Marshall Aaron M, Pai Vaibhav P, Sartor Maureen A, Horseman Nelson D
Systems Biology and Physiology Program, Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, OH 45267-0576, USA.
Cell Tissue Res. 2009 Feb;335(2):383-95. doi: 10.1007/s00441-008-0719-0. Epub 2008 Nov 13.
As demonstrated by a variety of animal studies, barrier function in the mammary epithelium is essential for a fully functioning and differentiated gland. However, there is a paucity of information on barrier function in human mammary epithelium. Here, we have established characteristics of a polarizing differentiating model of human mammary epithelial cells capable of forming a high-resistance/low-conductance barrier in a predictable manner, viz., by using MCF10A cells on permeable membranes. Inulin flux decreased and transepithelial electrical resistance (TEER) increased over the course of several days after seeding MCF10A cells on permeable membranes. MCF10A cells exhibited multipotent phenotypic differentiation into layers expressing basal and lumenal markers when placed on permeable membranes, with at least two distinct cell phenotypes. A clonal subline of MCF10A, generated by culturing stem-like cells under non-adherent conditions, also generated a barrier-forming epithelial membrane with cells expressing markers of both basal and lumenal differentiation (CD10 and MUC1, respectively). Progressive changes associated with differentiation, including wholesale inhibition of cell-cycle genes and stimulation of cell and tissue morphogenic genes, were observed by gene expression profiling. Clustering and gene ontology categorization of significantly altered genes revealed a pattern of lumenal epithelial-cell-specific differentiation.
正如各种动物研究所示,乳腺上皮中的屏障功能对于功能完备且分化的腺体至关重要。然而,关于人类乳腺上皮中屏障功能的信息却十分匮乏。在此,我们建立了一种人乳腺上皮细胞极化分化模型的特征,该模型能够以可预测的方式形成高电阻/低电导屏障,即通过在可渗透膜上使用MCF10A细胞。在将MCF10A细胞接种到可渗透膜上后的几天内,菊粉通量降低,跨上皮电阻(TEER)增加。当置于可渗透膜上时,MCF10A细胞表现出多能表型分化,形成表达基底和管腔标记物的细胞层,至少有两种不同的细胞表型。通过在非贴壁条件下培养类干细胞产生的MCF10A克隆亚系,也产生了一种形成屏障的上皮膜,其细胞表达基底和管腔分化的标记物(分别为CD10和MUC1)。通过基因表达谱分析观察到与分化相关的渐进性变化,包括对细胞周期基因的全面抑制以及对细胞和组织形态发生基因的刺激。对显著改变的基因进行聚类和基因本体分类,揭示了管腔上皮细胞特异性分化的模式。