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J Thromb Thrombolysis. 2014 Jan;37(1):24-31. doi: 10.1007/s11239-013-1032-7.
2
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本文引用的文献

1
Bioactive lipids and cationic antimicrobial peptides as new potential regulators for trafficking of bone marrow-derived stem cells in patients with acute myocardial infarction.生物活性脂质和阳离子抗菌肽作为急性心肌梗死后骨髓源性干细胞归巢的新的潜在调控因子。
Stem Cells Dev. 2013 Jun 1;22(11):1645-56. doi: 10.1089/scd.2012.0488. Epub 2013 Feb 19.
2
Cardiomyogenesis in the aging and failing human heart.衰老和衰竭人心肌生成。
Circulation. 2012 Oct 9;126(15):1869-81. doi: 10.1161/CIRCULATIONAHA.112.118380. Epub 2012 Sep 6.
3
S1P promotes murine progenitor cell egress and mobilization via S1P1-mediated ROS signaling and SDF-1 release.S1P 通过 S1P1 介导的 ROS 信号和 SDF-1 释放促进小鼠祖细胞迁出和动员。
Blood. 2012 Mar 15;119(11):2478-88. doi: 10.1182/blood-2011-06-358614. Epub 2012 Jan 25.
4
Therapeutic siRNA silencing in inflammatory monocytes in mice.在小鼠的炎症单核细胞中进行治疗性 siRNA 沉默。
Nat Biotechnol. 2011 Oct 9;29(11):1005-10. doi: 10.1038/nbt.1989.
5
The bone marrow-expressed antimicrobial cationic peptide LL-37 enhances the responsiveness of hematopoietic stem progenitor cells to an SDF-1 gradient and accelerates their engraftment after transplantation.骨髓表达的抗菌阳离子肽 LL-37 增强了造血干细胞祖细胞对 SDF-1 梯度的反应性,并加速了移植后的植入。
Leukemia. 2012 Apr;26(4):736-45. doi: 10.1038/leu.2011.252. Epub 2011 Sep 20.
6
Mobilization of stem and progenitor cells in cardiovascular diseases.心血管疾病中的干细胞和祖细胞动员。
Leukemia. 2012 Jan;26(1):23-33. doi: 10.1038/leu.2011.184. Epub 2011 Jul 26.
7
Conditioning for hematopoietic transplantation activates the complement cascade and induces a proteolytic environment in bone marrow: a novel role for bioactive lipids and soluble C5b-C9 as homing factors.造血移植的预处理会激活补体级联反应,并在骨髓中诱导产生蛋白水解环境:生物活性脂质和可溶性 C5b-C9 作为归巢因子的新作用。
Leukemia. 2012 Jan;26(1):106-16. doi: 10.1038/leu.2011.185. Epub 2011 Jul 19.
8
Rapid mobilization of hematopoietic progenitors by AMD3100 and catecholamines is mediated by CXCR4-dependent SDF-1 release from bone marrow stromal cells.AMD3100 和儿茶酚胺通过 CXCR4 依赖性 SDF-1 从骨髓基质细胞释放来快速动员造血祖细胞。
Leukemia. 2011 Aug;25(8):1286-1296. doi: 10.1038/leu.2011.62. Epub 2011 Apr 15.
9
Bone marrow-derived cell therapy stimulates endogenous cardiomyocyte progenitors and promotes cardiac repair.骨髓细胞疗法刺激内源性心肌祖细胞并促进心脏修复。
Cell Stem Cell. 2011 Apr 8;8(4):389-98. doi: 10.1016/j.stem.2011.02.002.
10
The ins and outs of hematopoietic stem cells: studies to improve transplantation outcomes.造血干细胞的来龙去脉:改善移植结果的研究。
Stem Cell Rev Rep. 2011 Sep;7(3):590-607. doi: 10.1007/s12015-010-9212-8.

生物活性脂质在心肌缺血期间干细胞动员中的新作用:血栓形成的新范例:新型介质和生物标志物。

A novel role for bioactive lipids in stem cell mobilization during cardiac ischemia: new paradigms in thrombosis: novel mediators and biomarkers.

机构信息

Gill Heart Institute, Lexington, KY, USA.

出版信息

J Thromb Thrombolysis. 2014 Jan;37(1):24-31. doi: 10.1007/s11239-013-1032-7.

DOI:10.1007/s11239-013-1032-7
PMID:24318213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4050642/
Abstract

Despite major advances in pharmacological and reperfusion therapies, regenerating and/or replacing the infarcted myocardial tissue is an enormous challenge and therefore ischemic heart disease (IHD) remains a major cause of mortality and morbidity worldwide. Adult bone marrow is home for a variety of hematopoietic and non-hematopoietic stem cells including a small subset of primitive cells that carry a promising regenerative potential. It is now well established that myocardial ischemia (MI) induces mobilization of bone marrow-derived cells including differentiated lineage as well as undifferentiated stem cells. While the numbers of stem cells carrying pluripotent features among the mobilized stem cells is small, their regenerative capacity appears immense. Therapies aimed at selective mobilization of these pluripotent stem cells during myocardial ischemia have a promising potential to regenerate the injured myocardium. Emerging evidence suggest that bioactive sphingolipids such as sphingosine-1-phosphate and ceramide-1-phosphate hold a great promise in selective mobilization of pluripotent stem cells to the infarcted region during MI. This review highlights the recent advances in the mechanisms of stem cell mobilization and provides newer evidence in support of bioactive lipids as potential therapeutic agents in the treatment of ischemic heart disease.

摘要

尽管在药理学和再灌注治疗方面取得了重大进展,但再生和/或替换梗死的心肌组织仍然是一个巨大的挑战,因此缺血性心脏病(IHD)仍然是全球死亡和发病的主要原因。成人骨髓是各种造血和非造血干细胞的家园,包括一小部分具有有前途的再生潜力的原始细胞。现在已经确定,心肌缺血(MI)会诱导骨髓来源的细胞包括分化谱系以及未分化的干细胞动员。虽然动员的干细胞中具有多能特征的干细胞数量很少,但它们的再生能力似乎很大。旨在选择性动员这些多能干细胞的治疗方法在心肌缺血期间具有很大的潜力来再生受损的心肌。新出现的证据表明,生物活性鞘脂,如鞘氨醇-1-磷酸和神经酰胺-1-磷酸,在 MI 期间将多能干细胞选择性动员到梗死区域方面具有很大的潜力。这篇综述强调了干细胞动员的机制的最新进展,并提供了新的证据支持生物活性脂质作为治疗缺血性心脏病的潜在治疗剂。