• 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

定位小脑浦肯野细胞的细胞和分子事件剖析:对math1基因敲除突变小鼠的研究

Dissection of the cellular and molecular events that position cerebellar Purkinje cells: a study of the math1 null-mutant mouse.

作者信息

Jensen Patricia, Zoghbi Huda Y, Goldowitz Dan

机构信息

University of Tennessee Health Science Center, Memphis, Tennessee 38163, USA.

出版信息

J Neurosci. 2002 Sep 15;22(18):8110-6. doi: 10.1523/JNEUROSCI.22-18-08110.2002.

DOI:10.1523/JNEUROSCI.22-18-08110.2002
PMID:12223565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6758078/
Abstract

Granule cell precursors in the external germinal layer (EGL) of the cerebellum have been proposed to be a major player in the migration and positioning of Purkinje cells through the expression of the Netrin-like receptor Unc5h3 and the extracellular matrix molecule Reelin. To explore the role of the EGL on these processes, we made use of the math1 null-mutant mouse in which the EGL does not form. In the absence of the EGL, we find three populations of ectopic Purkinje cells. First, we find 1% of all Purkinje cells in a supracerebellar position at the dorsal midline. Second, we find 7% of all Purkinje cells in the inferior colliculus, similar to what is seen in the Unc5h3 mutant. Our finding that Unc5h3 expression is not disrupted in these cells supports the proposed role of EGL granule cell precursors in establishing the anterior cerebellar boundary through the expression of Unc5h3. Third, we find 20% of all Purkinje cells positioned deep to the cerebellar cortex as seen in the reeler mutant. However, unlike the reeler mutant, where 5% of the Purkinje cells migrate successfully, we find that in the math1 null that 72% of the Purkinje cells migrate successfully. This finding demonstrates that Purkinje cell migration is not solely dependent on Reelin signaling from the EGL and is likely caused by Reelin signals emanating from the nuclear transitory zone or the ventricular zone, or both.

摘要

小脑外颗粒层(EGL)中的颗粒细胞前体被认为是浦肯野细胞迁移和定位的主要参与者,通过表达类Netrin受体Unc5h3和细胞外基质分子Reelin来实现。为了探究EGL在这些过程中的作用,我们利用了math1基因敲除突变小鼠,该小鼠不会形成EGL。在没有EGL的情况下,我们发现了三群异位的浦肯野细胞。首先,我们在背侧中线的小脑上位置发现了所有浦肯野细胞的1%。其次,我们在下丘中发现了所有浦肯野细胞的7%,这与在Unc5h3突变体中观察到的情况类似。我们发现这些细胞中Unc5h3的表达没有被破坏,这支持了EGL颗粒细胞前体通过表达Unc5h3在建立小脑前边界中所起的作用。第三,我们在小脑皮质深处发现了所有浦肯野细胞的20%,这与reeler突变体中的情况一样。然而,与reeler突变体不同,在reeler突变体中5%的浦肯野细胞成功迁移,而在math1基因敲除小鼠中,我们发现72%的浦肯野细胞成功迁移。这一发现表明,浦肯野细胞的迁移并不完全依赖于来自EGL的Reelin信号,可能是由来自核过渡区或脑室区或两者发出的Reelin信号引起的。

相似文献

1
Dissection of the cellular and molecular events that position cerebellar Purkinje cells: a study of the math1 null-mutant mouse.定位小脑浦肯野细胞的细胞和分子事件剖析:对math1基因敲除突变小鼠的研究
J Neurosci. 2002 Sep 15;22(18):8110-6. doi: 10.1523/JNEUROSCI.22-18-08110.2002.
2
Disruption of cerebellar granule cell development in the Pax6 mutant, Sey mouse.Pax6突变体Sey小鼠中小脑颗粒细胞发育的破坏。
Brain Res Dev Brain Res. 2005 Dec 7;160(2):176-93. doi: 10.1016/j.devbrainres.2005.09.005. Epub 2005 Nov 9.
3
Migration, early axonogenesis, and Reelin-dependent layer-forming behavior of early/posterior-born Purkinje cells in the developing mouse lateral cerebellum.发育中小鼠外侧小脑早期/后部出生的浦肯野细胞的迁移、早期轴突发生和依赖 Reelin 的层形成行为。
Neural Dev. 2010 Sep 1;5:23. doi: 10.1186/1749-8104-5-23.
4
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin.尽管存在reelin,但爬行突变小鼠中仍具有reeler所特有的小脑结构紊乱特征。
J Neurosci. 1997 Nov 15;17(22):8767-77. doi: 10.1523/JNEUROSCI.17-22-08767.1997.
5
Embryonic phenotype of Unc5h3 mutant mice suggests chemorepulsion during the formation of the rostral cerebellar boundary.Unc5h3突变小鼠的胚胎表型表明在小脑前缘边界形成过程中存在化学排斥作用。
Development. 1998 Jan;125(1):41-50. doi: 10.1242/dev.125.1.41.
6
The community effect and Purkinje cell migration in the cerebellar cortex: analysis of scrambler chimeric mice.小脑皮质中的群落效应与浦肯野细胞迁移:对扰频器嵌合小鼠的分析。
J Neurosci. 2002 Jan 15;22(2):464-70. doi: 10.1523/JNEUROSCI.22-02-00464.2002.
7
Analysis of cerebellar development in math1 null embryos and chimeras.math1基因敲除胚胎和嵌合体中小脑发育的分析。
J Neurosci. 2004 Mar 3;24(9):2202-11. doi: 10.1523/JNEUROSCI.3427-03.2004.
8
Regulation of Purkinje cell alignment by reelin as revealed with CR-50 antibody.用CR-50抗体揭示的Reelin对浦肯野细胞排列的调节作用。
J Neurosci. 1997 May 15;17(10):3599-609. doi: 10.1523/JNEUROSCI.17-10-03599.1997.
9
Role of Reelin in cell positioning in the cerebellum and the cerebellum-like structure in zebrafish.Reelin 在小脑和斑马鱼小脑样结构中细胞定位的作用。
Dev Biol. 2019 Nov 15;455(2):393-408. doi: 10.1016/j.ydbio.2019.07.010. Epub 2019 Jul 16.
10
Obstructed migration of Purkinje cells in the developing cerebellum of the reeler mutant mouse.在reeler突变小鼠发育中的小脑中,浦肯野细胞迁移受阻。
Anat Embryol (Berl). 1993 Oct;188(4):317-29. doi: 10.1007/BF00185941.

引用本文的文献

1
The Nuclear Transitory Zone: A Key Player in the Cerebellar Development.核过渡区:小脑发育中的关键角色。
Cerebellum. 2025 May 2;24(4):92. doi: 10.1007/s12311-025-01848-5.
2
Revisiting the development of cerebellar inhibitory interneurons in the light of single-cell genetic analyses.重新审视单细胞遗传分析对小脑抑制性中间神经元发育的认识。
Histochem Cell Biol. 2024 Jan;161(1):5-27. doi: 10.1007/s00418-023-02251-z. Epub 2023 Nov 8.
3
Regulation of cerebellar network development by granule cells and their molecules.颗粒细胞及其分子对小脑网络发育的调控
Front Mol Neurosci. 2023 Jul 14;16:1236015. doi: 10.3389/fnmol.2023.1236015. eCollection 2023.
4
Cerebellar development after preterm birth.早产后脑小脑发育。
Front Cell Dev Biol. 2022 Nov 29;10:1068288. doi: 10.3389/fcell.2022.1068288. eCollection 2022.
5
The Transcription Factor Pou3f1 Sheds Light on the Development and Molecular Diversity of Glutamatergic Cerebellar Nuclear Neurons in the Mouse.转录因子Pou3f1揭示了小鼠谷氨酸能小脑核神经元的发育和分子多样性。
Front Mol Neurosci. 2022 Jul 20;15:921901. doi: 10.3389/fnmol.2022.921901. eCollection 2022.
6
Upregulation of Neural Cell Adhesion Molecule 1 and Excessive Migration of Purkinje Cells in Cerebellar Cortex.神经细胞黏附分子1上调与小脑皮质浦肯野细胞过度迁移
Front Neurosci. 2022 Jan 21;15:804402. doi: 10.3389/fnins.2021.804402. eCollection 2021.
7
Maturation of Purkinje cell firing properties relies on neurogenesis of excitatory neurons.浦肯野细胞放电特性的成熟依赖于兴奋性神经元的神经发生。
Elife. 2021 Sep 20;10:e68045. doi: 10.7554/eLife.68045.
8
Heterochronic Developmental Shifts Underlying Squamate Cerebellar Diversity Unveil the Key Features of Amniote Cerebellogenesis.有鳞目动物小脑多样性背后的异时发育转变揭示了羊膜动物小脑发生的关键特征。
Front Cell Dev Biol. 2020 Oct 22;8:593377. doi: 10.3389/fcell.2020.593377. eCollection 2020.
9
Interactions Between Purkinje Cells and Granule Cells Coordinate the Development of Functional Cerebellar Circuits.浦肯野细胞与颗粒细胞的相互作用协调功能性小脑回路的发育。
Neuroscience. 2021 May 10;462:4-21. doi: 10.1016/j.neuroscience.2020.06.010. Epub 2020 Jun 14.
10
Cend1, a Story with Many Tales: From Regulation of Cell Cycle Progression/Exit of Neural Stem Cells to Brain Structure and Function.Cend1:一个有着诸多故事的蛋白:从神经干细胞细胞周期进程/退出的调控到脑结构与功能
Stem Cells Int. 2019 May 2;2019:2054783. doi: 10.1155/2019/2054783. eCollection 2019.

本文引用的文献

1
Estimation of nuclear population from microtome sections.从切片估计核数量。
Anat Rec. 1946 Feb;94:239-47. doi: 10.1002/ar.1090940210.
2
An autoradiographic analysis of histogenesis in the mouse cerebellum.小鼠小脑组织发生的放射自显影分析。
Exp Neurol. 1961 Oct;4:277-96. doi: 10.1016/0014-4886(61)90055-3.
3
Granule cells and cerebellar boundaries: analysis of Unc5h3 mutant chimeras.颗粒细胞与小脑边界:Unc5h3突变嵌合体分析
J Neurosci. 2000 Jun 1;20(11):4129-37. doi: 10.1523/JNEUROSCI.20-11-04129.2000.
4
A simple and sensitive antigen retrieval method for free-floating and slide-mounted tissue sections.一种用于游离和载玻片固定组织切片的简单且灵敏的抗原修复方法。
J Neurosci Methods. 1999 Nov 15;93(2):149-62. doi: 10.1016/s0165-0270(99)00142-9.
5
Mutant mice with scrambled brains: understanding the signaling pathways that control cell positioning in the CNS.大脑混乱的突变小鼠:理解控制中枢神经系统中细胞定位的信号通路。
Genes Dev. 1999 Nov 1;13(21):2758-73. doi: 10.1101/gad.13.21.2758.
6
Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2.在缺乏极低密度脂蛋白受体和载脂蛋白E受体2的基因敲除小鼠中,Reeler/Disabled样神经元迁移紊乱。
Cell. 1999 Jun 11;97(6):689-701. doi: 10.1016/s0092-8674(00)80782-5.
7
Math1: an essential gene for the generation of inner ear hair cells.Math1:内耳毛细胞生成所必需的基因。
Science. 1999 Jun 11;284(5421):1837-41. doi: 10.1126/science.284.5421.1837.
8
Cloning and mapping of the UNC5C gene to human chromosome 4q21-q23.UNC5C基因的克隆及在人类染色体4q21 - q23上的定位。
Genomics. 1998 Sep 1;52(2):205-8. doi: 10.1006/geno.1998.5425.
9
Quantitative analysis of cerebellar lobulation in normal and agranular rats.正常大鼠和无颗粒大鼠小脑叶的定量分析。
J Comp Neurol. 1998 Sep 28;399(3):306-20.
10
Disabled-1 acts downstream of Reelin in a signaling pathway that controls laminar organization in the mammalian brain.Disabled-1在一条控制哺乳动物大脑分层组织的信号通路中,作用于Reelin的下游。
Development. 1998 Sep;125(18):3719-29. doi: 10.1242/dev.125.18.3719.