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少突胶质前体细胞的特化受神经祖细胞-内皮细胞双向通讯调控。

Oligodendrocyte precursor cell specification is regulated by bidirectional neural progenitor-endothelial cell crosstalk.

机构信息

European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.

出版信息

Nat Neurosci. 2021 Apr;24(4):478-488. doi: 10.1038/s41593-020-00788-z. Epub 2021 Jan 28.

Abstract

Neural-derived signals are crucial regulators of CNS vascularization. However, whether the vasculature responds to these signals by means of elongating and branching or in addition by building a feedback response to modulate neurodevelopmental processes remains unknown. In this study, we identified bidirectional crosstalk between the neural and the vascular compartment of the developing CNS required for oligodendrocyte precursor cell specification. Mechanistically, we show that neural progenitor cells (NPCs) express angiopoietin-1 (Ang1) and that this expression is regulated by Sonic hedgehog. We demonstrate that NPC-derived Ang1 signals to its receptor, Tie2, on endothelial cells to induce the production of transforming growth factor beta 1 (TGFβ1). Endothelial-derived TGFβ1, in turn, acts as an angiocrine molecule and signals back to NPCs to induce their commitment toward oligodendrocyte precursor cells. This work demonstrates a true bidirectional collaboration between NPCs and the vasculature as a critical regulator of oligodendrogenesis.

摘要

神经源性信号是中枢神经系统血管生成的关键调节因子。然而,血管系统是否通过延长和分支来响应这些信号,或者是否通过建立反馈反应来调节神经发育过程,目前尚不清楚。在这项研究中,我们确定了发育中中枢神经系统的神经和血管区室之间的双向串扰对于少突胶质前体细胞特化是必需的。从机制上讲,我们表明神经祖细胞 (NPC) 表达血管生成素 1 (Ang1),并且这种表达受 Sonic hedgehog 调节。我们证明 NPC 衍生的 Ang1 信号转导到内皮细胞上的受体 Tie2,以诱导转化生长因子 β1 (TGFβ1) 的产生。内皮细胞衍生的 TGFβ1 反过来作为血管分泌分子作用并反向信号转导到 NPC 以诱导其向少突胶质前体细胞的分化。这项工作证明了 NPC 和血管之间的真正双向协作是少突胶质发生的关键调节因子。

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