INTERFERON-GAMMA INDUCES POLYMERIC IMMUNOGLOBULIN RECEPTOR MESSENGER-RNA IN HUMAN INTESTINAL EPITHELIAL-CELLS BY A PROTEIN-SYNTHESIS DEPENDENT MECHANISM

被引:68
作者
PISKURICH, JF
FRANCE, JA
TAMER, CM
WILLMER, CA
KAETZEL, CS
KAETZEL, DM
机构
[1] CASE WESTERN RESERVE UNIV, INST PATHOL, CLEVELAND, OH 44106 USA
[2] CASE WESTERN RESERVE UNIV, DEPT MED, CLEVELAND, OH 44106 USA
[3] CASE WESTERN RESERVE UNIV, DEPT PHARMACOL, CLEVELAND, OH 44106 USA
[4] DEPT VET AFFAIRS MED CTR, CLEVELAND, OH 44106 USA
关键词
D O I
10.1016/0161-5890(93)90071-I
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
Transport of secretory IgA into external fluids is mediated by the polymeric immunoglobulin receptor (pIgR) on the surface of mucosal epithelial cells. We studied the mechanism by which interferon-gamma (IFN-gamma) induces pIgR expression in HT-29.74 cells, a subclone of the HT-29 cell line selected for high concns of pIgR. Here we report the isolation of genomic DNA and cDNA clones encoding human pIgR and development of a sensitive ribonuclease protection assay for pIgR mRNA. This assay was used to determine if induction of pIgR by IFN-gamma is mediated by accumulation of pIgR mRNA. After an initial lag of 12 hr, pIgR mRNA increased seven-fold in response to IFN-gamma, reaching a plateau at 24 hr. Concentrations of pIgR protein also increased seven-fold, but the increase was delayed until 48 hr following stimulation with IFN-gamma. Cycloheximide treatment abolished the IFN-gamma induced increase in pIgR mRNA, indicating that induction of pIgR mRNA by IFN-gamma requires de novo protein synthesis. These results suggest that induction of pIgR expression by IFN-gamma involves an increase in steady-state concns of pIgR mRNA via a protein synthesis dependent mechanism.
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收藏
页码:413 / 421
页数:9
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