• 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
Notch1 and Notch2 inhibit myeloid differentiation in response to different cytokines.Notch1和Notch2在响应不同细胞因子时会抑制髓系分化。
Mol Cell Biol. 1998 Apr;18(4):2324-33. doi: 10.1128/MCB.18.4.2324.
2
Notch signaling enhances survival and alters differentiation of 32D myeloblasts.Notch信号通路增强32D成髓细胞的存活能力并改变其分化。
J Immunol. 2000 Oct 15;165(8):4428-36. doi: 10.4049/jimmunol.165.8.4428.
3
Phosphorylation of Ser2078 modulates the Notch2 function in 32D cell differentiation.
J Biol Chem. 2001 Nov 30;276(48):44873-80. doi: 10.1074/jbc.M104703200. Epub 2001 Sep 27.
4
Function of Delta4 gene and its effects on 32D cell differentiation.Delta4基因的功能及其对32D细胞分化的影响。
Chin Med J (Engl). 2004 Nov;117(11):1687-92.
5
Notch signalling via RBP-J promotes myeloid differentiation.通过RBP-J的Notch信号通路促进髓系分化。
EMBO J. 2000 Jun 1;19(11):2558-68. doi: 10.1093/emboj/19.11.2558.
6
Notch1 inhibits differentiation of hematopoietic cells by sustaining GATA-2 expression.Notch1通过维持GATA-2的表达来抑制造血细胞的分化。
Blood. 2001 Dec 1;98(12):3283-9. doi: 10.1182/blood.v98.12.3283.
7
The Notch ligand, Delta-1, inhibits the differentiation of monocytes into macrophages but permits their differentiation into dendritic cells.Notch配体Delta-1可抑制单核细胞向巨噬细胞的分化,但允许其向树突状细胞分化。
Blood. 2001 Sep 1;98(5):1402-7. doi: 10.1182/blood.v98.5.1402.
8
Multipotent hematopoietic cell lines derived from C/EBPalpha(-/-) knockout mice display granulocyte macrophage-colony-stimulating factor, granulocyte- colony-stimulating factor, and retinoic acid-induced granulocytic differentiation.源自C/EBPα(-/-)基因敲除小鼠的多能造血细胞系表现出粒细胞巨噬细胞集落刺激因子、粒细胞集落刺激因子以及视黄酸诱导的粒细胞分化。
Blood. 2001 Oct 15;98(8):2382-8. doi: 10.1182/blood.v98.8.2382.
9
Inhibition of granulocytic differentiation by mNotch1.mNotch1对粒细胞分化的抑制作用。
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13014-9. doi: 10.1073/pnas.93.23.13014.
10
PU.1 regulates both cytokine-dependent proliferation and differentiation of granulocyte/macrophage progenitors.PU.1调节粒细胞/巨噬细胞祖细胞的细胞因子依赖性增殖和分化。
EMBO J. 1998 Aug 3;17(15):4456-68. doi: 10.1093/emboj/17.15.4456.

引用本文的文献

1
Neurobeachin regulates hematopoietic progenitor differentiation and survival by modulating Notch activity.神经海滩蛋白通过调节Notch活性来调控造血祖细胞的分化和存活。
Blood Adv. 2024 Aug 13;8(15):4129-4143. doi: 10.1182/bloodadvances.2023012426.
2
Jagged2 targeting in lung cancer activates anti-tumor immunity via Notch-induced functional reprogramming of tumor-associated macrophages.Jagged2 靶向治疗肺癌通过 Notch 诱导的肿瘤相关巨噬细胞功能重编程激活抗肿瘤免疫。
Immunity. 2024 May 14;57(5):1124-1140.e9. doi: 10.1016/j.immuni.2024.03.020. Epub 2024 Apr 17.
3
Viral transduction of primary human lymphoma B cells reveals mechanisms of NOTCH-mediated immune escape.原发性人淋巴瘤 B 细胞的病毒转导揭示了 NOTCH 介导的免疫逃逸机制。
Nat Commun. 2022 Oct 20;13(1):6220. doi: 10.1038/s41467-022-33739-2.
4
Propranolol Inhibits the Proliferation of Human Glioblastoma Cell Lines through Notch1 and Hes1 Signaling System.普萘洛尔通过Notch1和Hes1信号系统抑制人胶质母细胞瘤细胞系的增殖。
J Korean Neurosurg Soc. 2021 Sep;64(5):716-725. doi: 10.3340/jkns.2021.0068. Epub 2021 Aug 11.
5
The transcriptome of anterior regeneration in earthworm Eudrilus eugeniae.在蚯蚓 Eugeniae 的前再生转录组中。
Mol Biol Rep. 2021 Jan;48(1):259-283. doi: 10.1007/s11033-020-06044-8. Epub 2020 Dec 11.
6
Oncogenic role of lncRNA CRNDE in acute promyelocytic leukemia and NPM1-mutant acute myeloid leukemia.长链非编码RNA CRNDE在急性早幼粒细胞白血病和NPM1突变型急性髓系白血病中的致癌作用
Cell Death Discov. 2020 Nov 11;6(1):121. doi: 10.1038/s41420-020-00359-y.
7
Transcriptional Regulation of Natural Killer Cell Development and Functions.自然杀伤细胞发育与功能的转录调控
Cancers (Basel). 2020 Jun 16;12(6):1591. doi: 10.3390/cancers12061591.
8
Macrophages Promote Aortic Valve Cell Calcification and Alter STAT3 Splicing.巨噬细胞促进主动脉瓣细胞钙化并改变 STAT3 剪接。
Arterioscler Thromb Vasc Biol. 2020 Jun;40(6):e153-e165. doi: 10.1161/ATVBAHA.120.314360. Epub 2020 Apr 16.
9
Deregulated Notch and Wnt signaling activates early-stage myeloid regeneration pathways in leukemia. Notch 和 Wnt 信号失调激活白血病早期髓系再生途径。
J Exp Med. 2020 Mar 2;217(3). doi: 10.1084/jem.20190787.
10
Notch1 activation enhances proliferation via activation of cdc2 and delays differentiation of myeloid progenitors.Notch1激活通过激活cdc2增强增殖并延迟髓系祖细胞的分化。
Leuk Res. 2018 Sep;72:34-44. doi: 10.1016/j.leukres.2018.07.022. Epub 2018 Jul 30.

本文引用的文献

1
The human homolog of rat Jagged1 expressed by marrow stroma inhibits differentiation of 32D cells through interaction with Notch1.骨髓基质表达的大鼠Jagged1的人类同源物通过与Notch1相互作用抑制32D细胞的分化。
Immunity. 1998 Jan;8(1):43-55. doi: 10.1016/s1074-7613(00)80457-4.
2
Notch activity influences the alphabeta versus gammadelta T cell lineage decision.Notch信号活性影响αβ与γδ T细胞谱系决定。
Cell. 1997 Mar 21;88(6):833-43. doi: 10.1016/s0092-8674(00)81929-7.
3
Hematopoietic activity of a stromal cell transmembrane protein containing epidermal growth factor-like repeat motifs.一种含有表皮生长因子样重复基序的基质细胞跨膜蛋白的造血活性。
Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):4011-6. doi: 10.1073/pnas.94.8.4011.
4
Inhibition of granulocytic differentiation by mNotch1.mNotch1对粒细胞分化的抑制作用。
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13014-9. doi: 10.1073/pnas.93.23.13014.
5
An activated form of Notch influences the choice between CD4 and CD8 T cell lineages.Notch的激活形式影响CD4和CD8 T细胞谱系之间的选择。
Cell. 1996 Nov 1;87(3):483-92. doi: 10.1016/s0092-8674(00)81368-9.
6
The biology of hematopoietic stem cells.造血干细胞生物学
Annu Rev Cell Dev Biol. 1995;11:35-71. doi: 10.1146/annurev.cb.11.110195.000343.
7
Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene.Notch4/int-3是一种乳腺原癌基因,是一种内皮细胞特异性的哺乳动物Notch基因。
Development. 1996 Jul;122(7):2251-9. doi: 10.1242/dev.122.7.2251.
8
Signal transduction by activated mNotch: importance of proteolytic processing and its regulation by the extracellular domain.活化的mNotch的信号转导:蛋白水解加工的重要性及其受细胞外结构域的调控
Proc Natl Acad Sci U S A. 1996 Feb 20;93(4):1683-8. doi: 10.1073/pnas.93.4.1683.
9
The transcriptional control of hematopoiesis.造血作用的转录调控。
Blood. 1996 May 15;87(10):4025-39.
10
Use of a promoter-trap retrovirus to identify and isolate genes involved in differentiation of a myeloid progenitor cell line in vitro.利用启动子捕获逆转录病毒在体外鉴定和分离参与髓系祖细胞系分化的基因。
Blood. 1996 Mar 1;87(5):1771-9.

Notch1和Notch2在响应不同细胞因子时会抑制髓系分化。

Notch1 and Notch2 inhibit myeloid differentiation in response to different cytokines.

作者信息

Bigas A, Martin D I, Milner L A

机构信息

The Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.

出版信息

Mol Cell Biol. 1998 Apr;18(4):2324-33. doi: 10.1128/MCB.18.4.2324.

DOI:10.1128/MCB.18.4.2324
PMID:9528802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC121486/
Abstract

We have compared the ability of two mammalian Notch homologs, mouse Notchl and Notch2, to inhibit the granulocytic differentiation of 32D myeloid progenitor cells. 32D cells undergo granulocytic differentiation when stimulated with either granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF). Expression of the activated intracellular domain of Notch1 inhibits the differentiation induced by G-CSF but not by GM-CSF; conversely, the corresponding domain of Notch2 inhibits differentiation in response to GM-CSF but not to G-CSF. The region immediately C-terminal to the cdc10 domain of Notch confers cytokine specificity on the cdc10 domain. The cytokine response patterns of Notch1 and Notch2 are transferred with this region, which we have termed the Notch cytokine response (NCR) region. The NCR region is also associated with differences in posttranslational modification and subcellular localization of the different Notch molecules. These findings suggest that the multiple forms of Notch found in mammals have structural differences that allow their function to be modulated by specific differentiation signals.

摘要

我们比较了两种哺乳动物Notch同源物——小鼠Notch1和Notch2抑制32D髓系祖细胞向粒细胞分化的能力。当用粒细胞集落刺激因子(G-CSF)或粒细胞-巨噬细胞集落刺激因子(GM-CSF)刺激时,32D细胞会发生粒细胞分化。Notch1活化的细胞内结构域的表达可抑制G-CSF诱导的分化,但不能抑制GM-CSF诱导的分化;相反,Notch2的相应结构域可抑制对GM-CSF而非G-CSF的分化反应。Notch的cdc10结构域紧邻的C末端区域赋予cdc10结构域细胞因子特异性。Notch1和Notch2的细胞因子反应模式通过这个我们称为Notch细胞因子反应(NCR)区域的区域进行传递。NCR区域还与不同Notch分子的翻译后修饰和亚细胞定位差异有关。这些发现表明,哺乳动物中发现的多种Notch形式具有结构差异,使其功能能够被特定的分化信号调节。