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首页> 外文期刊>Journal of Immunological Methods >Comparison of short term in vitro cultured human mast cells from different progenitors - Peripheral blood-derived progenitors generate highly mature and functional mast cells.
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Comparison of short term in vitro cultured human mast cells from different progenitors - Peripheral blood-derived progenitors generate highly mature and functional mast cells.

机译:来自不同祖细胞的短期体外培养人类肥大细胞的比较-外周血来源的祖细胞生成高度成熟和功能正常的肥大细胞。

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During the last two decades different scientific groups have investigated the phenotype and function of in vitro generated human mast cells (MC). The cells have been shown to display variable surface markers and functional characteristics. The phenotypic differences may reflect different culture conditions, protocols or the use of different progenitors. To investigate the significance of different progenitors, we have compared MC generated from CD133(+) progenitor cells from cord blood (CBMC) or peripheral blood (PBMC). The progenitors were cultured for 7 weeks in the presence of IL-6 and SCF, with addition of IL-3 the first 3 weeks, and FCS during week 7. The phenotype of the established MC was characterized by surface marker expression levels, metachromasia, histamine and tryptase contents and their function was evaluated by receptor-mediated release of histamine and PGD(2). The generated metachromatic (99%) MC were 75% tryptase(+), regardless of the source of progenitor cell. Expression of c-kit/CD117, CD203c, and FcepsilonRI was comparable. The density of c-kit/CD117 receptors on CBMC was higher that of PBMC (p0.001). The density of CD203c and FcepsilonRI was higher on PBMC (p0.001). PBMC contained more histamine (p0.001), expressed more FcepsilonRI (p0.001) and released more histamine (p0.001) and PGD(2) (p0.001) upon ligation of FcepsilonRI, than CBMC. Culture with IL-4 increased expression of tryptase, FcepsilonRI, CD117 and CD203c, secretion of histamine and PGD(2) of PBMC, and histamine secretion of CBMC. Cord and peripheral blood may give rise to different types of MC. The question addressed should determine the progenitor cell and protocol to be used.
机译:在过去的二十年中,不同的科研小组研究了体外生成的人类肥大细胞(MC)的表型和功能。已经显示该细胞显示出可变的表面标记和功能特征。表型差异可能反映不同的培养条件,方案或不同祖细胞的使用。为了研究不同祖细胞的重要性,我们比较了脐带血(CBMC)或外周血(PBMC)从CD133(+)祖细胞产生的MC。将祖细胞在存在IL-6和SCF的情况下培养7周,在开始的3周内添加IL-3,并在第7周内添加FCS。表面标记物的表达水平,变色,组胺和类胰蛋白酶含量及其功能通过受体介导的组胺和PGD(2)释放来评估。不管祖细胞的来源如何,生成的变色(<99%)MC都是75%的类胰蛋白酶(+)。 c-kit / CD117,CD203c和FcepsilonRI的表达具有可比性。 CBMC上c-kit / CD117受体的密度高于PBMC(p <0.001)。在PBMC上,CD203c和FcepsilonRI的密度较高(p <0.001)。与CBMC相比,与FcepsilonRI连接后,PBMC包含更多的组胺(p <0.001),表达更多的FcepsilonRI(p <0.001)和释放更多的组胺(p <0.001)和PGD(2)(p <0.001)。用IL-4培养可增加类胰蛋白酶,FcepsilonRI,CD117和CD203c的表达,PBMC的组胺和PGD(2)的分泌以及CBMC的组胺的分泌。脐带血和外周血可能引起不同类型的MC。所解决的问题应确定要使用的祖细胞和方案。

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