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星形胶质细胞中的蛋白质合成:“自发”及环磷酸腺苷诱导的分化

Protein synthesis in astrocytes: 'spontaneous' and cyclic AMP-induced differentiation.

作者信息

Bridoux A M, Fages C, Couchie D, Nunez J, Tardy M

出版信息

Dev Neurosci. 1986;8(1):31-43. doi: 10.1159/000112239.

Abstract

Primary cultures of mouse astrocytes have been used to study astroglial protein synthesis during 'in vitro' differentiation. Spontaneous age-related differentiation was compared to the effect of DBcAMP or forskolin, a drug which directly stimulates the adenylate cyclase and induces 'morphological differentiation' in these cells. Cell differentiation was followed in parallel by phase contrast microscopy and immunofluorescence techniques. Two antisera, one raised against GFA, the other against microtubule-associated protein 2 (MAP2) were used. Anti-GFA serum labelled the cells as early as 7 days in vitro. Anti-MAP2 serum revealed a dense fibrous network at later stages of the culture, whereas the dividing astroblasts appeared poorly stained by this antibody. Both phase contrast microscopy and immunofluorescence techniques suggested that most of the cells spontaneously differentiate after 3 weeks of culture even in the absence of DBcAMP or forskolin. Forskolin, while accelerating differentiation after 7 days of culture, produced smaller cells than DBcAMP and had biphasic effects on cell morphology. Mono- and two-dimensional gel electrophoresis of the 35S-methionine labelled cells also showed that the major changes in protein synthetic activity occur spontaneously during the time course of the culture. Whatever the stage of the culture, DBcAMP or forskolin induced changes in the synthesis of only a few proteins. However, depending on the culture stage the proteins, which were positively or negatively controlled by these drugs, were not the same.

摘要

小鼠星形胶质细胞的原代培养物已被用于研究“体外”分化过程中的星形胶质细胞蛋白质合成。将自发的年龄相关分化与二丁酰环磷腺苷(DBcAMP)或福斯可林的作用进行了比较,福斯可林是一种直接刺激腺苷酸环化酶并诱导这些细胞“形态分化”的药物。通过相差显微镜和免疫荧光技术并行跟踪细胞分化。使用了两种抗血清,一种针对胶质纤维酸性蛋白(GFA),另一种针对微管相关蛋白2(MAP2)。抗GFA血清在体外培养7天时就可标记细胞。抗MAP2血清在培养后期显示出密集的纤维网络,而正在分裂的成星形细胞被该抗体染色较差。相差显微镜和免疫荧光技术均表明,即使在没有DBcAMP或福斯可林的情况下,大多数细胞在培养3周后也会自发分化。福斯可林虽然在培养7天后加速了分化,但产生的细胞比DBcAMP小,并且对细胞形态有双相作用。对用35S-甲硫氨酸标记的细胞进行的一维和二维凝胶电泳也表明,蛋白质合成活性的主要变化在培养过程中自发发生。无论培养处于哪个阶段,DBcAMP或福斯可林仅诱导少数蛋白质合成发生变化。然而,根据培养阶段的不同,受这些药物正向或负向调控的蛋白质并不相同。

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