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不同的神经配体和信号转导途径在少突胶质细胞分化的特定发育阶段刺激CREB磷酸化。

Different neuroligands and signal transduction pathways stimulate CREB phosphorylation at specific developmental stages along oligodendrocyte differentiation.

作者信息

Sato-Bigbee C, Pal S, Chu A K

机构信息

Department of Biochemistry and Molecular Biophysics, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond 23298-0614, USA.

出版信息

J Neurochem. 1999 Jan;72(1):139-47. doi: 10.1046/j.1471-4159.1999.0720139.x.

Abstract

We have shown previously that the pattern of expression of the transcription factor CREB (cyclic AMP-response element binding protein) in developing oligodendrocytes (OLGs) suggests a role during a period that precedes the peak of myelination in rat brain. We have now investigated the signaling pathways that could be responsible for activating CREB by phosphorylation at different stages along OLG maturation. CREB phosphorylation was studied in short-term cultures of immature OLG precursor cells and young OLGs isolated from 4- and 11-day-old rat cerebrum, respectively. The results indicated that at both developmental stages, CREB phosphorylation could be stimulated by either increased concentrations of cyclic AMP and cyclic AMP-dependent protein kinase activation or increased Ca2+ levels and a protein kinase C activity. The results also showed that CREB phosphorylation in immature OLG precursor cells could be up-regulated by treatment with histamine, carbachol, glutamate, and ATP (neuroligands known to increase Ca2+ levels in these cells), by signaling cascade(s) that involve a protein kinase C activity, as well as the mitogen-activated protein kinase pathway. In contrast, in cells isolated from 11-day-old rats, at a developmental stage that immediately precedes the beginning of the active period of myelin synthesis, CREB phosphorylation was only stimulated by treatment with the beta-adrenergic agonist isoproterenol in a process that appears to be mediated by a cyclic AMP/cyclic AMP-dependent protein kinase-dependent pathway. These results support the idea that CREB could be a mediator of neuronal signals that, coupled to specific signal transduction cascades, may play different regulatory roles at specific stages along OLG differentiation.

摘要

我们之前已经表明,转录因子CREB(环磷酸腺苷反应元件结合蛋白)在发育中的少突胶质细胞(OLGs)中的表达模式表明其在大鼠脑髓鞘形成高峰期之前的阶段发挥作用。我们现在研究了在OLG成熟的不同阶段可能通过磷酸化激活CREB的信号通路。分别在从4日龄和11日龄大鼠大脑分离的未成熟OLG前体细胞和年轻OLG的短期培养物中研究了CREB磷酸化。结果表明,在两个发育阶段,环磷酸腺苷浓度增加和环磷酸腺苷依赖性蛋白激酶激活或钙离子水平升高和蛋白激酶C活性增加均可刺激CREB磷酸化。结果还表明,未成熟OLG前体细胞中的CREB磷酸化可通过组胺、卡巴胆碱、谷氨酸和ATP(已知可增加这些细胞中钙离子水平的神经配体)处理,通过涉及蛋白激酶C活性以及丝裂原活化蛋白激酶途径的信号级联反应上调。相比之下,在从11日龄大鼠分离的细胞中,即在髓鞘合成活跃期开始之前的发育阶段,CREB磷酸化仅在β-肾上腺素能激动剂异丙肾上腺素处理下受到刺激,这一过程似乎由环磷酸腺苷/环磷酸腺苷依赖性蛋白激酶依赖性途径介导。这些结果支持这样一种观点,即CREB可能是神经元信号的介质,与特定的信号转导级联反应相结合,可能在OLG分化的特定阶段发挥不同的调节作用。

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