• 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

胶质细胞系源性神经营养因子(GDNF)缺陷小鼠的牙齿细胞分化受损。

Impaired dental cytodifferentiation in glial cell-line derived growth factor (GDNF) deficient mice.

作者信息

de Vicente J C, Cabo R, Ciriaco E, Laurà R, Naves F J, Silos-Santiago I, Vega J A

机构信息

Departamentos de Cirugía y Especialidades Médico-Quirúrgicas, Escuela de Estomatología, Oviedo, Spain

出版信息

Ann Anat. 2002 Jan;184(1):85-92. doi: 10.1016/S0940-9602(02)80041-3.

DOI:10.1016/S0940-9602(02)80041-3
PMID:11878293
Abstract

Glial cell line-derived neurotrophic factor promotes the survival of multiple neuron types in the central and peripheral nervous system. Moreover, it plays a key role in the development of the enteric nervous system and in the kidney organogenesis. Glial cell line-derived neurotrophic factor and their receptors are expressed in the developing tooth as well as in the trigeminal ganglion. However, the precise role of this growth factor in tooth morphogenesis and cell differentiation, or in the development of trigeminal ganglion cells, is still elusive. Using structural and ultrastructural techniques we analyzed in detail the first molar tooth germ of glial cell line-derived neurotrophic factor deficient mice as well as the neuronal density in trigeminal ganglion. The length and width of first molar tooth germ in knockout deficient animals showed no differences in the knockout animals in comparison with age-matched heterozygous or wild-type littermates. Nevertheless, in mice lacking glial cell line-derived neurotrophic factor, both ameloblasts and odontoblasts failed to fully develop and differentiate, and the enamel matrix and predentin layers were absent. On the other hand, the number of trigeminal sensory neurons and the structure of the nerves supplying first molar tooth germ were largely normal. Present results suggest a new non-neuronal role for glial cell line-derived neurotrophic factor in tooth development. Glial cell line-derived neurotrophic factor seems not to be involved in tooth initiation and morphogenesis, whereas it seems essential for cytodifferentiation. Conversely, neither development of trigeminal neuron nor nerve fibers supplying teeth are directly dependent on glial cell line-derived neutrophic factor.

摘要

胶质细胞系源性神经营养因子可促进中枢和外周神经系统中多种神经元类型的存活。此外,它在肠神经系统的发育和肾脏器官发生过程中发挥关键作用。胶质细胞系源性神经营养因子及其受体在发育中的牙齿以及三叉神经节中均有表达。然而,这种生长因子在牙齿形态发生和细胞分化,或在三叉神经节细胞发育中的精确作用仍不清楚。我们使用结构和超微结构技术,详细分析了胶质细胞系源性神经营养因子缺陷小鼠的第一磨牙牙胚以及三叉神经节中的神经元密度。与年龄匹配的杂合子或野生型同窝小鼠相比,基因敲除缺陷动物的第一磨牙牙胚的长度和宽度没有差异。然而,在缺乏胶质细胞系源性神经营养因子的小鼠中,成釉细胞和成牙本质细胞均未能充分发育和分化,且釉质基质和前期牙本质层缺失。另一方面,三叉神经感觉神经元的数量以及供应第一磨牙牙胚的神经结构基本正常。目前的结果表明,胶质细胞系源性神经营养因子在牙齿发育中具有一种新的非神经元作用。胶质细胞系源性神经营养因子似乎不参与牙齿的起始和形态发生,而对细胞分化似乎至关重要。相反,三叉神经元的发育和供应牙齿的神经纤维均不直接依赖于胶质细胞系源性神经营养因子。

相似文献

1
Impaired dental cytodifferentiation in glial cell-line derived growth factor (GDNF) deficient mice.胶质细胞系源性神经营养因子(GDNF)缺陷小鼠的牙齿细胞分化受损。
Ann Anat. 2002 Jan;184(1):85-92. doi: 10.1016/S0940-9602(02)80041-3.
2
Neurturin mRNA expression suggests roles in trigeminal innervation of the first branchial arch and in tooth formation.神经营养因子mRNA表达提示其在第一鳃弓三叉神经支配及牙齿形成中发挥作用。
Dev Dyn. 1998 Oct;213(2):207-19. doi: 10.1002/(SICI)1097-0177(199810)213:2<207::AID-AJA6>3.0.CO;2-K.
3
Expression of GDNF and its receptors in developing tooth is developmentally regulated and suggests multiple roles in innervation and organogenesis.胶质细胞源性神经营养因子(GDNF)及其受体在牙齿发育过程中的表达受到发育调控,并提示其在神经支配和器官发生中具有多种作用。
Dev Dyn. 1997 Dec;210(4):463-71. doi: 10.1002/(SICI)1097-0177(199712)210:4<463::AID-AJA9>3.0.CO;2-E.
4
Glial cell line-derived neurotrophic factor (GDNF) from adult rat tooth serves a distinct population of large-sized trigeminal neurons.成年大鼠牙齿中的胶质细胞源性神经营养因子(GDNF)作用于不同的大尺寸三叉神经元群体。
Eur J Neurosci. 2004 Apr;19(8):2089-98. doi: 10.1111/j.0953-816X.2004.03291.x.
5
Neural cells in the esophagus respond to glial cell line-derived neurotrophic factor and neurturin, and are RET-dependent.食管中的神经细胞对胶质细胞系衍生的神经营养因子和神经营养素起反应,且依赖于RET。
Dev Biol. 2004 Aug 1;272(1):118-33. doi: 10.1016/j.ydbio.2004.04.025.
6
Other neurotrophic factors: glial cell line-derived neurotrophic factor (GDNF).其他神经营养因子:胶质细胞源性神经营养因子(GDNF)。
Microsc Res Tech. 1999;45(4-5):292-302. doi: 10.1002/(SICI)1097-0029(19990515/01)45:4/5<292::AID-JEMT13>3.0.CO;2-8.
7
Semaphorin 3A controls timing and patterning of the dental pulp innervation.神经信号蛋白 3A 控制牙髓神经支配的时间和模式。
Differentiation. 2012 Dec;84(5):371-9. doi: 10.1016/j.diff.2012.09.003. Epub 2012 Nov 7.
8
Glial cell line-derived neurotrophic factor (GDNF) is a neurotrophic factor for sensory neurons: comparison with the effects of the neurotrophins.胶质细胞系源性神经营养因子(GDNF)是一种感觉神经元的神经营养因子:与神经营养素作用的比较。
J Neurobiol. 1997 Jan;32(1):22-32.
9
Glial cell line-derived neurotrophic factor (GDNF) is required for differentiation of pontine noradrenergic neurons and patterning of central respiratory output.胶质细胞系源性神经营养因子(GDNF)是脑桥去甲肾上腺素能神经元分化和中枢呼吸输出模式形成所必需的。
Neuroscience. 2005;130(1):95-105. doi: 10.1016/j.neuroscience.2004.08.036.
10
Possible involvement of glial cell line-derived neurotrophic factor and its receptor, GFRalpha1, in survival and maturation of thymocytes.胶质细胞源性神经营养因子及其受体GFRalpha1可能参与胸腺细胞的存活和成熟。
Eur J Immunol. 2003 Aug;33(8):2233-40. doi: 10.1002/eji.200323458.

引用本文的文献

1
A novel model of autologous tooth transplantation for the study of nerve recruitment.一种用于研究神经募集的自体牙移植新模型。
BMC Oral Health. 2024 Sep 27;24(1):1141. doi: 10.1186/s12903-024-04884-5.
2
The Genes Involved in Dentinogenesis.涉及牙本质生成的基因。
Organogenesis. 2022 Dec 31;18(1):1-19. doi: 10.1080/15476278.2021.2022373. Epub 2022 Jan 13.
3
Dental pulp stem cells stimulate neuronal differentiation of PC12 cells.牙髓干细胞刺激PC12细胞的神经元分化。
Neural Regen Res. 2021 Sep;16(9):1821-1828. doi: 10.4103/1673-5374.306089.
4
A dual-hit animal model for age-related parkinsonism.用于年龄相关性帕金森病的双重打击动物模型。
Prog Neurobiol. 2010 Feb 9;90(2):217-29. doi: 10.1016/j.pneurobio.2009.10.013. Epub 2009 Oct 21.