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人新生儿和婴儿胸腺间充质基质细胞的表征及血管生成潜力

Characterization and angiogenic potential of human neonatal and infant thymus mesenchymal stromal cells.

作者信息

Wang Shuyun, Mundada Lakshmi, Johnson Sean, Wong Joshua, Witt Russell, Ohye Richard G, Si Ming-Sing

机构信息

Department of Cardiac Surgery, Section of Pediatric Cardiovascular Surgery and Department of Pediatric Cardiology, University of Michigan, Ann Arbor, Michigan, USA; Department of General Surgery, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Department of Cardiac Surgery, Section of Pediatric Cardiovascular Surgery and Department of Pediatric Cardiology, University of Michigan, Ann Arbor, Michigan, USA; Department of General Surgery, Brigham and Women's Hospital, Boston, Massachusetts, USA

出版信息

Stem Cells Transl Med. 2015 Apr;4(4):339-50. doi: 10.5966/sctm.2014-0240. Epub 2015 Feb 23.

Abstract

Resident mesenchymal stromal cells (MSCs) are involved in angiogenesis during thymus regeneration. We have previously shown that MSCs can be isolated from enzymatically digested human neonatal and infant thymus tissue that is normally discarded during pediatric cardiac surgical procedures. In this paper, we demonstrate that thymus MSCs can also be isolated by explant culture of discarded thymus tissue and that these cells share many of the characteristics of bone marrow MSCs. Human neonatal thymus MSCs are clonogenic, demonstrate exponential growth in nearly 30 population doublings, have a characteristic surface marker profile, and express pluripotency genes. Furthermore, thymus MSCs have potent proangiogenic behavior in vitro with sprout formation and angiogenic growth factor production. Thymus MSCs promote neoangiogenesis and cooperate with endothelial cells to form functional human blood vessels in vivo. These characteristics make thymus MSCs a potential candidate for use as an angiogenic cell therapeutic agent and for vascularizing engineered tissues in vitro.

摘要

驻留间充质基质细胞(MSCs)参与胸腺再生过程中的血管生成。我们之前已经表明,可以从儿科心脏手术过程中通常被丢弃的经酶消化的人类新生儿和婴儿胸腺组织中分离出MSCs。在本文中,我们证明胸腺MSCs也可以通过对丢弃的胸腺组织进行外植体培养来分离,并且这些细胞具有许多骨髓MSCs的特征。人类新生儿胸腺MSCs具有克隆形成能力,在近30次群体倍增中呈指数增长,具有特征性的表面标志物谱,并表达多能性基因。此外,胸腺MSCs在体外具有强大的促血管生成行为,可形成芽并产生血管生成生长因子。胸腺MSCs在体内促进新生血管生成,并与内皮细胞协同形成功能性人类血管。这些特性使胸腺MSCs成为用作血管生成细胞治疗剂和体外使工程组织血管化的潜在候选者。

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