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胚胎大鼠神经球分化过程中激肽B2受体的表达与活性

Kinin-B2 receptor expression and activity during differentiation of embryonic rat neurospheres.

作者信息

Martins Antonio H, Alves Janaína M, Trujillo Cleber A, Schwindt Telma T, Barnabé Gabriela F, Motta Fabiana L T, Guimaraes Alessander O, Casarini Dulce E, Mello Luiz E, Pesquero João B, Ulrich Henning

机构信息

Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.

出版信息

Cytometry A. 2008 Apr;73(4):361-8. doi: 10.1002/cyto.a.20519.

Abstract

Neural progenitor cells were isolated from rat fetal telencephalon and proliferate as neurospheres in the presence of EGF, FGF-2, and heparin. In the absence of these growth factors, neurospheres differentiate into neurons, astrocytes, and oligodendrocytes. Using an embryonal carcinoma cell line as in vitro differentiation model, we have already demonstrated the presence of an autocrine loop system between kinin-B2 receptor activity and secretion of its ligand bradykinin (BK) as prerequisites for final neuronal differentiation (Martins et al., J Biol Chem 2005; 280: 19576-19586). The aim of this study was to verify the activity of the kallikrein-kinin system (KKS) during neural progenitor cell differentiation. Immunofluorescence studies and flow cytometry analysis revealed increases in glial fibrillary acidic protein and beta-3 tubulin expression and decrease in the number of nestin-positive cells along neurospheres differentiation, indicating the transition of neural progenitor cells to astrocytes and neurons. Kinin-B2 receptor expression and activity, secretion of BK into the medium, and presence of high-molecular weight kininogen suggest the participation of the KKS in neurosphere differentiation. Functional kinin-B2 receptors and BK secretion indicate an autocrine loop during neurosphere differentiation to neurons, astrocytes, and oligodendrocytes, reflecting events occurring during early brain development.

摘要

神经祖细胞从大鼠胚胎端脑中分离出来,在表皮生长因子(EGF)、成纤维细胞生长因子-2(FGF-2)和肝素存在的情况下增殖形成神经球。在缺乏这些生长因子时,神经球分化为神经元、星形胶质细胞和少突胶质细胞。我们利用胚胎癌细胞系作为体外分化模型,已经证明激肽B2受体活性与其配体缓激肽(BK)的分泌之间存在自分泌循环系统,这是最终神经元分化的先决条件(Martins等人,《生物化学杂志》2005年;280:19576 - 19586)。本研究的目的是验证激肽释放酶-激肽系统(KKS)在神经祖细胞分化过程中的活性。免疫荧光研究和流式细胞术分析显示,随着神经球分化,胶质纤维酸性蛋白和β-3微管蛋白表达增加,巢蛋白阳性细胞数量减少,这表明神经祖细胞向星形胶质细胞和神经元的转变。激肽B2受体的表达和活性、BK向培养基中的分泌以及高分子量激肽原的存在表明KKS参与了神经球的分化。功能性激肽B2受体和BK分泌表明在神经球向神经元、星形胶质细胞和少突胶质细胞分化过程中存在自分泌循环,反映了早期脑发育过程中发生的事件。

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