Literature DB >> 7977760

Transgenic models for study of pulmonary development and disease.

S W Glasser1, T R Korfhagen, S E Wert, J A Whitsett.   

Abstract

This review summarizes progress in the application of transgenic mouse technology to the study of lung development and disease. Since advances in molecular genetics have greatly facilitated the isolation of cDNA and genes, our ability to readily assess roles of both normal and mutated genes in transgenic mouse in vivo represents a major advance, bridging molecular biology and whole animal physiology. Strategies have been developed in which lung epithelial cell promoter elements are used to drive normal or mutated genes into specific subsets of respiratory epithelial cells in the lungs of developing and mature transgenic mice. These mice have been used to elucidate the cis-acting elements controlling lung epithelial cell gene expression, to discern the role of specific polypeptides in lung morphogenesis and tumorigenesis, and to create animal models of pulmonary disease. The ability to mutate genes at their precise chromosomal locations through gene targeting in embryonic stem cells has lead to the production of animal models of lung diseases such as cystic fibrosis. Both gene insertion and gene targeting create permanent mouse lines that pass the modified gene to their progeny, providing animals for the study of the pathogenesis and treatment of pulmonary disorders.

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Year:  1994        PMID: 7977760     DOI: 10.1152/ajplung.1994.267.5.L489

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  7 in total

1.  Induction and apoptotic regression of lung adenocarcinomas by regulation of a K-Ras transgene in the presence and absence of tumor suppressor genes.

Authors:  G H Fisher; S L Wellen; D Klimstra; J M Lenczowski; J W Tichelaar; M J Lizak; J A Whitsett; A Koretsky; H E Varmus
Journal:  Genes Dev       Date:  2001-12-15       Impact factor: 11.361

Review 2.  Genetically manipulated mouse models of lung disease: potential and pitfalls.

Authors:  Rebecca M Baron; Alexander J S Choi; Caroline A Owen; Augustine M K Choi
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2011-12-23       Impact factor: 5.464

3.  Glutaredoxin-1 attenuates S-glutathionylation of the death receptor fas and decreases resolution of Pseudomonas aeruginosa pneumonia.

Authors:  Vikas Anathy; Scott W Aesif; Sidra M Hoffman; Jenna L Bement; Amy S Guala; Karolyn G Lahue; Laurie W Leclair; Benjamin T Suratt; Carlyne D Cool; Matthew J Wargo; Yvonne M W Janssen-Heininger
Journal:  Am J Respir Crit Care Med       Date:  2014-02-15       Impact factor: 21.405

4.  Protein transfection of mouse lung.

Authors:  Patrick Geraghty; Robert Foronjy
Journal:  J Vis Exp       Date:  2013-05-15       Impact factor: 1.355

5.  Pulmonary epithelial cell expression of GM-CSF corrects the alveolar proteinosis in GM-CSF-deficient mice.

Authors:  J A Huffman; W M Hull; G Dranoff; R C Mulligan; J A Whitsett
Journal:  J Clin Invest       Date:  1996-02-01       Impact factor: 14.808

Review 6.  Transgenic animals as models for human disease.

Authors:  R M Petters; J R Sommer
Journal:  Transgenic Res       Date:  2000       Impact factor: 3.145

Review 7.  Rodent models of cardiopulmonary disease: their potential applicability in studies of air pollutant susceptibility.

Authors:  U P Kodavanti; D L Costa; P A Bromberg
Journal:  Environ Health Perspect       Date:  1998-02       Impact factor: 9.031

  7 in total

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