Gene expression profiles of normal proliferating and differentiating human intestinal epithelial cells: A comparison with the Caco-2 cell model

• Published in: Journal of cellular biochemistry Vol. 99; no. 4; pp. 1175 - 1186
• Main Authors: Tremblay, Eric, Auclair, Joëlle, Delvin, Edgar, Levy, Emile, Ménard, Daniel, Pshezhetsky, Alexey V., Rivard, Nathalie, Seidman, Ernest G., Sinnett, Daniel, Vachon, Pierre H., Beaulieu, Jean-François
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.11.2006
• Subjects: Caco-2 Cells; Cell Differentiation; Cell Proliferation; Cluster Analysis; Enterocytes - cytology; Enterocytes - metabolism; Gene Expression Profiling; Genes; genomics; growth and differentiation; human intestine; Humans; Microarray Analysis; Reproducibility of Results
• ISSN: 0730-2312; 1097-4644; 1097-4644
• DOI: 10.1002/jcb.21015

cDNA microarray technology enables detailed analysis of gene expression throughout complex processes such as differentiation. The aim of this study was to analyze the gene expression profile of normal human intestinal epithelial cells using cell models that recapitulate the crypt‐villus axis of intestinal differentiation in comparison with the widely used Caco‐2 cell model. cDNA microarrays (19,200 human genes) and a clustering algorithm were used to identify patterns of gene expression in the crypt‐like proliferative HIEC and tsFHI cells, and villus epithelial cells as well as Caco‐2/15 cells at two distinct stages of differentiation. Unsupervised hierarchical clustering analysis of global gene expression among the cell lines identified two branches: one for the HIEC cells versus a second comprised of two sub‐groups: (a) the proliferative Caco‐2 cells and (b) the differentiated Caco‐2 cells and closely related villus epithelial cells. At the gene level, supervised hierarchical clustering with 272 differentially expressed genes revealed distinct expression patterns specific to each cell phenotype. We identified several upregulated genes that could lead to the identification of new regulatory pathways involved in cell differentiation and carcinogenesis. The combined use of microarray analysis and human intestinal cell models thus provides a powerful tool for establishing detailed gene expression profiles of proliferative to terminally differentiated intestinal cells. Furthermore, the molecular differences between the normal human intestinal cell models and Caco‐2 cells clearly point out the strengths and limitations of this widely used experimental model for studying intestinal cell proliferation and differentiation. J. Cell. Biochem. 99: 1175–1186, 2006. © 2006 Wiley‐Liss, Inc.