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Isolation and Characterization of Human Trophoblast Side-Population (SP) Cells in Primary Villous Cytotrophoblasts and HTR-8/SVneo Cell Line

机译:原发性绒毛滋养细胞和HTR-8 / SVneo细胞系中人类滋养层侧群(SP)细胞的分离和鉴定

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摘要

Recently, numerous studies have identified that immature cell populations including stem cells and progenitor cells can be found among “side-population” (SP) cells. Although SP cells isolated from some adult tissues have been reported elsewhere, isolation and characterization of human trophoblast SP remained to be reported. In this study, HTR-8/SVneo cells and human primary villous cytotrophoblasts (vCTBs) were stained with Hoechst 33342 and SP and non-SP (NSP) fractions were isolated using a cell sorter. A small population of SP cells was identified in HTR-8/SVneo cells and in vCTBs. SP cells expressed several vCTB-specific markers and failed to express syncytiotrophoblast (STB) or extravillous cytotrophopblast (EVT)-specific differentiation markers. SP cells formed colonies and proliferated on mouse embryonic fibroblast (MEF) feeder cells or in MEF conditioned medium supplemented with heparin/FGF2, and they also showed long-term repopulating property. SP cells could differentiate into both STB and EVT cell lineages and expressed several differentiation markers. Microarray analysis revealed that IL7R and IL1R2 were exclusively expressed in SP cells and not in NSP cells. vCTB cells sorted as positive for both IL7R and IL1R2 failed to express trophoblast differentiation markers and spontaneously differentiated into both STB and EVT in basal medium. These features shown by the SP cells suggested that IL7R and IL1R2 are available as markers to detect the SP cells and that vCTB progenitor cells and trophoblast stem cells were involved in the SP cell population.
机译:最近,许多研究已经发现,在“侧群”(SP)细胞中可以发现包括干细胞和祖细胞在内的未成熟细胞群体。尽管从其他成年组织分离出的SP细胞在其他地方已有报道,但人类滋养层SP的分离和鉴定仍有待报道。在这项研究中,用Hoechst 33342对HTR-8 / SVneo细胞和人原发绒毛成纤维细胞(vCTBs)进行了染色,并使用细胞分选仪分离了SP和非SP(NSP)组分。在HTR-8 / SVneo细胞和vCTB中鉴定出少量SP细胞。 SP细胞表达了几种vCTB特异性标记,但未能表达合体滋养层细胞(STB)或绒毛外滋养层细胞(EVT)特异性分化标记。 SP细胞形成集落并在小鼠胚胎成纤维细胞(MEF)饲养细胞或添加了肝素/ FGF2的MEF条件培养基中增殖,它们还显示出长期的繁殖特性。 SP细胞可以分化为STB和EVT细胞谱系,并表达几种分化标记。基因芯片分析显示IL7R和IL1R2仅在SP细胞中表达,而不在NSP细胞中表达。被分类为IL7R和IL1R2阳性的vCTB细胞未能表达滋养细胞分化标记,并在基础培养基中自发分化为STB和EVT。 SP细胞显示的这些特征表明,IL7R和IL1R2可作为检测SP细胞的标志物,并且vCTB祖细胞和滋养层干细胞参与了SP细胞群体。

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