Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin

Growth and reproduction are closely related. Growth hormone (GH)-transgenic common carp exhibit accelerated growth and delayed reproductive development, which provides an amenable model to study hormone cross talk between the growth and reproductive axes. We analyzed the energy status and reproducti...

Full description

Bibliographic Details
Main Authors: Ji Chen, Mengxi Cao, Aidi Zhang, Mijuan Shi, Binbin Tao, Yongming Li, Yaping Wang, Zuoyan Zhu, Vance L. Trudeau, Wei Hu
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fendo.2018.00131/full
id doaj-57e88433c23b4cb6971ac47a45bcecec
record_format Article
spelling doaj-57e88433c23b4cb6971ac47a45bcecec2020-11-24T23:49:32ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922018-03-01910.3389/fendo.2018.00131341019Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on LeptinJi Chen0Mengxi Cao1Mengxi Cao2Aidi Zhang3Mijuan Shi4Binbin Tao5Yongming Li6Yaping Wang7Zuoyan Zhu8Vance L. Trudeau9Wei Hu10State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaInstitute of Environment and Health, Jianghan University, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaDepartment of Biology, University of Ottawa, Ottawa, ON, CanadaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaGrowth and reproduction are closely related. Growth hormone (GH)-transgenic common carp exhibit accelerated growth and delayed reproductive development, which provides an amenable model to study hormone cross talk between the growth and reproductive axes. We analyzed the energy status and reproductive development in GH-transgenic common carp by using multi-tissue RNA sequencing, real-time-PCR, Western blotting, ELISA, immunofluorescence, and in vitro incubation. The expression of gys (glycogen synthase) and igfbp1 (insulin-like growth factor binding protein) as well as blood glucose concentrations are lower in GH-transgenic carp. Agrp1 (agouti-related protein 1) and sla (somatolactin a), which are related to appetite and lipid catabolism, are significantly higher in GH-transgenic carp. Low glucose content and increased appetite indicate disrupted metabolic and energy deprivation status in GH-transgenic carp. Meanwhile, the expression of genes, such as gnrhr2 (gonadotropin-releasing hormone receptor 2), gthα (gonadotropin hormone, alpha polypeptide), fshβ (follicle stimulating hormone, beta polypeptide), lhβ [luteinizing hormone, beta polypeptide] in the pituitary, cyp19a1a (aromatase A) in the gonad, and cyp19a1b (aromatase B) in the hypothalamus, are decreased in GH-transgenic carp. In contrast, pituitary gnih (gonadotropin inhibitory hormone), drd1 (dopamine receptor D1), drd3 (dopamine receptor D3), and drd4 (dopamine receptor D4) exhibit increased expression, which were associated with the retarded reproductive development. Leptin receptor mRNA was detected by fluorescence in situ hybridization in the pituitary including the pars intermedia and proximal pars distalis, suggesting a direct effect of leptin on LH. Recombinant carp Leptin protein was shown to stimulate pituitary gthα, fshβ, lhβ expression, and ovarian germinal vesicle breakdown in vitro. In addition to neuroendocrine factors, we suggest that reduced hepatic leptin signaling to the pituitary might be part of the response to overexpression of GH and the resulting delay in puberty onset.http://journal.frontiersin.org/article/10.3389/fendo.2018.00131/fullcommon carpgrowth hormonereproductive regulationenergy balanceleptin
collection DOAJ
language English
format Article
sources DOAJ
author Ji Chen
Mengxi Cao
Mengxi Cao
Aidi Zhang
Mijuan Shi
Binbin Tao
Yongming Li
Yaping Wang
Zuoyan Zhu
Vance L. Trudeau
Wei Hu
spellingShingle Ji Chen
Mengxi Cao
Mengxi Cao
Aidi Zhang
Mijuan Shi
Binbin Tao
Yongming Li
Yaping Wang
Zuoyan Zhu
Vance L. Trudeau
Wei Hu
Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin
Frontiers in Endocrinology
common carp
growth hormone
reproductive regulation
energy balance
leptin
author_facet Ji Chen
Mengxi Cao
Mengxi Cao
Aidi Zhang
Mijuan Shi
Binbin Tao
Yongming Li
Yaping Wang
Zuoyan Zhu
Vance L. Trudeau
Wei Hu
author_sort Ji Chen
title Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin
title_short Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin
title_full Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin
title_fullStr Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin
title_full_unstemmed Growth Hormone Overexpression Disrupts Reproductive Status Through Actions on Leptin
title_sort growth hormone overexpression disrupts reproductive status through actions on leptin
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2018-03-01
description Growth and reproduction are closely related. Growth hormone (GH)-transgenic common carp exhibit accelerated growth and delayed reproductive development, which provides an amenable model to study hormone cross talk between the growth and reproductive axes. We analyzed the energy status and reproductive development in GH-transgenic common carp by using multi-tissue RNA sequencing, real-time-PCR, Western blotting, ELISA, immunofluorescence, and in vitro incubation. The expression of gys (glycogen synthase) and igfbp1 (insulin-like growth factor binding protein) as well as blood glucose concentrations are lower in GH-transgenic carp. Agrp1 (agouti-related protein 1) and sla (somatolactin a), which are related to appetite and lipid catabolism, are significantly higher in GH-transgenic carp. Low glucose content and increased appetite indicate disrupted metabolic and energy deprivation status in GH-transgenic carp. Meanwhile, the expression of genes, such as gnrhr2 (gonadotropin-releasing hormone receptor 2), gthα (gonadotropin hormone, alpha polypeptide), fshβ (follicle stimulating hormone, beta polypeptide), lhβ [luteinizing hormone, beta polypeptide] in the pituitary, cyp19a1a (aromatase A) in the gonad, and cyp19a1b (aromatase B) in the hypothalamus, are decreased in GH-transgenic carp. In contrast, pituitary gnih (gonadotropin inhibitory hormone), drd1 (dopamine receptor D1), drd3 (dopamine receptor D3), and drd4 (dopamine receptor D4) exhibit increased expression, which were associated with the retarded reproductive development. Leptin receptor mRNA was detected by fluorescence in situ hybridization in the pituitary including the pars intermedia and proximal pars distalis, suggesting a direct effect of leptin on LH. Recombinant carp Leptin protein was shown to stimulate pituitary gthα, fshβ, lhβ expression, and ovarian germinal vesicle breakdown in vitro. In addition to neuroendocrine factors, we suggest that reduced hepatic leptin signaling to the pituitary might be part of the response to overexpression of GH and the resulting delay in puberty onset.
topic common carp
growth hormone
reproductive regulation
energy balance
leptin
url http://journal.frontiersin.org/article/10.3389/fendo.2018.00131/full
work_keys_str_mv AT jichen growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT mengxicao growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT mengxicao growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT aidizhang growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT mijuanshi growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT binbintao growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT yongmingli growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT yapingwang growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT zuoyanzhu growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT vanceltrudeau growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
AT weihu growthhormoneoverexpressiondisruptsreproductivestatusthroughactionsonleptin
_version_ 1725481898934796288