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Advancing the detection of maternal haematopoietic microchimeric cells in fetal immune organs in mice by flow cytometry

机译:流式细胞仪促进小鼠胎儿免疫器官中母体造血微嵌合细胞的检测

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摘要

Maternal microchimerism, which occurs naturally during gestation in hemochorial placental mammals upon transplacental migration of maternal cells into the fetus, is suggested to significantly influence the fetal immune system. In our previous publication, we explored the sensitivity of quantitative polymerase chain reaction and flow cytometry to detect cellular microchimerism. With that purpose, we created mixed cells suspensions in vitro containing reciprocal frequencies of wild type cells and cellspositive for enhanced green fluorescent protein or CD45.1+, respectively. Here, we now introduce the H-2 complex, which defines the major histocompatibility complex in mice and is homologous to HLA in human, as an additional target to detect maternal microchimerism among fetal haploidentical cells. We envision that this advanced approach to detect maternal microchimeric cells by flow cytometry facilitates the pursuit of phenotypic, gene expression and functional analysis of microchimeric cells in future studies.
机译:母体微嵌合体现象在母体细胞经胎盘向胎儿的胎盘迁移后自然会在妊娠期出血的胎盘哺乳动物中自然发生,这被认为会显着影响胎儿的免疫系统。在我们以前的出版物中,我们探讨了定量聚合酶链反应和流式细胞仪检测细胞微嵌合体的敏感性。出于这个目的,我们在体外创建了混合细胞悬液,其中分别包含野生型细胞和增强绿色荧光蛋白或CD45.1 +阳性细胞的倒数频率。在这里,我们现在介绍H-2复合物,它定义了小鼠中的主要组织相容性复合物,并且与人的HLA同源,作为检测胎儿单倍体细胞中母亲微嵌合体的另一个目标。我们设想,通过流式细胞术检测母体微嵌合细胞的这种先进方法有助于在未来的研究中追求微嵌合细胞的表型,基因表达和功能分析。

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