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足突细胞样蛋白1是人类c-kit(阳性)心脏干细胞的相关标志物。

Podocalyxin-like protein 1 is a relevant marker for human c-kit(pos) cardiac stem cells.

作者信息

Moscoso Isabel, Tejados Naiara, Barreiro Olga, Sepúlveda Pilar, Izarra Alberto, Calvo Enrique, Dorronsoro Akaitz, Salcedo Juan Manuel, Sádaba Rafael, Díez-Juan Antonio, Trigueros César, Bernad Antonio

机构信息

Cardiovascular Development and Repair, Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid, Spain.

Inbiomed Foundation, San Sebastian, Spain.

出版信息

J Tissue Eng Regen Med. 2016 Jul;10(7):580-90. doi: 10.1002/term.1795. Epub 2013 Jul 30.

Abstract

Cardiac progenitor cells (CPCs) from adult myocardium offer an alternative cell therapy approach for ischaemic heart disease. Improved clinical performance of CPCs in clinical trials requires a comprehensive definition of their biology and specific interactions with the environment. In this work we characterize specific human CPC surface markers and study some of their related functions. c-kit(pos) human CPCs (hCPCs) were characterized for cell surface marker expression, pluripotency, early and late cardiac differentiation markers and therapeutic activity in a rat model of acute myocardial infarction. The results indicate that hCPCs are a mesenchymal stem cell (MSC)-like population, with a similar immunoregulatory capacity. A partial hCPC membrane proteome was analysed by liquid chromatography-mass spectrometry/mass spectrometry and 36 proteins were identified. Several, including CD26, myoferlin and podocalyxin-like protein 1 (PODXL), have been previously described in other stem-cell systems. Suppression and overexpression analysis demonstrated that PODXL regulates hCPC activation, migration and differentiation; it also modulates their local immunoregulatory capacity. Therefore, hCPCs are a resident cardiac population that shares many features with hMSCs, including their capacity for local immunoregulation. Expression of PODXL appears to favour the immature state of hCPCs, while its downregulation facilitates their differentiation. Copyright © 2016 John Wiley & Sons, Ltd.

摘要

来自成年心肌的心脏祖细胞(CPCs)为缺血性心脏病提供了一种替代性的细胞治疗方法。在临床试验中提高CPCs的临床疗效需要全面定义其生物学特性以及与环境的特定相互作用。在这项研究中,我们对特定的人类CPC表面标志物进行了表征,并研究了它们的一些相关功能。对c-kit阳性人类CPCs(hCPCs)进行了细胞表面标志物表达、多能性、早期和晚期心脏分化标志物以及急性心肌梗死大鼠模型中的治疗活性的表征。结果表明,hCPCs是一种间充质干细胞(MSC)样群体,具有相似的免疫调节能力。通过液相色谱-质谱联用/质谱对部分hCPC膜蛋白质组进行了分析,鉴定出36种蛋白质。其中几种,包括CD26、肌铁蛋白和足突蛋白样蛋白1(PODXL),此前已在其他干细胞系统中有所描述。抑制和过表达分析表明,PODXL调节hCPC的激活、迁移和分化;它还调节其局部免疫调节能力。因此,hCPCs是一种驻留心脏群体,与hMSCs有许多共同特征,包括其局部免疫调节能力。PODXL的表达似乎有利于hCPCs的未成熟状态,而其下调则促进其分化。版权所有© 2016约翰威立父子有限公司。

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