Regulation of gut-derived resistin-like molecule β expression by nutrients

Abstract Resistin was initially identified as a protein, secreted by adipocytes, which inhibits insulin action and adipose differentiation. The three proteins homologous to resistin were identified and given the names resistin-like molecules (RELM) α, β and γ. Resistin and RELMα are abundantly expre...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Diabetes research and clinical practice 2008-01, Vol.79 (1), p.2-10
Hauptverfasser: Fujio, Junko, Kushiyama, Akifumi, Sakoda, Hideyuki, Fujishiro, Midori, Ogihara, Takehide, Fukushima, Yasushi, Anai, Motonobu, Horike, Nanao, Kamata, Hideaki, Uchijima, Yasunobu, Kurihara, Hiroki, Asano, Tomoichiro
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10
container_issue 1
container_start_page 2
container_title Diabetes research and clinical practice
container_volume 79
creator Fujio, Junko
Kushiyama, Akifumi
Sakoda, Hideyuki
Fujishiro, Midori
Ogihara, Takehide
Fukushima, Yasushi
Anai, Motonobu
Horike, Nanao
Kamata, Hideaki
Uchijima, Yasunobu
Kurihara, Hiroki
Asano, Tomoichiro
description Abstract Resistin was initially identified as a protein, secreted by adipocytes, which inhibits insulin action and adipose differentiation. The three proteins homologous to resistin were identified and given the names resistin-like molecules (RELM) α, β and γ. Resistin and RELMα are abundantly expressed in adipose, but RELMβ and RELMγ are secreted mainly from the gut. Since nutrient composition greatly affects insulin sensitivity, we investigated the regulatory effects of various nutritional factors in food on the expressions of resistin family proteins. First, mice were given diets with different nutritional compositions (high-carbohydrate, high-protein and high-fat) for 2 weeks. RELMβ mRNA expression in the intestines was markedly suppressed by the high-protein and high-carbohydrate diets, while slightly but not significantly upregulated by the high-fat diet. In the epididymal fat, resistin expression was unchanged, while RELMα expression was markedly decreased by the high-carbohydrate diet. Taking into consideration that humans have neither RELMα nor RELMγ, our subsequent studies focused on RELMβ expression. We used the human colon cancer cell line LS174T. Treatments with insulin and TNFα as well as stearic acid, a saturated free fatty acid, upregulated RELMβ expression, while d -glucose downregulated RELMβ. These results suggest RELMβ expression to be regulated directly by nutrients such as glucose and saturated free fatty acids including stearic acid, as well as by hormones including insulin and TNFα. These regulations may play an important role in the nutrient-associated induction of insulin resistance.
doi_str_mv 10.1016/j.diabres.2007.04.015
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70185260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S016882270700424X</els_id><sourcerecordid>70185260</sourcerecordid><originalsourceid>FETCH-LOGICAL-c418t-1b612181e176585d990baf063813b65c41672c516c23a2268ee15fc510a6ec373</originalsourceid><addsrcrecordid>eNqFkc9u1DAQhy0EotvCI4By4pYw48R_9gJCVSmISkgtSNwsx5lU3nqTxU6q7mvxIDwTDrtSJS6cbNnfb8b-hrFXCBUCyrebqvO2jZQqDqAqaCpA8YStUCteas7VU7bKnP67P2GnKW0AQNaNeM5OUK1rWa_1in25pts52MmPQzH2xe08lR1Ff09dkWv7NPmhDP6Oiu0YyM2Bit-_CnrY5cu0ZNp9McxT9DRM6QV71tuQ6OVxPWPfP158O_9UXn29_Hz-4ap0DeqpxFYiR42ESgotuvUaWtvnp2msWykyJBV3AqXjteVcaiIUfT4AK8nVqj5jbw51d3H8OVOazNYnRyHYgcY5GQWoBZeQQXEAXRxTitSbXfRbG_cGwSwWzcYcLZrFooHGZIs59_rYYG631D2mjtoy8P4AUP7mvadokssKHHU-kptMN_r_tnj3TwUX_OCdDXe0p7QZ5zhkhwZN4gbMzTLKZZKgABre_Kj_AJ1vmxU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70185260</pqid></control><display><type>article</type><title>Regulation of gut-derived resistin-like molecule β expression by nutrients</title><source>Elsevier ScienceDirect Journals Complete - AutoHoldings</source><source>MEDLINE</source><creator>Fujio, Junko ; Kushiyama, Akifumi ; Sakoda, Hideyuki ; Fujishiro, Midori ; Ogihara, Takehide ; Fukushima, Yasushi ; Anai, Motonobu ; Horike, Nanao ; Kamata, Hideaki ; Uchijima, Yasunobu ; Kurihara, Hiroki ; Asano, Tomoichiro</creator><creatorcontrib>Fujio, Junko ; Kushiyama, Akifumi ; Sakoda, Hideyuki ; Fujishiro, Midori ; Ogihara, Takehide ; Fukushima, Yasushi ; Anai, Motonobu ; Horike, Nanao ; Kamata, Hideaki ; Uchijima, Yasunobu ; Kurihara, Hiroki ; Asano, Tomoichiro</creatorcontrib><description>Abstract Resistin was initially identified as a protein, secreted by adipocytes, which inhibits insulin action and adipose differentiation. The three proteins homologous to resistin were identified and given the names resistin-like molecules (RELM) α, β and γ. Resistin and RELMα are abundantly expressed in adipose, but RELMβ and RELMγ are secreted mainly from the gut. Since nutrient composition greatly affects insulin sensitivity, we investigated the regulatory effects of various nutritional factors in food on the expressions of resistin family proteins. First, mice were given diets with different nutritional compositions (high-carbohydrate, high-protein and high-fat) for 2 weeks. RELMβ mRNA expression in the intestines was markedly suppressed by the high-protein and high-carbohydrate diets, while slightly but not significantly upregulated by the high-fat diet. In the epididymal fat, resistin expression was unchanged, while RELMα expression was markedly decreased by the high-carbohydrate diet. Taking into consideration that humans have neither RELMα nor RELMγ, our subsequent studies focused on RELMβ expression. We used the human colon cancer cell line LS174T. Treatments with insulin and TNFα as well as stearic acid, a saturated free fatty acid, upregulated RELMβ expression, while d -glucose downregulated RELMβ. These results suggest RELMβ expression to be regulated directly by nutrients such as glucose and saturated free fatty acids including stearic acid, as well as by hormones including insulin and TNFα. These regulations may play an important role in the nutrient-associated induction of insulin resistance.</description><identifier>ISSN: 0168-8227</identifier><identifier>EISSN: 1872-8227</identifier><identifier>DOI: 10.1016/j.diabres.2007.04.015</identifier><identifier>PMID: 17936398</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animal Feed ; Animals ; Diet ; Dietary Carbohydrates - pharmacology ; Dietary Fats - pharmacology ; Dietary Proteins - pharmacology ; Eating ; Endocrinology &amp; Metabolism ; Fasting ; Fatty Acids, Nonesterified - pharmacology ; Gene Expression Regulation - drug effects ; Gene Expression Regulation - physiology ; Glucose - pharmacology ; Hormones, Ectopic - genetics ; Insulin resistance ; Intestines - physiology ; Mice ; Mice, Inbred C57BL ; Nutrient compositions ; RELMβ ; Resistin - genetics ; RNA, Messenger - genetics ; Stearic Acids - pharmacology ; Tumor Necrosis Factor-alpha - pharmacology</subject><ispartof>Diabetes research and clinical practice, 2008-01, Vol.79 (1), p.2-10</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2007 Elsevier Ireland Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-1b612181e176585d990baf063813b65c41672c516c23a2268ee15fc510a6ec373</citedby><cites>FETCH-LOGICAL-c418t-1b612181e176585d990baf063813b65c41672c516c23a2268ee15fc510a6ec373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.diabres.2007.04.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17936398$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujio, Junko</creatorcontrib><creatorcontrib>Kushiyama, Akifumi</creatorcontrib><creatorcontrib>Sakoda, Hideyuki</creatorcontrib><creatorcontrib>Fujishiro, Midori</creatorcontrib><creatorcontrib>Ogihara, Takehide</creatorcontrib><creatorcontrib>Fukushima, Yasushi</creatorcontrib><creatorcontrib>Anai, Motonobu</creatorcontrib><creatorcontrib>Horike, Nanao</creatorcontrib><creatorcontrib>Kamata, Hideaki</creatorcontrib><creatorcontrib>Uchijima, Yasunobu</creatorcontrib><creatorcontrib>Kurihara, Hiroki</creatorcontrib><creatorcontrib>Asano, Tomoichiro</creatorcontrib><title>Regulation of gut-derived resistin-like molecule β expression by nutrients</title><title>Diabetes research and clinical practice</title><addtitle>Diabetes Res Clin Pract</addtitle><description>Abstract Resistin was initially identified as a protein, secreted by adipocytes, which inhibits insulin action and adipose differentiation. The three proteins homologous to resistin were identified and given the names resistin-like molecules (RELM) α, β and γ. Resistin and RELMα are abundantly expressed in adipose, but RELMβ and RELMγ are secreted mainly from the gut. Since nutrient composition greatly affects insulin sensitivity, we investigated the regulatory effects of various nutritional factors in food on the expressions of resistin family proteins. First, mice were given diets with different nutritional compositions (high-carbohydrate, high-protein and high-fat) for 2 weeks. RELMβ mRNA expression in the intestines was markedly suppressed by the high-protein and high-carbohydrate diets, while slightly but not significantly upregulated by the high-fat diet. In the epididymal fat, resistin expression was unchanged, while RELMα expression was markedly decreased by the high-carbohydrate diet. Taking into consideration that humans have neither RELMα nor RELMγ, our subsequent studies focused on RELMβ expression. We used the human colon cancer cell line LS174T. Treatments with insulin and TNFα as well as stearic acid, a saturated free fatty acid, upregulated RELMβ expression, while d -glucose downregulated RELMβ. These results suggest RELMβ expression to be regulated directly by nutrients such as glucose and saturated free fatty acids including stearic acid, as well as by hormones including insulin and TNFα. These regulations may play an important role in the nutrient-associated induction of insulin resistance.</description><subject>Animal Feed</subject><subject>Animals</subject><subject>Diet</subject><subject>Dietary Carbohydrates - pharmacology</subject><subject>Dietary Fats - pharmacology</subject><subject>Dietary Proteins - pharmacology</subject><subject>Eating</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Fasting</subject><subject>Fatty Acids, Nonesterified - pharmacology</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Gene Expression Regulation - physiology</subject><subject>Glucose - pharmacology</subject><subject>Hormones, Ectopic - genetics</subject><subject>Insulin resistance</subject><subject>Intestines - physiology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Nutrient compositions</subject><subject>RELMβ</subject><subject>Resistin - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>Stearic Acids - pharmacology</subject><subject>Tumor Necrosis Factor-alpha - pharmacology</subject><issn>0168-8227</issn><issn>1872-8227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQhy0EotvCI4By4pYw48R_9gJCVSmISkgtSNwsx5lU3nqTxU6q7mvxIDwTDrtSJS6cbNnfb8b-hrFXCBUCyrebqvO2jZQqDqAqaCpA8YStUCteas7VU7bKnP67P2GnKW0AQNaNeM5OUK1rWa_1in25pts52MmPQzH2xe08lR1Ff09dkWv7NPmhDP6Oiu0YyM2Bit-_CnrY5cu0ZNp9McxT9DRM6QV71tuQ6OVxPWPfP158O_9UXn29_Hz-4ap0DeqpxFYiR42ESgotuvUaWtvnp2msWykyJBV3AqXjteVcaiIUfT4AK8nVqj5jbw51d3H8OVOazNYnRyHYgcY5GQWoBZeQQXEAXRxTitSbXfRbG_cGwSwWzcYcLZrFooHGZIs59_rYYG631D2mjtoy8P4AUP7mvadokssKHHU-kptMN_r_tnj3TwUX_OCdDXe0p7QZ5zhkhwZN4gbMzTLKZZKgABre_Kj_AJ1vmxU</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Fujio, Junko</creator><creator>Kushiyama, Akifumi</creator><creator>Sakoda, Hideyuki</creator><creator>Fujishiro, Midori</creator><creator>Ogihara, Takehide</creator><creator>Fukushima, Yasushi</creator><creator>Anai, Motonobu</creator><creator>Horike, Nanao</creator><creator>Kamata, Hideaki</creator><creator>Uchijima, Yasunobu</creator><creator>Kurihara, Hiroki</creator><creator>Asano, Tomoichiro</creator><general>Elsevier Ireland Ltd</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>20080101</creationdate><title>Regulation of gut-derived resistin-like molecule β expression by nutrients</title><author>Fujio, Junko ; Kushiyama, Akifumi ; Sakoda, Hideyuki ; Fujishiro, Midori ; Ogihara, Takehide ; Fukushima, Yasushi ; Anai, Motonobu ; Horike, Nanao ; Kamata, Hideaki ; Uchijima, Yasunobu ; Kurihara, Hiroki ; Asano, Tomoichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-1b612181e176585d990baf063813b65c41672c516c23a2268ee15fc510a6ec373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animal Feed</topic><topic>Animals</topic><topic>Diet</topic><topic>Dietary Carbohydrates - pharmacology</topic><topic>Dietary Fats - pharmacology</topic><topic>Dietary Proteins - pharmacology</topic><topic>Eating</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Fasting</topic><topic>Fatty Acids, Nonesterified - pharmacology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Gene Expression Regulation - physiology</topic><topic>Glucose - pharmacology</topic><topic>Hormones, Ectopic - genetics</topic><topic>Insulin resistance</topic><topic>Intestines - physiology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nutrient compositions</topic><topic>RELMβ</topic><topic>Resistin - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>Stearic Acids - pharmacology</topic><topic>Tumor Necrosis Factor-alpha - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujio, Junko</creatorcontrib><creatorcontrib>Kushiyama, Akifumi</creatorcontrib><creatorcontrib>Sakoda, Hideyuki</creatorcontrib><creatorcontrib>Fujishiro, Midori</creatorcontrib><creatorcontrib>Ogihara, Takehide</creatorcontrib><creatorcontrib>Fukushima, Yasushi</creatorcontrib><creatorcontrib>Anai, Motonobu</creatorcontrib><creatorcontrib>Horike, Nanao</creatorcontrib><creatorcontrib>Kamata, Hideaki</creatorcontrib><creatorcontrib>Uchijima, Yasunobu</creatorcontrib><creatorcontrib>Kurihara, Hiroki</creatorcontrib><creatorcontrib>Asano, Tomoichiro</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>Diabetes research and clinical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujio, Junko</au><au>Kushiyama, Akifumi</au><au>Sakoda, Hideyuki</au><au>Fujishiro, Midori</au><au>Ogihara, Takehide</au><au>Fukushima, Yasushi</au><au>Anai, Motonobu</au><au>Horike, Nanao</au><au>Kamata, Hideaki</au><au>Uchijima, Yasunobu</au><au>Kurihara, Hiroki</au><au>Asano, Tomoichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of gut-derived resistin-like molecule β expression by nutrients</atitle><jtitle>Diabetes research and clinical practice</jtitle><addtitle>Diabetes Res Clin Pract</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>79</volume><issue>1</issue><spage>2</spage><epage>10</epage><pages>2-10</pages><issn>0168-8227</issn><eissn>1872-8227</eissn><abstract>Abstract Resistin was initially identified as a protein, secreted by adipocytes, which inhibits insulin action and adipose differentiation. The three proteins homologous to resistin were identified and given the names resistin-like molecules (RELM) α, β and γ. Resistin and RELMα are abundantly expressed in adipose, but RELMβ and RELMγ are secreted mainly from the gut. Since nutrient composition greatly affects insulin sensitivity, we investigated the regulatory effects of various nutritional factors in food on the expressions of resistin family proteins. First, mice were given diets with different nutritional compositions (high-carbohydrate, high-protein and high-fat) for 2 weeks. RELMβ mRNA expression in the intestines was markedly suppressed by the high-protein and high-carbohydrate diets, while slightly but not significantly upregulated by the high-fat diet. In the epididymal fat, resistin expression was unchanged, while RELMα expression was markedly decreased by the high-carbohydrate diet. Taking into consideration that humans have neither RELMα nor RELMγ, our subsequent studies focused on RELMβ expression. We used the human colon cancer cell line LS174T. Treatments with insulin and TNFα as well as stearic acid, a saturated free fatty acid, upregulated RELMβ expression, while d -glucose downregulated RELMβ. These results suggest RELMβ expression to be regulated directly by nutrients such as glucose and saturated free fatty acids including stearic acid, as well as by hormones including insulin and TNFα. These regulations may play an important role in the nutrient-associated induction of insulin resistance.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>17936398</pmid><doi>10.1016/j.diabres.2007.04.015</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0168-8227
ispartof Diabetes research and clinical practice, 2008-01, Vol.79 (1), p.2-10
issn 0168-8227
1872-8227
language eng
recordid cdi_proquest_miscellaneous_70185260
source Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects Animal Feed
Animals
Diet
Dietary Carbohydrates - pharmacology
Dietary Fats - pharmacology
Dietary Proteins - pharmacology
Eating
Endocrinology & Metabolism
Fasting
Fatty Acids, Nonesterified - pharmacology
Gene Expression Regulation - drug effects
Gene Expression Regulation - physiology
Glucose - pharmacology
Hormones, Ectopic - genetics
Insulin resistance
Intestines - physiology
Mice
Mice, Inbred C57BL
Nutrient compositions
RELMβ
Resistin - genetics
RNA, Messenger - genetics
Stearic Acids - pharmacology
Tumor Necrosis Factor-alpha - pharmacology
title Regulation of gut-derived resistin-like molecule β expression by nutrients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T13%3A01%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regulation%20of%20gut-derived%20resistin-like%20molecule%20%CE%B2%20expression%20by%20nutrients&rft.jtitle=Diabetes%20research%20and%20clinical%20practice&rft.au=Fujio,%20Junko&rft.date=2008-01-01&rft.volume=79&rft.issue=1&rft.spage=2&rft.epage=10&rft.pages=2-10&rft.issn=0168-8227&rft.eissn=1872-8227&rft_id=info:doi/10.1016/j.diabres.2007.04.015&rft_dat=%3Cproquest_cross%3E70185260%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70185260&rft_id=info:pmid/17936398&rft_els_id=1_s2_0_S016882270700424X&rfr_iscdi=true