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少突胶质细胞神经束蛋白独立调节中枢神经系统髓鞘的靶向和鞘生长。

Oligodendrocyte Neurofascin Independently Regulates Both Myelin Targeting and Sheath Growth in the CNS.

机构信息

Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH16 4SB, UK.

Department of Cell and Developmental Biology, University College London, London WC1E 6BT, UK.

出版信息

Dev Cell. 2019 Dec 16;51(6):730-744.e6. doi: 10.1016/j.devcel.2019.10.016. Epub 2019 Nov 21.

Abstract

Selection of the correct targets for myelination and regulation of myelin sheath growth are essential for central nervous system (CNS) formation and function. Through a genetic screen in zebrafish and complementary analyses in mice, we find that loss of oligodendrocyte Neurofascin leads to mistargeting of myelin to cell bodies, without affecting targeting to axons. In addition, loss of Neurofascin reduces CNS myelination by impairing myelin sheath growth. Time-lapse imaging reveals that the distinct myelinating processes of individual oligodendrocytes can engage in target selection and sheath growth at the same time and that Neurofascin concomitantly regulates targeting and growth. Disruption to Caspr, the neuronal binding partner of oligodendrocyte Neurofascin, also impairs myelin sheath growth, likely reflecting its association in an adhesion complex at the axon-glial interface with Neurofascin. Caspr does not, however, affect myelin targeting, further indicating that Neurofascin independently regulates distinct aspects of CNS myelination by individual oligodendrocytes in vivo.

摘要

髓鞘形成的正确靶点选择和髓鞘生长的调控对于中枢神经系统(CNS)的形成和功能至关重要。通过在斑马鱼中的遗传筛选和在小鼠中的互补分析,我们发现少突胶质细胞 Neurofascin 的缺失导致髓鞘错误靶向到细胞体,而不影响其靶向到轴突。此外,Neurofascin 的缺失通过损害髓鞘鞘生长来减少 CNS 的髓鞘形成。延时成像揭示,单个少突胶质细胞的不同髓鞘形成过程可以同时进行靶点选择和鞘生长,并且 Neurofascin 同时调节靶向和生长。少突胶质细胞 Neurofascin 的神经元结合伴侣 Caspr 的破坏也会损害髓鞘鞘生长,这可能反映了它在轴突-胶质界面的粘附复合物中与 Neurofascin 的关联。然而,Caspr 并不影响髓鞘靶向,这进一步表明,Neurofascin 独立地通过体内的单个少突胶质细胞调节 CNS 髓鞘形成的不同方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6230/6912162/b54fce741910/fx1.jpg

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