• 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

相似文献

1
STATus and Context within the Mammalian Nervous System.哺乳动物神经系统中的状态和语境。
Mol Med. 2011 Sep-Oct;17(9-10):965-73. doi: 10.2119/molmed.2010.00259. Epub 2011 May 20.
2
HIV-1-infected and immune-activated macrophages induce astrocytic differentiation of human cortical neural progenitor cells via the STAT3 pathway.HIV-1 感染和免疫激活的巨噬细胞通过 STAT3 通路诱导人皮质神经祖细胞的星形胶质细胞分化。
PLoS One. 2011;6(5):e19439. doi: 10.1371/journal.pone.0019439. Epub 2011 May 27.
3
Hippocalcin Promotes Neuronal Differentiation and Inhibits Astrocytic Differentiation in Neural Stem Cells.海马钙结合蛋白促进神经干细胞的神经元分化并抑制其星形胶质细胞分化。
Stem Cell Reports. 2017 Jan 10;8(1):95-111. doi: 10.1016/j.stemcr.2016.11.009. Epub 2016 Dec 22.
4
Qingnaoyizhi decoction suppresses the formation of glial fibrillary acidic protein-positive cells in cultured neural stem cells by inhibiting the Janus kinase 2/signal transducer and activator of transcription 3 signaling pathway.清脑益智汤通过抑制Janus激酶2/信号转导及转录激活因子3信号通路,抑制培养的神经干细胞中胶质纤维酸性蛋白阳性细胞的形成。
J Tradit Chin Med. 2015 Feb;35(1):69-76. doi: 10.1016/s0254-6272(15)30011-x.
5
Thyroid hormone promotes neuronal differentiation of embryonic neural stem cells by inhibiting STAT3 signaling through TRα1.甲状腺激素通过 TRα1 抑制 STAT3 信号通路促进胚胎神经干细胞的神经元分化。
Stem Cells Dev. 2012 Sep 20;21(14):2667-81. doi: 10.1089/scd.2012.0023. Epub 2012 May 9.
6
Stage-dependent STAT3 activation is involved in the differentiation of rat hippocampus neural stem cells.阶段依赖性 STAT3 激活参与大鼠海马神经干细胞的分化。
Neurosci Lett. 2011 Apr 8;493(1-2):18-23. doi: 10.1016/j.neulet.2011.02.006. Epub 2011 Feb 17.
7
Astrocytic endothelin-1 overexpression promotes neural progenitor cells proliferation and differentiation into astrocytes via the Jak2/Stat3 pathway after stroke.星形胶质细胞内皮素-1 过表达通过 Jak2/Stat3 通路促进卒中后神经祖细胞增殖和分化为星形胶质细胞。
J Neuroinflammation. 2019 Nov 16;16(1):227. doi: 10.1186/s12974-019-1597-y.
8
Signal transducer and activator of transcription-3 maintains the stemness of radial glia at mid-neurogenesis.信号转导子和转录激活子 3 维持了神经发生中期放射状胶质细胞的干性。
J Neurosci. 2015 Jan 21;35(3):1011-23. doi: 10.1523/JNEUROSCI.2119-14.2015.
9
A growth-promoting signaling component cyclin D1 in neural stem cells has antiastrogliogenic function to execute self-renewal.神经干细胞中具有促生长信号作用的细胞周期蛋白 D1 具有抗星形胶质发生功能,以执行自我更新。
Stem Cells. 2014 Jun;32(6):1602-15. doi: 10.1002/stem.1613.
10
Lithium suppresses astrogliogenesis by neural stem and progenitor cells by inhibiting STAT3 pathway independently of glycogen synthase kinase 3 beta.锂通过抑制 STAT3 通路而不依赖于糖原合成酶激酶 3β抑制神经干细胞和祖细胞的星形胶质细胞发生。
PLoS One. 2011;6(9):e23341. doi: 10.1371/journal.pone.0023341. Epub 2011 Sep 9.

引用本文的文献

1
Cellular responses to Sindbis virus infection of neural progenitors derived from human embryonic stem cells.源自人类胚胎干细胞的神经祖细胞对辛德毕斯病毒感染的细胞反应。
BMC Res Notes. 2014 Oct 24;7:757. doi: 10.1186/1756-0500-7-757.
2
Involvement of hypothalamic PI3K-STAT3 signalling in regulating appetite suppression mediated by amphetamine.下丘脑PI3K-STAT3信号通路参与调节苯丙胺介导的食欲抑制。
Br J Pharmacol. 2014 Jul;171(13):3223-33. doi: 10.1111/bph.12667.
3
Modeling to optimize terminal stem cell differentiation.建模以优化终末干细胞分化。
Scientifica (Cairo). 2013;2013:574354. doi: 10.1155/2013/574354. Epub 2013 Feb 11.
4
PLZF regulates fibroblast growth factor responsiveness and maintenance of neural progenitors.PLZF 调节成纤维细胞生长因子反应性和神经祖细胞的维持。
PLoS Biol. 2013 Oct;11(10):e1001676. doi: 10.1371/journal.pbio.1001676. Epub 2013 Oct 8.

本文引用的文献

1
Inhibition of notch signaling blocks growth of glioblastoma cell lines and tumor neurospheres.Notch信号通路的抑制可阻断胶质母细胞瘤细胞系和肿瘤神经球的生长。
Genes Cancer. 2010 Aug;1(8):822-35. doi: 10.1177/1947601910383564.
2
Targeting Stat3 in the myeloid compartment drastically improves the in vivo antitumor functions of adoptively transferred T cells.靶向髓系细胞中的 Stat3 可显著改善过继转移 T 细胞的体内抗肿瘤功能。
Cancer Res. 2010 Oct 1;70(19):7455-64. doi: 10.1158/0008-5472.CAN-10-0736. Epub 2010 Sep 14.
3
Transcriptional profiling of intrinsic PNS factors in the postnatal mouse.在出生后小鼠中进行内在 PNS 因子的转录谱分析。
Mol Cell Neurosci. 2011 Jan;46(1):32-44. doi: 10.1016/j.mcn.2010.07.015. Epub 2010 Aug 7.
4
The DNA methylome of glioblastoma multiforme.胶质母细胞瘤的 DNA 甲基组。
Neurobiol Dis. 2010 Jul;39(1):40-6. doi: 10.1016/j.nbd.2009.12.030. Epub 2010 Jan 11.
5
The transcriptional network for mesenchymal transformation of brain tumours.脑肿瘤间质转化的转录网络。
Nature. 2010 Jan 21;463(7279):318-25. doi: 10.1038/nature08712. Epub 2009 Dec 23.
6
The neuronal microRNA miR-326 acts in a feedback loop with notch and has therapeutic potential against brain tumors.神经元微小RNA miR-326与Notch形成反馈回路,并具有抗脑肿瘤的治疗潜力。
J Neurosci. 2009 Dec 2;29(48):15161-8. doi: 10.1523/JNEUROSCI.4966-09.2009.
7
Notch promotes radioresistance of glioma stem cells.Notch 促进脑胶质瘤干细胞的放射抵抗性。
Stem Cells. 2010 Jan;28(1):17-28. doi: 10.1002/stem.261.
8
MicroRNA-34a inhibits glioblastoma growth by targeting multiple oncogenes.微小RNA-34a通过靶向多个癌基因抑制胶质母细胞瘤的生长。
Cancer Res. 2009 Oct 1;69(19):7569-76. doi: 10.1158/0008-5472.CAN-09-0529. Epub 2009 Sep 22.
9
In vivo delivery of siRNA to immune cells by conjugation to a TLR9 agonist enhances antitumor immune responses.通过与 TLR9 激动剂缀合将 siRNA 递送至免疫细胞体内可增强抗肿瘤免疫反应。
Nat Biotechnol. 2009 Oct;27(10):925-32. doi: 10.1038/nbt.1564. Epub 2009 Sep 13.
10
Targeting interleukin 6 signaling suppresses glioma stem cell survival and tumor growth.靶向白介素 6 信号通路抑制神经胶质瘤干细胞存活和肿瘤生长。
Stem Cells. 2009 Oct;27(10):2393-404. doi: 10.1002/stem.188.

哺乳动物神经系统中的状态和语境。

STATus and Context within the Mammalian Nervous System.

机构信息

Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, USA.

出版信息

Mol Med. 2011 Sep-Oct;17(9-10):965-73. doi: 10.2119/molmed.2010.00259. Epub 2011 May 20.

DOI:10.2119/molmed.2010.00259
PMID:21607287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3188880/
Abstract

Effective manipulation of human disease processes may be achieved by understanding transcriptional, posttranscriptional and epigenetic events that orchestrate cellular events. The levels of activation of specific molecules, spatial distribution and concentrations of relevant networks of signaling molecules along with the receptiveness of the chromatin to these signals are some of the parameters which dictate context. Effects elicited by the transcription factor signal transducers and activator of transcription 3 (Stat3) are discussed with respect to the context within which Stat3-mediated effects are elicited within the developing and adult mammalian nervous system. Stat3 signals are pivotal to the proliferation and differentiation of neural stem cells. They also participate in neuronal regeneration and cancers of the nervous system. An analysis of the context in which Stat3 activation occurs in these processes provides a potential predictive paradigm with which novel methods for intervention may be designed.

摘要

通过理解转录、转录后和表观遗传事件来协调细胞事件,可能实现对人类疾病过程的有效干预。特定分子的激活水平、信号分子相关网络的空间分布和浓度以及染色质对这些信号的敏感性是决定上下文的一些参数。本文讨论了转录因子信号转导和转录激活因子 3(Stat3)的作用,以及 Stat3 介导的作用在发育中和成年哺乳动物神经系统中被引发的背景。Stat3 信号对神经干细胞的增殖和分化至关重要。它们还参与神经元再生和神经系统癌症。对 Stat3 激活在这些过程中发生的背景进行分析,为干预提供了一种潜在的预测范例,可能设计出新的干预方法。