Devriese Sarah, Van den Bossche Lien, Van Welden Sophie, Holvoet Tom, Pinheiro Iris, Hindryckx Pieter, De Vos Martine, Laukens Debby
Department of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
ProDigest BVBA, Technologiepark 3, 9052, Ghent, Belgium.
Histochem Cell Biol. 2017 Jul;148(1):85-93. doi: 10.1007/s00418-017-1539-7. Epub 2017 Mar 6.
Colonic adenocarcinoma-derived Caco-2 and T84 epithelial cell lines are frequently used as in vitro model systems of functional epithelial barriers. Both are utilised interchangeably despite evidence that differentiated Caco-2 cells are more reminiscent of small intestinal enterocytes than of colonocytes, whereas differentiated T84 cells are less well characterised. The aim of this study was, therefore, to further characterise and compare differentiated Caco-2 and T84 cells. The objectives were to (1) compare the brush border morphology, (2) measure the expression of enterocyte- and colonocyte-specific genes and (3) compare their response to butyrate, which is dependent on the monocarboxylate transporter 1 (MCT1), an apical protein expressed primarily in colonocytes. T84 microvilli were significantly shorter than those of Caco-2 cells, which is a characteristic difference between small intestinal enterocytes and colonocytes. Also, enterocyte-associated brush border enzymes expressed in differentiated Caco-2 cells were not increased during T84 maturation, whereas colonic markers such as MCT1 were more abundant in differentiated T84 cells compared to differentiated Caco-2 cells. Consequently, T84 cells displayed a dose-responsive improvement of barrier function towards butyrate, which was absent in Caco-2 cells. On the other hand, differences in epithelial toll-like receptor expression between Caco-2 and T84 monolayers did not result in a corresponding differential functional response. We conclude that differentiated Caco-2 and T84 cells have distinct morphological, biochemical and functional characteristics, suggesting that T84 cells do not acquire the biochemical signature of mature small intestinal enterocytes like Caco-2 cells, but retain much of their original colonic characteristics throughout differentiation. These findings can help investigators select the appropriate intestinal epithelial cell line for specific in vitro research purposes.
结肠腺癌来源的Caco-2和T84上皮细胞系常被用作功能性上皮屏障的体外模型系统。尽管有证据表明分化的Caco-2细胞更类似于小肠肠上皮细胞而非结肠细胞,而分化的T84细胞的特征尚不明确,但二者仍被交替使用。因此,本研究的目的是进一步表征和比较分化的Caco-2和T84细胞。目标包括:(1)比较刷状缘形态;(2)测量肠上皮细胞和结肠细胞特异性基因的表达;(3)比较它们对丁酸盐的反应,丁酸盐的反应依赖于单羧酸转运蛋白1(MCT1),这是一种主要在结肠细胞中表达的顶端蛋白。T84微绒毛明显短于Caco-2细胞的微绒毛,这是小肠肠上皮细胞和结肠细胞之间的一个特征性差异。此外,在分化的Caco-2细胞中表达的与肠上皮细胞相关的刷状缘酶在T84细胞成熟过程中并未增加,而与结肠相关的标志物如MCT1在分化的T84细胞中比在分化的Caco-2细胞中更为丰富。因此,T84细胞对丁酸盐的屏障功能呈现剂量依赖性改善,而Caco-2细胞则没有。另一方面,Caco-2和T84单层上皮细胞中Toll样受体表达的差异并未导致相应的功能差异反应。我们得出结论,分化的Caco-2和T84细胞具有不同的形态、生化和功能特征,这表明T84细胞不像Caco-2细胞那样获得成熟小肠肠上皮细胞的生化特征,而是在整个分化过程中保留了许多其原始的结肠特征。这些发现有助于研究人员为特定的体外研究目的选择合适的肠上皮细胞系。