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新型永生化人基质细胞系可增强脐带血造血干细胞的体外扩增。

New immortalized human stromal cell lines enhancing in vitro expansion of cord blood hematopoietic stem cells.

作者信息

De Angeli Sergio, Di Liddo Rosa, Buoro Sabrina, Toniolo Luana, Conconi Maria Teresa, Belloni Anna S, Parnigotto Pier Paolo, Nussdorfer Gastone G

机构信息

Cell Culture Laboratory, Transfusional Center, Treviso Regional Hospital, I-31100 Treviso, Italy.

出版信息

Int J Mol Med. 2004 Mar;13(3):363-71.

Abstract

One of the most promising technique for the in vitro expansion of cord blood (CB) hematopoietic stem cells (SCs) seems to be their co-culture with stromal feeder-layers. Hence, we developed and immortalized by retroviral transduction with the temperature-sensitive SV40 large T antigen three new human cell lines, two derived from bone marrow (HM1-SV40 and HM2-SV40) and one from umbilical cord (HCB1-SV40), and investigated the inductive capacity of their conditioned culture media on clonal growth of CB hematopoietic SCs. Immunocytochemistry showed that cell lines were positive to either cytokeratins or stromal markers, as well as to epidermal growth factor (EGF), fibroblast growth factor (FGF) and adrenomedullin. Moreover, cell lines expressed interleukin (IL)-1 beta, IL-6, granulocyte macrophage-colony stimulating factor (GM-CSF), G-CSF and stem cell factor (SCF), and secreted variable amount of IL-1 beta, IL-6 and GM-CSF. Collectively, these findings indicate that cell lines possess the stromal-cell phenotype. The conditioned supernatants of the three cell lines induced similar increases in the clonal growth of both fresh and cryopreserved-thawed CB hematopoietic SCs cultured on semisolid media deprived of growth factors and cytokines. However, the inductive capacity was significantly higher in the case of cryopreserved cells, where the rise in clonal growth reached that induced by the addition to the culture media of IL-3, GM-CSF and SCF. Our findings allow us to conclude that our new human stromal cell lines could be used as feeder-layers for CB hematopoietic SC expansion in vitro.

摘要

脐带血(CB)造血干细胞(SCs)体外扩增最有前景的技术之一似乎是将其与基质饲养层共培养。因此,我们通过用温度敏感型SV40大T抗原进行逆转录病毒转导,开发并永生化了三种新的人类细胞系,其中两种源自骨髓(HM1-SV40和HM2-SV40),一种源自脐带(HCB1-SV40),并研究了它们的条件培养基对CB造血SCs克隆生长的诱导能力。免疫细胞化学显示,这些细胞系对细胞角蛋白或基质标志物呈阳性,对表皮生长因子(EGF)、成纤维细胞生长因子(FGF)和肾上腺髓质素也呈阳性。此外,细胞系表达白细胞介素(IL)-1β、IL-6、粒细胞巨噬细胞集落刺激因子(GM-CSF)、G-CSF和干细胞因子(SCF),并分泌不同量的IL-1β、IL-6和GM-CSF。总体而言,这些发现表明细胞系具有基质细胞表型。这三种细胞系的条件上清液在无生长因子和细胞因子的半固体培养基上培养时,对新鲜和冷冻解冻后的CB造血SCs的克隆生长均诱导了相似的增加。然而,对于冷冻保存的细胞,诱导能力显著更高,其克隆生长的增加达到了向培养基中添加IL-3、GM-CSF和SCF所诱导的水平。我们的研究结果使我们能够得出结论,我们新的人类基质细胞系可作为体外CB造血SCs扩增的饲养层。

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