Irisin inhibition of growth hormone secretion in cultured tilapia pituitary cells
Irisin, the product of fibronectin type III domain-containing protein 5 (FNDC5) gene, is well-documented to be a regulator of energy metabolism. At present, not much is known about its biological function in non-mammalian species. In this study, a full-length tilapia FDNC5 was cloned and its tissue...
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Veröffentlicht in: | Molecular and cellular endocrinology 2017-01, Vol.439, p.395-406 |
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description | Irisin, the product of fibronectin type III domain-containing protein 5 (FNDC5) gene, is well-documented to be a regulator of energy metabolism. At present, not much is known about its biological function in non-mammalian species. In this study, a full-length tilapia FDNC5 was cloned and its tissue expression pattern has been confirmed. Based on the sequence obtained, we produced and purified recombinant irisin which could induce uncoupling protein 1 (UCP1) gene expression in tilapia hepatocytes. Further, the rabbit polyclonal irisin antiserum was produced and its specificity was confirmed by antiserum preabsorption. In tilapia pituitary cells, irisin inhibited growth hormone (GH) gene expression and secretion and triggered rapid phosphorylation of Akt, Erk1/2, and p38 MAPK. Furthermore, irisin-inhibited GH mRNA expression could be prevented by inhibiting PI3K/Akt, MEK1/2, and p38 MAPK, respectively. Apparently, fish irisin can act directly at the pituitary level to inhibit GH transcript expression via multiple signaling pathways.
•Cloning of tilapia FNDC5 and examination of its tissue expression pattern.•Production of recombinant irisin and confirmation of its biological activity.•The antiserum produced was highly specific for tilapia irisin.•Irisin inhibited GH gene expression and secretion in tilapia pituitary cells.•Irisin reduced GH transcript expression via multiple signaling pathways. |
doi_str_mv | 10.1016/j.mce.2016.09.030 |
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•Cloning of tilapia FNDC5 and examination of its tissue expression pattern.•Production of recombinant irisin and confirmation of its biological activity.•The antiserum produced was highly specific for tilapia irisin.•Irisin inhibited GH gene expression and secretion in tilapia pituitary cells.•Irisin reduced GH transcript expression via multiple signaling pathways.</description><identifier>ISSN: 0303-7207</identifier><identifier>EISSN: 1872-8057</identifier><identifier>DOI: 10.1016/j.mce.2016.09.030</identifier><identifier>PMID: 27693813</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Biological Assay ; Cells, Cultured ; Cloning, Molecular ; DNA, Complementary - genetics ; Fibronectins - chemistry ; Fibronectins - genetics ; Fibronectins - metabolism ; Fibronectins - pharmacology ; Gene Expression Profiling ; Gene Expression Regulation - drug effects ; Growth hormone ; Growth Hormone - genetics ; Growth Hormone - metabolism ; Growth Hormone - secretion ; Hepatocytes ; Humans ; Immune Sera - metabolism ; Irisin ; MAP Kinase Signaling System - drug effects ; MAP Kinase Signaling System - genetics ; Pituitary cells ; Pituitary Gland - cytology ; Recombinant Proteins - pharmacology ; Sequence Alignment ; Tilapia ; Tilapia - genetics ; Tilapia - metabolism ; Uncoupling Protein 1 - metabolism</subject><ispartof>Molecular and cellular endocrinology, 2017-01, Vol.439, p.395-406</ispartof><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-111502a4028d9301dc5f7b7e116bcca848dd3ddb8a328ebefd18a1d0a3414e493</citedby><cites>FETCH-LOGICAL-c353t-111502a4028d9301dc5f7b7e116bcca848dd3ddb8a328ebefd18a1d0a3414e493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mce.2016.09.030$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27693813$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lian, Anji</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Jiang, Quan</creatorcontrib><title>Irisin inhibition of growth hormone secretion in cultured tilapia pituitary cells</title><title>Molecular and cellular endocrinology</title><addtitle>Mol Cell Endocrinol</addtitle><description>Irisin, the product of fibronectin type III domain-containing protein 5 (FNDC5) gene, is well-documented to be a regulator of energy metabolism. At present, not much is known about its biological function in non-mammalian species. In this study, a full-length tilapia FDNC5 was cloned and its tissue expression pattern has been confirmed. Based on the sequence obtained, we produced and purified recombinant irisin which could induce uncoupling protein 1 (UCP1) gene expression in tilapia hepatocytes. Further, the rabbit polyclonal irisin antiserum was produced and its specificity was confirmed by antiserum preabsorption. In tilapia pituitary cells, irisin inhibited growth hormone (GH) gene expression and secretion and triggered rapid phosphorylation of Akt, Erk1/2, and p38 MAPK. Furthermore, irisin-inhibited GH mRNA expression could be prevented by inhibiting PI3K/Akt, MEK1/2, and p38 MAPK, respectively. Apparently, fish irisin can act directly at the pituitary level to inhibit GH transcript expression via multiple signaling pathways.
•Cloning of tilapia FNDC5 and examination of its tissue expression pattern.•Production of recombinant irisin and confirmation of its biological activity.•The antiserum produced was highly specific for tilapia irisin.•Irisin inhibited GH gene expression and secretion in tilapia pituitary cells.•Irisin reduced GH transcript expression via multiple signaling pathways.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological Assay</subject><subject>Cells, Cultured</subject><subject>Cloning, Molecular</subject><subject>DNA, Complementary - genetics</subject><subject>Fibronectins - chemistry</subject><subject>Fibronectins - genetics</subject><subject>Fibronectins - metabolism</subject><subject>Fibronectins - pharmacology</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Growth hormone</subject><subject>Growth Hormone - genetics</subject><subject>Growth Hormone - metabolism</subject><subject>Growth Hormone - secretion</subject><subject>Hepatocytes</subject><subject>Humans</subject><subject>Immune Sera - metabolism</subject><subject>Irisin</subject><subject>MAP Kinase Signaling System - drug effects</subject><subject>MAP Kinase Signaling System - genetics</subject><subject>Pituitary cells</subject><subject>Pituitary Gland - cytology</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Sequence Alignment</subject><subject>Tilapia</subject><subject>Tilapia - genetics</subject><subject>Tilapia - metabolism</subject><subject>Uncoupling Protein 1 - metabolism</subject><issn>0303-7207</issn><issn>1872-8057</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PxCAQhonR6Lr6A7yYHr20MtBuaTwZ41diYkz0TChMXTZtWYFq_Peyrnr0BGEe3pl5CDkBWgCFxfmqGDQWLF0L2hSU0x0yA1GzXNCq3iWz9MLzmtH6gByGsKKU1hUT--SA1YuGC-Az8nTvbbBjZselbW20bsxcl7169xGX2dL5wY2YBdQev2uJ1FMfJ48mi7ZXa6uytY2Tjcp_Zhr7PhyRvU71AY9_zjl5ubl-vrrLHx5v768uH3LNKx5zAKgoUyVlwjScgtFVV7c1AixarZUohTHcmFYozgS22BkQCgxVvIQSy4bPydk2d-3d24QhysGGzQRqRDcFCSL1qYBBlVDYotq7EDx2cu3tkCaWQOXGpFzJZFJuTErayI23OTn9iZ_aAc3fj191CbjYApiWfLfoZdAWR43GetRRGmf_if8CdsyEyA</recordid><startdate>20170105</startdate><enddate>20170105</enddate><creator>Lian, Anji</creator><creator>Li, Xin</creator><creator>Jiang, Quan</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170105</creationdate><title>Irisin inhibition of growth hormone secretion in cultured tilapia pituitary cells</title><author>Lian, Anji ; Li, Xin ; Jiang, Quan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-111502a4028d9301dc5f7b7e116bcca848dd3ddb8a328ebefd18a1d0a3414e493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological Assay</topic><topic>Cells, Cultured</topic><topic>Cloning, Molecular</topic><topic>DNA, Complementary - genetics</topic><topic>Fibronectins - chemistry</topic><topic>Fibronectins - genetics</topic><topic>Fibronectins - metabolism</topic><topic>Fibronectins - pharmacology</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Growth hormone</topic><topic>Growth Hormone - genetics</topic><topic>Growth Hormone - metabolism</topic><topic>Growth Hormone - secretion</topic><topic>Hepatocytes</topic><topic>Humans</topic><topic>Immune Sera - metabolism</topic><topic>Irisin</topic><topic>MAP Kinase Signaling System - drug effects</topic><topic>MAP Kinase Signaling System - genetics</topic><topic>Pituitary cells</topic><topic>Pituitary Gland - cytology</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Sequence Alignment</topic><topic>Tilapia</topic><topic>Tilapia - genetics</topic><topic>Tilapia - metabolism</topic><topic>Uncoupling Protein 1 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lian, Anji</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Jiang, Quan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lian, Anji</au><au>Li, Xin</au><au>Jiang, Quan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Irisin inhibition of growth hormone secretion in cultured tilapia pituitary cells</atitle><jtitle>Molecular and cellular endocrinology</jtitle><addtitle>Mol Cell Endocrinol</addtitle><date>2017-01-05</date><risdate>2017</risdate><volume>439</volume><spage>395</spage><epage>406</epage><pages>395-406</pages><issn>0303-7207</issn><eissn>1872-8057</eissn><abstract>Irisin, the product of fibronectin type III domain-containing protein 5 (FNDC5) gene, is well-documented to be a regulator of energy metabolism. At present, not much is known about its biological function in non-mammalian species. In this study, a full-length tilapia FDNC5 was cloned and its tissue expression pattern has been confirmed. Based on the sequence obtained, we produced and purified recombinant irisin which could induce uncoupling protein 1 (UCP1) gene expression in tilapia hepatocytes. Further, the rabbit polyclonal irisin antiserum was produced and its specificity was confirmed by antiserum preabsorption. In tilapia pituitary cells, irisin inhibited growth hormone (GH) gene expression and secretion and triggered rapid phosphorylation of Akt, Erk1/2, and p38 MAPK. Furthermore, irisin-inhibited GH mRNA expression could be prevented by inhibiting PI3K/Akt, MEK1/2, and p38 MAPK, respectively. Apparently, fish irisin can act directly at the pituitary level to inhibit GH transcript expression via multiple signaling pathways.
•Cloning of tilapia FNDC5 and examination of its tissue expression pattern.•Production of recombinant irisin and confirmation of its biological activity.•The antiserum produced was highly specific for tilapia irisin.•Irisin inhibited GH gene expression and secretion in tilapia pituitary cells.•Irisin reduced GH transcript expression via multiple signaling pathways.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>27693813</pmid><doi>10.1016/j.mce.2016.09.030</doi><tpages>12</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Biological Assay Cells, Cultured Cloning, Molecular DNA, Complementary - genetics Fibronectins - chemistry Fibronectins - genetics Fibronectins - metabolism Fibronectins - pharmacology Gene Expression Profiling Gene Expression Regulation - drug effects Growth hormone Growth Hormone - genetics Growth Hormone - metabolism Growth Hormone - secretion Hepatocytes Humans Immune Sera - metabolism Irisin MAP Kinase Signaling System - drug effects MAP Kinase Signaling System - genetics Pituitary cells Pituitary Gland - cytology Recombinant Proteins - pharmacology Sequence Alignment Tilapia Tilapia - genetics Tilapia - metabolism Uncoupling Protein 1 - metabolism |
title | Irisin inhibition of growth hormone secretion in cultured tilapia pituitary cells |
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