Literature DB >> 11014209

Prolactin (PRL) receptor gene expression in mouse adipose tissue: increases during lactation and in PRL-transgenic mice.

C Ling1, G Hellgren, M Gebre-Medhin, K Dillner, H Wennbo, B Carlsson, H Billig.   

Abstract

There are indications that PRL may exert important metabolic actions on adipose tissue in different species. However, with the exception of birds, the receptor has not been identified in white adipose tissue. The present study was designed to examine the possible expression and regulation of the PRL receptor (PRLR) in mouse adipose tissue. The long PRLR messenger RNA (mRNA) splice form (L-PRLR) and two short splice forms (S2- and S3-PRLR) were detected in mouse adipose tissue by RT-PCR. Furthermore, L-PRLR mRNA was detected by ribonuclease protection assay. Immunoreactive PRLR with a relative molecular mass of 95,000 was revealed by immunoblotting. Furthermore, L-PRLR mRNA expression was demonstrated in primary isolated adipocytes. In mouse adipose tissue, the level of L-PRLR mRNA expression increased 2.3-fold during lactation compared with those in virgin and pregnant mice. In contrast, in the liver the expression of L-PRLR increased 3.4-fold during pregnancy compared with those in virgin and lactating mice. When comparing the levels of L-PRLR expression in virgin female and male mice, no difference was detected in adipose tissue. However, in virgin female liver the expression was 4.5-fold higher than that in male liver. As PRL up-regulates its own receptor in some tissues, we analyzed L-PRLR expression in PRL-transgenic female and male mice. In PRL-transgenic mice L-PRLR expression was significantly increased in both adipose tissue (1.4-fold in females and 2.4-fold in males) and liver (1.9-fold in females and 2.7-fold in males) compared with that in control mice. Furthermore, in female PRL-transgenic mice retroperitoneal adipose tissue was decreased in weight compared with that in control mice. However, no difference was detected when comparing the masses of parametrial adipose tissue. Our results suggest a direct role for PRL, mediated by PRLR, in modulating physiological events in adipose tissue.

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Year:  2000        PMID: 11014209     DOI: 10.1210/endo.141.10.7691

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  21 in total

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Review 2.  Effects of growth hormone and prolactin on adipose tissue development and function.

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Review 3.  Extrapituitary production of anterior pituitary hormones: an overview.

Authors:  S Harvey; C Arámburo; E J Sanders
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4.  Paternal recognition of adult offspring mediated by newly generated CNS neurons.

Authors:  Gloria K Mak; Samuel Weiss
Journal:  Nat Neurosci       Date:  2010-05-09       Impact factor: 24.884

5.  Completely humanizing prolactin rescues infertility in prolactin knockout mice and leads to human prolactin expression in extrapituitary mouse tissues.

Authors:  Heather R Christensen; Michael K Murawsky; Nelson D Horseman; Tara A Willson; Karen A Gregerson
Journal:  Endocrinology       Date:  2013-09-12       Impact factor: 4.736

6.  Prolactin activation of the long form of its cognate receptor causes increased visceral fat and obesity in males as shown in transgenic mice expressing only this receptor subtype.

Authors:  J A Le; H M Wilson; A Shehu; Y S Devi; T Aguilar; G Gibori
Journal:  Horm Metab Res       Date:  2011-10-11       Impact factor: 2.936

7.  The role of adipocyte XBP1 in metabolic regulation during lactation.

Authors:  Margaret F Gregor; Emily S Misch; Ling Yang; Sarah Hummasti; Karen E Inouye; Ann-Hwee Lee; Brian Bierie; Gökhan S Hotamisligil
Journal:  Cell Rep       Date:  2013-04-25       Impact factor: 9.423

8.  Adipocyte Versus Somatotrope Leptin: Regulation of Metabolic Functions in the Mouse.

Authors:  Angela Katherine Odle; Melody Allensworth-James; Anessa Haney; Noor Akhter; Mohsin Syed; Gwen V Childs
Journal:  Endocrinology       Date:  2016-02-09       Impact factor: 4.736

9.  Body composition of prolactin-, growth hormone, and thyrotropin-deficient Ames dwarf mice.

Authors:  Mark L Heiman; Frank C Tinsley; Julie A Mattison; Steven Hauck; Andrzej Bartke
Journal:  Endocrine       Date:  2003 Feb-Mar       Impact factor: 3.633

10.  Effects of lactogen resistance and GH deficiency on mouse metabolism: pancreatic hormones, adipocytokines, and expression of adiponectin and insulin receptors.

Authors:  Ramamani Arumugam; Don Fleenor; Michael Freemark
Journal:  Endocrine       Date:  2007-11-02       Impact factor: 3.633

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