Pulmonary epithelial expression of human α1-antitrypsin in transgenic mice results in delivery of α1-antitrypsin protein to the interstitium

被引:31
作者
Dhami, R [1 ]
Zay, K [1 ]
Gilks, B [1 ]
Porter, S [1 ]
Wright, JL [1 ]
Churg, A [1 ]
机构
[1] Univ British Columbia, Dept Pathol, Vancouver, BC V6T 2B5, Canada
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 1999年 / 77卷 / 04期
基金
英国医学研究理事会;
关键词
alpha(1)-antitrypsin; lung; surfactant protein C promoter; Clara cell protein 10 promoter; haptoglobin promoter;
D O I
10.1007/s001090050364
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
alpha(1)-Antitrypsin (alpha(1)AT) therapy is used as a treatment for alpha(1)AT deficiency. It has also been proposed as a therapy for cigarette smoke-induced emphysema, although the efficacy of such therapy is as yet unproven. Moreover, the optimal route of delivery of alpha(1)AT to the lung interstitium, the crucial locus of action, is unknown. We created transgenic mice with expression of the human alpha(1)AT gene directed by a human surfactant protein C (SpC) promoter fragment or a rat Clara cell 10-kDa protein (CC10) promoter fragment in order to examine the ability of pulmonary epithelial cell expression of alpha(1)AT to deliver protein to the interstitium, and to produce a model that would allow studies on the efficacy of alpha(1)AT in preventing lung damage after cigarette smoke exposure. Four transgenic lines were studied. In situ hybridization and light microscopic immunohistochemistry showed that two CC10 driven lines expressed human alpha(1)AT in type II alveolar cells and airway epithelial cells; alpha(1)AT expression was seen in the alveolar parenchyma in two SpC driven lines, and in small airway epithelium in one of the SpC lines. Electron microscopic immunochemistry showed the presence of the human alpha(1)AT protein in the interstitium in all lines. Mean levels of human protein varied from 0.37 to 2.9 mu g/g lung protein and serum levels from 0.72 to 1.3 mu g/ml, compared to normal human serum alpha(1)AT levels of 2-5 mg/ml. We conclude that transgene-mediated expression of alpha(1)AT in pulmonary epithelial cells results in diffuse expression of the transgene in the alveolar parenchyma and reproducibly leads to transfer of protein to the interstitium. The present model is, however, limited by low levels of protein production; limited protein production may be a problem in other forms of gene therapy in which relatively large amounts of extracellular protein are needed in the lung for a therapeutic effect.
引用
收藏
页码:377 / 385
页数:9
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