| Literature DB >> 34797529 |
Yanrong Qian1, Darlene E Berryman1,2, Reetobrata Basu1, Edward O List1, Shigeru Okada1,3, Jonathan A Young1,2, Elizabeth A Jensen1,2,4, Stephen R C Bell1,2, Prateek Kulkarni1,5,6, Silvana Duran-Ortiz1, Patricia Mora-Criollo1,4, Samuel C Mathes1, Alison L Brittain1,2,6, Mat Buchman1,2, Emily Davis1,5,6, Kevin R Funk1,5,6, Jolie Bogart1,5, Diego Ibarra1,7, Isaac Mendez-Gibson1,8, Julie Slyby1,5, Joseph Terry1,5, John J Kopchick9,10.
Abstract
Much of our understanding of GH's action stems from animal models and the generation and characterization of genetically altered or modified mice. Manipulation of genes in the GH/IGF1 family in animals started in 1982 when the first GH transgenic mice were produced. Since then, multiple laboratories have altered mouse DNA to globally disrupt Gh, Ghr, and other genes upstream or downstream of GH or its receptor. The ability to stay current with the various genetically manipulated mouse lines within the realm of GH/IGF1 research has been daunting. As such, this review attempts to consolidate and summarize the literature related to the initial characterization of many of the known gene-manipulated mice relating to the actions of GH, PRL and IGF1. We have organized the mouse lines by modifications made to constituents of the GH/IGF1 family either upstream or downstream of GHR or to the GHR itself. Available data on the effect of altered gene expression on growth, GH/IGF1 levels, body composition, reproduction, diabetes, metabolism, cancer, and aging are summarized. For the ease of finding this information, key words are highlighted in bold throughout the main text for each mouse line and this information is summarized in Tables 1, 2, 3 and 4. Most importantly, the collective data derived from and reported for these mice have enhanced our understanding of GH action.Entities:
Keywords: Aging; Cancer; Growth hormone; Insulin-like growth factor 1; Knockout mice; Metabolism; Prolactin; Transgenic mice
Mesh:
Substances:
Year: 2021 PMID: 34797529 PMCID: PMC8603657 DOI: 10.1007/s11102-021-01191-y
Source DB: PubMed Journal: Pituitary ISSN: 1386-341X Impact factor: 4.107