Up-regulation of the tight-junction protein ZO-1 by substance P and IGF-1 in A431 cells

被引:28
作者
Ko, Ji-Ae [1 ]
Murata, Shizuka [1 ]
Nishida, Teruo [1 ]
机构
[1] Yamaguchi Univ, Grad Sch Med, Dept Ophthalmol, Ube, Yamaguchi 7558505, Japan
关键词
A431; cells; substance P; IGF-1; ZO-1; tight junction; VASOACTIVE INTESTINAL POLYPEPTIDE; CULTURED HUMAN KERATINOCYTES; EPIDERMAL-GROWTH-FACTOR; ATOPIC-DERMATITIS; BETA-CATENIN; SKIN; NEUROPEPTIDES; ACTIN; EPITHELIA; RECEPTORS;
D O I
10.1002/cbf.1587
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The formation of a barrier by tight junctions is important in epithelia of various tissues. Substance P (SP) and insulin-like growth factor (IGF)-1 synergistically promote barrier function in the corneal epithelium. We have now examined the effects of SP and IGF-1 on expression of the tight-junction protein zonula occludens (ZO)-1 in A431 human epidermoid carcinoma cells. Reverse transcription-polymerase chain reaction (RT-PCR) and immunoblot analyses revealed that SP and IGF-1 increased the amounts of ZO-1 mRNA and protein in these cells in a concentration-dependent manner, with neither SP nor IGF-1 alone having such an effect. The SP- and IGF-1-induced up-regulation of ZO-1 was accompanied by phosphorylation of extracellular signal-regulated kinase (ERK), and both of these effects were blocked by PD98059, an inhibitor of ERK activation. SP and IGF-1 also increased the transepithelial electrical resistance (TER) (an indicator of barrier function) of an A431 cell monolayer in a manner sensitive to PD98059. Our results thus suggest that the synergistic induction of ZO-1 expression by SP and IGF-1 may promote barrier function in skin epithelial cells. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:388 / 394
页数:7
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