Prolactin (PRL) Receptor Gene Expression in Mouse Adipose Tissue: Increases during Lactation and in PRL-Transgenic Mice1
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...
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Veröffentlicht in: | Endocrinology (Philadelphia) 2000-10, Vol.141 (10), p.3564-3572 |
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Sprache: | eng ; jpn |
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Zusammenfassung: | 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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ISSN: | 0013-7227 1945-7170 |
DOI: | 10.1210/endo.141.10.7691 |