• 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

Pax6影响腹侧神经管中神经胶质前体细胞的起源时间和位置。

Pax6 influences the time and site of origin of glial precursors in the ventral neural tube.

作者信息

Sun T, Pringle N P, Hardy A P, Richardson W D, Smith H K

机构信息

Department of Biology, University College London, Gower Street, London, WC1E 6BT.

出版信息

Mol Cell Neurosci. 1998 Nov;12(4-5):228-39. doi: 10.1006/mcne.1998.0711.

DOI:10.1006/mcne.1998.0711
PMID:9828088
Abstract

Neuroepithelial precursors in the ventral ventricular zone (VZ) of the spinal cord generate motor neurons (MNs) and interneurons, and then a subset of precursors starts to produce oligodendrocyte progenitors (OLPs). We show that OLPs originate in the ventral-most part of the Pax6-positive VZ, which at earlier times generates somatic (Isl2/Lim3-positive) MNs. In Small eye (Pax6-deficient) mice, the origin of OLPs is shifted dorsally and both OLPs and Isl2/Lim3 MNs are delayed. We suggest that somatic MNs and OLPs are generated sequentially from a common set of MN-OL precursors whose position in the VZ is influenced by Pax6. Neuron-glia fate switching might be a preprogrammed property of these precursors or a response to feedback from newly generated neurons. OLs developed normally in explants of Isl1(-/-) spinal cords, which lack MNs, arguing against feedback control and suggesting that the neuron-glia switch is an intrinsic developmental program in a specific subset of neural precursors.

摘要

脊髓腹侧脑室区(VZ)的神经上皮前体细胞可生成运动神经元(MNs)和中间神经元,随后一部分前体细胞开始产生少突胶质细胞前体细胞(OLPs)。我们发现,OLPs起源于Pax6阳性VZ的最腹侧部分,该部分在早期产生躯体(Isl2/Lim3阳性)MNs。在小眼(Pax6缺陷)小鼠中,OLPs的起源向背侧偏移,且OLPs和Isl2/Lim3 MNs均出现延迟。我们认为,躯体MNs和OLPs是由一组共同的MN-OL前体细胞依次产生的,这些前体细胞在VZ中的位置受Pax6影响。神经元-胶质细胞命运转换可能是这些前体细胞的预编程特性,或是对新生成神经元反馈的一种反应。OLs在缺乏MNs的Isl1(-/-)脊髓外植体中正常发育,这与反馈控制相悖,并表明神经元-胶质细胞转换是特定神经前体细胞亚群的内在发育程序。

相似文献

1
Pax6 influences the time and site of origin of glial precursors in the ventral neural tube.Pax6影响腹侧神经管中神经胶质前体细胞的起源时间和位置。
Mol Cell Neurosci. 1998 Nov;12(4-5):228-39. doi: 10.1006/mcne.1998.0711.
2
Gliogenic radial glial cells show heterogeneity in the developing mouse spinal cord.神经胶质源性放射状胶质细胞在发育中的小鼠脊髓中表现出异质性。
Dev Neurosci. 2005;27(6):364-77. doi: 10.1159/000088452.
3
Ventralized dorsal telencephalic progenitors in Pax6 mutant mice generate GABA interneurons of a lateral ganglionic eminence fate.Pax6突变小鼠中腹侧化的背侧端脑祖细胞产生具有外侧神经节隆起命运的GABA中间神经元。
Proc Natl Acad Sci U S A. 2005 May 17;102(20):7374-9. doi: 10.1073/pnas.0500819102. Epub 2005 May 6.
4
The on/off of Pax6 controls the tempo of neuronal differentiation in the developing spinal cord.Pax6的开启和关闭控制着发育中脊髓神经元分化的节奏。
Dev Biol. 2007 May 15;305(2):659-73. doi: 10.1016/j.ydbio.2007.02.012. Epub 2007 Feb 16.
5
Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling.Pax6 根据梯度性 Sonic Hedgehog(Shh)信号控制祖细胞特性和神经元命运。
Cell. 1997 Jul 11;90(1):169-80. doi: 10.1016/s0092-8674(00)80323-2.
6
Spatially distinct functions of PAX6 and NKX2.2 during gliogenesis in the ventral spinal cord.脊髓腹侧神经胶质生成过程中PAX6和NKX2.2的空间特异性功能。
Biochem Biophys Res Commun. 2009 Apr 24;382(1):69-73. doi: 10.1016/j.bbrc.2009.02.134. Epub 2009 Mar 1.
7
Pax6 is expressed in subsets of V0 and V2 interneurons in the ventral spinal cord in mice.Pax6在小鼠脊髓腹侧的V0和V2中间神经元亚群中表达。
Gene Expr Patterns. 2013 Dec;13(8):328-34. doi: 10.1016/j.gep.2013.06.004. Epub 2013 Jun 29.
8
Ventral neurogenesis and the neuron-glial switch.腹侧神经发生与神经元-胶质细胞转换
Neuron. 2001 Sep 13;31(5):677-80. doi: 10.1016/s0896-6273(01)00430-5.
9
Expression pattern of PAX3 and PAX6 genes during human embryogenesis.人胚胎发育过程中PAX3和PAX6基因的表达模式。
Int J Dev Biol. 1999 Sep;43(6):501-8.
10
Homeobox gene Nkx2.2 and specification of neuronal identity by graded Sonic hedgehog signalling.同源框基因Nkx2.2与由梯度音猬因子信号传导决定的神经元身份
Nature. 1999 Apr 15;398(6728):622-7. doi: 10.1038/19315.

引用本文的文献

1
Development of Oligodendroglia and Myelin.少突胶质细胞与髓鞘的发育
Adv Neurobiol. 2025;43:61-79. doi: 10.1007/978-3-031-87919-7_3.
2
Basal forebrain cholinergic signalling: development, connectivity and roles in cognition.基底前脑胆碱能信号传递:发育、连接及在认知中的作用。
Nat Rev Neurosci. 2023 Apr;24(4):233-251. doi: 10.1038/s41583-023-00677-x. Epub 2023 Feb 23.
3
Developmental Cues and Molecular Drivers in Myelinogenesis: Revisiting Early Life to Re-Evaluate the Integrity of CNS Myelin.髓鞘形成中的发育线索和分子驱动因素:回顾早期生命以重新评估中枢神经系统髓鞘的完整性
Curr Issues Mol Biol. 2022 Jul 19;44(7):3208-3237. doi: 10.3390/cimb44070222.
4
Genetic Regulation of Vertebrate Forebrain Development by Homeobox Genes.同源框基因对脊椎动物前脑发育的遗传调控
Front Neurosci. 2022 Apr 25;16:843794. doi: 10.3389/fnins.2022.843794. eCollection 2022.
5
Oligodendrocyte Dysfunction in Amyotrophic Lateral Sclerosis: Mechanisms and Therapeutic Perspectives.肌萎缩侧索硬化症中的少突胶质细胞功能障碍:机制和治疗展望。
Cells. 2021 Mar 5;10(3):565. doi: 10.3390/cells10030565.
6
The transcription factor NKX2-2 regulates oligodendrocyte differentiation through domain-specific interactions with transcriptional corepressors.转录因子 NKX2-2 通过与转录核心抑制物的特定结构域相互作用来调节少突胶质细胞分化。
J Biol Chem. 2020 Feb 14;295(7):1879-1888. doi: 10.1074/jbc.RA119.011163. Epub 2020 Jan 13.
7
Hedgehog: A Key Signaling in the Development of the Oligodendrocyte Lineage.刺猬蛋白:少突胶质细胞谱系发育中的关键信号通路
J Dev Biol. 2016 Sep 8;4(3):28. doi: 10.3390/jdb4030028.
8
Utx is required for proper induction of ectoderm and mesoderm during differentiation of embryonic stem cells.Utx 对于胚胎干细胞分化过程中外胚层和中胚层的正常诱导是必需的。
PLoS One. 2013;8(4):e60020. doi: 10.1371/journal.pone.0060020. Epub 2013 Apr 3.
9
Endogenous proliferation after spinal cord injury in animal models.动物模型中的脊髓损伤后内源性增殖。
Stem Cells Int. 2012;2012:387513. doi: 10.1155/2012/387513. Epub 2012 Dec 20.
10
Neuron-oligodendrocyte myelination co-culture derived from embryonic rat spinal cord and cerebral cortex.源自胚胎大鼠脊髓和大脑皮层的神经元-少突胶质细胞髓鞘共培养物。
Brain Behav. 2012 Jan;2(1):53-67. doi: 10.1002/brb3.33.