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单核细胞募集阻断与间充质干细胞移植协同治疗心肌梗死。

Monocytes recruitment blocking synergizes with mesenchymal stem cell transplantation for treating myocardial infarction.

作者信息

Wang Qian, Wang Ke, Zhao Xianxian

机构信息

Department of Cardiology, Changhai Hospital, Naval Medical University, No.168 Changhai Road, Shanghai 200433, China.

出版信息

Regen Med. 2021 Jan;16(1):9-17. doi: 10.2217/rme-2020-0047. Epub 2021 Feb 9.

DOI:10.2217/rme-2020-0047
PMID:33560157
Abstract

Mesenchymal stem cell (MSC) transplantation is a promising therapeutic approach for acute myocardial infarction (AMI), however, research to date has demonstrated unsatisfactory results. An AMI mouse model was established via left coronary artery ligation. AMI mice were treated with MSCs, anti-CCR2 or MSCs + anti-CCR2 and the effects of each treatment group were compared. Macrophage infiltration was analyzed by immunofluorescence staining and flow cytometry. Implantation of MSCs + anti-CCR2 yielded a greater improvement in cardiac function and significantly reduced macrophage accumulation in the infarct site of AMI mice compared with the injection of MSCs or anti-CCR2 alone. Moreover, reduced macrophage infiltration was accompanied by reduced pro-inflammatory cytokine secretion in the injury sites and the low inflammatory response favored tissue regeneration. Treatment with MSCs and anti-CCR2 in combination may be a promising therapeutic strategy for AMI.

摘要

间充质干细胞(MSC)移植是治疗急性心肌梗死(AMI)的一种很有前景的治疗方法,然而,迄今为止的研究结果并不理想。通过左冠状动脉结扎建立AMI小鼠模型。用MSC、抗CCR2或MSC +抗CCR2治疗AMI小鼠,并比较各治疗组的效果。通过免疫荧光染色和流式细胞术分析巨噬细胞浸润情况。与单独注射MSC或抗CCR2相比,植入MSC +抗CCR2能使AMI小鼠的心脏功能有更大改善,并显著减少梗死部位的巨噬细胞聚集。此外,巨噬细胞浸润减少伴随着损伤部位促炎细胞因子分泌减少,且低炎症反应有利于组织再生。联合使用MSC和抗CCR2治疗可能是一种有前景的AMI治疗策略。

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Monocytes recruitment blocking synergizes with mesenchymal stem cell transplantation for treating myocardial infarction.单核细胞募集阻断与间充质干细胞移植协同治疗心肌梗死。
Regen Med. 2021 Jan;16(1):9-17. doi: 10.2217/rme-2020-0047. Epub 2021 Feb 9.
2
Photoluminescent Mesoporous Silicon Nanoparticles with siCCR2 Improve the Effects of Mesenchymal Stromal Cell Transplantation after Acute Myocardial Infarction.具有siCCR2的光致发光介孔硅纳米颗粒改善急性心肌梗死后间充质基质细胞移植的效果。
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Effect of intravenous transplantation of hUCB-MSCs on M1/M2 subtype conversion in monocyte/macrophages of AMI mice.静脉移植人脐带来源间充质干细胞对 AMI 小鼠单核细胞/巨噬细胞 M1/M2 亚型转化的影响。
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Combinatorial treatment of acute myocardial infarction using stem cells and their derived exosomes resulted in improved heart performance.联合应用干细胞及其衍生的外泌体治疗急性心肌梗死可改善心脏功能。
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Macrophage subpopulations are essential for infarct repair with and without stem cell therapy.巨噬细胞亚群对于梗死修复是必不可少的,无论是否进行干细胞治疗。
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Induction of a monocyte/macrophage phenotype switch by mesenchymal stem cells might contribute to improved infarct healing postacute myocardial infarction.间充质干细胞诱导单核细胞/巨噬细胞表型转换可能有助于改善急性心肌梗死后的梗死愈合。
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Intravenous injection of allogeneic umbilical cord-derived multipotent mesenchymal stromal cells reduces the infarct area and ameliorates cardiac function in a porcine model of acute myocardial infarction.静脉注射同种异体脐带源多能间充质基质细胞可减少猪急性心肌梗死模型的梗死面积并改善心功能。
Stem Cell Res Ther. 2018 May 11;9(1):129. doi: 10.1186/s13287-018-0888-z.

引用本文的文献

1
Monocytes presenting a pro-inflammatory profile persist in patients submitted to a long-term pharmacological treatment after acute myocardial infarction.在急性心肌梗死后接受长期药物治疗的患者中,呈现促炎特征的单核细胞持续存在。
Front Physiol. 2023 Jan 20;13:1056466. doi: 10.3389/fphys.2022.1056466. eCollection 2022.
2
Identification of GLS as a cuproptosis-related diagnosis gene in acute myocardial infarction.鉴定谷氨酸盐代谢酶作为急性心肌梗死中与铜死亡相关的诊断基因。
Front Cardiovasc Med. 2022 Nov 11;9:1016081. doi: 10.3389/fcvm.2022.1016081. eCollection 2022.
3
Strategies to Overcome the Barrier of Ischemic Microenvironment in Cell Therapy of Cardiovascular Disease.
克服细胞治疗心血管疾病中缺血微环境障碍的策略。
Int J Mol Sci. 2021 Feb 25;22(5):2312. doi: 10.3390/ijms22052312.