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经冠状动脉内注射间充质干细胞衍生的生长因子可改善梗死心脏的功能和心肌修复。

Improved function and myocardial repair of infarcted heart by intracoronary injection of mesenchymal stem cell-derived growth factors.

机构信息

Cardiac Surgery, Montreal University Hospital Centre (CHUM), Montreal, QC, Canada.

出版信息

J Cardiovasc Transl Res. 2010 Oct;3(5):547-58. doi: 10.1007/s12265-010-9171-0. Epub 2010 Feb 26.

Abstract

Transplantation of mesenchymal stem cells (MSC) improves repair and function recovery following myocardial infarction (MI), but underlying mechanisms remain to be elucidated. We hypothesize that MSC could achieve protection by paracrine effects through released mediators rather than direct cardiac regeneration. We sought to characterize the effects of MSC-secreted growth factors on extent of early recovery from MI. Swine subjected to acute MI by temporary balloon occlusion of the left anterior descending coronary artery using percutaneous techniques received intracoronary injection of either concentrated MSC-derived growth factors or control medium. Animals were killed at 7 days to evaluate early effects. Treatment with MSC-derived factors significantly reduced cardiac troponin-T elevation and improved echocardiographic parameters, including fractional area shortening, stroke volume, cardiac output, and wall motion score index. Quantitative evaluation of fibrosis by Verhoff staining revealed a reduction of the fibrotic area in the infarcted zone. Similarly, Masson's trichrome staining revealed reduced myocardial damage as demonstrated by areas of relatively preserved myocardium in the infarcted area. TUNEL assay demonstrated less cardiomyocyte apoptosis. Protein array detected the presence of angiogenic (vascular endothelial growth factor, endothelin, and epiregulin), anti-apoptotic (Galectin-3, Smad-5, sRFP-1, and sRFP-4) and anti-remodeling factors. Reverse transcription polymerase chain reaction confirmed the expression of these factors. In summary, a single intracoronary injection of concentrated biologically active factors secreted by MSC could achieve early protection of ischemic myocardium and improve cardiac repair and contractility. MSC-derived growth factors injection (rather than MSC themselves) should be evaluated as a novel therapy to treat ischemic heart disease, avoiding many practical and technical issues of cell therapy.

摘要

间充质干细胞(MSC)移植可改善心肌梗死(MI)后的修复和功能恢复,但潜在机制仍需阐明。我们假设 MSC 可以通过释放的介质发挥旁分泌作用来实现保护,而不是直接进行心脏再生。我们试图描述 MSC 分泌的生长因子对 MI 早期恢复程度的影响。通过经皮技术暂时闭塞左前降支冠状动脉,使猪发生急性 MI,然后通过冠状动脉内注射浓缩的 MSC 衍生生长因子或对照培养基。在 7 天时处死动物,以评估早期影响。用 MSC 衍生的因子处理可显著降低心肌肌钙蛋白 T 的升高,并改善超声心动图参数,包括射血分数缩短率、每搏输出量、心输出量和室壁运动评分指数。通过 Verhoff 染色进行纤维化的定量评估显示,梗死区的纤维化面积减少。同样,Masson 三色染色显示梗死区相对保留的心肌区域较多,表明心肌损伤减少。TUNEL 检测表明心肌细胞凋亡减少。蛋白芯片检测到了血管生成(血管内皮生长因子、内皮素和表皮调节素)、抗凋亡(半乳糖凝集素-3、Smad-5、sRFP-1 和 sRFP-4)和抗重塑因子。逆转录聚合酶链反应证实了这些因子的表达。总之,单次冠状动脉内注射浓缩的 MSC 分泌的具有生物活性的因子可实现缺血心肌的早期保护,并改善心脏修复和收缩功能。应评估 MSC 衍生生长因子注射(而不是 MSC 本身)作为治疗缺血性心脏病的一种新疗法,从而避免细胞治疗的许多实际和技术问题。

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