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Am J Physiol Lung Cell Mol Physiol 282: L757-L765, 2002; doi:10.1152/ajplung.00271.2001
1040-0605/02 $5.00
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Vol. 282, Issue 4, L757-L765, April 2002

Cell-specific involvement of HNF-1beta in alpha 1-antitrypsin gene expression in human respiratory epithelial cells

Chaobin Hu and David H. Perlmutter

Departments of Pediatrics and Cell Biology and Physiology, Washington University School of Medicine, and Division of Gastroenterology and Nutrition, St. Louis Children's Hospital, St. Louis, Missouri 63110

The synergistic action of hepatocyte nuclear factor (HNF)-1alpha and HNF-4 plays an important role in expression of the alpha 1-antitrypsin (alpha 1-AT) gene in human hepatic and intestinal epithelial cells. Recent studies have indicated that the alpha 1-AT gene is also expressed in human pulmonary alveolar epithelial cells, a potentially important local site of the lung antiprotease defense. In this study, we examined the possibility that alpha 1-AT gene expression in a human pulmonary epithelial cell line H441 was also directed by the synergistic action of HNF-1alpha and HNF-4 and/or by the action of HNF-3, which has been shown to play a dominant role in gene expression in H441 cells. The results show that alpha 1-AT gene expression in H441 cells is predominantly driven by HNF-1beta , even though HNF-1beta has no effect on alpha 1-AT gene expression in human hepatic Hep G2 and human intestinal epithelial Caco-2 cell lines. Expression of alpha 1-AT and HNF-1beta was also demonstrated in primary cultures of human respiratory epithelial cells. HNF-4 has no effect on alpha 1-AT gene expression in H441 cells, even when it is cotransfected with HNF-1beta or HNF-1alpha . HNF-3 by itself has little effect on alpha 1-AT gene expression in H441, Hep G2, or Caco-2 cells but tends to have an upregulating effect when cotransfected with HNF-1 in Hep G2 and Caco-2 cells. These results indicate the unique involvement of HNF-1beta in alpha 1-AT gene expression in a cell line and primary cultures derived from human respiratory epithelium.

protease inhibitors; pneumocytes; tissue-specific gene expression


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