Widespread Cell-Specific Prolactin Receptor Expression in Multiple Murine Organs

Author:

Aoki Mari1,Wartenberg Philipp1,Grünewald Ramona1,Phillipps Hollian R2,Wyatt Amanda1,Grattan David R2,Boehm Ulrich1ORCID

Affiliation:

1. Experimental Pharmacology, Center for Molecular Signaling, Saarland University School of Medicine, Homburg, Germany

2. Centre for Neuroendocrinology and Department of Anatomy, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand

Abstract

AbstractThe 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.

Funder

Bundesministerium für Bildung und Forschung

Health Research Council of New Zealand

Deutsche Forschungsgemeinschaft

Publisher

The Endocrine Society

Subject

Endocrinology

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