• 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

NSG小鼠骨骼和横纹肌微循环的体内功能与形态学特征

In vivo functional and morphological characterization of bone and striated muscle microcirculation in NSG mice.

作者信息

Mussawy Haider, Viezens Lennart, Hauenherm Gerrit, Schroeder Malte, Schaefer Christian

机构信息

Department of Orthopaedic Surgery, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Department of Trauma-, Hand-, and Reconstructive Surgery, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

出版信息

PLoS One. 2017 Aug 11;12(8):e0183186. doi: 10.1371/journal.pone.0183186. eCollection 2017.

DOI:10.1371/journal.pone.0183186
PMID:28800593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5553939/
Abstract

Organ-specific microcirculation plays a central role in tumor growth, tumor cell homing, tissue engineering, and wound healing. Mouse models are widely used to study these processes; however, these mouse strains often possess unique microhemodynamic parameters, making it difficult to directly compare experiments. The full functional characterization of bone and striated muscle microcirculatory parameters in non-obese diabetic-severe combined immunodeficiency/y-chain; NOD-Prkds IL2rg (NSG) mice has not yet been reported. Here, we established either a dorsal skinfold chamber or femur window in NSG mice (n = 23), allowing direct analysis of microcirculatory parameters in vivo by intravital fluorescence microscopy at 7, 14, 21, and 28 days after chamber preparation. Organ-specific differences were observed. Bone had a significantly lower vessel density but a higher vessel diameter than striated muscle. Bone also showed higher effective vascular permeability than striated muscle. The centerline velocity values were similar in the femur window and dorsal skinfold chamber, with a higher volumetric blood flow in bone. Interestingly, bone and striated muscle showed similar tissue perfusion rates. Knowledge of physiological microhemodynamic values of bone and striated muscle in NSG mice makes it possible to analyze pathophysiological processes at these anatomic sites, such as tumor growth, tumor metastasis, and tumor microcirculation, as well as the response to therapeutic agents.

摘要

器官特异性微循环在肿瘤生长、肿瘤细胞归巢、组织工程和伤口愈合中起着核心作用。小鼠模型被广泛用于研究这些过程;然而,这些小鼠品系往往具有独特的微血流动力学参数,使得直接比较实验变得困难。非肥胖糖尿病严重联合免疫缺陷/γ链;NOD-Prkds IL2rg(NSG)小鼠的骨骼和横纹肌微循环参数的完整功能特征尚未见报道。在此,我们在NSG小鼠(n = 23)中建立了背部皮褶室或股骨窗口,通过活体荧光显微镜在室制备后7、14、21和28天对体内微循环参数进行直接分析。观察到了器官特异性差异。骨骼的血管密度显著低于横纹肌,但血管直径更大。骨骼的有效血管通透性也高于横纹肌。股骨窗口和背部皮褶室的中心线速度值相似,骨骼中的体积血流量更高。有趣的是,骨骼和横纹肌的组织灌注率相似。了解NSG小鼠骨骼和横纹肌的生理微血流动力学值使得分析这些解剖部位的病理生理过程成为可能,如肿瘤生长、肿瘤转移和肿瘤微循环,以及对治疗药物的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/9036a6cb0db0/pone.0183186.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/a8a5522c4947/pone.0183186.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/dc8d1cbfc33e/pone.0183186.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/9036a6cb0db0/pone.0183186.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/a8a5522c4947/pone.0183186.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/dc8d1cbfc33e/pone.0183186.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d15/5553939/9036a6cb0db0/pone.0183186.g003.jpg

相似文献

1
In vivo functional and morphological characterization of bone and striated muscle microcirculation in NSG mice.NSG小鼠骨骼和横纹肌微循环的体内功能与形态学特征
PLoS One. 2017 Aug 11;12(8):e0183186. doi: 10.1371/journal.pone.0183186. eCollection 2017.
2
The bone microenvironment promotes tumor growth and tissue perfusion compared with striated muscle in a preclinical model of prostate cancer in vivo.在体内前列腺癌的临床前模型中,骨微环境促进肿瘤生长和组织灌注,优于横纹肌。
BMC Cancer. 2018 Oct 16;18(1):979. doi: 10.1186/s12885-018-4905-5.
3
Femur window--a new approach to microcirculation of living bone in situ.股骨窗——一种用于活体骨原位微循环研究的新方法。
J Orthop Res. 2005 Sep;23(5):1073-82. doi: 10.1016/j.orthres.2005.02.013.
4
Dorsal skinfold chamber technique for intravital microscopy in nude mice.裸鼠活体显微镜检查的背部皮褶小室技术。
Am J Pathol. 1993 Oct;143(4):1055-62.
5
Perfusion of single tumor microvessels: application to vascular permeability measurement.单个肿瘤微血管的灌注:在血管通透性测量中的应用
Microcirculation. 1996 Dec;3(4):349-57. doi: 10.3109/10739689609148307.
6
Microvascular response to shock wave application in striated skin muscle.平滑肌组织中冲击波应用的微血管反应。
J Surg Res. 2011 Nov;171(1):347-54. doi: 10.1016/j.jss.2009.12.011. Epub 2010 Jan 5.
7
Static magnetic fields affect capillary flow of red blood cells in striated skin muscle.静磁场影响横纹皮肤肌肉中红细胞的毛细血管流动。
Microcirculation. 2008 Jan;15(1):15-26. doi: 10.1080/10739680701410850.
8
The impact of topical antiseptics on skin microcirculation.局部抗菌剂对皮肤微循环的影响。
Eur J Med Res. 2004 Sep 29;9(9):449-54.
9
Angiogenesis, microvascular architecture, microhemodynamics, and interstitial fluid pressure during early growth of human adenocarcinoma LS174T in SCID mice.人腺癌LS174T在SCID小鼠体内早期生长过程中的血管生成、微血管结构、微循环动力学及组织液压力
Cancer Res. 1992 Dec 1;52(23):6553-60.
10
Angiopoietin-1 regulates microvascular reactivity and protects the microcirculation during acute endothelial dysfunction: role of eNOS and VE-cadherin.血管生成素-1调节微血管反应性并在急性内皮功能障碍期间保护微循环:内皮型一氧化氮合酶和血管内皮钙黏蛋白的作用。
Pharmacol Res. 2014 Feb;80:43-51. doi: 10.1016/j.phrs.2013.12.008. Epub 2014 Jan 7.

引用本文的文献

1
analysis of noise dependent activation of white blood cells and microvascular dysfunction in mice.小鼠中白细胞噪声依赖性激活及微血管功能障碍的分析
MethodsX. 2021 Oct 8;8:101540. doi: 10.1016/j.mex.2021.101540. eCollection 2021.
2
The bone microenvironment promotes tumor growth and tissue perfusion compared with striated muscle in a preclinical model of prostate cancer in vivo.在体内前列腺癌的临床前模型中,骨微环境促进肿瘤生长和组织灌注,优于横纹肌。
BMC Cancer. 2018 Oct 16;18(1):979. doi: 10.1186/s12885-018-4905-5.

本文引用的文献

1
Sunitinib treatment reduces tumor growth and limits changes in microvascular properties after minor surgical intervention in an in vivo model of secondary breast cancer growth in bone.在骨转移继发性乳腺癌生长的体内模型中,舒尼替尼治疗可减少肿瘤生长,并限制小型手术干预后微血管特性的变化。
J Surg Oncol. 2016 Apr;113(5):515-21. doi: 10.1002/jso.24185. Epub 2016 Jan 27.
2
Human tumor infiltrating lymphocytes cooperatively regulate prostate tumor growth in a humanized mouse model.人源肿瘤浸润淋巴细胞在人源化小鼠模型中协同调控前列腺肿瘤生长。
J Immunother Cancer. 2015 Apr 21;3:12. doi: 10.1186/s40425-015-0056-2. eCollection 2015.
3
Higher susceptibility of NOD/LtSz-scid Il2rg (-/-) NSG mice to xenotransplanted lung cancer cell lines.
NOD/LtSz-scid Il2rg(-/-) NSG 小鼠对异种移植肺癌细胞系更敏感。
Cancer Manag Res. 2014 Oct 21;6:431-6. doi: 10.2147/CMAR.S71185. eCollection 2014.
4
Imaging cell biology in live animals: ready for prime time.在活体动物中进行细胞生物学成像:准备好进入黄金时代。
J Cell Biol. 2013 Jun 24;201(7):969-79. doi: 10.1083/jcb.201212130.
5
Generation of islet-like cells from mouse gall bladder by direct ex vivo reprogramming.通过直接体外重编程从小鼠胆囊生成胰岛样细胞。
Stem Cell Res. 2013 Jul;11(1):503-15. doi: 10.1016/j.scr.2013.02.005. Epub 2013 Feb 18.
6
Comparison of childhood leukemia initiating cell populations in NOD/SCID and NSG mice.NOD/SCID和NSG小鼠中儿童白血病起始细胞群体的比较。
Leukemia. 2012 Feb;26(2):376-80. doi: 10.1038/leu.2011.212. Epub 2011 Aug 23.
7
Superior human leukocyte reconstitution and susceptibility to vaginal HIV transmission in humanized NOD-scid IL-2Rγ(-/-) (NSG) BLT mice.人源化 NOD-scid IL-2Rγ(-/-) (NSG) BLT 小鼠中人白细胞重建更完全,且对阴道 HIV 传播更易感。
Virology. 2011 Aug 15;417(1):154-60. doi: 10.1016/j.virol.2011.05.013.
8
Primary tumor dependent inhibition of tumor growth, angiogenesis, and perfusion of secondary breast cancer in bone.原发肿瘤依赖性抑制骨转移乳腺癌的生长、血管生成和灌注。
J Orthop Res. 2011 Aug;29(8):1251-8. doi: 10.1002/jor.21402. Epub 2011 Mar 4.
9
Microcirculation of secondary bone tumors in vivo: the impact of minor surgery at a distal site.体内继发性骨肿瘤的微循环:远端部位小手术的影响。
J Orthop Res. 2010 Nov;28(11):1515-21. doi: 10.1002/jor.21166.
10
Tumor-initiating cells are rare in many human tumors.肿瘤起始细胞在许多人类肿瘤中较为罕见。
Cell Stem Cell. 2010 Sep 3;7(3):279-82. doi: 10.1016/j.stem.2010.08.009.