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Morphological analysis of ghrelin and its receptor distribution in the rat pancreas
Ghrelin, a novel peptide isolated from stomach tissue of rats and humans, has been identified as the endogenous ligand for the growth hormone secretagogue receptor (GHS-R). In addition to its secretion from the stomach, ghrelin is also expressed in the hypothalamic arcuate nucleus, intestine, kidney...
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Published in: | Regulatory peptides 2005-03, Vol.126 (1), p.67-71 |
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creator | Kageyama, Haruaki Funahashi, Hisayuki Hirayama, Masami Takenoya, Fumiko Kita, Tetsuro Kato, Sachi Sakurai, Junko Lee, Eun Young Inoue, Shuji Date, Yukari Nakazato, Masamitsu Kangawa, Kenji Shioda, Seiji |
description | Ghrelin, a novel peptide isolated from stomach tissue of rats and humans, has been identified as the endogenous ligand for the growth hormone secretagogue receptor (GHS-R). In addition to its secretion from the stomach, ghrelin is also expressed in the hypothalamic arcuate nucleus, intestine, kidney, placenta, and pancreas. GHS-R mRNA, on the other hand, is expressed in the hypothalamus, pituitary, heart, lung, liver, pancreas, stomach, intestine, and adipose tissue. Ghrelin is considered to have important roles in feeding regulation and energy metabolism as well as in the release of growth hormone (GH). Recent physiological experiments on the pancreas have shown that ghrelin regulates insulin secretion. However, sites of action of ghrelin in the pancreas are yet to be identified. In this study, to gain insight into the role of ghrelin in rat pancreatic islets, we used immunohistochemistry to determine the localization of ghrelin and GHS-R in islet cells. Double fluorescence immunohistochemistry revealed that weak GHS-R-like immunoreactivity was found in B cells containing insulin. GHS-R immunoreactivity overlapped that of glucagon-like immunoreactive cells. Moreover, both ghrelin and GHS-R-like immunoreactivities were detected mostly in the same cells in the periphery of the islets of Langerhans. These observations suggest that ghrelin is synthesized and secreted from A cells, and acts back on A cells in an autocrine and/or paracrine manner. In addition, ghrelin may act on B cells via GHS-R to regulate insulin secretion. |
doi_str_mv | 10.1016/j.regpep.2004.08.031 |
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In addition to its secretion from the stomach, ghrelin is also expressed in the hypothalamic arcuate nucleus, intestine, kidney, placenta, and pancreas. GHS-R mRNA, on the other hand, is expressed in the hypothalamus, pituitary, heart, lung, liver, pancreas, stomach, intestine, and adipose tissue. Ghrelin is considered to have important roles in feeding regulation and energy metabolism as well as in the release of growth hormone (GH). Recent physiological experiments on the pancreas have shown that ghrelin regulates insulin secretion. However, sites of action of ghrelin in the pancreas are yet to be identified. In this study, to gain insight into the role of ghrelin in rat pancreatic islets, we used immunohistochemistry to determine the localization of ghrelin and GHS-R in islet cells. Double fluorescence immunohistochemistry revealed that weak GHS-R-like immunoreactivity was found in B cells containing insulin. GHS-R immunoreactivity overlapped that of glucagon-like immunoreactive cells. Moreover, both ghrelin and GHS-R-like immunoreactivities were detected mostly in the same cells in the periphery of the islets of Langerhans. These observations suggest that ghrelin is synthesized and secreted from A cells, and acts back on A cells in an autocrine and/or paracrine manner. In addition, ghrelin may act on B cells via GHS-R to regulate insulin secretion.</description><identifier>ISSN: 0167-0115</identifier><identifier>EISSN: 1873-1686</identifier><identifier>DOI: 10.1016/j.regpep.2004.08.031</identifier><identifier>PMID: 15620416</identifier><identifier>CODEN: REPPDY</identifier><language>eng</language><publisher>Shannon: Elsevier B.V</publisher><subject>A cell ; Animals ; Biological and medical sciences ; Fundamental and applied biological sciences. 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In addition to its secretion from the stomach, ghrelin is also expressed in the hypothalamic arcuate nucleus, intestine, kidney, placenta, and pancreas. GHS-R mRNA, on the other hand, is expressed in the hypothalamus, pituitary, heart, lung, liver, pancreas, stomach, intestine, and adipose tissue. Ghrelin is considered to have important roles in feeding regulation and energy metabolism as well as in the release of growth hormone (GH). Recent physiological experiments on the pancreas have shown that ghrelin regulates insulin secretion. However, sites of action of ghrelin in the pancreas are yet to be identified. In this study, to gain insight into the role of ghrelin in rat pancreatic islets, we used immunohistochemistry to determine the localization of ghrelin and GHS-R in islet cells. Double fluorescence immunohistochemistry revealed that weak GHS-R-like immunoreactivity was found in B cells containing insulin. GHS-R immunoreactivity overlapped that of glucagon-like immunoreactive cells. Moreover, both ghrelin and GHS-R-like immunoreactivities were detected mostly in the same cells in the periphery of the islets of Langerhans. These observations suggest that ghrelin is synthesized and secreted from A cells, and acts back on A cells in an autocrine and/or paracrine manner. In addition, ghrelin may act on B cells via GHS-R to regulate insulin secretion.</description><subject>A cell</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ghrelin</subject><subject>Growth Hormone - metabolism</subject><subject>Growth hormone secretagogue receptor (GHS-R)</subject><subject>Immunohistochemistry</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Islets of Langerhans - cytology</subject><subject>Islets of Langerhans - metabolism</subject><subject>Male</subject><subject>Pancreas</subject><subject>Peptide Hormones - biosynthesis</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, G-Protein-Coupled - biosynthesis</subject><subject>Receptors, Ghrelin</subject><subject>Vertebrates: endocrinology</subject><issn>0167-0115</issn><issn>1873-1686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp90E2LFDEQgOEgijuu_gORXPTWbVWnO8lJkMUvWPGgnkMmqcxk6Om0SUbYf2-GGdibp0DxVhEexl4j9Ago3x_6TLuV1n4AGHvQPQh8wjaolehQavmUbVqmOkCcbtiLUg4AOCklnrMbnOQAI8oN-_k95XWf5rSLzs7cLnZ-KLHwFPhun2mOS5t5HmvhmRytNWXuY6k5bk81poW3oO6JZ1v5aheXyZaX7Fmwc6FX1_eW_f786dfd1-7-x5dvdx_vOzdOsna4VU64QYPS2k4YBGmLAV2wY_DSk9SEWk_CAYUJxeQ9DmFQAF4LGgSJW_bucnfN6c-JSjXHWBzNs10onYqRSgiBGls4XkKXUymZgllzPNr8YBDMGdMczAXTnDENaNMw29qb6_3T9kj-cemq14K318CWphdyA4jlsZOjUBrOhz5cOmoafyNlU1ykxZGPDbUan-L_f_IPJ8OVLw</recordid><startdate>20050315</startdate><enddate>20050315</enddate><creator>Kageyama, Haruaki</creator><creator>Funahashi, Hisayuki</creator><creator>Hirayama, Masami</creator><creator>Takenoya, Fumiko</creator><creator>Kita, Tetsuro</creator><creator>Kato, Sachi</creator><creator>Sakurai, Junko</creator><creator>Lee, Eun Young</creator><creator>Inoue, Shuji</creator><creator>Date, Yukari</creator><creator>Nakazato, Masamitsu</creator><creator>Kangawa, Kenji</creator><creator>Shioda, Seiji</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>20050315</creationdate><title>Morphological analysis of ghrelin and its receptor distribution in the rat pancreas</title><author>Kageyama, Haruaki ; Funahashi, Hisayuki ; Hirayama, Masami ; Takenoya, Fumiko ; Kita, Tetsuro ; Kato, Sachi ; Sakurai, Junko ; Lee, Eun Young ; Inoue, Shuji ; Date, Yukari ; Nakazato, Masamitsu ; Kangawa, Kenji ; Shioda, Seiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-1b7c3c280788a51f3e8a1f1cfa4fd6de68e18853c0ef5135dd12f2700d83e23e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>A cell</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ghrelin</topic><topic>Growth Hormone - metabolism</topic><topic>Growth hormone secretagogue receptor (GHS-R)</topic><topic>Immunohistochemistry</topic><topic>Insulin - metabolism</topic><topic>Insulin Secretion</topic><topic>Islets of Langerhans - cytology</topic><topic>Islets of Langerhans - metabolism</topic><topic>Male</topic><topic>Pancreas</topic><topic>Peptide Hormones - biosynthesis</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, G-Protein-Coupled - biosynthesis</topic><topic>Receptors, Ghrelin</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kageyama, Haruaki</creatorcontrib><creatorcontrib>Funahashi, Hisayuki</creatorcontrib><creatorcontrib>Hirayama, Masami</creatorcontrib><creatorcontrib>Takenoya, Fumiko</creatorcontrib><creatorcontrib>Kita, Tetsuro</creatorcontrib><creatorcontrib>Kato, Sachi</creatorcontrib><creatorcontrib>Sakurai, Junko</creatorcontrib><creatorcontrib>Lee, Eun Young</creatorcontrib><creatorcontrib>Inoue, Shuji</creatorcontrib><creatorcontrib>Date, Yukari</creatorcontrib><creatorcontrib>Nakazato, Masamitsu</creatorcontrib><creatorcontrib>Kangawa, Kenji</creatorcontrib><creatorcontrib>Shioda, Seiji</creatorcontrib><collection>Pascal-Francis</collection><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>Regulatory peptides</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kageyama, Haruaki</au><au>Funahashi, Hisayuki</au><au>Hirayama, Masami</au><au>Takenoya, Fumiko</au><au>Kita, Tetsuro</au><au>Kato, Sachi</au><au>Sakurai, Junko</au><au>Lee, Eun Young</au><au>Inoue, Shuji</au><au>Date, Yukari</au><au>Nakazato, Masamitsu</au><au>Kangawa, Kenji</au><au>Shioda, Seiji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological analysis of ghrelin and its receptor distribution in the rat pancreas</atitle><jtitle>Regulatory peptides</jtitle><addtitle>Regul Pept</addtitle><date>2005-03-15</date><risdate>2005</risdate><volume>126</volume><issue>1</issue><spage>67</spage><epage>71</epage><pages>67-71</pages><issn>0167-0115</issn><eissn>1873-1686</eissn><coden>REPPDY</coden><abstract>Ghrelin, a novel peptide isolated from stomach tissue of rats and humans, has been identified as the endogenous ligand for the growth hormone secretagogue receptor (GHS-R). In addition to its secretion from the stomach, ghrelin is also expressed in the hypothalamic arcuate nucleus, intestine, kidney, placenta, and pancreas. GHS-R mRNA, on the other hand, is expressed in the hypothalamus, pituitary, heart, lung, liver, pancreas, stomach, intestine, and adipose tissue. Ghrelin is considered to have important roles in feeding regulation and energy metabolism as well as in the release of growth hormone (GH). Recent physiological experiments on the pancreas have shown that ghrelin regulates insulin secretion. However, sites of action of ghrelin in the pancreas are yet to be identified. In this study, to gain insight into the role of ghrelin in rat pancreatic islets, we used immunohistochemistry to determine the localization of ghrelin and GHS-R in islet cells. Double fluorescence immunohistochemistry revealed that weak GHS-R-like immunoreactivity was found in B cells containing insulin. GHS-R immunoreactivity overlapped that of glucagon-like immunoreactive cells. Moreover, both ghrelin and GHS-R-like immunoreactivities were detected mostly in the same cells in the periphery of the islets of Langerhans. These observations suggest that ghrelin is synthesized and secreted from A cells, and acts back on A cells in an autocrine and/or paracrine manner. In addition, ghrelin may act on B cells via GHS-R to regulate insulin secretion.</abstract><cop>Shannon</cop><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15620416</pmid><doi>10.1016/j.regpep.2004.08.031</doi><tpages>5</tpages></addata></record> |
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subjects | A cell Animals Biological and medical sciences Fundamental and applied biological sciences. Psychology Ghrelin Growth Hormone - metabolism Growth hormone secretagogue receptor (GHS-R) Immunohistochemistry Insulin - metabolism Insulin Secretion Islets of Langerhans - cytology Islets of Langerhans - metabolism Male Pancreas Peptide Hormones - biosynthesis Rats Rats, Sprague-Dawley Receptors, G-Protein-Coupled - biosynthesis Receptors, Ghrelin Vertebrates: endocrinology |
title | Morphological analysis of ghrelin and its receptor distribution in the rat pancreas |
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