Solano Maria Emilia, Thiele Kristin, Stelzer Ina Annelies, Mittrücker Hans-Willi, Arck Petra Clara
a Laboratory for Experimental Feto-maternal Medicine; Department of Obstetrics and Fetal Medicine ; University Medical Center Hamburg-Eppendorf ; Hamburg , Germany.
b Department of Immunology ; University Medical Center Hamburg-Eppendorf ; Hamburg , Germany.
Chimerism. 2014;5(3-4):99-102. doi: 10.4161/19381956.2014.959827. Epub 2014 Oct 30.
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 cells positive 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.
母源微嵌合体在妊娠期间自然发生于血绒毛膜胎盘哺乳动物,此时母细胞经胎盘迁移至胎儿体内,据推测其会显著影响胎儿免疫系统。在我们之前的出版物中,我们探讨了定量聚合酶链反应和流式细胞术检测细胞微嵌合体的敏感性。为此,我们在体外创建了混合细胞悬液,分别包含野生型细胞与增强型绿色荧光蛋白阳性细胞或CD45.1(+)细胞的相互频率。在此,我们现在引入H-2复合体,其定义了小鼠的主要组织相容性复合体且与人类的HLA同源,作为在胎儿单倍体相同细胞中检测母源微嵌合体的额外靶点。我们设想,这种通过流式细胞术检测母源微嵌合细胞的先进方法将有助于在未来研究中对微嵌合细胞进行表型、基因表达和功能分析。