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In vitro proliferation of mononucleated suspension and adherent cells from mouse and human peripheral blood system

机译:小鼠和人外周血系统的单核悬浮液和贴壁细胞的体外增殖

摘要

Primary cells have a limited proliferative capacity with a finite number of times as compared with cell line which can grow indefinitely. Therefore, this study was carried out to identify the proliferative capacity of primary mononucleated cells from mouse and human. The mononucleated cells were isolated from mouse and human peripheral blood by density gradient centrifugation using Ficoll-Paque™ Plus. The two types of cells i.e. suspension and adherent forms were obtained after culturing the isolated mononucleated cells for 4 days in the complete medium consists of Alpha Minimal Essential Medium, 10% newborn calf serum and 2% penicillin/streptomycin. The cells were then cultured for another 10 days to observe cell viability using trypan blue exclusion assay (suspension form) and MTT assay (adherent form). NSO and MC3T3-E1 cell lines were selected as control cell for suspension and adherent cells, respectively. Our results showed that the proliferation rate of mouse suspension mononucleated cells increased from 1.31 ± 0.24 cells/day (day 5) to 2.69 ± 0.42 cells/day (day 10) whilst, for human suspension cells, the proliferation rate slightly increased from 0.56 ± 0.20 cells/day (day 5) to 0.76 ± 0.29 cells/day (day 10). However, the proliferation rate of mouse adherent mononucleated cells decreased from 0.23 ± 0.02 cells/day (day 5) to 0.17 ± 0.01 cells/day (day 10). Meanwhile, human adherent cells maintained proliferation rate at approximately 0.67 ± 0.18 cells/day. In conclusion, adherent primary mononucleated cells from both mouse and human have limited capacity to generate more cells in vitro as compared with suspension mononucleated cells.
机译:与可以无限期生长的细胞系相比,原代细胞的增殖能力有限,只有有限的次数。因此,进行了这项研究以鉴定来自小鼠和人的原代单核细胞的增殖能力。通过使用Ficoll-Paque™Plus进行密度梯度离心,从小鼠和人外周血中分离出单核细胞。在由Alpha基本必需培养基,10%新生小牛血清和2%青霉素/链霉素组成的完全培养基中培养分离的单核细胞4天后,获得了两种类型的细胞,即悬浮细胞和贴壁形式。然后将细胞再培养10天,以使用锥虫蓝排除试验(悬浮液形式)和MTT测定法(贴壁形式)观察细胞活力。将NSO和MC3T3-E1细胞系分别选作悬浮细胞和贴壁细胞的对照细胞。我们的结果表明,小鼠悬浮单核细胞的增殖速率从1.31±0.24细胞/天(第5天)增加到2.69±0.42细胞/天(第10天),而对于人类悬浮细胞,增殖速率则从0.56±轻微增加。 0.20个细胞/天(第5天)至0.76±0.29个细胞/天(第10天)。但是,小鼠粘附的单核细胞的增殖速率从0.23±0.02细胞/天(第5天)降低到0.17±0.01细胞/天(第10天)。同时,人类贴壁细胞将增殖速率维持在约0.67±0.18细胞/天。总之,与悬浮单核细胞相比,来自小鼠和人的贴壁初级单核细胞在体外产生更多细胞的能力有限。

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