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本文引用的文献

1
Plasma microRNAs to predict the response of radiotherapy in esophageal squamous cell carcinoma patients.血浆微小RNA用于预测食管鳞状细胞癌患者的放疗反应。
Am J Transl Res. 2015 Oct 15;7(10):2060-71. eCollection 2015.
2
Hematopoietic stem and progenitor cells regulate the regeneration of their niche by secreting Angiopoietin-1.造血干细胞和祖细胞通过分泌血管生成素-1来调节其微环境的再生。
Elife. 2015 Mar 30;4:e05521. doi: 10.7554/eLife.05521.
3
Bone marrow vascular niche: home for hematopoietic stem cells.骨髓血管龛:造血干细胞的家园。
Bone Marrow Res. 2014;2014:128436. doi: 10.1155/2014/128436. Epub 2014 Apr 14.
4
Signal transduction by vascular endothelial growth factor receptors.血管内皮生长因子受体的信号转导。
Cold Spring Harb Perspect Med. 2012 Jul;2(7):a006502. doi: 10.1101/cshperspect.a006502.
5
The Notch pathway in the developing hematopoietic system.发育中的造血系统中的Notch信号通路。
Int J Dev Biol. 2010;54(6-7):1175-88. doi: 10.1387/ijdb.093049ab.
6
Angiopoietin-1/Tie2 receptor signaling in vascular quiescence and angiogenesis.血管静止和血管生成中的血管生成素-1/Tie2 受体信号。
Histol Histopathol. 2010 Mar;25(3):387-96. doi: 10.14670/HH-25.387.
7
Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes.Notch信号通路的起源与进化:真核生物基因组概述
BMC Evol Biol. 2009 Oct 13;9:249. doi: 10.1186/1471-2148-9-249.
8
Tie2 is tied at the cell-cell contacts and to extracellular matrix by angiopoietin-1.血管生成素-1将Tie2固定在细胞间接触部位以及细胞外基质上。
Exp Mol Med. 2009 Mar 31;41(3):133-9. doi: 10.3858/emm.2009.41.3.016.
9
Angiopoietin-1 requires p190 RhoGAP to protect against vascular leakage in vivo.血管生成素-1在体内需要p190 RhoGAP来防止血管渗漏。
J Biol Chem. 2007 Aug 17;282(33):23910-8. doi: 10.1074/jbc.M702169200. Epub 2007 Jun 11.
10
Endothelial cell migration during angiogenesis.血管生成过程中的内皮细胞迁移。
Circ Res. 2007 Mar 30;100(6):782-94. doi: 10.1161/01.RES.0000259593.07661.1e.

血管生成素-1促进辐射小鼠造血功能的恢复。

Angiopoietin-1 facilitates recovery of hematopoiesis in radiated mice.

作者信息

Sun Lan, Zhang Huaibao, Bi Laixi, Shi Yi-Fen, Xing Chongyun, Tang Liyuan, Jiang Songfu, Yu Kang

机构信息

Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University NanBai Xiang, Ouhai District, Wenzhou 325000, China.

Department of Orthopaedics, The First Affiliated Hospital of Wenzhou Medical University NanBai Xiang, Ouhai District, Wenzhou 325000, China.

出版信息

Am J Transl Res. 2016 May 15;8(5):2011-21. eCollection 2016.

PMID:27347310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4891415/
Abstract

Angiopoietin-1 (Ang-1) plays a critical role in the regulation of endothelial cell survival and vascular maturation and stability. However, its role in hematopoiesis is not clear. Here, we determined effect of Ang-1 on the recovery of hematopoiesis in radiated mice. By injecting an Ang-1 plasmid, we found that Ang-1 was preferentially expressed in bone marrow (BM) of femur from radiated mice. This injection resulted in elevated blood counts and serum VEGF level. The blockade in S phase of cell cycle in mouse BM stromal cells following radiation was attenuated by injection of Ang-1 plasmid. In addition, injection of Ang-1 plasmid attenuated the radiation-mediated inhibition of Tie2 expression. Furthermore, through analyzing Notch1 expression, we found that injection of Ang-1 plasmid increased Notch mRNA expression in radiated mice. In conclusion, these findings suggest that Ang-1 facilitates the recovery of hematopoiesis in radiated mice with the involvement of Notch signaling pathway.

摘要

血管生成素-1(Ang-1)在调节内皮细胞存活、血管成熟和稳定性方面发挥着关键作用。然而,其在造血过程中的作用尚不清楚。在此,我们确定了Ang-1对辐射小鼠造血恢复的影响。通过注射Ang-1质粒,我们发现Ang-1在辐射小鼠股骨的骨髓(BM)中优先表达。这种注射导致血细胞计数和血清VEGF水平升高。注射Ang-1质粒减弱了辐射后小鼠骨髓基质细胞细胞周期S期的阻滞。此外,注射Ang-1质粒减弱了辐射介导的Tie2表达抑制。此外,通过分析Notch1表达,我们发现注射Ang-1质粒增加了辐射小鼠中Notch mRNA的表达。总之,这些发现表明,Ang-1通过Notch信号通路促进辐射小鼠的造血恢复。