Vectorial TGFβ Signaling in Polarized Intestinal Epithelial Cells

被引:13
|
作者
Yakovich, Adam J. [1 ]
Huang, Qin
Du, Jianguo [1 ]
Jiang, Bo [1 ]
Barnard, John A. [1 ,2 ,3 ]
机构
[1] Nationwide Childrens Hosp, Res Inst, Ctr Cell & Dev Biol, Columbus, OH 43205 USA
[2] Ohio State Univ, Coll Med, Dept Pulm Allergy Crit Care & Sleep, Columbus, OH USA
[3] Ohio State Univ, Coll Med, Dept Pediat, Columbus, OH USA
关键词
INFLAMMATORY-BOWEL-DISEASE; CANINE KIDNEY-CELLS; GROWTH-FACTOR; COLORECTAL-CANCER; II RECEPTOR; PROTEIN; PATHWAY; BARRIER; CLONING; DOMAIN;
D O I
10.1002/jcp.22135
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Polarized gastrointestinal epithelial cells form tight junctions that spatially separate apical and basolateral cell membrane domains. These domains harbor functionally distinct proteins that contribute to cellular homeostasis and morphogenesis. Transforming growth factor beta (TGF beta) is a critical regulator of gastrointestinal epithelial cell growth and differentiation. Functional assays of vectorial TGF beta signaling and immunofluorescence techniques were used to determine the localization of TGF beta receptors and ligand secretion in polarizing Caco-2 cells, a colon cancer cell line. Results were compared to the nontransformed MDCK cell line. In both Caco-2 and MDCK cells, addition of TGF beta 1 to the basolateral medium resulted in phosphorylation of Smad2. No phosphorylation was observed when TGF beta 1 was added to the apical chamber, indicating that receptor signaling is localized at the basolateral membrane. In support of this, immunofluorescence and biotinylation assays show receptor localization along the basolateral membrane. Secretion of TGF beta 1 from MDCK and Caco-2 cells into the apical or basolateral medium was measured by ELISA. Interestingly, secretion was exclusively apical in the nontransformed MDCK line and basolateral in transformed Caco-2 cells. Collectively, these results show basolateral domain specificity in localization of the TGF beta receptor signaling apparatus. These observations have important implications for understanding the biology of TGF beta in polarized epithelia, including elements of communication between epithelial and mesenchymal layers, and will prove useful in the design of therapeutics that target TGF beta function. J. Cell. Physiol. 224: 398-404, 2010. (C) 2010 Wiley-Liss, Inc.
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页码:398 / 404
页数:7
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