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少突胶质细胞的存活以及髓鞘紧密化和完整性的维持需要星形胶质细胞。

Astrocytes Are Required for Oligodendrocyte Survival and Maintenance of Myelin Compaction and Integrity.

作者信息

Tognatta Reshmi, Karl Molly T, Fyffe-Maricich Sharyl L, Popratiloff Anastas, Garrison Eric D, Schenck Jessica K, Abu-Rub Mohammad, Miller Robert H

机构信息

School of Medicine and Health Sciences, George Washington University, Washington, DC, United States.

Gladstone Institute of Neurological Diseases, San Francisco, CA, United States.

出版信息

Front Cell Neurosci. 2020 Apr 2;14:74. doi: 10.3389/fncel.2020.00074. eCollection 2020.

Abstract

Astrocytes have been implicated in regulating oligodendrocyte development and myelination , although their functions remain less well defined. Using a novel approach to locally ablate GFAP+ astrocytes, we demonstrate that astrocytes are required for normal CNS myelin compaction during development, and for maintaining myelin integrity in the adult. Transient ablation of GFAP+ astrocytes in the mouse spinal cord during the first postnatal week reduced the numbers of mature oligodendrocytes and inhibited myelin formation, while prolonged ablation resulted in myelin that lacked compaction and structural integrity. Ablation of GFAP+ astrocytes in the adult spinal cord resulted in the rapid, local loss of myelin integrity and regional demyelination. The loss of myelin integrity induced by astrocyte ablation was greatly reduced by NMDA receptor antagonists, both and , suggesting that myelin stability was affected by elevation of local glutamate levels following astrocyte ablation. Furthermore, targeted delivery of glutamate into adult spinal cord white matter resulted in reduction of myelin basic protein expression and localized disruption of myelin compaction which was also reduced by NMDA receptor blockade. The pathology induced by localized astrocyte loss and elevated exogenous glutamate, supports the concept that astrocytes are critical for maintenance of myelin integrity in the adult CNS and may be primary targets in the initiation of demyelinating diseases of the CNS, such as Neuromyelitis Optica (NMO).

摘要

星形胶质细胞被认为参与调节少突胶质细胞的发育和髓鞘形成,尽管它们的功能仍不太明确。我们采用一种新方法对GFAP+星形胶质细胞进行局部消融,结果表明,星形胶质细胞对于发育过程中中枢神经系统正常的髓鞘压实以及维持成体髓鞘完整性是必需的。在出生后第一周对小鼠脊髓中的GFAP+星形胶质细胞进行短暂消融,会减少成熟少突胶质细胞的数量并抑制髓鞘形成,而长期消融则会导致髓鞘缺乏压实和结构完整性。对成体脊髓中的GFAP+星形胶质细胞进行消融,会导致髓鞘完整性迅速局部丧失和区域性脱髓鞘。NMDA受体拮抗剂(和)可大大减轻星形胶质细胞消融引起的髓鞘完整性丧失,这表明髓鞘稳定性受星形胶质细胞消融后局部谷氨酸水平升高的影响。此外,将谷氨酸靶向递送至成体脊髓白质会导致髓鞘碱性蛋白表达减少以及髓鞘压实的局部破坏,而NMDA受体阻断也可减轻这种破坏。局部星形胶质细胞丧失和外源性谷氨酸升高所引发的病理变化,支持了星形胶质细胞对于维持成体中枢神经系统髓鞘完整性至关重要这一观点,并且星形胶质细胞可能是中枢神经系统脱髓鞘疾病(如视神经脊髓炎,NMO)发病起始阶段的主要靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df1/7142332/1fb6ae853338/fncel-14-00074-g001.jpg

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