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胸腺素 β4 与心脏再生:我们是否错失了关键?

Thymosin β4 and cardiac regeneration: are we missing a beat?

机构信息

Cardiovascular Regenerative Medicine, Cardiovascular Research Center, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1030, New York, NY 10029, USA.

出版信息

Stem Cell Rev Rep. 2013 Jun;9(3):303-12. doi: 10.1007/s12015-012-9378-3.

Abstract

Epicardial resident stem cells are known to differentiate into cardiomyocytes during cardiac development, amongst other cell types. Whether epicardium-derived progenitor cells (EPDCs) retain this plasticity in the adult heart has been the topic of heated scientific debate. Priming with thymosin beta 4, a peptide which has been suggested to be critical for cardiac development and to have cardio-protective properties, was recently shown to induce differentiation of EPDCs into cardiomyocytes in a small animal model of myocardial infarction. This finding is in stark contrast to another recent study in which thymosin beta 4 treatment following myocardial infarction did not induce cardiomyocyte differentiation of EPDCs. While EPDCs seem to exhibit overall cardio-protective effects on the heart following myocardial infarction, they have not been shown to differentiate into cardiomyocytes in a clinically relevant setting. It will be important to understand why the ability of one therapeutic agent to induce cardiomyocyte differentiation of EPDCs seemingly depends on a single variable, i.e. the time of administration. Furthermore, in light of a recent report, it appears that thymosin beta 4 may be dispensable for cardiac development.

摘要

心外膜常驻干细胞在心脏发育过程中可分化为心肌细胞以及其他类型的细胞。心外膜衍生祖细胞(EPDC)在成人心脏中是否保留这种可塑性一直是激烈科学争论的主题。最近的一项研究表明,用胸腺肽β4(一种被认为对心脏发育至关重要且具有心脏保护特性的肽)进行预处理,可以在心肌梗死的小动物模型中诱导 EPDC 分化为心肌细胞。这一发现与另一项最近的研究形成鲜明对比,即在心肌梗死后使用胸腺肽β4 治疗并未诱导 EPDC 的心肌细胞分化。虽然 EPDC 在心肌梗死后对心脏表现出总体的心脏保护作用,但它们尚未在临床相关环境中分化为心肌细胞。了解为什么一种治疗剂诱导 EPDC 分化为心肌细胞的能力似乎取决于一个单一变量(即给药时间)非常重要。此外,鉴于最近的一份报告,胸腺肽β4 似乎对于心脏发育并非必需。

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