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中枢神经系统髓鞘形成之前的轴突-胶质细胞相互作用受双向 Eph-ephrin 信号调控。

Axo-Glia Interaction Preceding CNS Myelination Is Regulated by Bidirectional Eph-Ephrin Signaling.

作者信息

Linneberg Cecilie, Harboe Mette, Laursen Lisbeth S

机构信息

Department of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej, Aarhus, Denmark.

Department of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej, Aarhus, Denmark

出版信息

ASN Neuro. 2015 Sep 8;7(5). doi: 10.1177/1759091415602859. Print 2015 Sep-Oct.

Abstract

In the central nervous system, myelination of axons is required to ensure fast saltatory conduction and for survival of neurons. However, not all axons are myelinated, and the molecular mechanisms involved in guiding the oligodendrocyte processes toward the axons to be myelinated are not well understood. Only a few negative or positive guidance clues that are involved in regulating axo-glia interaction prior to myelination have been identified. One example is laminin, known to be required for early axo-glia interaction, which functions through α6β1 integrin. Here, we identify the Eph-ephrin family of guidance receptors as novel regulators of the initial axo-glia interaction, preceding myelination. We demonstrate that so-called forward and reverse signaling, mediated by members of both Eph and ephrin subfamilies, has distinct and opposing effects on processes extension and myelin sheet formation. EphA forward signaling inhibits oligodendrocyte process extension and myelin sheet formation, and blocking of bidirectional signaling through this receptor enhances myelination. Similarly, EphB forward signaling also reduces myelin membrane formation, but in contrast to EphA forward signaling, this occurs in an integrin-dependent manner, which can be reversed by overexpression of a constitutive active β1-integrin. Furthermore, ephrin-B reverse signaling induced by EphA4 or EphB1 enhances myelin sheet formation. Combined, this suggests that the Eph-ephrin receptors are important mediators of bidirectional signaling between axons and oligodendrocytes. It further implies that balancing Eph-ephrin forward and reverse signaling is important in the selection process of axons to be myelinated.

摘要

在中枢神经系统中,轴突的髓鞘形成对于确保快速跳跃式传导以及神经元的存活是必需的。然而,并非所有轴突都有髓鞘,而且引导少突胶质细胞突起朝向待髓鞘化轴突的分子机制尚未完全清楚。目前仅鉴定出少数几个在髓鞘形成前调节轴突与胶质细胞相互作用的负性或正性导向线索。一个例子是层粘连蛋白,已知它是早期轴突与胶质细胞相互作用所必需的,其通过α6β1整合素发挥作用。在此,我们确定Eph-ephrin家族的导向受体是髓鞘形成前初始轴突与胶质细胞相互作用的新型调节因子。我们证明,由Eph和ephrin亚家族成员介导的所谓正向和反向信号传导,对突起延伸和髓鞘片层形成具有不同且相反的作用。EphA正向信号传导抑制少突胶质细胞突起延伸和髓鞘片层形成,通过该受体阻断双向信号传导可增强髓鞘形成。同样,EphB正向信号传导也会减少髓鞘膜形成,但与EphA正向信号传导不同的是,这是以整合素依赖的方式发生的,可通过组成型活性β1整合素的过表达来逆转。此外,由EphA4或EphB1诱导的ephrin-B反向信号传导可增强髓鞘片层形成。综合来看,这表明Eph-ephrin受体是轴突与少突胶质细胞之间双向信号传导的重要介质。这进一步意味着,在待髓鞘化轴突的选择过程中,平衡Eph-ephrin正向和反向信号传导很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8027/4568937/c9ed3beb8087/10.1177_1759091415602859-fig1.jpg

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