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靶向视神经少突胶质细胞凋亡导致持续脱髓鞘。

Targeted Oligodendrocyte Apoptosis in Optic Nerve Leads to Persistent Demyelination.

机构信息

Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, 20037, USA.

出版信息

Neurochem Res. 2020 Mar;45(3):580-590. doi: 10.1007/s11064-019-02754-z. Epub 2019 Mar 8.

Abstract

The optic nerve represents one of the simplest regions of the CNS and has been useful in developing an understanding of glial development and myelination. While the visual system is frequently affected in demyelinating conditions, utilizing the optic nerve to model demyelination/remyelination studies has been difficult due to its accessibility, relatively small size, and dense nature that makes direct injections challenging. Taking advantage of the lack of oligodendrocytes and myelination in the mouse retina, we have developed a model in which the induction of apoptosis in mature oligodendrocytes allows for the selective, non-invasive generation of demyelinating lesions in optic nerve. Delivery of an inducer of oligodendrocyte apoptosis by intravitreous injection minimizes trauma to the optic nerve and allows for the assessment of oligodendrocyte death in the absence of injury related factors. Here we show that following induction of apoptosis, oligodendrocytes are lost within 3 days. The loss of oligodendrocytes is associated with limited microglial and astrocyte response, is patchy along the nerve, and results in localized myelin loss. Unlike in other regions of the murine CNS, where local demyelination stimulates activation of local oligodendrocyte precursors and remyelination, optic nerve demyelination induced by oligodendrocyte apoptosis fails to recover and results in persistent areas of myelin loss. Over time these chronic lesions change cellular composition and ultimately become devoid of GFAP+ astrocytes and OPCs. Why the optic nerve lesions fail to repair may reflect the lack of early immune responsiveness and provide a novel model of chronic demyelination.

摘要

视神经代表中枢神经系统中最简单的区域之一,对于了解神经胶质细胞的发育和髓鞘形成非常有用。虽然脱髓鞘疾病经常影响视觉系统,但由于视神经易于接近、体积相对较小且结构致密,直接注射较为困难,因此利用视神经来模拟脱髓鞘/髓鞘再生研究一直具有挑战性。利用小鼠视网膜中少突胶质细胞和髓鞘的缺乏,我们开发了一种模型,该模型通过诱导成熟少突胶质细胞凋亡,可以选择性地、非侵入性地在视神经中产生脱髓鞘病变。通过玻璃体内注射递送至少突胶质细胞凋亡的诱导剂可最大程度地减少对视神经的创伤,并允许在没有损伤相关因素的情况下评估少突胶质细胞的死亡。在这里,我们发现诱导凋亡后,少突胶质细胞在 3 天内消失。少突胶质细胞的丢失与小胶质细胞和星形胶质细胞的反应有限有关,沿神经呈斑片状,并导致局部髓鞘丢失。与其他小鼠中枢神经系统区域不同,局部脱髓鞘会刺激局部少突胶质前体细胞的激活和髓鞘再生,而由少突胶质细胞凋亡诱导的视神经脱髓鞘无法恢复,导致持续的髓鞘丢失区域。随着时间的推移,这些慢性病变改变了细胞组成,最终导致 GFAP+星形胶质细胞和 OPC 缺失。为什么视神经病变无法修复可能反映了缺乏早期免疫反应性,并为慢性脱髓鞘提供了一种新的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75dd/7058578/33eb3960cd97/11064_2019_2754_Fig1_HTML.jpg

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