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...
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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 |
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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 & 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 & 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 & 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> |
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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 |
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