Transcriptional modulation of genes encoding structural characteristics of differentiating Enterocytes during development of a polarized epithelium in vitro

被引:57
作者
Halbleib, Jennifer M. [1 ]
Saeaef, Annika M.
Brown, Patrick O.
Nelson, W. James
机构
[1] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
关键词
D O I
10.1091/mbc.E07-04-0308
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although there is considerable evidence implicating posttranslational mechanisms in the development of epithelial cell polarity, little is known about the patterns of gene expression and transcriptional regulation during this process. We characterized the temporal program of gene expression during cell-cell adhesion-initiated polarization of human Caco-2 cells in tissue culture, which develop structural and functional polarity similar to that of enterocytes in vivo. A distinctive switch in gene expression patterns occurred upon formation of cell-cell contacts between neighboring cells. Expression of genes involved in cell proliferation was down-regulated concomitant with induction of genes necessary for functional specialization of polarized epithelial cells. Transcriptional up-regulation of these latter genes correlated with formation of important structural and functional features in enterocyte differentiation and establishment of structural and functional cell polarity; components of the apical microvilli were induced as the brush border formed during polarization; as barrier function was established, expression of tight junction transmembrane proteins peaked; transcripts encoding components of the apical, but not the basal-lateral trafficking machinery were increased during polarization. Coordinated expression of genes encoding components of functional cell structures were often observed indicating temporal control of expression and assembly of multiprotein complexes.
引用
收藏
页码:4261 / 4278
页数:18
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