Metabolic regulation of ghrelin O-acyl transferase (GOAT) expression in the mouse hypothalamus, pituitary, and stomach
Ghrelin acts as an endocrine link connecting physiological processes regulating food intake, body composition, growth, and energy balance. Ghrelin is the only peptide known to undergo octanoylation. The enzyme mediating this process, ghrelin O-acyltransferase (GOAT), is expressed in the gastrointest...
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creator | Gahete, Manuel D. Córdoba-Chacón, Jose Salvatori, Roberto Castaño, Justo P. Kineman, Rhonda D. Luque, Raul M. |
description | Ghrelin acts as an endocrine link connecting physiological processes regulating food intake, body composition, growth, and energy balance. Ghrelin is the only peptide known to undergo octanoylation. The enzyme mediating this process, ghrelin O-acyltransferase (GOAT), is expressed in the gastrointestinal tract (GI; primary source of circulating ghrelin) as well as other tissues. The present study demonstrates that stomach GOAT mRNA levels correlate with circulating acylated-ghrelin levels in fasted and diet-induced obese mice. In addition, GOAT was found to be expressed in both the pituitary and hypothalamus (two target tissues of ghrelin's actions), and regulated in response to metabolic status. Using primary pituitary cell cultures as a model system to study the regulation of GOAT expression, we found that acylated-ghrelin, but not desacyl-ghrelin, increased GOAT expression. In addition, growth-hormone-releasing hormone (GHRH) and leptin increased, while somatostatin (SST) decreased GOAT expression. The physiologic relevance of these later results is supported by the observation that pituitary GOAT expression in mice lacking GHRH, SST and leptin showed opposite changes to those observed after
in vitro treatment with the corresponding peptides. Therefore, it seems plausible that these hormones directly contribute to the regulation of pituitary GOAT. Interestingly, in all the models studied, pituitary GOAT expression paralleled changes in the expression of a dominant spliced-variant of ghrelin (In2-ghrelin) and therefore this transcript may be a primary substrate for pituitary GOAT. Collectively, these observations support the notion that the GI tract is not the only source of acylated-ghrelin, but in fact locally produced des-acylated-ghrelin could be converted to acylated-ghrelin within target tissues by locally active GOAT, to mediate its tissue-specific effects. |
doi_str_mv | 10.1016/j.mce.2009.12.023 |
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in vitro treatment with the corresponding peptides. Therefore, it seems plausible that these hormones directly contribute to the regulation of pituitary GOAT. Interestingly, in all the models studied, pituitary GOAT expression paralleled changes in the expression of a dominant spliced-variant of ghrelin (In2-ghrelin) and therefore this transcript may be a primary substrate for pituitary GOAT. Collectively, these observations support the notion that the GI tract is not the only source of acylated-ghrelin, but in fact locally produced des-acylated-ghrelin could be converted to acylated-ghrelin within target tissues by locally active GOAT, to mediate its tissue-specific effects.</description><identifier>ISSN: 0303-7207</identifier><identifier>EISSN: 1872-8057</identifier><identifier>EISSN: 0303-7207</identifier><identifier>DOI: 10.1016/j.mce.2009.12.023</identifier><identifier>PMID: 20035826</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Acyltransferases - genetics ; Acyltransferases - metabolism ; Animals ; Cells, Cultured ; Fasting ; Gene Dosage ; Gene Expression Regulation, Enzymologic - drug effects ; Ghrelin - pharmacology ; Ghrelin O-acyl transferase (GOAT) ; Growth Hormone-Releasing Hormone - pharmacology ; Hypothalamus ; Hypothalamus - drug effects ; Hypothalamus - enzymology ; Insulin - pharmacology ; Insulin-Like Growth Factor I - pharmacology ; Leptin - pharmacology ; Mice ; Mouse models (fasting, obesity, knockouts) ; Neuropeptide Y - pharmacology ; Obesity - enzymology ; Pituitary ; Pituitary Gland - cytology ; Pituitary Gland - drug effects ; Pituitary Gland - enzymology ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Somatostatin - pharmacology ; Stomach ; Stomach - drug effects ; Stomach - enzymology</subject><ispartof>Molecular and cellular endocrinology, 2010-04, Vol.317 (1), p.154-160</ispartof><rights>2010 Elsevier Ireland Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c582t-de0a8d79ed5b2fdeb48ee72b9ff69a69006a924e27e8d2a1afbc75b3d8ed45313</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0303720709006546$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20035826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00559596$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gahete, Manuel D.</creatorcontrib><creatorcontrib>Córdoba-Chacón, Jose</creatorcontrib><creatorcontrib>Salvatori, Roberto</creatorcontrib><creatorcontrib>Castaño, Justo P.</creatorcontrib><creatorcontrib>Kineman, Rhonda D.</creatorcontrib><creatorcontrib>Luque, Raul M.</creatorcontrib><title>Metabolic regulation of ghrelin O-acyl transferase (GOAT) expression in the mouse hypothalamus, pituitary, and stomach</title><title>Molecular and cellular endocrinology</title><addtitle>Mol Cell Endocrinol</addtitle><description>Ghrelin acts as an endocrine link connecting physiological processes regulating food intake, body composition, growth, and energy balance. Ghrelin is the only peptide known to undergo octanoylation. The enzyme mediating this process, ghrelin O-acyltransferase (GOAT), is expressed in the gastrointestinal tract (GI; primary source of circulating ghrelin) as well as other tissues. The present study demonstrates that stomach GOAT mRNA levels correlate with circulating acylated-ghrelin levels in fasted and diet-induced obese mice. In addition, GOAT was found to be expressed in both the pituitary and hypothalamus (two target tissues of ghrelin's actions), and regulated in response to metabolic status. Using primary pituitary cell cultures as a model system to study the regulation of GOAT expression, we found that acylated-ghrelin, but not desacyl-ghrelin, increased GOAT expression. In addition, growth-hormone-releasing hormone (GHRH) and leptin increased, while somatostatin (SST) decreased GOAT expression. The physiologic relevance of these later results is supported by the observation that pituitary GOAT expression in mice lacking GHRH, SST and leptin showed opposite changes to those observed after
in vitro treatment with the corresponding peptides. Therefore, it seems plausible that these hormones directly contribute to the regulation of pituitary GOAT. Interestingly, in all the models studied, pituitary GOAT expression paralleled changes in the expression of a dominant spliced-variant of ghrelin (In2-ghrelin) and therefore this transcript may be a primary substrate for pituitary GOAT. Collectively, these observations support the notion that the GI tract is not the only source of acylated-ghrelin, but in fact locally produced des-acylated-ghrelin could be converted to acylated-ghrelin within target tissues by locally active GOAT, to mediate its tissue-specific effects.</description><subject>Acyltransferases - genetics</subject><subject>Acyltransferases - metabolism</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Fasting</subject><subject>Gene Dosage</subject><subject>Gene Expression Regulation, Enzymologic - drug effects</subject><subject>Ghrelin - pharmacology</subject><subject>Ghrelin O-acyl transferase (GOAT)</subject><subject>Growth Hormone-Releasing Hormone - pharmacology</subject><subject>Hypothalamus</subject><subject>Hypothalamus - drug effects</subject><subject>Hypothalamus - enzymology</subject><subject>Insulin - pharmacology</subject><subject>Insulin-Like Growth Factor I - pharmacology</subject><subject>Leptin - pharmacology</subject><subject>Mice</subject><subject>Mouse models (fasting, obesity, knockouts)</subject><subject>Neuropeptide Y - pharmacology</subject><subject>Obesity - enzymology</subject><subject>Pituitary</subject><subject>Pituitary Gland - cytology</subject><subject>Pituitary Gland - drug effects</subject><subject>Pituitary Gland - enzymology</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Somatostatin - pharmacology</subject><subject>Stomach</subject><subject>Stomach - drug effects</subject><subject>Stomach - enzymology</subject><issn>0303-7207</issn><issn>1872-8057</issn><issn>0303-7207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV-L1DAUxYso7rj6AXyRvOnCdkzSpk1YEIZFd4WReVmfQ5rcTjO0TU3Swfn2psy6qA8-BXJ_59w_J8veErwmmFQfD-tBw5piLNaErjEtnmUrwmuac8zq59kKF7jIa4rri-xVCAeMcc0of5ldJEnBOK1W2fEbRNW43mrkYT_3Klo3IteifeehtyPa5UqfehS9GkMLXgVAH-52m4crBD8nDyEsfOJiB2hwcyp3p8nFTvVqmMM1mmycbVT-dI3UaFCIblC6e529aFUf4M3je5l9__L54fY-3-7uvt5utrlO48XcAFbc1AIMa2hroCk5QE0b0baVUJXAuFKClkBr4IYqotpG16wpDAdTsoIUl9mns-80NwMYDWNapJeTt0MaSTpl5d-V0XZy746SciJwhZPB1dmg-0d2v9nK5Q9jxgQT1XFp9v6xmXc_ZghRDjZo6Hs1QrqM5KIiXLCyTCQ5k9q7EDy0T9YEyyVaeZApWrlEKwmVKdqkeffnKk-K31km4OYMQDro0YKXQVsYNRjrQUdpnP2P_S8ESbb_</recordid><startdate>20100412</startdate><enddate>20100412</enddate><creator>Gahete, Manuel D.</creator><creator>Córdoba-Chacón, Jose</creator><creator>Salvatori, Roberto</creator><creator>Castaño, Justo P.</creator><creator>Kineman, Rhonda D.</creator><creator>Luque, Raul M.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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>7TK</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope></search><sort><creationdate>20100412</creationdate><title>Metabolic regulation of ghrelin O-acyl transferase (GOAT) expression in the mouse hypothalamus, pituitary, and stomach</title><author>Gahete, Manuel D. ; Córdoba-Chacón, Jose ; Salvatori, Roberto ; Castaño, Justo P. ; Kineman, Rhonda D. ; Luque, Raul M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c582t-de0a8d79ed5b2fdeb48ee72b9ff69a69006a924e27e8d2a1afbc75b3d8ed45313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acyltransferases - genetics</topic><topic>Acyltransferases - metabolism</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Fasting</topic><topic>Gene Dosage</topic><topic>Gene Expression Regulation, Enzymologic - drug effects</topic><topic>Ghrelin - pharmacology</topic><topic>Ghrelin O-acyl transferase (GOAT)</topic><topic>Growth Hormone-Releasing Hormone - pharmacology</topic><topic>Hypothalamus</topic><topic>Hypothalamus - drug effects</topic><topic>Hypothalamus - enzymology</topic><topic>Insulin - pharmacology</topic><topic>Insulin-Like Growth Factor I - pharmacology</topic><topic>Leptin - pharmacology</topic><topic>Mice</topic><topic>Mouse models (fasting, obesity, knockouts)</topic><topic>Neuropeptide Y - pharmacology</topic><topic>Obesity - enzymology</topic><topic>Pituitary</topic><topic>Pituitary Gland - cytology</topic><topic>Pituitary Gland - drug effects</topic><topic>Pituitary Gland - enzymology</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Somatostatin - pharmacology</topic><topic>Stomach</topic><topic>Stomach - drug effects</topic><topic>Stomach - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gahete, Manuel D.</creatorcontrib><creatorcontrib>Córdoba-Chacón, Jose</creatorcontrib><creatorcontrib>Salvatori, Roberto</creatorcontrib><creatorcontrib>Castaño, Justo P.</creatorcontrib><creatorcontrib>Kineman, Rhonda D.</creatorcontrib><creatorcontrib>Luque, Raul M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular and cellular endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gahete, Manuel D.</au><au>Córdoba-Chacón, Jose</au><au>Salvatori, Roberto</au><au>Castaño, Justo P.</au><au>Kineman, Rhonda D.</au><au>Luque, Raul M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic regulation of ghrelin O-acyl transferase (GOAT) expression in the mouse hypothalamus, pituitary, and stomach</atitle><jtitle>Molecular and cellular endocrinology</jtitle><addtitle>Mol Cell Endocrinol</addtitle><date>2010-04-12</date><risdate>2010</risdate><volume>317</volume><issue>1</issue><spage>154</spage><epage>160</epage><pages>154-160</pages><issn>0303-7207</issn><eissn>1872-8057</eissn><eissn>0303-7207</eissn><abstract>Ghrelin acts as an endocrine link connecting physiological processes regulating food intake, body composition, growth, and energy balance. Ghrelin is the only peptide known to undergo octanoylation. The enzyme mediating this process, ghrelin O-acyltransferase (GOAT), is expressed in the gastrointestinal tract (GI; primary source of circulating ghrelin) as well as other tissues. The present study demonstrates that stomach GOAT mRNA levels correlate with circulating acylated-ghrelin levels in fasted and diet-induced obese mice. In addition, GOAT was found to be expressed in both the pituitary and hypothalamus (two target tissues of ghrelin's actions), and regulated in response to metabolic status. Using primary pituitary cell cultures as a model system to study the regulation of GOAT expression, we found that acylated-ghrelin, but not desacyl-ghrelin, increased GOAT expression. In addition, growth-hormone-releasing hormone (GHRH) and leptin increased, while somatostatin (SST) decreased GOAT expression. The physiologic relevance of these later results is supported by the observation that pituitary GOAT expression in mice lacking GHRH, SST and leptin showed opposite changes to those observed after
in vitro treatment with the corresponding peptides. Therefore, it seems plausible that these hormones directly contribute to the regulation of pituitary GOAT. Interestingly, in all the models studied, pituitary GOAT expression paralleled changes in the expression of a dominant spliced-variant of ghrelin (In2-ghrelin) and therefore this transcript may be a primary substrate for pituitary GOAT. Collectively, these observations support the notion that the GI tract is not the only source of acylated-ghrelin, but in fact locally produced des-acylated-ghrelin could be converted to acylated-ghrelin within target tissues by locally active GOAT, to mediate its tissue-specific effects.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>20035826</pmid><doi>10.1016/j.mce.2009.12.023</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acyltransferases - genetics Acyltransferases - metabolism Animals Cells, Cultured Fasting Gene Dosage Gene Expression Regulation, Enzymologic - drug effects Ghrelin - pharmacology Ghrelin O-acyl transferase (GOAT) Growth Hormone-Releasing Hormone - pharmacology Hypothalamus Hypothalamus - drug effects Hypothalamus - enzymology Insulin - pharmacology Insulin-Like Growth Factor I - pharmacology Leptin - pharmacology Mice Mouse models (fasting, obesity, knockouts) Neuropeptide Y - pharmacology Obesity - enzymology Pituitary Pituitary Gland - cytology Pituitary Gland - drug effects Pituitary Gland - enzymology RNA, Messenger - genetics RNA, Messenger - metabolism Somatostatin - pharmacology Stomach Stomach - drug effects Stomach - enzymology |
title | Metabolic regulation of ghrelin O-acyl transferase (GOAT) expression in the mouse hypothalamus, pituitary, and stomach |
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