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与内皮细胞共培养的干细胞的生存能力提高、血管分化和伤口愈合潜能。

Improved survival, vascular differentiation and wound healing potential of stem cells co-cultured with endothelial cells.

机构信息

Centre for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.

出版信息

PLoS One. 2011 Jan 24;6(1):e16114. doi: 10.1371/journal.pone.0016114.

DOI:10.1371/journal.pone.0016114
PMID:21283630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3026015/
Abstract

In this study, we developed a methodology to improve the survival, vascular differentiation and regenerative potential of umbilical cord blood (UCB)-derived hematopoietic stem cells (CD34(+) cells), by co-culturing the stem cells in a 3D fibrin gel with CD34(+)-derived endothelial cells (ECs). ECs differentiated from CD34(+) cells appear to have superior angiogenic properties to fully differentiated ECs, such as human umbilical vein endothelial cells (HUVECs). Our results indicate that the pro-survival effect of CD34(+)-derived ECs on CD34(+) cells is mediated, at least in part, by bioactive factors released from ECs. This effect likely involves the secretion of novel cytokines, including interleukin-17 (IL-17) and interleukin-10 (IL-10), and the activation of the ERK 1/2 pathway in CD34(+) cells. We also show that the endothelial differentiation of CD34(+) cells in co-culture with CD34(+)-derived ECs is mediated by a combination of soluble and insoluble factors. The regenerative potential of this co-culture system was demonstrated in a chronic wound diabetic animal model. The co-transplantation of CD34(+) cells with CD34(+)-derived ECs improved the wound healing relatively to controls, by decreasing the inflammatory reaction and increasing the neovascularization of the wound.

摘要

在这项研究中,我们开发了一种方法,通过将脐带血(UCB)来源的造血干细胞(CD34+细胞)与 CD34+衍生的内皮细胞(ECs)共培养在 3D 纤维蛋白凝胶中,来提高干细胞的存活率、血管分化和再生潜能。与完全分化的 ECs(如人脐静脉内皮细胞 [HUVECs])相比,由 CD34+细胞分化而来的 ECs 似乎具有更好的血管生成特性。我们的结果表明,CD34+衍生的 ECs 对 CD34+细胞的促生存作用至少部分是由 ECs 释放的生物活性因子介导的。这种作用可能涉及到新型细胞因子的分泌,包括白细胞介素-17(IL-17)和白细胞介素-10(IL-10),以及 CD34+细胞中 ERK 1/2 途径的激活。我们还表明,在与 CD34+衍生的 ECs 共培养中,CD34+细胞的内皮分化是由可溶性和不可溶性因子的组合介导的。在慢性伤口糖尿病动物模型中,证明了这种共培养系统的再生潜力。与对照组相比,CD34+细胞与 CD34+衍生的 ECs 的共移植通过减少炎症反应和增加伤口的新生血管化,相对提高了伤口愈合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8af4/3026015/33d5dc01fb7b/pone.0016114.g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8af4/3026015/1e9953705717/pone.0016114.g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8af4/3026015/33d5dc01fb7b/pone.0016114.g007.jpg

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