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PRDM16 通过在发育中的大脑中的神经分化来协调血管生成。

PRDM16 orchestrates angiogenesis via neural differentiation in the developing brain.

机构信息

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Cell Death Differ. 2020 Aug;27(8):2313-2329. doi: 10.1038/s41418-020-0504-5. Epub 2020 Feb 3.

Abstract

Angiogenesis plays crucial roles in maintaining the complex operation of central nervous system (CNS) development. The architecture of communication between neurogenesis and angiogenesis is essential to maintain normal brain development and function. Hence, any disruption of neuron-vascular communications may lead to the pathophysiology of cerebrovascular diseases and blood-brain barrier (BBB) dysfunction. Here we demonstrate that neural differentiation and communication are required for vascular development. Regarding the cellular and molecular mechanism, our results show that PRDM16 activity determines the production of mature neurons and their specific positions in the neocortex. In the cortical plate (CP), aberrant neurons fail to secrete modular calcium-binding protein 1 (SMOC1), an important neuronal signal that participates in neurovascular communication to regulate CNS angiogenesis. Neuronal SMOC1 interacts with TGFBR1 by activating the transcription factors phospho-Smad2/3 to convey intercellular signals to endothelial cells (ECs) in the TGF-β-Smad signaling pathway. Together, our results highlight a crucial coordinated neurovascular development process orchestrated by PRDM16 and reveal the importance of intimate communication for building the neurovascular network during brain development.

摘要

血管生成在维持中枢神经系统(CNS)发育的复杂运作中起着至关重要的作用。神经发生和血管生成之间的通讯结构对于维持正常的大脑发育和功能至关重要。因此,神经元-血管通讯的任何中断都可能导致脑血管疾病和血脑屏障(BBB)功能障碍的病理生理学。在这里,我们证明了神经分化和通讯对于血管发育是必需的。关于细胞和分子机制,我们的结果表明 PRDM16 活性决定了成熟神经元的产生及其在新皮层中的特定位置。在皮质板(CP)中,异常神经元不能分泌模块化钙结合蛋白 1(SMOC1),SMOC1 是一种重要的神经元信号,参与神经血管通讯以调节中枢神经系统血管生成。神经元 SMOC1 通过激活转录因子磷酸化 Smad2/3 与 TGFBR1 相互作用,在 TGF-β-Smad 信号通路中向内皮细胞(ECs)传递细胞间信号。总之,我们的结果强调了 PRDM16 协调的神经血管发育过程的重要性,并揭示了在大脑发育过程中建立神经血管网络的紧密通讯的重要性。

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