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钙调神经磷酸酶信号通路通过拮抗 BMP 通路调控神经诱导。

Calcineurin signaling regulates neural induction through antagonizing the BMP pathway.

机构信息

Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California 94305, USA.

Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.

出版信息

Neuron. 2014 Apr 2;82(1):109-124. doi: 10.1016/j.neuron.2014.02.015.

Abstract

Development of the nervous system begins with neural induction, which is controlled by complex signaling networks functioning in concert with one another. Fine-tuning of the bone morphogenetic protein (BMP) pathway is essential for neural induction in the developing embryo. However, the molecular mechanisms by which cells integrate the signaling pathways that contribute to neural induction have remained unclear. We find that neural induction is dependent on the Ca(2+)-activated phosphatase calcineurin (CaN). Fibroblast growth factor (FGF)-regulated Ca(2+) entry activates CaN, which directly and specifically dephosphorylates BMP-regulated Smad1/5 proteins. Genetic and biochemical analyses revealed that CaN adjusts the strength and transcriptional output of BMP signaling and that a reduction of CaN activity leads to an increase of Smad1/5-regulated transcription. As a result, FGF-activated CaN signaling opposes BMP signaling during gastrulation, thereby promoting neural induction and the development of anterior structures.

摘要

神经系统的发育始于神经诱导,这一过程受到彼此协调作用的复杂信号网络的控制。精细调节骨形态发生蛋白(BMP)途径对于胚胎发育中的神经诱导至关重要。然而,细胞整合有助于神经诱导的信号通路的分子机制仍不清楚。我们发现神经诱导依赖于钙激活的磷酸酶钙调神经磷酸酶(CaN)。成纤维细胞生长因子(FGF)调节的 Ca2+内流激活 CaN,其直接且特异性地去磷酸化 BMP 调节的 Smad1/5 蛋白。遗传和生化分析表明,CaN 调节 BMP 信号的强度和转录输出,而 CaN 活性的降低导致 Smad1/5 调节的转录增加。因此,FGF 激活的 CaN 信号在原肠胚形成过程中与 BMP 信号相反,从而促进神经诱导和前体结构的发育。

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Bone morphogenetic proteins.骨形态发生蛋白
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