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Vascular Wall-Resident CD44+ Multipotent Stem Cells Give Rise to Pericytes and Smooth Muscle Cells and Contribute to New Vessel Maturation

机译:驻留在血管壁的CD44 +多能干细胞使周细胞和平滑肌细胞增加并促进新血管的成熟

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摘要

Here, we identify CD44(+)CD90(+)CD73(+)CD34(−)CD45(−) cells within the adult human arterial adventitia with properties of multipotency which were named vascular wall-resident multipotent stem cells (VW-MPSCs). VW-MPSCs exhibit typical mesenchymal stem cell characteristics including cell surface markers in immunostaining and flow cytometric analyses, and differentiation into adipocytes, chondrocytes and osteocytes under culture conditions. Particularly, TGFß1 stimulation up-regulates smooth muscle cell markers in VW-MPSCs. Using fluorescent cell labelling and co-localisation studies we show that VW-MPSCs differentiate to pericytes/smooth muscle cells which cover the wall of newly formed endothelial capillary-like structures in vitro. Co-implantation of EGFP-labelled VW-MPSCs and human umbilical vein endothelial cells into SCID mice subcutaneously via Matrigel results in new vessels formation which were covered by pericyte- or smooth muscle-like cells generated from implanted VW-MPSCs. Our results suggest that VW-MPSCs are of relevance for vascular morphogenesis, repair and self-renewal of vascular wall cells and for local capacity of neovascularization in disease processes.
机译:在这里,我们确定了成年人类动脉外膜内具有多能特性的CD44(+)CD90(+)CD73(+)CD34(-)CD45(-)细胞,这些细胞被称为血管壁驻留多能干细胞(VW-MPSCs) 。 VW-MPSCs具有典型的间充质干细胞特征,包括免疫染色和流式细胞术分析中的细胞表面标记,以及在培养条件下可分化为脂肪细胞,软骨细胞和骨细胞。特别是,TGFβ1刺激上调了VW-MPSC中的平滑肌细胞标志物。使用荧光细胞标记和共定位研究,我们发现VW-MPSCs分化为周细胞/平滑肌细胞,该细胞覆盖了体外新形成的内皮毛细管样结构的壁。通过Matrigel将EGFP标记的VW-MPSCs和人脐静脉内皮细胞共植入皮下SCID小鼠中,导致新血管形成,这些血管被植入的VW-MPSCs产生的周细胞或平滑肌样细胞覆盖。我们的结果表明,VW-MPSC与血管形态发生,血管壁细胞的修复和自我更新以及疾病过程中新血管形成的局部能力有关。

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