首页> 外文期刊>Journal of Neuropathology and Experimental Neurology: Official Journal of the American Association of Neuropathologists, Inc >Arrested oligodendrocyte lineage progression during human cerebral white matter development: dissociation between the timing of progenitor differentiation and myelinogenesis.
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Arrested oligodendrocyte lineage progression during human cerebral white matter development: dissociation between the timing of progenitor differentiation and myelinogenesis.

机译:人类脑白质发育过程中少突胶质细胞谱系的进展:祖细胞分化的时间和髓鞘生成之间的分离。

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Immature oligodendrocytes (OLs) derive from a large pool of late OL progenitors that populate human cerebral white matter throughout the latter half of gestation. We recently reported that a minor population of immature OLs are present in human cerebral white matter for at least 3 months before these cells commit to myelinogenesis around 30 wk postconceptional age. Since this finding supports dissociation between the events that regulate human immature OL maturation and their commitment to myelinogenesis, we characterized here the cellular sequence of events that characterize immature OLs during the transition from a premyelinating to a myelinating state. Commitment of immature OLs to myelinogenesis in human cerebral white matter correlated with the longitudinal extension of specialized processes, designated "pioneer processes," that made multiple types of apparent contacts with axons. This event coincided with the appearance of 3 distinct populations of sheaths that varied in their labeling for myelin basic protein (MBP). Since few axons initially labeled for MBP, this supported the occurrence in vivo of O4-negative, O1-positive premyelin sheaths that precede MBP-positive compacted myelin. These observations identify 3 sequential stages of early myelinogenesis: 1) the initial ensheathment of axons by premyelin sheaths generated by immature OLs; 2) the initial insertion of MBP into transitional sheaths; and 3) the generation of MBP-rich mature myelin.
机译:未成熟的少突胶质细胞(OL)来源于大量的晚期OL祖细胞,这些祖细胞在整个妊娠的后半段都分布在人脑白质中。我们最近报道说,在人类脑白质中,少数未成熟OL存在至少3个月,然后这些细胞在受孕后30周左右开始发生髓鞘形成。由于此发现支持调节人类未成熟OL成熟的事件与其对髓鞘生成的承诺之间的分离,因此在此我们表征了细胞事件的序列,这些事件表征了从前髓鞘转变为髓鞘状态期间未成熟OL的特征。未成熟OLs对人脑白质中髓鞘形成的承诺与特定过程的纵向延伸有关,该过程被称为“先锋过程”,使轴突与多种类型的表面接触。该事件与3种不同鞘的出现相吻合,它们的髓鞘碱性蛋白(MBP)标记有所不同。由于最初为MBP标记的轴突很少,因此这支持了在体内出现O4阴性,O1阳性的前髓鞘,而后者在MBP阳性的紧密髓鞘之前。这些发现确定了早期髓鞘形成的三个连续阶段:1)不成熟的OLs产生的髓鞘前鞘最初包裹了轴突。 2)MBP最初插入过渡鞘中; 3)富含MBP的成熟髓磷脂的生成。

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