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Gene markers of cellular aging in human multipotent stromal cells in culture.培养的人多能基质细胞中细胞衰老的基因标志物
Stem Cell Res Ther. 2014 Apr 28;5(2):59. doi: 10.1186/scrt448.
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MSC-based product characterization for clinical trials: an FDA perspective.基于 MSC 的临床试验产品特征分析:FDA 的观点。
Cell Stem Cell. 2014 Feb 6;14(2):141-5. doi: 10.1016/j.stem.2014.01.013.
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Bioluminescence imaging of cardiomyogenic and vascular differentiation of cardiac and subcutaneous adipose tissue-derived progenitor cells in fibrin patches in a myocardium infarct model.纤维蛋白贴片中心肌梗死模型中心房和皮下脂肪组织源性祖细胞的成心肌和血管分化的生物发光成像。
Int J Cardiol. 2013 Nov 15;169(4):288-95. doi: 10.1016/j.ijcard.2013.09.013. Epub 2013 Oct 6.
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CD105 (endoglin)-negative murine mesenchymal stromal cells define a new multipotent subpopulation with distinct differentiation and immunomodulatory capacities.CD105(内皮糖蛋白)阴性的鼠间质基质细胞定义了一个具有独特分化和免疫调节能力的新的多能亚群。
PLoS One. 2013 Oct 4;8(10):e76979. doi: 10.1371/journal.pone.0076979. eCollection 2013.
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Essential components for ex vivo proliferation of mesenchymal stromal cells.间质基质细胞体外增殖的基本成分。
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Comparison of allogeneic platelet lysate and fetal bovine serum for in vitro expansion of equine bone marrow-derived mesenchymal stem cells.比较异体血小板裂解物和胎牛血清在体外扩增马骨髓间充质干细胞中的应用。
Res Vet Sci. 2013 Oct;95(2):693-8. doi: 10.1016/j.rvsc.2013.04.024. Epub 2013 May 16.
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Growth, differentiation capacity, and function of mesenchymal stem cells expanded in serum-free medium developed via combinatorial screening.通过组合筛选开发的无血清培养基中扩增的间充质干细胞的生长、分化能力和功能。
Exp Cell Res. 2013 Jun 10;319(10):1409-18. doi: 10.1016/j.yexcr.2013.04.004. Epub 2013 Apr 15.
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Development of fully defined xeno-free culture system for the preparation and propagation of cell therapy-compliant human adipose stem cells.用于制备和扩增符合细胞治疗要求的人脂肪干细胞的完全限定无血清培养体系的开发。
Stem Cell Res Ther. 2013 Mar 7;4(2):27. doi: 10.1186/scrt175.
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Comparison of human adipose-derived stem cells and bone marrow-derived stem cells in a myocardial infarction model.人脂肪来源干细胞与骨髓来源干细胞在心肌梗死模型中的比较。
Cell Transplant. 2014 Feb;23(2):195-206. doi: 10.3727/096368912X659871. Epub 2012 Dec 4.
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Effects of medium supplements on proliferation, differentiation potential, and in vitro expansion of mesenchymal stem cells.培养基补充剂对间充质干细胞增殖、分化潜能和体外扩增的影响。
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用于治疗的快速增殖脂肪组织间充质样细胞。

Fast-proliferating adipose tissue mesenchymal-stromal-like cells for therapy.

作者信息

Aguilar Elisabet, Bagó Julio Rodriguez, Soler-Botija Carol, Alieva Maria, Rigola Maria Angeles, Fuster Carme, Vila Olaia F, Rubio Nuria, Blanco Jeronimo

机构信息

1 Human DNA Variability Department, GENYO-Centre for Genomic and Oncological Research (Pfizer/University of Granada/Andalusian Regional Government) , PTS Granada, Granada, Spain .

出版信息

Stem Cells Dev. 2014 Dec 1;23(23):2908-20. doi: 10.1089/scd.2014.0231. Epub 2014 Aug 13.

DOI:10.1089/scd.2014.0231
PMID:25019281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4235596/
Abstract

Human mesenchymal stromal cells, whether from the bone marrow or adipose tissue (hASCs), are promising cell therapy agents. However, generation of abundant cells for therapy remains to be a challenge, due to the need of lengthy expansion and the risk of accumulating genomic defects during the process. We show that hASCs can be easily induced to a reversible fast-proliferating phenotype (FP-ASCs) that allows rapid generation of a clinically useful quantity of cells in <2 weeks of culture. Expanded FP-ASCs retain their finite expansion capacity and pluripotent properties. Despite the high proliferation rate, FP-ASCs show genomic stability by array-comparative genomic hybridization, and did not generate tumors when implanted for a long time in an SCID mouse model. Comparative analysis of gene expression patterns revealed a set of genes that can be used to characterize FP-ASCs and distinguish them from hASCs. As potential candidate therapeutic agents, FP-ASCs displayed high vasculogenic capacity in Matrigel assays. Moreover, application of hASCs and FP-ASCs in a fibrin scaffold over a myocardium infarct model in SCID mice showed that both cell types can differentiate to endothelial and myocardium lineages, although FP-ASCs were more potent angiogenesis inducers than hASCs, at promoting myocardium revascularization.

摘要

人骨髓间充质干细胞以及脂肪组织来源的人间充质干细胞(hASC)都是很有前景的细胞治疗制剂。然而,由于需要长时间的扩增以及在此过程中积累基因组缺陷的风险,为治疗生成大量细胞仍然是一个挑战。我们发现,hASC可以很容易地被诱导成一种可逆的快速增殖表型(FP-ASC),这种表型能够在不到2周的培养时间内快速生成临床上可用数量的细胞。扩增后的FP-ASC保留了其有限的扩增能力和多能特性。尽管增殖率很高,但通过阵列比较基因组杂交分析,FP-ASC显示出基因组稳定性,并且在SCID小鼠模型中长期植入时不会产生肿瘤。基因表达模式的比较分析揭示了一组可用于表征FP-ASC并将其与hASC区分开来的基因。作为潜在的候选治疗制剂,FP-ASC在基质胶试验中显示出高血管生成能力。此外,在SCID小鼠心肌梗死模型的纤维蛋白支架中应用hASC和FP-ASC表明,尽管在促进心肌血管再生方面,FP-ASC比hASC是更强的血管生成诱导剂,但两种细胞类型都可以分化为内皮细胞和心肌细胞谱系。