Naruse Masae, Ishizaki Yasuki, Ikenaka Kazuhiro, Tanaka Aoi, Hitoshi Seiji
Division of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki, Japan.
Department of Molecular and Cellular Neurobiology, Gunma University Graduate School of Medicine, Maebashi, Japan.
J Physiol Sci. 2017 Jan;67(1):63-70. doi: 10.1007/s12576-016-0479-7. Epub 2016 Aug 29.
Oligodendrocyte precursor cells (OPCs) appear in the late embryonic brain, mature into oligodendrocytes (OLs), and form myelin in the postnatal brain. It has been proposed that early born OPCs derived from the ventral forebrain are eliminated postnatally and late-born OLs predominate in the adult mouse cortex. However, the temporal and regional niche for cortical OL generation, which persists throughout life in adult mammals, remains to be determined. Our recent study provides new insight into self-renewing and multipotent neural stem cells (NSCs). Our results, together with previous studies, suggest that NSCs at the dorsoventral boundary are uniquely specialized to produce myelin-forming OLs in the cortex during a restricted temporal window. These findings may help identify transcription factors or gene expression patterns which confer neural precursors with the characteristic ability of dorsoventral boundary NSCs to differentiate into OLs, and facilitate the development of new strategies for regenerative medicine of the damaged brain.
少突胶质前体细胞(OPCs)出现在胚胎晚期的大脑中,成熟为少突胶质细胞(OLs),并在出生后的大脑中形成髓鞘。有人提出,源自腹侧前脑的早期出生的OPCs在出生后被清除,而晚期出生的OLs在成年小鼠皮质中占主导地位。然而,成年哺乳动物一生中持续存在的皮质OL生成的时间和区域生态位仍有待确定。我们最近的研究为自我更新和多能神经干细胞(NSCs)提供了新的见解。我们的结果与之前的研究一起表明,背腹边界的NSCs在一个有限的时间窗口内独特地专门用于在皮质中产生形成髓鞘的OLs。这些发现可能有助于识别赋予神经前体细胞背腹边界NSCs分化为OLs特征能力的转录因子或基因表达模式,并促进受损大脑再生医学新策略的开发。