Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice

Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice
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人囊性纤维化跨膜电导调节剂针对转基因小鼠呼吸道上皮细胞

DOI:
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发表时间:
1992
期刊:
影响因子:
30.8
通讯作者:
J. Engelhardt
J. Engelhardt
中科院分区:
生物学1区
文献类型:
--
作者:
J. Whitsett;C. Dey;B. Stripp;K. Wikenheiser;Jean C. Clark;S. Wert;R. Gregory;Alan E. Smith;J. Cohn;James M. Wilson;J. Engelhardt

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在转基因小鼠中表达人囊性纤维化跨膜传导调节因子(CFTR),其受来自人表面活性蛋白C(SP-C)基因的转录元件控制。hCFTR mRNA在肺和睾丸中表达:在肺中,我们在细支气管和肺泡上皮细胞中发现hCFTR mRNA,在呼吸道上皮细胞中发现CFTR蛋白。虽然hCFTR mRNA的表达水平不同,但在几个品系的肺上皮细胞中检测到hCFTR mRNA和蛋白。肺重量,形态,体细胞生长和生殖能力没有改变表达hCFTR在肺和睾丸的转基因。我们的研究结果表明,hCFTR可以安全地转移到肺上皮细胞的CF治疗。
Human cystic fibrosis transmembrane conductance regulator (CFTR) was expressed in transgenic mice under the control of transcriptional elements derived from the human surfactant protein C (SP–C) gene. The hCFTR mRNA was expressed in lungs and testes: in the lung, we found hCFTR mRNA in bronchiolar and alveolar epithelial cells, and CFTR protein in respiratory epithelial cells. While the level of expression of hCFTR mRNA varied, hCFTR mRNA and protein were detected in pulmonary epithelial cells of several lines. Lung weight, morphology, somatic growth and reproductive capacity were not altered by expression hCFTR in lung and testes of the transgenics. Our findings suggest that hCFTR can be safely transferred to lung epithelial cells for CF therapy.
DOI: 10.1126/science.2475911
发表时间: 1989-09
期刊: Science
影响因子: 56.9
作者:
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期刊: The American journal of physiology
影响因子: --
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DOI: --
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