demonstrate that both c-Jun and NGF are exclusively expressed in reactive astrocytes but not in microglia or in GABAergic basal forebrain neurons. These observations support the hypothesis that reactive astrocytes synthesize neurotrophic substances in vivo in response to neuronal degeneration in the basal forebrain.
胆碱能基底前脑神经元是皮质胆碱能神经支配的主要来源。这些神经元的数量在发育过程中受神经生长因子(NGF)可用性的调节,而在成年期,它们的胆碱能活性受NGF调节。在先前的研究中,我们已经表明,基底前脑神经元的胆碱能免疫损伤会增加变性区域的局部即早基因表达和NGF合成。在本研究中,我们通过将c-Jun和NGF的双重免疫标记与神经元和胶质细胞标记物相结合,确定了c-Jun和NGF表达的细胞来源。我们证明,c-Jun和NGF仅在反应性星形胶质细胞中表达,而在小胶质细胞或GABA能基底前脑神经元中不表达。这些观察结果支持以下假设:反应性星形胶质细胞在体内响应基底前脑的神经元变性而合成神经营养物质。