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诱导人皮质球体形成髓鞘少突胶质细胞。

Induction of myelinating oligodendrocytes in human cortical spheroids.

机构信息

Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA.

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

出版信息

Nat Methods. 2018 Sep;15(9):700-706. doi: 10.1038/s41592-018-0081-4. Epub 2018 Jul 25.

Abstract

Cerebral organoids provide an accessible system for investigations of cellular composition, interactions, and organization but have lacked oligodendrocytes, the myelinating glia of the central nervous system. Here we reproducibly generated oligodendrocytes and myelin in 'oligocortical spheroids' derived from human pluripotent stem cells. Molecular features consistent with those of maturing oligodendrocytes and early myelin appeared by week 20 in culture, with further maturation and myelin compaction evident by week 30. Promyelinating drugs enhanced the rate and extent of oligodendrocyte generation and myelination, and spheroids generated from human subjects with a genetic myelin disorder recapitulated human disease phenotypes. Oligocortical spheroids provide a versatile platform for studies of myelination of the developing central nervous system and offer new opportunities for disease modeling and therapeutic development.

摘要

类脑器官为研究细胞组成、相互作用和组织提供了一种易于获取的系统,但缺乏中枢神经系统的髓鞘形成胶质细胞——少突胶质细胞。在这里,我们从人类多能干细胞中可重复地生成少突胶质细胞和髓鞘形成于“少突胶质细胞球体”中。在培养的第 20 周,出现了与成熟少突胶质细胞和早期髓鞘相一致的分子特征,在第 30 周时,可见进一步的成熟和髓鞘紧缩。促髓鞘生成药物可提高少突胶质细胞生成和髓鞘形成的速度和程度,并且来自具有遗传髓鞘疾病的人类供体的球体再现了人类疾病表型。少突胶质细胞球体为研究发育中中枢神经系统的髓鞘形成提供了一个多功能平台,并为疾病建模和治疗开发提供了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8784/6508550/e4a4cca8126c/nihms-979721-f0001.jpg

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