• 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

髓鞘形成过程中少突胶质细胞突起树突的渐进性重塑。

Progressive remodeling of the oligodendrocyte process arbor during myelinogenesis.

作者信息

Hardy R J, Friedrich V L

机构信息

Brookdale Center for Molecular Biology, Mount Sinai Medical School, New York, NY 10029, USA.

出版信息

Dev Neurosci. 1996;18(4):243-54. doi: 10.1159/000111414.

DOI:10.1159/000111414
PMID:8911764
Abstract

Myelin sheaths develop in the central nervous system (CNS) as elaborations of the processes of oligodendrocytes. Although many details of the spiral wrapping of oligodendrocyte processes around axons and their subsequent transformation into myelin sheaths are known from thin-section electron-microscopic studies, the three-dimensional architecture of the myelin-forming cells is incompletely understood. To characterize this aspect of oligodendrocyte development, we labeled thick (100- to 300-microns) sections of developing murine CNS with oligodendrocyte marker antibodies, recorded individual cells in serial optical sections by confocal microscopy, and created whole-cell reconstructions of oligodendrocytes before and during the initiation of myelination. We distinguish three stages in the maturation of oligodendrocytes, which at all three stages are labeled by the O4, O1 and Ranscht monoclonals and by antibodies against the myelin-specific proteins CNP and myelin basic protein. Premyelinating oligodendrocytes, present before axonal ensheathment begins, emit multiple irregular processes which have predominant radial orientation. These processes, which generally terminate within 50 microns of the cell body, have a surface area 3-8 times or more that of the cell body itself and may represent a mechanism for sampling the local environment of each cell and for identifying target axons. Transitional cells have initiated one or more myelin sheaths; these cells progressively reduce the number of their radial processes as they increase the number of their myelin internodes. The radial processes of each transitional cell are most reduced in parts of the process arbor where ensheathment has begun, suggesting directional control in the elaboration or stability of the radial processes. Mature myelin-bearing oligodendrocytes entirely lack the radial processes and instead emit a few sparsely branching processes which connect cell bodies with myelin internodes. Three-dimensional analysis of the earliest stages in myelin sheath formation reveals two distinct phases. The initiating event in the formation of myelin internodes is the growth of thin unbranched processes, termed 'initiator processes', along axons. The second phase, spiral ensheathment of target axons, begins through the elaboration from each initiator process of lamellar extensions which extend circumferentially around the target axon and thereby form the first turn of its myelin sheath.

摘要

髓鞘在中枢神经系统(CNS)中作为少突胶质细胞突起的精细结构而发育形成。尽管通过薄切片电子显微镜研究已经了解到少突胶质细胞突起围绕轴突进行螺旋缠绕以及随后转变为髓鞘的许多细节,但对形成髓鞘细胞的三维结构仍未完全理解。为了表征少突胶质细胞发育的这一方面,我们用少突胶质细胞标记抗体标记发育中小鼠CNS的厚切片(100至300微米),通过共聚焦显微镜在连续光学切片中记录单个细胞,并在髓鞘形成开始之前和期间创建少突胶质细胞的全细胞重建。我们区分了少突胶质细胞成熟的三个阶段,在所有这三个阶段,少突胶质细胞都被O4、O1和Ranscht单克隆抗体以及针对髓鞘特异性蛋白CNP和髓鞘碱性蛋白的抗体标记。在轴突被包裹开始之前出现的前髓鞘形成少突胶质细胞发出多个不规则突起,这些突起主要呈径向取向。这些突起通常在细胞体50微米范围内终止,其表面积是细胞体本身的3至8倍或更多,可能代表了一种对每个细胞局部环境进行采样和识别靶轴突的机制。过渡细胞已经开始形成一个或多个髓鞘;随着髓鞘节段数量的增加,这些细胞逐渐减少其径向突起的数量。每个过渡细胞的径向突起在包裹开始的突起树突部分减少最多,这表明在径向突起的形成或稳定性方面存在方向控制。成熟的带有髓鞘的少突胶质细胞完全没有径向突起,而是发出一些稀疏分支的突起,这些突起将细胞体与髓鞘节段连接起来。对髓鞘形成最早阶段的三维分析揭示了两个不同的阶段。髓鞘节段形成的起始事件是沿着轴突生长出细的无分支突起,称为“起始突起”。第二阶段,即靶轴突的螺旋包裹,通过从每个起始突起延伸出的层状延伸开始,这些层状延伸围绕靶轴突周向延伸,从而形成其髓鞘的第一圈。

相似文献

1
Progressive remodeling of the oligodendrocyte process arbor during myelinogenesis.髓鞘形成过程中少突胶质细胞突起树突的渐进性重塑。
Dev Neurosci. 1996;18(4):243-54. doi: 10.1159/000111414.
2
The relationship between developing oligodendrocyte units and maturing axons during myelinogenesis in the anterior medullary velum of neonatal rats.新生大鼠延髓前帆髓鞘形成过程中发育中的少突胶质细胞单位与成熟轴突之间的关系。
J Neurocytol. 1997 May;26(5):327-38. doi: 10.1023/a:1018556702353.
3
Arrested oligodendrocyte lineage progression during human cerebral white matter development: dissociation between the timing of progenitor differentiation and myelinogenesis.人类脑白质发育过程中少突胶质细胞谱系进展受阻:祖细胞分化时间与髓鞘形成之间的分离。
J Neuropathol Exp Neurol. 2002 Feb;61(2):197-211. doi: 10.1093/jnen/61.2.197.
4
The role of oligodendrocytes and myelin on axon maturation in the developing rat retinofugal pathway.少突胶质细胞和髓鞘在发育中的大鼠视网膜神经纤维通路轴突成熟中的作用。
J Neurosci. 1994 May;14(5 Pt 1):2594-605. doi: 10.1523/JNEUROSCI.14-05-02594.1994.
5
Oligodendrocytes and the control of myelination in vivo: new insights from the rat anterior medullary velum.少突胶质细胞与体内髓鞘形成的调控:来自大鼠延髓前帆的新见解
J Neurosci Res. 2000 Feb 15;59(4):477-88. doi: 10.1002/(SICI)1097-4547(20000215)59:4<477::AID-JNR2>3.0.CO;2-J.
6
Myelinogenesis and axonal recognition by oligodendrocytes in brain are uncoupled in Olig1-null mice.在少突胶质细胞转录因子1基因缺失的小鼠中,大脑中少突胶质细胞的髓鞘形成和轴突识别功能相互分离。
J Neurosci. 2005 Feb 9;25(6):1354-65. doi: 10.1523/JNEUROSCI.3034-04.2005.
7
Growth of regenerating goldfish axons is inhibited by rat oligodendrocytes and CNS myelin but not but not by goldfish optic nerve tract oligodendrocytelike cells and fish CNS myelin.再生金鱼轴突的生长受到大鼠少突胶质细胞和中枢神经系统髓磷脂的抑制,但不受金鱼视神经束少突胶质细胞样细胞和鱼类中枢神经系统髓磷脂的抑制。
J Neurosci. 1991 Mar;11(3):626-40. doi: 10.1523/JNEUROSCI.11-03-00626.1991.
8
Double myelination of axons in the sympathetic nervous system of the mouse. II. Mechanisms of formation.小鼠交感神经系统中轴突的双重髓鞘形成。II. 形成机制。
J Neurocytol. 1988 Apr;17(2):263-76. doi: 10.1007/BF01674212.
9
CNS myelinogenesis in vitro: time course and pattern of rat oligodendrocyte development.体外中枢神经系统髓鞘形成:大鼠少突胶质细胞发育的时间进程和模式
J Neurosci Res. 1995 Mar 1;40(4):519-34. doi: 10.1002/jnr.490400411.
10
Individual neuronal subtypes control initial myelin sheath growth and stabilization.特定神经元亚型控制初始髓鞘生长和稳定。
Neural Dev. 2020 Sep 28;15(1):12. doi: 10.1186/s13064-020-00149-3.

引用本文的文献

1
Synaptic vesicle release regulates pre-myelinating oligodendrocyte-axon interactions in a neuron subtype-specific manner.突触小泡释放以神经元亚型特异性方式调节少突胶质前体细胞与轴突之间的相互作用。
Front Cell Neurosci. 2024 May 22;18:1386352. doi: 10.3389/fncel.2024.1386352. eCollection 2024.
2
A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes.活性依赖性髓鞘形成和少突胶质细胞髓鞘损伤的形态学分析。
Sci Rep. 2021 May 5;11(1):9588. doi: 10.1038/s41598-021-88887-0.
3
Neuron-Oligodendrocyte Communication in Myelination of Cortical GABAergic Cells.
皮质GABA能细胞髓鞘形成过程中的神经元-少突胶质细胞通讯
Life (Basel). 2021 Mar 9;11(3):216. doi: 10.3390/life11030216.
4
Myelin Deficits Caused by Olig2 Deficiency Lead to Cognitive Dysfunction and Increase Vulnerability to Social Withdrawal in Adult Mice.少突胶质细胞特异性转录因子 2 缺乏导致髓鞘缺陷,进而引起成年小鼠认知功能障碍,并增加其对社交回避的易感性。
Neurosci Bull. 2020 Apr;36(4):419-426. doi: 10.1007/s12264-019-00449-7. Epub 2019 Nov 22.
5
The oligodendrocyte growth cone and its actin cytoskeleton: A fundamental element for progenitor cell migration and CNS myelination.少突胶质细胞生长锥及其肌动蛋白细胞骨架:祖细胞迁移和中枢神经系统髓鞘形成的基本要素。
Glia. 2020 Jul;68(7):1329-1346. doi: 10.1002/glia.23735. Epub 2019 Nov 7.
6
Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes.小鼠原代少突胶质细胞的快速特异性免疫磁珠分离
J Vis Exp. 2018 May 21(135):57543. doi: 10.3791/57543.
7
Novel schizophrenia risk factor pathways regulate FEZ1 to advance oligodendroglia development.新型精神分裂症风险因素通路调控 FEZ1 促进少突胶质细胞发育。
Transl Psychiatry. 2017 Dec 18;7(12):1293. doi: 10.1038/s41398-017-0028-z.
8
Inducible Expression of a Truncated Form of Tau in Oligodendrocytes Elicits Gait Abnormalities and a Decrease in Myelin: Implications for Selective CNS Degenerative Diseases.少突胶质细胞中截短形式的 Tau 蛋白的诱导表达引发步态异常和髓鞘减少:对中枢神经系统选择性退行性疾病的启示。
Neurochem Res. 2015 Nov;40(11):2188-99. doi: 10.1007/s11064-015-1707-x. Epub 2015 Sep 22.
9
Focal adhesion kinase can play unique and opposing roles in regulating the morphology of differentiating oligodendrocytes.黏着斑激酶在调节分化少突胶质细胞的形态方面可以发挥独特且相反的作用。
J Neurochem. 2010 Oct;115(1):269-82. doi: 10.1111/j.1471-4159.2010.06926.x. Epub 2010 Aug 19.
10
Distinct mechanisms of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrimidine resistance revealed by transcriptome mapping in mouse striatum.通过小鼠纹状体转录组图谱揭示的1-甲基-4-苯基-1,2,3,6-四氢嘧啶抗性的不同机制。
Neuroscience. 2008 Sep 9;155(4):1174-94. doi: 10.1016/j.neuroscience.2008.06.064. Epub 2008 Jul 8.