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首页> 外文期刊>Journal of cell biology >MAP2 is required for dendrite elongation, PKA anchoring in dendrites, and proper PKA signal transduction
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MAP2 is required for dendrite elongation, PKA anchoring in dendrites, and proper PKA signal transduction

机译:MAP2是枝晶延伸,PKA固定在树突中以及适当的PKA信号转导所必需的

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摘要

Microtubule-associated protein 2 (MAP2) is a major component of cross-bridges between microtubules in dendrites, and is known to stabilize microtubules. MAP2 also has a binding domain for the regulatory subunit II of cAMP-dependent protein kinase (PKA). We found that there is reduction in microtubule density in dendrites and a reduction of dendritic length in MAP2-deficient mice. Moreover, there is a significant reduction of various subunits of PKA in dendrites and total amounts of various PKA subunits in hippocampal tissue and cultured neurons. In MAP2-deficient cultured neurons, the induction rate of phosphorylated CREB after forskolin stimulation was much lower than in wild-type neurons. Therefore, MAP2 is an anchoring protein of PKA in dendrites, whose loss leads to reduced amount of dendritic and total PKA and reduced activation of CREB.
机译:微管相关蛋白2(MAP2)是树突中微管之间的跨桥的主要成分,已知可以稳定微管。 MAP2还具有cAMP依赖性蛋白激酶(PKA)调节亚基II的结合域。我们发现在MAP2缺陷小鼠中,树突中的微管密度降低,树突长度降低。而且,树突中PKA的各种亚基显着减少,海马组织和培养的神经元中各种PKA的亚基总量显着减少。在缺乏MAP2的培养神经元中,毛喉素刺激后磷酸化CREB的诱导率远低于野生型神经元。因此,MAP2是树突状细胞中PKA的锚定蛋白,其丢失导致树突状和总PKA的量减少以及CREB的活化减少。

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