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Differential involvement of cAMP/PKA-, PLC/PKC- and Ca 2+ /calmodulin-dependent pathways in GnRH-induced prolactin secretion and gene expression in grass carp pituitary cells.

Authors :
Li W
Ye C
He M
Ko WKW
Cheng CHK
Chan YW
Wong AOL
Source :
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2024 Jun 04; Vol. 15, pp. 1399274. Date of Electronic Publication: 2024 Jun 04 (Print Publication: 2024).
Publication Year :
2024

Abstract

Gonadotropin-releasing hormone (GnRH) is a key stimulator for gonadotropin secretion in the pituitary and its pivotal role in reproduction is well conserved in vertebrates. In fish models, GnRH can also induce prolactin (PRL) release, but little is known for the corresponding effect on PRL gene expression as well as the post-receptor signalling involved. Using grass carp as a model, the functional role of GnRH and its underlying signal transduction for PRL regulation were examined at the pituitary level. Using laser capture microdissection coupled with RT-PCR, GnRH receptor expression could be located in carp lactotrophs. In primary cell culture prepared from grass carp pituitaries, the native forms of GnRH, GnRH2 and GnRH3, as well as the GnRH agonist [D-Arg <superscript>6</superscript> , Pro <superscript>9</superscript> , NEt]-sGnRH were all effective in elevating PRL secretion, PRL mRNA level, PRL cell content and total production. In pituitary cells prepared from the rostral pars distalis, the region in the carp pituitary enriched with lactotrophs, GnRH not only increased cAMP synthesis with parallel CREB phosphorylation and nuclear translocation but also induced a rapid rise in cytosolic Ca <superscript>2+</superscript> by Ca <superscript>2+</superscript> influx via L-type voltage-sensitive Ca <superscript>2+</superscript> channel (VSCC) with subsequent CaM expression and NFAT <subscript>2</subscript> dephosphorylation. In carp pituitary cells prepared from whole pituitaries, GnRH-induced PRL secretion was reduced/negated by inhibiting cAMP/PKA, PLC/PKC and Ca <superscript>2+</superscript> /CaM/CaMK-II pathways but not the signalling events via IP <subscript>3</subscript> and CaN/NFAT. The corresponding effect on PRL mRNA expression, however, was blocked by inhibiting cAMP/PKA/CREB/CBP and Ca <superscript>2+</superscript> /CaM/CaN/NFAT <subscript>2</subscript> signalling but not PLC/IP <subscript>3</subscript> /PKC pathway. At the pituitary cell level, activation of cAMP/PKA pathway could also induce CaM expression and Ca <superscript>2+</superscript> influx via VSCC with parallel rises in PRL release and gene expression in a Ca <superscript>2+</superscript> /CaM-dependent manner. These findings, as a whole, suggest that the cAMP/PKA-, PLC/PKC- and Ca <superscript>2+</superscript> /CaM-dependent cascades are differentially involved in GnRH-induced PRL secretion and PRL transcript expression in carp lactotrophs. During the process, a functional crosstalk between the cAMP/PKA- and Ca <superscript>2+</superscript> /CaM-dependent pathways may occur with PRL release linked with CaMK-II and PKC activation and PRL gene transcription caused by nuclear action of CREB/CBP and CaN/NFAT <subscript>2</subscript> signalling.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.<br /> (Copyright © 2024 Li, Ye, He, Ko, Cheng, Chan and Wong.)

Details

Language :
English
ISSN :
1664-2392
Volume :
15
Database :
MEDLINE
Journal :
Frontiers in endocrinology
Publication Type :
Academic Journal
Accession number :
38894746
Full Text :
https://doi.org/10.3389/fendo.2024.1399274