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施万细胞的发育、成熟与再生:聚焦经典及新出现的细胞内信号通路

Schwann cell development, maturation and regeneration: a focus on classic and emerging intracellular signaling pathways.

作者信息

Castelnovo Luca Franco, Bonalume Veronica, Melfi Simona, Ballabio Marinella, Colleoni Deborah, Magnaghi Valerio

机构信息

Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Milan, Italy.

出版信息

Neural Regen Res. 2017 Jul;12(7):1013-1023. doi: 10.4103/1673-5374.211172.

Abstract

The development, maturation and regeneration of Schwann cells (SCs), the main glial cells of the peripheral nervous system, require the coordinate and complementary interaction among several factors, signals and intracellular pathways. These regulatory molecules consist of integrins, neuregulins, growth factors, hormones, neurotransmitters, as well as entire intracellular pathways including protein-kinase A, C, Akt, Erk/MAPK, Hippo, mTOR, . For instance, Hippo pathway is overall involved in proliferation, apoptosis, regeneration and organ size control, being crucial in cancer proliferation process. In SCs, Hippo is linked to merlin and YAP/TAZ signaling and it seems to respond to mechanic/physical challenges. Recently, among factors regulating SCs, also the signaling intermediates Src tyrosine kinase and focal adhesion kinase (FAK) proved relevant for SC fate, participating in the regulation of adhesion, motility, migration and myelination. In SCs, the factors Src and FAK are regulated by the neuroactive steroid allopregnanolone, thus corroborating the importance of this steroid in the control of SC maturation. In this review, we illustrate some old and novel signaling pathways modulating SC biology and functions during the different developmental, mature and regenerative states.

摘要

施万细胞(SCs)是周围神经系统的主要神经胶质细胞,其发育、成熟和再生需要多种因子、信号和细胞内途径之间的协同和互补相互作用。这些调节分子包括整合素、神经调节蛋白、生长因子、激素、神经递质,以及包括蛋白激酶A、C、Akt、Erk/MAPK、Hippo、mTOR等在内的整个细胞内途径。例如,Hippo途径总体上参与细胞增殖、凋亡、再生和器官大小控制,在癌症增殖过程中至关重要。在施万细胞中,Hippo与默林和YAP/TAZ信号传导相关,似乎对机械/物理挑战有反应。最近,在调节施万细胞的因子中,信号中间体Src酪氨酸激酶和粘着斑激酶(FAK)也被证明与施万细胞命运相关,参与调节粘附、运动、迁移和髓鞘形成。在施万细胞中,Src和FAK因子受神经活性类固醇别孕烯醇酮调节,从而证实了这种类固醇在控制施万细胞成熟中的重要性。在这篇综述中,我们阐述了一些在不同发育、成熟和再生状态下调节施万细胞生物学和功能的新旧信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f04/5558472/d2c896679215/NRR-12-1013-g001.jpg

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