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本文引用的文献

1
Hippo pathway effectors control cardiac progenitor cell fate by acting as dynamic sensors of substrate mechanics and nanostructure.Hippo 通路效应物通过作为基质力学和纳米结构的动态传感器来控制心脏祖细胞的命运。
ACS Nano. 2014 Mar 25;8(3):2033-47. doi: 10.1021/nn4058984. Epub 2014 Feb 7.
2
Human umbilical cord tissue-derived mesenchymal stromal cells attenuate remodeling after myocardial infarction by proangiogenic, antiapoptotic, and endogenous cell-activation mechanisms.人脐带组织来源的间充质基质细胞通过促血管生成、抗凋亡和内源性细胞激活机制减轻心肌梗死后的重塑。
Stem Cell Res Ther. 2014 Jan 10;5(1):5. doi: 10.1186/scrt394.
3
Stable phenotype and function of immortalized Lin-Sca-1+ cardiac progenitor cells in long-term culture: a step closer to standardization.永生化Lin-Sca-1+心脏祖细胞在长期培养中的稳定表型和功能:向标准化迈进了一步。
Stem Cells Dev. 2014 May 1;23(9):1012-26. doi: 10.1089/scd.2013.0305. Epub 2014 Feb 14.
4
Tissue-resident Sca1+ PDGFRα+ mesenchymal progenitors are the cellular source of fibrofatty infiltration in arrhythmogenic cardiomyopathy.组织驻留Sca1+ PDGFRα+间充质祖细胞是致心律失常性心肌病中纤维脂肪浸润的细胞来源。
F1000Res. 2013 Jun 19;2:141. doi: 10.12688/f1000research.2-141.v1. eCollection 2013.
5
Distinct fibroblast lineages determine dermal architecture in skin development and repair.不同的成纤维细胞谱系决定了皮肤发育和修复过程中的皮肤结构。
Nature. 2013 Dec 12;504(7479):277-281. doi: 10.1038/nature12783.
6
Sca1-derived cells are a source of myocardial renewal in the murine adult heart.Sca1 阳性细胞是成年鼠心脏再生的细胞来源。
Stem Cell Reports. 2013 Oct 24;1(5):397-410. doi: 10.1016/j.stemcr.2013.09.004. eCollection 2013.
7
Origin, development, and differentiation of cardiac fibroblasts.心脏成纤维细胞的起源、发展和分化。
J Mol Cell Cardiol. 2014 May;70:2-8. doi: 10.1016/j.yjmcc.2013.11.003. Epub 2013 Nov 11.
8
Direct isolation of myofibroblasts and fibroblasts from bleomycin-injured lungs reveals their functional similarities and differences.从博来霉素损伤的肺中直接分离肌成纤维细胞和成纤维细胞,揭示了它们在功能上的异同。
Fibrogenesis Tissue Repair. 2013 Aug 8;6(1):15. doi: 10.1186/1755-1536-6-15.
9
Progenitor cells identified by PDGFR-alpha expression in the developing and diseased human heart.在发育中和病变的人心肌中通过 PDGFR-α 表达鉴定的祖细胞。
Stem Cells Dev. 2013 Jul 1;22(13):1932-43. doi: 10.1089/scd.2012.0542. Epub 2013 Mar 26.
10
Cardiomyocyte proliferation and progenitor cell recruitment underlie therapeutic regeneration after myocardial infarction in the adult mouse heart.心肌细胞增殖和祖细胞募集是成年鼠心肌梗死后治疗性再生的基础。
EMBO Mol Med. 2013 Feb;5(2):191-209. doi: 10.1002/emmm.201201737. Epub 2013 Jan 29.

Sca-1+心脏祖细胞与心脏形成:关键概述

Sca-1+ cardiac progenitor cells and heart-making: a critical synopsis.

作者信息

Valente Mariana, Nascimento Diana Santos, Cumano Ana, Pinto-do-Ó Perpétua

机构信息

1 Stem-Cell Microenvironments in Repair/Regeneration Team, Microenvironments for NewTherapies Group, INEB-Instituto Nacional de Engenharia Biomédica, Universidade do Porto , Porto, Portugal .

出版信息

Stem Cells Dev. 2014 Oct 1;23(19):2263-73. doi: 10.1089/scd.2014.0197. Epub 2014 Jul 14.

DOI:10.1089/scd.2014.0197
PMID:24926741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4172562/
Abstract

The identification, in the adult, of cardiomyocyte turnover events and of cardiac progenitor cells (CPCs) has revolutionized the field of cardiovascular medicine. However, the low rate of CPCs differentiation events reported both in vitro and in vivo, even after injury, raised concerns on the biological significance of these subsets. In this Comprehensive Review, we discuss the current understanding of cardiac Lin(-)Sca-1(+) cells in light of what is also known for cellular compartments with similar phenotypes in other organs. The Lin(-)Sca-1(+) heart subset is heterogeneous and displays a mesenchymal profile, characterized by a limited ability to generate cardiomyocytes in vitro and in vivo, even after injury. There is no evidence for Sca-1 expression in embryonic cardiovascular progenitors. In other organs, Sca-1 expression is mainly observed on mesoderm-derived cells, although it is not restricted to stem/progenitor cell populations. It is urgent to determine, at a single cell level, to which extent cardiac Lin(-)Sca-1(+) cells overlap with the fibroblast compartment.

摘要

在成体中对心肌细胞更新事件和心脏祖细胞(CPCs)的识别,彻底改变了心血管医学领域。然而,无论是在体外还是体内,即使在损伤后,所报道的CPCs分化事件发生率都很低,这引发了人们对这些细胞亚群生物学意义的担忧。在这篇综述中,我们根据在其他器官中具有相似表型的细胞区室的已知情况,讨论对心脏Lin(-)Sca-1(+)细胞的当前认识。心脏Lin(-)Sca-1(+)细胞亚群是异质性的,呈现间充质特征,其特点是即使在损伤后,在体外和体内产生心肌细胞的能力也有限。在胚胎心血管祖细胞中没有Sca-1表达的证据。在其他器官中,虽然Sca-1表达不限于干/祖细胞群体,但主要在中胚层来源的细胞上观察到。迫切需要在单细胞水平上确定心脏Lin(-)Sca-1(+)细胞与成纤维细胞区室的重叠程度。