• 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

外周神经系统多能祖细胞中命运决定的上下文依赖性调控。

Context-dependent regulation of fate decisions in multipotent progenitor cells of the peripheral nervous system.

作者信息

Sommer L

机构信息

Institute of Cell Biology, Swiss Federal Institute of Technology, ETH-Hönggerberg, Zürich.

出版信息

Cell Tissue Res. 2001 Aug;305(2):211-6. doi: 10.1007/s004410000331.

DOI:10.1007/s004410000331
PMID:11545258
Abstract

A challenging problem in neural crest development is to understand how a migratory population of multipotent stem cells gives rise to a diverse array of differentiated cell types in the correct spatiotemporal manner. There is now ample evidence that this process involves the generation of postmigratory progenitor cells present in a variety of neural crest targets. When individual progenitors are challenged by instructive growth factors they are able to produce neural and non-neural cells, raising the question of how fate restrictions appropriate to a given embryonic location are regulated in multipotent postmigratory progenitor cells. Although some of the extracellular cues involved have been identified, it is likely that fate decisions in progenitor cells are controlled by the combinatorial action of multiple environmental signals. Moreover, cell type specificity is thought to be regulated by an interplay between extracellular and intracellular cues. We are just beginning to unravel some of the mechanisms that allow the context-dependent integration of cell-extrinsic and cell-intrinsic signals in multipotent progenitor cells.

摘要

神经嵴发育过程中的一个具有挑战性的问题是,要理解一群迁移性的多能干细胞如何以正确的时空方式产生多种多样的分化细胞类型。现在有充分的证据表明,这一过程涉及在各种神经嵴靶标中存在的迁移后祖细胞的产生。当单个祖细胞受到诱导性生长因子的刺激时,它们能够产生神经细胞和非神经细胞,这就提出了一个问题:在多能迁移后祖细胞中,如何调节与特定胚胎位置相适应的命运限制。尽管已经确定了一些相关的细胞外信号,但祖细胞中的命运决定可能是由多种环境信号的组合作用所控制的。此外,细胞类型特异性被认为是由细胞外和细胞内信号之间的相互作用所调节的。我们才刚刚开始揭示一些机制,这些机制能够使多能祖细胞中细胞外信号和细胞内信号进行依赖于环境的整合。

相似文献

1
Context-dependent regulation of fate decisions in multipotent progenitor cells of the peripheral nervous system.外周神经系统多能祖细胞中命运决定的上下文依赖性调控。
Cell Tissue Res. 2001 Aug;305(2):211-6. doi: 10.1007/s004410000331.
2
Cell-intrinsic and cell-extrinsic cues regulating lineage decisions in multipotent neural crest-derived progenitor cells.调节多能神经嵴衍生祖细胞谱系决定的细胞内在和细胞外在线索。
Int J Dev Biol. 2002 Jan;46(1):193-200.
3
P0 and PMP22 mark a multipotent neural crest-derived cell type that displays community effects in response to TGF-beta family factors.P0和PMP22标记了一种多能性神经嵴衍生细胞类型,该细胞类型对转化生长因子-β家族因子表现出群体效应。
Development. 1999 Sep;126(17):3781-94. doi: 10.1242/dev.126.17.3781.
4
A gene regulatory network orchestrates neural crest formation.一个基因调控网络协调神经嵴的形成。
Nat Rev Mol Cell Biol. 2008 Jul;9(7):557-68. doi: 10.1038/nrm2428. Epub 2008 Jun 4.
5
Autonomic neurogenesis and apoptosis are alternative fates of progenitor cell communities induced by TGFbeta.自主神经发生和凋亡是由转化生长因子β诱导的祖细胞群落的两种不同命运。
Dev Biol. 2000 Dec 1;228(1):57-72. doi: 10.1006/dbio.2000.9936.
6
Multipotent caudal neural progenitors derived from human pluripotent stem cells that give rise to lineages of the central and peripheral nervous system.源自人类多能干细胞的多能尾神经祖细胞,可分化为中枢和外周神经系统谱系。
Stem Cells. 2015 Jun;33(6):1759-70. doi: 10.1002/stem.1991.
7
Xenopus Id3 is required downstream of Myc for the formation of multipotent neural crest progenitor cells.非洲爪蟾的Id3在Myc下游对于多能神经嵴祖细胞的形成是必需的。
Development. 2005 Apr;132(8):1831-41. doi: 10.1242/dev.01734. Epub 2005 Mar 16.
8
[Phenotypic plasticity of neural crest-derived melanocytes and Schwann cells].[神经嵴衍生的黑素细胞和雪旺细胞的表型可塑性]
Biol Aujourdhui. 2011;205(1):53-61. doi: 10.1051/jbio/2011008. Epub 2011 Apr 19.
9
Signaling pathways bridging fate determination of neural crest cells to glial lineages in the developing peripheral nervous system.神经嵴细胞命运决定与发育周围神经系统神经胶质谱系之间的信号通路。
Cell Signal. 2014 Apr;26(4):673-82. doi: 10.1016/j.cellsig.2013.12.007. Epub 2013 Dec 27.
10
Environmental signals and neural crest cells.
J Physiol Paris. 1994;88(4):265-9. doi: 10.1016/0928-4257(94)90090-6.

引用本文的文献

1
Therapeutic strategies for peripheral nerve injury: decellularized nerve conduits and Schwann cell transplantation.周围神经损伤的治疗策略:去细胞神经导管与雪旺细胞移植
Neural Regen Res. 2019 Aug;14(8):1343-1351. doi: 10.4103/1673-5374.253511.
2
Neural crest: The fourth germ layer.神经嵴:第四胚层。
J Oral Maxillofac Pathol. 2015 May-Aug;19(2):221-9. doi: 10.4103/0973-029X.164536.
3
In vivo evidence for transdifferentiation of peripheral neurons.体内证据表明外周神经元的转分化。
Development. 2010 Sep;137(18):3047-56. doi: 10.1242/dev.052696. Epub 2010 Aug 4.
4
Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin.具有干细胞特征的神经嵴衍生细胞可追溯至成年皮肤中的多个谱系。
J Cell Biol. 2006 Dec 18;175(6):1005-15. doi: 10.1083/jcb.200606062. Epub 2006 Dec 11.
5
Mouse models of childhood cancer of the nervous system.儿童神经系统癌症的小鼠模型。
J Clin Pathol. 2004 Jun;57(6):561-76. doi: 10.1136/jcp.2003.009910.
6
Efficient isolation and gene expression profiling of small numbers of neural crest stem cells and developing Schwann cells.少量神经嵴干细胞和发育中的施万细胞的高效分离及基因表达谱分析。
J Neurosci. 2004 Mar 10;24(10):2357-65. doi: 10.1523/JNEUROSCI.4083-03.2004.
7
Lineage-specific requirements of beta-catenin in neural crest development.β-连环蛋白在神经嵴发育中的谱系特异性需求。
J Cell Biol. 2002 Dec 9;159(5):867-80. doi: 10.1083/jcb.200209039.