• 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

直接比较源自脂肪组织和骨髓的人间充质干细胞在介导血管新生以应对血管缺血方面的作用。

Direct comparison of human mesenchymal stem cells derived from adipose tissues and bone marrow in mediating neovascularization in response to vascular ischemia.

作者信息

Kim Yeon, Kim Hoe, Cho Hyun, Bae Yong, Suh Kuen, Jung Jin

机构信息

Department of Physiology, School of Medicine, Pusan National University, Pusan, Korea.

出版信息

Cell Physiol Biochem. 2007;20(6):867-76. doi: 10.1159/000110447.

DOI:10.1159/000110447
PMID:17982269
Abstract

BACKGROUND/AIM: Although transplantation of MSC derived from bone marrow or adipose tissues has been shown in proangiogenic action in hindlimb ischemia model of nude mice, little information is available regarding comparison of the angiogenic potency between human adipose stromal cells (hADSC) and bone marrow stromal cells (hBMSC). We compared their therapeutic potential by transplantation of equal numbers of hADSC or hBMSC in a nude mice model of hindlimb ischemia.

METHODS AND RESULTS

One day after creating hindlimb ischemia, mice were randomized to receive hADSC transplantation (hADSC group), hBMSC transplantation (hBMSC group), or vehicle transplantation (Control group). Two weeks after transplantation, the laser Doppler perfusion index was significantly higher in the hADSC group and hBMSC group than in the control group. Comparison between hADSC and hBMSC group showed better recovery of blood flow in hADSC group than in hBMSC group. Conditioned media from hADSC (hADSC-CM) showed better in vitro tube formation of hADSC than conditioned media from hBMSC (hBMSC-CM). hADSC showed higher expression of MMP3 and MMP9 than hBMSC. A MMP inhibitor, GM6001, and the transfection of MMP3 or MMP9 siRNA oligonucleotides inhibited in vitro tube formation of hADSC. Transplantation of MMP3 or MMP9 siRNA oligonucleotieds-transfected hADSC showed lower blood flow recovery and higher tissue injury than control oligonucelotide-transfected cells.

CONCLUSION

This study showed that hADSC can be an ideal source for therapeutic angiogenesis in ischemic disease in terms of efficacy, accessibility and available tissue amounts.

摘要

背景/目的:尽管已证明源自骨髓或脂肪组织的间充质干细胞移植在裸鼠后肢缺血模型中具有促血管生成作用,但关于人脂肪基质细胞(hADSC)和骨髓基质细胞(hBMSC)之间血管生成能力比较的信息却很少。我们通过在裸鼠后肢缺血模型中移植等量的hADSC或hBMSC来比较它们的治疗潜力。

方法与结果

在造成后肢缺血一天后,将小鼠随机分为接受hADSC移植组(hADSC组)、hBMSC移植组(hBMSC组)或载体移植组(对照组)。移植两周后,hADSC组和hBMSC组的激光多普勒灌注指数显著高于对照组。hADSC组和hBMSC组之间的比较显示,hADSC组的血流恢复情况优于hBMSC组。来自hADSC的条件培养基(hADSC-CM)比来自hBMSC的条件培养基(hBMSC-CM)在体外显示出更好的hADSC管形成能力。hADSC比hBMSC显示出更高的MMP3和MMP9表达。一种MMP抑制剂GM6001以及MMP3或MMP9 siRNA寡核苷酸的转染抑制了hADSC的体外管形成。移植MMP3或MMP9 siRNA寡核苷酸转染的hADSC显示出比对照寡核苷酸转染细胞更低的血流恢复和更高的组织损伤。

结论

本研究表明,就疗效、可及性和可用组织量而言,hADSC可以成为缺血性疾病治疗性血管生成的理想来源。

相似文献

1
Direct comparison of human mesenchymal stem cells derived from adipose tissues and bone marrow in mediating neovascularization in response to vascular ischemia.直接比较源自脂肪组织和骨髓的人间充质干细胞在介导血管新生以应对血管缺血方面的作用。
Cell Physiol Biochem. 2007;20(6):867-76. doi: 10.1159/000110447.
2
Human adipose tissue-derived mesenchymal stem cells improve postnatal neovascularization in a mouse model of hindlimb ischemia.人脂肪组织来源的间充质干细胞可改善后肢缺血小鼠模型的出生后血管新生。
Cell Physiol Biochem. 2006;17(5-6):279-90. doi: 10.1159/000094140. Epub 2006 Jun 20.
3
Enhancement of long-term angiogenic efficacy of adipose stem cells by delivery of FGF2.通过递送 FGF2 增强脂肪干细胞的长期血管生成功效。
Microvasc Res. 2012 Jul;84(1):1-8. doi: 10.1016/j.mvr.2012.04.004. Epub 2012 Apr 23.
4
Transplantation of modified human adipose derived stromal cells expressing VEGF165 results in more efficient angiogenic response in ischemic skeletal muscle.表达 VEGF165 的人脂肪来源基质细胞的移植导致缺血骨骼肌中更有效的血管生成反应。
J Transl Med. 2013 Jun 6;11:138. doi: 10.1186/1479-5876-11-138.
5
Direct comparison of the potency of human mesenchymal stem cells derived from amnion tissue, bone marrow and adipose tissue at inducing dermal fibroblast responses to cutaneous wounds.直接比较源自羊膜组织、骨髓和脂肪组织的人骨髓间充质干细胞在诱导皮肤成纤维细胞对皮肤创伤反应中的效力。
Int J Mol Med. 2013 Feb;31(2):407-15. doi: 10.3892/ijmm.2012.1199. Epub 2012 Nov 30.
6
Migration of culture-expanded human mesenchymal stem cells through bone marrow endothelium is regulated by matrix metalloproteinase-2 and tissue inhibitor of metalloproteinase-3.经培养扩增的人间充质干细胞穿过骨髓内皮的迁移受基质金属蛋白酶-2和金属蛋白酶组织抑制剂-3调控。
Haematologica. 2007 Apr;92(4):440-9. doi: 10.3324/haematol.10475.
7
Enhancing Retention of Human Bone Marrow Mesenchymal Stem Cells with Prosurvival Factors Promotes Angiogenesis in a Mouse Model of Limb Ischemia.使用生存促进因子增强人骨髓间充质干细胞的保留可促进肢体缺血小鼠模型中的血管生成。
Stem Cells Dev. 2019 Jan 15;28(2):114-119. doi: 10.1089/scd.2018.0090. Epub 2018 Dec 18.
8
Comparison of angiogenic potency between mesenchymal stem cells and mononuclear cells in a rat model of hindlimb ischemia.大鼠后肢缺血模型中间充质干细胞与单核细胞血管生成能力的比较。
Cardiovasc Res. 2005 Jun 1;66(3):543-51. doi: 10.1016/j.cardiores.2005.02.006. Epub 2005 Mar 2.
9
Fat extract promotes angiogenesis in a murine model of limb ischemia: a novel cell-free therapeutic strategy.脂肪提取物促进肢体缺血模型中的血管生成:一种新型的无细胞治疗策略。
Stem Cell Res Ther. 2018 Nov 8;9(1):294. doi: 10.1186/s13287-018-1014-y.
10
Monitoring of diffusion properties and transverse relaxation time of mouse ischaemic muscle after administration of human mesenchymal stromal cells derived from adipose tissue.监测人脂肪来源间充质基质细胞给药后小鼠缺血肌肉的扩散性质和横向弛豫时间。
Cell Prolif. 2019 Nov;52(6):e12672. doi: 10.1111/cpr.12672. Epub 2019 Aug 23.

引用本文的文献

1
Categories, applications, and potential of stem cells in bone regeneration: an overview.干细胞在骨再生中的分类、应用及潜力:综述
Front Med (Lausanne). 2025 Aug 20;12:1606100. doi: 10.3389/fmed.2025.1606100. eCollection 2025.
2
Therapeutic Potential of Local and Systemic Adipose-Derived Mesenchymal Stem Cell Injections in a Rat Model of Experimental Periodontitis: Implications for Cardiac Function.局部和全身注射脂肪来源间充质干细胞在实验性牙周炎大鼠模型中的治疗潜力:对心脏功能的影响
Int J Mol Sci. 2025 Apr 23;26(9):3984. doi: 10.3390/ijms26093984.
3
Development and Validation of a Multiparametric Semiquantitative Scoring System for the Histopathological Assessment of Ischaemia Severity in Skeletal Muscle.
用于骨骼肌缺血严重程度组织病理学评估的多参数半定量评分系统的开发与验证
J Tissue Eng Regen Med. 2023 Mar 16;2023:5592455. doi: 10.1155/2023/5592455. eCollection 2023.
4
Systematic review and meta-analysis of the effect of bone marrow-derived cell therapies on hind limb perfusion.系统评价和骨髓细胞疗法对下肢灌注影响的荟萃分析。
Dis Model Mech. 2024 May 1;17(5). doi: 10.1242/dmm.050632. Epub 2024 May 24.
5
In Vitro Enhanced Osteogenic Potential of Human Mesenchymal Stem Cells Seeded in a Poly (Lactic--Glycolic) Acid Scaffold: A Systematic Review.聚(乳酸-乙醇酸)酸支架接种人骨髓间充质干细胞的体外成骨潜能增强:一项系统评价
Craniomaxillofac Trauma Reconstr. 2024 Mar;17(1):61-73. doi: 10.1177/19433875231157454. Epub 2023 Feb 13.
6
The comparison of adipose-derived stromal cells (ADSCs) delivery method in a murine model of hindlimb ischemia.脂肪来源的基质细胞(ADSCs)在小鼠后肢缺血模型中的递送方法比较。
Stem Cell Res Ther. 2024 Feb 2;15(1):27. doi: 10.1186/s13287-024-03634-2.
7
Adipose-derived Mesenchymal Stem Cells are Ideal for the Cell-based Treatment of Refractory Wounds: Strong Potential for Angiogenesis.脂肪来源间充质干细胞是治疗难治性创面的理想细胞疗法:具有很强的血管生成潜力。
Stem Cell Rev Rep. 2024 Jan;20(1):313-328. doi: 10.1007/s12015-023-10641-y. Epub 2023 Oct 24.
8
Proliferation-Related Features of the Human Mesenchymal Stem Cells Derived from Palatine Tonsils, Adipose Tissues, and Bone Marrow.人腭扁桃体、脂肪组织和骨髓间充质干细胞的增殖相关特征。
Tissue Eng Regen Med. 2023 Dec;20(7):1119-1132. doi: 10.1007/s13770-023-00564-7. Epub 2023 Aug 18.
9
Stem cell transplantation therapy for diabetic foot ulcer: a narrative review.糖尿病足溃疡的干细胞移植治疗:一项叙述性综述。
Asian Biomed (Res Rev News). 2021 Feb 21;15(1):3-18. doi: 10.2478/abm-2021-0002. eCollection 2021 Feb.
10
Anti-aging mechanism of different age donor-matched adipose-derived stem cells.不同年龄供体匹配脂肪来源干细胞的抗衰老机制。
Stem Cell Res Ther. 2023 Aug 2;14(1):192. doi: 10.1186/s13287-023-03415-3.