首页> 外文期刊>Journal of Immunological Methods >The establishment of a combined serum-free and serum-supplemented culture method of obtaining functional cord blood-derived human mast cells.
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The establishment of a combined serum-free and serum-supplemented culture method of obtaining functional cord blood-derived human mast cells.

机译:建立获得功能性脐带血源性人肥大细胞的无血清和血清补充的联合培养方法。

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Background: Serum-free cultures supplemented with stem cell factor (SCF) and IL-6 is reported to support the extensive growth of less functional human cord blood-derived mast cells. Objective: To obtain more functional mast cells from cord blood, we developed a culture system combining a serum-free condition for 0-8 weeks of culture, and followed by a serum-supplemented culture condition and examined the function of the cells compared to the cells cultured continuously in serum-free condition. Methods: Human cord blood progenitors were purified with anti-CD133 antibody. They were cultured in a serum-free medium StemSpan supplemented with SCF at 100 ng/ml and IL-6 at 50 ng/ml for 8 weeks. Then, an aliquot of the cultured cells were cultured in the above condition but further supplemented with 10% fetal calf serum (FCS). Results: The addition of FCS after 8 weeks of culture significantly increased the amount of histamine per mast cell (3.8 pg/cell) when compared to the serum-free condition (0.7 pg/cell). The cells cultured with FCS after 8 weeks expressed more FcvarepsilonRI alpha and released >30% of the histamine content upon anti-IgE stimulation than those cultured without serum. Conclusion: It is uncertain why FCS enhanced the functional maturation of mast cells when added after week 8 of culture but suppressed mast cell development when added at day 0 of culture. Yet, the present method combining a serum-free culture system with a serum-supplemented culture system seems to be beneficial for most of the laboratories to obtain functional human mast cells.
机译:背景:据报道,补充有干细胞因子(SCF)和IL-6的无血清培养物可支持功能较弱的人脐带血来源的肥大细胞的广泛生长。目的:为了从脐带血中获得更多功能的肥大细胞,我们开发了一种培养系统,该系统结合了无血清条件,可进行0-8周的培养,然后再添加血清,并对其培养功能进行了比较。细胞在无血清条件下连续培养。方法:用抗CD133抗体纯化人脐带血祖细胞。将它们在补充有100 ng / ml SCF和50 ng / ml IL-6的无血清培养基StemSpan中培养8周。然后,将培养细胞的等分试样在上述条件下培养,但进一步补充10%胎牛血清(FCS)。结果:与无血清条件(0.7 pg /细胞)相比,培养8周后添加FCS显着增加了每个肥大细胞的组胺量(3.8 pg /细胞)。与未血清培养的细胞相比,用FCS培养8周后的细胞表达更多的FcvarepsilonRIα,并且在抗IgE刺激下释放的组胺含量> 30%。结论:尚不确定为何FCS在培养的第8周后添加会增强肥大细胞的功能成熟,而在培养的第0天添加时会抑制肥大细胞的发育。然而,将无血清培养系统与补充了血清的培养系统相结合的本方法对于大多数实验室获得功能性人类肥大细胞似乎是有益的。

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