Siavashi Vahid, Nassiri Seyed Mahdi, Rahbarghazi Reza, Vafaei Rana, Sariri Reyhaneh
Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.
Department of Clinical Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
J Cell Biochem. 2016 Aug;117(8):1934-46. doi: 10.1002/jcb.25492. Epub 2016 Feb 2.
Preserving self-renewal, multipotent capacity, and large-scale expansion of highly functional progenitor cells, including endothelial progenitor cells (EPCs), is a controversial issue. These current limitations, therefore, raise the need of developing promising in vitro conditions for prolonged expansion of EPCs without loss of their stemness feature. In the current study, the possible role of three different natural extracellular substrates, including collagen, gelatin, and fibronectin, on multiple parameters of EPCs such as cell morphology, phenotype, clonogenic, and vasculogenic properties was scrutinized. Next, EPCs from GFP-positive mice were pre-expanded on each of these ECM substrates and then systemically transplanted into sublethaly irradiated mice to analyze the potency of these cells for marrow reconstitution. Our results revealed considerable promise for fibronectin for EPC expansion with maintenance of stemness characteristics, whereas gelatin and collagen matrices directed the cells toward a mature endothelial phenotype. Transplantation of EPCs pre-expanded on fibronectin resulted in widespread distribution and appropriate engraftment to various tissues with habitation in close association with the microvasculature. In addition, fibronectin pre-expanded cells were gradually enriched in the bone marrow after transplantation, resulting in marrow repopulation and hematologic recovery, leading to improved survival of recipient mice whereas gelatin- and collagen-expanded cells failed to reconstitute the bone marrow. This study demonstrated that, cell characteristics of in vitro expanded EPCs are determined by the subjacent matrix. Fibronectin-expanded EPCs are heralded as a source of great promise for bone marrow reconstitution and neo-angiogenesis in therapeutic bone marrow transplantation. J. Cell. Biochem. 117: 1934-1946, 2016. © 2016 Wiley Periodicals, Inc.
保留包括内皮祖细胞(EPCs)在内的高功能祖细胞的自我更新、多能能力以及大规模扩增,是一个存在争议的问题。因此,这些当前的局限性引发了对开发有前景的体外条件的需求,以便在不丧失其干性特征的情况下长时间扩增EPCs。在当前研究中,仔细研究了三种不同的天然细胞外基质,包括胶原蛋白、明胶和纤连蛋白,对EPCs多个参数的影响,如细胞形态、表型、克隆形成和血管生成特性。接下来,将来自绿色荧光蛋白(GFP)阳性小鼠的EPCs在这些细胞外基质中的每一种上进行预扩增,然后全身移植到亚致死剂量照射的小鼠体内,以分析这些细胞进行骨髓重建的能力。我们的结果显示,纤连蛋白在维持干性特征的情况下对EPCs扩增具有相当大的前景,而明胶和胶原蛋白基质则使细胞趋向于成熟的内皮表型。在纤连蛋白上预扩增的EPCs移植后导致广泛分布并适当地植入各种组织,与微血管紧密相关。此外,移植后纤连蛋白预扩增的细胞在骨髓中逐渐富集,导致骨髓再填充和血液学恢复,从而提高受体小鼠的存活率,而明胶和胶原蛋白扩增的细胞未能重建骨髓。这项研究表明,体外扩增的EPCs的细胞特性由下层基质决定。纤连蛋白扩增的EPCs被誉为治疗性骨髓移植中骨髓重建和新生血管形成的极有前景的来源。《细胞生物化学杂志》117: 1934 - 1946, 2016。© 2016威利期刊公司