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中华细胞与干细胞杂志(电子版) ›› 2022, Vol. 12 ›› Issue (02) : 105 -109. doi: 10.3877/cma.j.issn.2095-1221.2022.02.007

综述

静脉输注间充质干细胞治疗缺血性心脏病的研究进展
齐婷婷1, 许晓明1, 夏云龙1, 郭永珍1, 樊苗苗1, 贺媛1, 陈迈1, 陶凌1, 闫文俊1, 范延红1,()   
  1. 1. 710032 西安,空军军医大学西京医院心血管内科
  • 收稿日期:2021-09-09 出版日期:2022-04-01
  • 通信作者: 范延红
  • 基金资助:
    国家重点研发计划(2018YFA0107400); 国家自然科学基金优秀青年科学基金(82022004); 国家自然科学基金面上项目(81970212); 国家自然科学基金青年项目(81900241、82100362)

Research progress of intravenous infusion of mesenchymal stromal cells in the treatment of ischemic heart disease

Tingting Qi1, Xiaoming Xu1, Yunlong Xia1, Yongzhen Guo1, Miaomiao Fan1, Yuan He1, Mai Chen1, Ling Tao1, Wenjun Yan1, Yanhong Fan1,()   

  1. 1. Department of Cardiology, Xijing Hospital of Air Force Military Medical University, Xi'an 710032, China
  • Received:2021-09-09 Published:2022-04-01
  • Corresponding author: Yanhong Fan
引用本文:

齐婷婷, 许晓明, 夏云龙, 郭永珍, 樊苗苗, 贺媛, 陈迈, 陶凌, 闫文俊, 范延红. 静脉输注间充质干细胞治疗缺血性心脏病的研究进展[J]. 中华细胞与干细胞杂志(电子版), 2022, 12(02): 105-109.

Tingting Qi, Xiaoming Xu, Yunlong Xia, Yongzhen Guo, Miaomiao Fan, Yuan He, Mai Chen, Ling Tao, Wenjun Yan, Yanhong Fan. Research progress of intravenous infusion of mesenchymal stromal cells in the treatment of ischemic heart disease[J]. Chinese Journal of Cell and Stem Cell(Electronic Edition), 2022, 12(02): 105-109.

缺血性心脏病(IHD)是一种高危凶险的疾病。近年来,间充质干细胞(MSCs)因具有心肌保护作用和低免疫原性,在IHD治疗中的潜力越来越受到人们关注。MSCs治疗IHD的移植途径包括心肌内注射、冠状血管注射和静脉注射,其中静脉注射侵入性最低,可多次注射,但存在心肌靶向归巢率低的问题,导致心肌保护作用不佳。如何提高静脉注射MSCs的心肌靶向归巢率是提高MSCs心肌保护的关键问题,也是目前研究的热点。本文总结了MSCs在IHD治疗中的现状,静脉注射MSCs心肌靶向归巢的研究进展,并探讨静脉注射MSCs在临床应用中的前景。

Ischemic heart disease (IHD) is one of the dangerous and severe disease. Recently, mesenchymal stromal cells (MSCs) have been more popular in the treatment of IHD due to their cardioprotective effect and low immunogenicity. The routes of MSCs transplantation for IHD therapy include intramyocardial injection, coronary artery/vein injection, and intravenous injection. Intravenous delivery is the least invasive and can be done multiple times. However, the problem of low homing rate of targeted myocardium may lead to poor myocardial protection. How to improve the targeted cardiac homing of intravenously injected MSCs is the key problem to improve the cardioprotection of MSCs, and it becomes more popular at present. The paper summarizes the status quo of MSCs in IHD treatment, research progress of the myocardial homing of intravenous MSCs, and the clinical application of intravenously injected MSCs for IHD.

图1 MSCs向缺血心肌靶向归巢的5个步骤注:Galectin为半乳糖凝集素;P-selectin为P-选择素;CCR2为趋化因子C-C-基元受体2;CXCR4、7为C-X-C趋化因子受体4、7;MCP1、3为单核细胞趋化蛋白1、3;SDF-1为基质细胞衍生因子-1;VCAM-1为血管细胞黏附分子-1;ICAM-1为细胞间黏附分子1;VLA4为迟现抗原4;TIMP2、3为组织金属蛋白酶抑制因子2、3;MMP2、9为基质金属蛋白酶2、9;MT1-MMP为膜型基质金属蛋白酶;PDGF-AB为血小板衍化生长因子-AB;IGF-1为胰岛素样生长因子1;RANTES又称CCL5,趋化因子C-C基元配体5
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