• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1002/glia.20006
PMID:15048854
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。

相似文献

1
Transient upregulation of Nkx2.2 expression in oligodendrocyte lineage cells during remyelination.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。
Glia. 2004 May;46(3):311-22. doi: 10.1002/glia.20006.
2
Nkx2.2 expression in differentiation of oligodendrocyte precursor cells and inhibitory factors for differentiation of oligodendrocytes after traumatic spinal cord injury.Nkx2.2在少突胶质前体细胞分化中的表达及创伤性脊髓损伤后少突胶质细胞分化的抑制因子
J Neurotrauma. 2007 Jun;24(6):1013-25. doi: 10.1089/neu.2006.0151.
3
Increased expression of Nkx2.2 and Olig2 identifies reactive oligodendrocyte progenitor cells responding to demyelination in the adult CNS.Nkx2.2和Olig2表达增加可识别成年中枢神经系统中对脱髓鞘作出反应的反应性少突胶质前体细胞。
Mol Cell Neurosci. 2004 Nov;27(3):247-54. doi: 10.1016/j.mcn.2004.06.015.
4
Endogenous Nkx2.2+/Olig2+ oligodendrocyte precursor cells fail to remyelinate the demyelinated adult rat spinal cord in the absence of astrocytes.在没有星形胶质细胞的情况下,内源性Nkx2.2+/Olig2+少突胶质前体细胞无法使成年大鼠脱髓鞘的脊髓重新髓鞘化。
Exp Neurol. 2005 Mar;192(1):11-24. doi: 10.1016/j.expneurol.2004.05.038.
5
nkx2.2a promotes specification and differentiation of a myelinating subset of oligodendrocyte lineage cells in zebrafish.nkx2.2a促进斑马鱼少突胶质细胞谱系细胞的一个髓鞘形成亚群的特化和分化。
Neuron Glia Biol. 2008 May;4(2):71-81. doi: 10.1017/S1740925X09990123.
6
Genetic evidence that Nkx2.2 and Pdgfra are major determinants of the timing of oligodendrocyte differentiation in the developing CNS.遗传证据表明,Nkx2.2 和 Pdgfra 是中枢神经系统发育中少突胶质细胞分化时间的主要决定因素。
Development. 2014 Feb;141(3):548-55. doi: 10.1242/dev.095323.
7
Co-localization of Nkx6.2 and Nkx2.2 homeodomain proteins in differentiated myelinating oligodendrocytes.Nkx6.2 和 Nkx2.2 同源结构域蛋白在分化的髓鞘形成少突胶质细胞中的共定位。
Glia. 2010 Mar;58(4):458-68. doi: 10.1002/glia.20937.
8
Conditional Deletion of the L-Type Calcium Channel Cav1.2 in NG2-Positive Cells Impairs Remyelination in Mice.在NG2阳性细胞中条件性删除L型钙通道Cav1.2会损害小鼠的髓鞘再生。
J Neurosci. 2017 Oct 18;37(42):10038-10051. doi: 10.1523/JNEUROSCI.1787-17.2017. Epub 2017 Sep 12.
9
A functional role of NMDA receptor in regulating the differentiation of oligodendrocyte precursor cells and remyelination.NMDA 受体在调控少突胶质前体细胞分化和髓鞘再生中的功能作用。
Glia. 2013 May;61(5):732-49. doi: 10.1002/glia.22469. Epub 2013 Feb 26.
10
The remyelinating potential and in vitro differentiation of MOG-expressing oligodendrocyte precursors isolated from the adult rat CNS.从成年大鼠中枢神经系统分离出的表达髓鞘少突胶质细胞糖蛋白(MOG)的少突胶质前体细胞的髓鞘再生潜力及体外分化
Eur J Neurosci. 2004 Sep;20(6):1445-60. doi: 10.1111/j.1460-9568.2004.03606.x.

引用本文的文献

1
Spinal Cord Injury Remyelination: Pathways to Therapies.脊髓损伤再髓鞘化:治疗途径
Int J Mol Sci. 2025 Jul 26;26(15):7249. doi: 10.3390/ijms26157249.
2
The interplay of inflammation and remyelination: rethinking MS treatment with a focus on oligodendrocyte progenitor cells.炎症与髓鞘修复的相互作用:以少突胶质前体细胞为焦点,重新思考多发性硬化症的治疗。
Mol Neurodegener. 2024 Jul 12;19(1):53. doi: 10.1186/s13024-024-00742-8.
3
Cleavage of VAMP2/3 Affects Oligodendrocyte Lineage Development in the Developing Mouse Spinal Cord.VAMP2/3 的裂解影响发育中鼠脊髓中的少突胶质前体细胞谱系发育。
J Neurosci. 2023 Sep 27;43(39):6592-6608. doi: 10.1523/JNEUROSCI.2206-21.2023. Epub 2023 Aug 24.
4
The Initial Myelination in the Central Nervous System.中枢神经系统的初始髓鞘形成。
ASN Neuro. 2023 Jan-Dec;15:17590914231163039. doi: 10.1177/17590914231163039.
5
Delayed Maturation of Oligodendrocyte Progenitors by Microgravity: Implications for Multiple Sclerosis and Space Flight.微重力导致少突胶质前体细胞成熟延迟:对多发性硬化症和太空飞行的影响
Life (Basel). 2022 May 27;12(6):797. doi: 10.3390/life12060797.
6
Laminin regulates oligodendrocyte development and myelination.层粘连蛋白调节少突胶质细胞的发育和髓鞘形成。
Glia. 2022 Mar;70(3):414-429. doi: 10.1002/glia.24117. Epub 2021 Nov 12.
7
Life-long oligodendrocyte development and plasticity.终生少突胶质细胞发育与可塑性。
Semin Cell Dev Biol. 2021 Aug;116:25-37. doi: 10.1016/j.semcdb.2021.02.004. Epub 2021 Mar 16.
8
Effects of the transcription factor Olig1 on the differentiation and remyelination of oligodendrocyte precursor cells after focal cerebral ischemia in rats.转录因子 Olig1 对大鼠局灶性脑缺血后少突胶质前体细胞分化和髓鞘再生的影响。
Mol Med Rep. 2019 Nov;20(5):4603-4611. doi: 10.3892/mmr.2019.10713. Epub 2019 Sep 26.
9
Aging restricts the ability of mesenchymal stem cells to promote the generation of oligodendrocytes during remyelination.衰老限制了间充质干细胞在髓鞘再生过程中促进少突胶质细胞生成的能力。
Glia. 2019 Aug;67(8):1510-1525. doi: 10.1002/glia.23624. Epub 2019 Apr 30.
10
Intracellular Protein Shuttling: A Mechanism Relevant for Myelin Repair in Multiple Sclerosis?细胞内蛋白质穿梭:一种与多发性硬化症髓鞘修复相关的机制?
Int J Mol Sci. 2015 Jul 3;16(7):15057-85. doi: 10.3390/ijms160715057.