| Literature DB >> 31373638 |
Mari Aoki1, Philipp Wartenberg1, Ramona Grünewald1, Hollian R Phillipps2, Amanda Wyatt1, David R Grattan2, Ulrich Boehm1.
Abstract
The prolactin receptor (Prlr) mediates not only the multiple effects of prolactin, but also those of the placental lactogens and, in humans, some actions of growth hormone. Although Prlr expression has been reported to be widespread in the body, specific cellular expression patterns within tissues are undefined for many organs. One persisting problem in investigating Prlr function is that the protein is difficult to detect using conventional methods. To allow investigation of Prlr expression with a single cell resolution, we have recently developed a knock-in mouse strain in which Cre recombinase is expressed together with the long isoform of the Prlr using an internal ribosome entry site. When crossed to a Cre-dependent reporter mouse strain, Cre-mediated recombination will genetically label cells that acutely express the Prlr as well as cells that have transiently expressed the Prlr during development. We report here the anatomical distribution of cells which express the fluorescent reporter τ green fluorescent protein in a total of 38 organs prepared from young adult male and female Prlr reporter mice. Our results establish a resource for dissecting the functional role of Prlr in multiple murine tissues.Entities:
Year: 2019 PMID: 31373638 DOI: 10.1210/en.2019-00234
Source DB: PubMed Journal: Endocrinology ISSN: 0013-7227 Impact factor: 4.736