What Can Transgenic and Gene-targeted Mouse Models Teach Us about Salivary Gland Physiology?

Author:

Melvin J.E.1,Nguyen H.-V.2,Evans R.L.2,Shull G.E.3

Affiliation:

1. Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Aab Institute of Biomedical Sciences, Medical Center Box 611, 601 Elmwood Avenue, Rochester, NY 14642, USA,

2. Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Aab Institute of Biomedical Sciences, Medical Center Box 611, 601 Elmwood Avenue, Rochester, NY 14642, USA

3. Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Cincinnati, OH 45267

Abstract

Thousands of genetically modified mice have been developed since the first reports of stable expression of recombinant DNA in this species nearly 20 years ago. This mammalian model system has revolutionized the study of whole-animal, organ, and cell physiology. Transgenic and gene-targeted mice have been widely used to characterize salivary-gland-specific expression and to identify genes associated with tumorigenesis. Moreover, several of these mouse lines have proved to be useful models of salivary gland disease related to impaired immunology, i.e., Sjogren's syndrome, and disease states associated with pathogens. Despite the availability of genetically modified mice, few investigators have taken advantage of this resource to better their understanding of salivary gland function as it relates to the production of saliva. In this article, we describe the methods used to generate transgenic and gene-targeted mice and provide an overview of the advantages of and potential difficulties with these models. Finally, using these mouse models, we discuss the advances made in our understanding of the salivary gland secretion process.

Publisher

SAGE Publications

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Molecular identification of Ca2+-activated K+ channels in parotid acinar cells;American Journal of Physiology-Cell Physiology;2003-02-01

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