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在髓鞘再生过程中,少突胶质细胞谱系细胞中Nkx2.2表达的短暂上调。

Transient upregulation of Nkx2.2 expression in oligodendrocyte lineage cells during remyelination.

作者信息

Watanabe Masahiko, Hadzic Tarik, Nishiyama Akiko

机构信息

Department of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut 06269, USA.

出版信息

Glia. 2004 May;46(3):311-22. doi: 10.1002/glia.20006.

Abstract

While numerous oligodendrocyte progenitor cells (OPCs) exist in the adult central nervous system (CNS), the molecular signals that promote or inhibit their differentiation into mature oligodendrocytes (OLs) are not known. To investigate whether remyelination in the adult CNS is regulated by the same mechanisms that promote developmental myelination, we used an acute demyelinating/remyelinating lesion in the adult rat spinal cord to examine the expression of the homeodomain transcription factor Nkx2.2, which has previously been implicated in oligodendrocyte differentiation during embryonic development. After a demyelinating insult, Nkx2.2 expression was upregulated first in NG2-expressing OPCs surrounding the lesion and subsequently in both precursors and OLs that appeared inside the lesion prior to the onset of remyelination. The temporal and spatial pattern of Nkx2.2 upregulation coincided with that of oligodendrocyte differentiation characterized in our previous study. A similar increase in the level of Nkx2.2 expression was observed in the postnatal developing optic nerve in a wave from the proximal to the distal retinal end. In vitro Nkx2.2 was expressed in OPCs and immature OLs isolated from postnatal rat spinal cord but was absent from mature OLs. These observations indicate that the process of generating new OLs in a remyelinating lesion recapitulates the developmental program involving activation of the Nkx2.2 gene, which may trigger the existing NG2-expressing precursors in the adult CNS to undergo terminal differentiation into remyelinating OLs.

摘要

虽然成年中枢神经系统(CNS)中存在大量少突胶质前体细胞(OPC),但促进或抑制它们分化为成熟少突胶质细胞(OL)的分子信号尚不清楚。为了研究成年CNS中的髓鞘再生是否受促进发育性髓鞘形成的相同机制调控,我们利用成年大鼠脊髓中的急性脱髓鞘/髓鞘再生损伤来检测同源结构域转录因子Nkx2.2的表达,该转录因子先前已被证明在胚胎发育过程中与少突胶质细胞分化有关。脱髓鞘损伤后,Nkx2.2表达首先在损伤周围表达NG2的OPC中上调,随后在髓鞘再生开始前出现在损伤内部的前体细胞和OL中上调。Nkx2.2上调的时空模式与我们先前研究中所描述的少突胶质细胞分化模式一致。在出生后发育中的视神经中,从视网膜近端到远端也观察到了类似的Nkx2.2表达水平升高。在体外,Nkx2.2在从出生后大鼠脊髓分离的OPC和未成熟OL中表达,但在成熟OL中不表达。这些观察结果表明,在髓鞘再生损伤中产生新OL的过程重现了涉及Nkx2.2基因激活的发育程序,这可能会触发成年CNS中现有的表达NG2的前体细胞终末分化为参与髓鞘再生的OL。

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