• 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

Molecular mechanisms mediating axon pathway formation.

作者信息

Johansen J, Johansen K M

机构信息

Department of Zoology and Genetics, Iowa State University, Ames 50011, USA.

出版信息

Crit Rev Eukaryot Gene Expr. 1997;7(1-2):95-116. doi: 10.1615/critreveukargeneexpr.v7.i1-2.60.

DOI:10.1615/critreveukargeneexpr.v7.i1-2.60
PMID:9034717
Abstract

During nervous system formation nerve cells extend axons in order to form precise patterns of neuronal connectivity. These connections are often established after the neuronal growth cones have pioneered or navigated through complex pathways to their target area both within the CNS and to and from the periphery. Recent studies have provided evidence that the process of specific pathway formation may rely on a number of molecular guidance mechanisms and cues such as selective adhesion, growth cone avoidance, surface gradients, guidepost cells, and chemotropism. Analysis of the molecular basis for these guidance mechanisms show that the molecules involved often belong to distinct multigene families and that they can provide both short- and long-range attractive as well as repulsive cues. Many of these molecules have a modular structure that is made up of different tandemly arranged domains that allow for multiple functional interactions with a range of other molecules. This allows the same molecule to be multifunctional, for example, by attracting certain neurons while repelling others. This review is an overview of the molecular structure, as it relates to function and mechanisms of action of some of the major gene families thought to be mediating specific axonal guidance and pathway formation.

摘要

相似文献

1
Molecular mechanisms mediating axon pathway formation.
Crit Rev Eukaryot Gene Expr. 1997;7(1-2):95-116. doi: 10.1615/critreveukargeneexpr.v7.i1-2.60.
2
Signaling at the growth cone: ligand-receptor complexes and the control of axon growth and guidance.生长锥中的信号传导:配体-受体复合物与轴突生长和导向的控制
Annu Rev Neurosci. 2003;26:509-63. doi: 10.1146/annurev.neuro.26.010302.081139. Epub 2003 Mar 28.
3
Axon guidance at the midline choice point.轴突在中线选择点处的导向
Dev Dyn. 2001 Jun;221(2):154-81. doi: 10.1002/dvdy.1143.
4
Axon guidance: motor-way madness.
Curr Biol. 1996 Jul 1;6(7):794-7. doi: 10.1016/s0960-9822(02)00597-3.
5
Netrin, Slit and Wnt receptors allow axons to choose the axis of migration.Netrin、Slit和Wnt受体使轴突能够选择迁移的轴。
Dev Biol. 2008 Nov 15;323(2):143-51. doi: 10.1016/j.ydbio.2008.08.027. Epub 2008 Sep 5.
6
Molecular cues that guide the development of neural connectivity.引导神经连接发育的分子线索。
Essays Biochem. 1998;33:1-13. doi: 10.1042/bse0330001.
7
Immunolocalization studies of putative guidance molecules used by axons and growth cones of intersegemental interneurons in the chick embryo spinal cord.对鸡胚脊髓节间中间神经元轴突和生长锥所使用的假定导向分子的免疫定位研究。
J Comp Neurol. 1991 Aug 8;310(2):234-52. doi: 10.1002/cne.903100208.
8
Slit and Receptor Tyrosine Phosphatase 69D Confer Spatial Specificity to Axon Branching via Dscam1.Slit和受体酪氨酸磷酸酶69D通过Dscam1赋予轴突分支空间特异性。
Cell. 2015 Aug 27;162(5):1140-54. doi: 10.1016/j.cell.2015.08.003.
9
Tyrosine phosphorylation and axon guidance: of mice and flies.
Curr Opin Neurobiol. 1997 Feb;7(1):70-4. doi: 10.1016/s0959-4388(97)80122-5.
10
Axon guidance at the midline of the developing CNS.发育中中枢神经系统中线处的轴突导向
Anat Rec. 2000 Oct 15;261(5):176-97. doi: 10.1002/1097-0185(20001015)261:5<176::AID-AR7>3.0.CO;2-R.

引用本文的文献

1
Differential glycosylation of tractin and LeechCAM, two novel Ig superfamily members, regulates neurite extension and fascicle formation.两种新型免疫球蛋白超家族成员——束丝蛋白(tractin)和水蛭细胞粘附分子(LeechCAM)的差异糖基化作用调节神经突延伸和神经束形成。
J Cell Biol. 1997 Jul 14;138(1):143-57. doi: 10.1083/jcb.138.1.143.