• 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

Prox1功能是小鼠淋巴系统发育所必需的。

Prox1 function is required for the development of the murine lymphatic system.

作者信息

Wigle J T, Oliver G

机构信息

Department of Genetics, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Cell. 1999 Sep 17;98(6):769-78. doi: 10.1016/s0092-8674(00)81511-1.

DOI:10.1016/s0092-8674(00)81511-1
PMID:10499794
Abstract

The lack of specific markers has raised problems in documenting the precise manner by which the lymphatic system develops. Here we report that the homeobox gene Prox1 is expressed in a subpopulation of endothelial cells that by budding and sprouting give rise to the lymphatic system. The initial localization of these cells in the veins and their subsequent budding are both polarized, suggesting that unidentified guidance signals regulate this process. In Prox1 null mice, budding and sprouting is arrested, although vasculogenesis and angiogenesis of the vascular system is unaffected. These findings suggest that Prox1 is a specific and required regulator of the development of the lymphatic system and that the vascular and lymphatic systems develop independently.

摘要

缺乏特异性标志物给记录淋巴系统发育的确切方式带来了问题。在此我们报告,同源盒基因Prox1在一部分内皮细胞中表达,这些内皮细胞通过出芽和芽生形成淋巴系统。这些细胞最初在静脉中的定位及其随后的出芽都是极化的,这表明存在尚未确定的引导信号调节这一过程。在Prox1基因敲除小鼠中,出芽和芽生过程受阻,尽管血管系统的血管发生和血管生成未受影响。这些发现表明,Prox1是淋巴系统发育的特异性且必需的调节因子,并且血管系统和淋巴系统是独立发育的。

相似文献

1
Prox1 function is required for the development of the murine lymphatic system.Prox1功能是小鼠淋巴系统发育所必需的。
Cell. 1999 Sep 17;98(6):769-78. doi: 10.1016/s0092-8674(00)81511-1.
2
Prox1, master regulator of the lymphatic vasculature phenotype.Prox1,淋巴管表型的主要调节因子。
Cell Tissue Res. 2003 Oct;314(1):85-92. doi: 10.1007/s00441-003-0747-8. Epub 2003 Jul 22.
3
An essential role for Prox1 in the induction of the lymphatic endothelial cell phenotype.Prox1在诱导淋巴管内皮细胞表型中起重要作用。
EMBO J. 2002 Apr 2;21(7):1505-13. doi: 10.1093/emboj/21.7.1505.
4
Prox1 is a master control gene in the program specifying lymphatic endothelial cell fate.Prox1是决定淋巴管内皮细胞命运程序中的一个主控基因。
Dev Dyn. 2002 Nov;225(3):351-7. doi: 10.1002/dvdy.10163.
5
Prox1 is a marker of ectodermal placodes, endodermal compartments, lymphatic endothelium and lymphangioblasts.Prox1是外胚层基板、内胚层隔室、淋巴管内皮和淋巴成血管细胞的标志物。
Anat Embryol (Berl). 2001 Nov;204(5):399-406. doi: 10.1007/s00429-001-0214-9.
6
Prox1 induces lymphatic endothelial differentiation via integrin alpha9 and other signaling cascades.Prox1通过整合素α9和其他信号级联反应诱导淋巴管内皮分化。
Mol Biol Cell. 2007 Apr;18(4):1421-9. doi: 10.1091/mbc.e06-09-0780. Epub 2007 Feb 7.
7
Prox1 promotes lineage-specific expression of fibroblast growth factor (FGF) receptor-3 in lymphatic endothelium: a role for FGF signaling in lymphangiogenesis.Prox1促进淋巴管内皮细胞中纤维母细胞生长因子(FGF)受体-3的谱系特异性表达:FGF信号在淋巴管生成中的作用
Mol Biol Cell. 2006 Feb;17(2):576-84. doi: 10.1091/mbc.e05-04-0368. Epub 2005 Nov 16.
8
T1alpha/podoplanin deficiency disrupts normal lymphatic vasculature formation and causes lymphedema.T1α/血小板反应蛋白1缺乏会破坏正常的淋巴管系统形成并导致淋巴水肿。
EMBO J. 2003 Jul 15;22(14):3546-56. doi: 10.1093/emboj/cdg342.
9
Identification of targets of Prox1 during in vitro vascular differentiation from embryonic stem cells: functional roles of HoxD8 in lymphangiogenesis.从胚胎干细胞体外血管分化过程中识别 Prox1 的靶标:HoxD8 在淋巴管生成中的功能作用。
J Cell Sci. 2009 Nov 1;122(Pt 21):3923-30. doi: 10.1242/jcs.052324. Epub 2009 Oct 13.
10
Lymphangioblasts in embryonic lymphangiogenesis.胚胎淋巴管生成中的成淋巴管细胞
Lymphat Res Biol. 2003;1(1):33-40. doi: 10.1089/15396850360495673.

引用本文的文献

1
Single-Cell Characterization of Anterior Segment Development: Cell Types, Pathways, and Signals Driving Formation of the Trabecular Meshwork and Schlemm's Canal.眼前节发育的单细胞特征:驱动小梁网和施莱姆管形成的细胞类型、途径和信号
bioRxiv. 2025 Aug 21:2025.08.15.670438. doi: 10.1101/2025.08.15.670438.
2
Morphology of the glymphatic and meningeal lymphatic structures of the bottlenose dolphin.宽吻海豚脑周淋巴系统和脑膜淋巴结构的形态学
Sci Rep. 2025 Aug 18;15(1):30216. doi: 10.1038/s41598-025-14840-0.
3
Characteristics and advances in signaling pathways, cellular communication, cell junctions, and oxidative stress in lymphedema.
淋巴水肿中信号通路、细胞通讯、细胞连接及氧化应激的特征与进展
Front Cell Dev Biol. 2025 Jul 22;13:1521320. doi: 10.3389/fcell.2025.1521320. eCollection 2025.
4
Zebrafish Models of Induced Lymphangiogenesis: Current Advancements and Therapeutic Discovery.诱导性淋巴管生成的斑马鱼模型:当前进展与治疗发现
Pharmaceuticals (Basel). 2025 Jul 21;18(7):1076. doi: 10.3390/ph18071076.
5
Case Report: Surgical management of primary lymphedema with a novel PROX1 mutation involving upper and lower limbs.病例报告:原发性淋巴水肿的手术治疗,伴有涉及上肢和下肢的新型PROX1突变。
Front Genet. 2025 Jul 3;16:1560471. doi: 10.3389/fgene.2025.1560471. eCollection 2025.
6
Targeted Therapy for Complex Lymphatic Anomalies in Patients with Noonan Syndrome and Related Disorders.努南综合征及相关疾病患者复杂淋巴管异常的靶向治疗
Int J Mol Sci. 2025 Jun 26;26(13):6126. doi: 10.3390/ijms26136126.
7
Neurovascular plasticity as a modulator of hypothalamic function.神经血管可塑性作为下丘脑功能的调节因子。
Rev Endocr Metab Disord. 2025 Jun 21. doi: 10.1007/s11154-025-09982-5.
8
Single-Cell Transcriptomics and Lineage Tracing Unveil Parallels in Lymphatic Muscle and Venous Smooth Muscle Development, Identity, and Function.单细胞转录组学与谱系追踪揭示淋巴管平滑肌和静脉平滑肌发育、特征及功能的相似之处
Arterioscler Thromb Vasc Biol. 2025 Jul;45(7):1207-1225. doi: 10.1161/ATVBAHA.125.322567. Epub 2025 May 15.
9
Lymphatic endothelial mTORC1 instructs metabolic and developmental signaling during lymphangiogenesis.淋巴管生成过程中,淋巴管内皮细胞中的mTORC1指导代谢和发育信号传导。
Dev Cell. 2025 May 2. doi: 10.1016/j.devcel.2025.04.012.
10
Tissue engineering approaches for lymphedema: biomaterial innovations and clinical potential.淋巴水肿的组织工程学方法:生物材料创新与临床潜力
Front Cell Dev Biol. 2025 Apr 15;13:1537050. doi: 10.3389/fcell.2025.1537050. eCollection 2025.