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本文引用的文献

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NDRG2: a newly identified mediator of insulin cardioprotection against myocardial ischemia-reperfusion injury.NDRG2:一种新发现的胰岛素心肌缺血再灌注损伤保护作用的中介物。
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Adipose stromal cells primed with hypoxia and inflammation enhance cardiomyocyte proliferation rate in vitro through STAT3 and Erk1/2.缺氧和炎症预处理的脂肪基质细胞通过 STAT3 和 Erk1/2 增强体外心肌细胞的增殖率。
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Sca-1-positive cardiac stem cell migration in a cardiac infarction model.Sca-1 阳性心脏干细胞在心肌梗死模型中的迁移。
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Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury.间充质干细胞衍生的外泌体可提高三磷酸腺苷(ATP)水平,降低氧化应激,并激活磷脂酰肌醇-3-激酶/蛋白激酶B(PI3K/Akt)信号通路,从而增强心肌活力,预防心肌缺血/再灌注损伤后的不良重塑。
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Rosuvastatin enhances the therapeutic efficacy of adipose-derived mesenchymal stem cells for myocardial infarction via PI3K/Akt and MEK/ERK pathways.瑞舒伐他汀通过 PI3K/Akt 和 MEK/ERK 通路增强脂肪间充质干细胞治疗心肌梗死的疗效。
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mTORC1 inhibition restricts inflammation-associated gastrointestinal tumorigenesis in mice.mTORC1 抑制限制了小鼠炎症相关的胃肠道肿瘤发生。
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Cardiomyocyte proliferation contributes to heart growth in young humans.心肌细胞增殖有助于人类幼体心脏生长。
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9
Human mesenchymal stem cell grafts enhance normal and impaired wound healing by recruiting existing endogenous tissue stem/progenitor cells.人间质干细胞移植物通过募集现有的内源性组织干细胞/祖细胞增强正常和受损的伤口愈合。
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Mammalian heart renewal by pre-existing cardiomyocytes.哺乳动物的心肌再生由预先存在的心肌细胞完成。
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适应炎症微环境的细胞再生治疗缺血性心血管疾病。

Adaptive inflammatory microenvironment for cell-based regeneration in ischemic cardiovascular disease.

机构信息

Department of Cardiology & Molecular Imaging Program; Xijing Hospital; Fourth Military Medical University; Xi'an, PR China.

出版信息

Organogenesis. 2013 Jul-Sep;9(3):121-4. doi: 10.4161/org.25586. Epub 2013 Jul 3.

DOI:10.4161/org.25586
PMID:23974172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3896581/
Abstract

Cell-based therapy has emerged to be a promising strategy for alleviating the heavy burden of ischemic cardiovascular disease for nearly two decades, despite a variety of pending questions about its availability and efficacy. One question is whether and how the cells behave for regeneration in vivo, which could be limited or potentiated by the inflammatory microenvironment following myocardial infarction or critical limb ischemia. To this end, we hypothesize that the "adaptive inflammatory microenvironment" is pertinent to the cell-based regeneration, and make a brief comment on it based upon recent evidence.

摘要

细胞治疗作为一种有前途的策略,近二十年来已经出现,旨在缓解缺血性心血管疾病的沉重负担,尽管关于其可用性和疗效仍存在许多悬而未决的问题。其中一个问题是细胞在体内是否以及如何进行再生,这可能受到心肌梗死或严重肢体缺血后炎症微环境的限制或增强。为此,我们假设“适应性炎症微环境”与基于细胞的再生有关,并根据最近的证据对此进行简要评论。