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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Veröffentlicht in:Molecular and cellular endocrinology 2010-04, Vol.317 (1), p.154-160
Hauptverfasser: Gahete, Manuel D., Córdoba-Chacón, Jose, Salvatori, Roberto, Castaño, Justo P., Kineman, Rhonda D., Luque, Raul M.
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container_end_page 160
container_issue 1
container_start_page 154
container_title Molecular and cellular endocrinology
container_volume 317
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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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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