Patatin‐like phospholipase domain‐containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease
PNPLA3 (adiponutrin), a novel patatin‐like phospholipase domain‐containing enzyme, is expressed at high level in fat, but also in other tissues including liver. Polymorphisms in PNPLA3 have been linked to obesity and insulin sensitivity. Notably, a nonsynonymous variant rs738409(G) allele of the PNP...
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Veröffentlicht in: | Hepatology (Baltimore, Md.) Md.), 2010-09, Vol.52 (3), p.1134-1142 |
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description | PNPLA3 (adiponutrin), a novel patatin‐like phospholipase domain‐containing enzyme, is expressed at high level in fat, but also in other tissues including liver. Polymorphisms in PNPLA3 have been linked to obesity and insulin sensitivity. Notably, a nonsynonymous variant rs738409(G) allele of the PNPLA3 gene was found to be strongly associated with both nonalcoholic and alcoholic fatty liver disease. We have generated Pnpla3−/− mice by gene targeting. Loss of Pnpla3 has no effect on body weight or composition, adipose mass, or development, whether the mice were fed regular chow or high‐fat diet or bred into the genetic obese Lepob/ob background. Plasma and liver triglyceride content and plasma aspartate aminotransferase and alanine aminotransferase levels were not different between Pnpla3+/+ and Pnpla3−/− mice while they were on regular chow, fed three different fatty liver‐inducing diets, or after they were bred into Lepob/ob background. Hepatic Pnpla5 messenger RNA (mRNA) levels were similar in wild‐type and Pnpla3−/− mice, although adipose Pnpla5 mRNA level was increased in Pnpla3−/− mice. A high‐sucrose lipogenic diet stimulated hepatic Pnpla3 and Pnpla5 mRNA levels to a similar degree, but it did not affect adipose or liver triglyceride lipase (ATGL, known also as Pnpla2) mRNA in Pnpla3+/+ and Pnpla3−/− mice. Finally, Pnpla3+/+ and Pnpla3−/− mice displayed similar glucose tolerance and insulin tolerance tests while on regular chow or three different fatty liver–inducing diets. Conclusion: Loss of Pnpla3 does not cause fatty liver, liver enzyme elevation, or insulin resistance in mice. (HEPATOLOGY 2010) |
doi_str_mv | 10.1002/hep.23812 |
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Polymorphisms in PNPLA3 have been linked to obesity and insulin sensitivity. Notably, a nonsynonymous variant rs738409(G) allele of the PNPLA3 gene was found to be strongly associated with both nonalcoholic and alcoholic fatty liver disease. We have generated Pnpla3−/− mice by gene targeting. Loss of Pnpla3 has no effect on body weight or composition, adipose mass, or development, whether the mice were fed regular chow or high‐fat diet or bred into the genetic obese Lepob/ob background. Plasma and liver triglyceride content and plasma aspartate aminotransferase and alanine aminotransferase levels were not different between Pnpla3+/+ and Pnpla3−/− mice while they were on regular chow, fed three different fatty liver‐inducing diets, or after they were bred into Lepob/ob background. Hepatic Pnpla5 messenger RNA (mRNA) levels were similar in wild‐type and Pnpla3−/− mice, although adipose Pnpla5 mRNA level was increased in Pnpla3−/− mice. A high‐sucrose lipogenic diet stimulated hepatic Pnpla3 and Pnpla5 mRNA levels to a similar degree, but it did not affect adipose or liver triglyceride lipase (ATGL, known also as Pnpla2) mRNA in Pnpla3+/+ and Pnpla3−/− mice. Finally, Pnpla3+/+ and Pnpla3−/− mice displayed similar glucose tolerance and insulin tolerance tests while on regular chow or three different fatty liver–inducing diets. Conclusion: Loss of Pnpla3 does not cause fatty liver, liver enzyme elevation, or insulin resistance in mice. (HEPATOLOGY 2010)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.23812</identifier><identifier>PMID: 20648554</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adipose Tissue - metabolism ; Alanine Transaminase - blood ; Animals ; Aspartate Aminotransferases - blood ; Biological and medical sciences ; Body Composition ; Body Weight ; Disease Models, Animal ; Enzymes ; Fatty Liver - etiology ; Fatty Liver - metabolism ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepatology ; Hyperglycemia ; Insulin Resistance ; Liver ; Liver - metabolism ; Liver diseases ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; Mice ; Mice, Knockout ; Obesity - etiology ; Obesity - metabolism ; Other diseases. Semiology ; Phospholipases A2, Calcium-Independent - genetics ; Phospholipases A2, Calcium-Independent - metabolism ; Rodents ; Triglycerides - metabolism</subject><ispartof>Hepatology (Baltimore, Md.), 2010-09, Vol.52 (3), p.1134-1142</ispartof><rights>Copyright © 2010 American Association for the Study of Liver Diseases</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4502-6006df678b49fc48b9549f0d7a5ac90b9030a3cf8159fb326010134eda0f8d3f3</citedby><cites>FETCH-LOGICAL-c4502-6006df678b49fc48b9549f0d7a5ac90b9030a3cf8159fb326010134eda0f8d3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.23812$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.23812$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23218634$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20648554$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Weiqin</creatorcontrib><creatorcontrib>Chang, Benny</creatorcontrib><creatorcontrib>Li, Lan</creatorcontrib><creatorcontrib>Chan, Lawrence</creatorcontrib><title>Patatin‐like phospholipase domain‐containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>PNPLA3 (adiponutrin), a novel patatin‐like phospholipase domain‐containing enzyme, is expressed at high level in fat, but also in other tissues including liver. Polymorphisms in PNPLA3 have been linked to obesity and insulin sensitivity. Notably, a nonsynonymous variant rs738409(G) allele of the PNPLA3 gene was found to be strongly associated with both nonalcoholic and alcoholic fatty liver disease. We have generated Pnpla3−/− mice by gene targeting. Loss of Pnpla3 has no effect on body weight or composition, adipose mass, or development, whether the mice were fed regular chow or high‐fat diet or bred into the genetic obese Lepob/ob background. Plasma and liver triglyceride content and plasma aspartate aminotransferase and alanine aminotransferase levels were not different between Pnpla3+/+ and Pnpla3−/− mice while they were on regular chow, fed three different fatty liver‐inducing diets, or after they were bred into Lepob/ob background. Hepatic Pnpla5 messenger RNA (mRNA) levels were similar in wild‐type and Pnpla3−/− mice, although adipose Pnpla5 mRNA level was increased in Pnpla3−/− mice. A high‐sucrose lipogenic diet stimulated hepatic Pnpla3 and Pnpla5 mRNA levels to a similar degree, but it did not affect adipose or liver triglyceride lipase (ATGL, known also as Pnpla2) mRNA in Pnpla3+/+ and Pnpla3−/− mice. Finally, Pnpla3+/+ and Pnpla3−/− mice displayed similar glucose tolerance and insulin tolerance tests while on regular chow or three different fatty liver–inducing diets. Conclusion: Loss of Pnpla3 does not cause fatty liver, liver enzyme elevation, or insulin resistance in mice. (HEPATOLOGY 2010)</description><subject>Adipose Tissue - metabolism</subject><subject>Alanine Transaminase - blood</subject><subject>Animals</subject><subject>Aspartate Aminotransferases - blood</subject><subject>Biological and medical sciences</subject><subject>Body Composition</subject><subject>Body Weight</subject><subject>Disease Models, Animal</subject><subject>Enzymes</subject><subject>Fatty Liver - etiology</subject><subject>Fatty Liver - metabolism</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hepatology</subject><subject>Hyperglycemia</subject><subject>Insulin Resistance</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Liver diseases</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Obesity - etiology</subject><subject>Obesity - metabolism</subject><subject>Other diseases. Semiology</subject><subject>Phospholipases A2, Calcium-Independent - genetics</subject><subject>Phospholipases A2, Calcium-Independent - metabolism</subject><subject>Rodents</subject><subject>Triglycerides - metabolism</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90c1qFTEUB_AgFnutLnwBCYhoF9N7ksxkkqWUaoWCXeh6yOTDmzqTjJOM5YILH8Fn9ElMe68VCroIOSE_zkn4I_SMwAkBoOuNnU4oE4Q-QCvS0LZirIGHaAW0hUoSJg_R45SuAEDWVDxChxR4LZqmXqHvlyqr7MOvHz8H_8XiaRNTWYOfVLLYxFHd3ukYcql8-IzZWhk_xbDk2QdsrPPa26C3uJxGry32CYeYsUopaq-yNfja5w12KuctHvw3O2Pjky39n6ADp4Zkn-73I_Tp7dnH0_Pq4sO796dvLipdN0ArDsCN463oa-l0LXrZlAJMqxqlJfQSGCimnSCNdD2jHAgQVlujwAnDHDtCr3Z9pzl-XWzK3eiTtsOggo1L6tqGSdkC4UW-_q8kbct5eQ9rC31xj17FZQ7lH0VxLiiRIIo63ik9x5Rm67pp9qOatx2B7ia8roTX3YZX7PN9x6UfrbmTf9Iq4OUeqKTV4GYVtE9_HaNEcHbj1jt37Qe7_ffE7vzscjf6Nx7Dsp4</recordid><startdate>201009</startdate><enddate>201009</enddate><creator>Chen, Weiqin</creator><creator>Chang, Benny</creator><creator>Li, Lan</creator><creator>Chan, Lawrence</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wolters Kluwer Health, Inc</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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201009</creationdate><title>Patatin‐like phospholipase domain‐containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease</title><author>Chen, Weiqin ; Chang, Benny ; Li, Lan ; Chan, Lawrence</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4502-6006df678b49fc48b9549f0d7a5ac90b9030a3cf8159fb326010134eda0f8d3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adipose Tissue - metabolism</topic><topic>Alanine Transaminase - blood</topic><topic>Animals</topic><topic>Aspartate Aminotransferases - blood</topic><topic>Biological and medical sciences</topic><topic>Body Composition</topic><topic>Body Weight</topic><topic>Disease Models, Animal</topic><topic>Enzymes</topic><topic>Fatty Liver - etiology</topic><topic>Fatty Liver - metabolism</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hepatology</topic><topic>Hyperglycemia</topic><topic>Insulin Resistance</topic><topic>Liver</topic><topic>Liver - metabolism</topic><topic>Liver diseases</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Obesity - etiology</topic><topic>Obesity - metabolism</topic><topic>Other diseases. Semiology</topic><topic>Phospholipases A2, Calcium-Independent - genetics</topic><topic>Phospholipases A2, Calcium-Independent - metabolism</topic><topic>Rodents</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Weiqin</creatorcontrib><creatorcontrib>Chang, Benny</creatorcontrib><creatorcontrib>Li, Lan</creatorcontrib><creatorcontrib>Chan, Lawrence</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>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Weiqin</au><au>Chang, Benny</au><au>Li, Lan</au><au>Chan, Lawrence</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patatin‐like phospholipase domain‐containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2010-09</date><risdate>2010</risdate><volume>52</volume><issue>3</issue><spage>1134</spage><epage>1142</epage><pages>1134-1142</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>PNPLA3 (adiponutrin), a novel patatin‐like phospholipase domain‐containing enzyme, is expressed at high level in fat, but also in other tissues including liver. Polymorphisms in PNPLA3 have been linked to obesity and insulin sensitivity. Notably, a nonsynonymous variant rs738409(G) allele of the PNPLA3 gene was found to be strongly associated with both nonalcoholic and alcoholic fatty liver disease. We have generated Pnpla3−/− mice by gene targeting. Loss of Pnpla3 has no effect on body weight or composition, adipose mass, or development, whether the mice were fed regular chow or high‐fat diet or bred into the genetic obese Lepob/ob background. Plasma and liver triglyceride content and plasma aspartate aminotransferase and alanine aminotransferase levels were not different between Pnpla3+/+ and Pnpla3−/− mice while they were on regular chow, fed three different fatty liver‐inducing diets, or after they were bred into Lepob/ob background. Hepatic Pnpla5 messenger RNA (mRNA) levels were similar in wild‐type and Pnpla3−/− mice, although adipose Pnpla5 mRNA level was increased in Pnpla3−/− mice. A high‐sucrose lipogenic diet stimulated hepatic Pnpla3 and Pnpla5 mRNA levels to a similar degree, but it did not affect adipose or liver triglyceride lipase (ATGL, known also as Pnpla2) mRNA in Pnpla3+/+ and Pnpla3−/− mice. Finally, Pnpla3+/+ and Pnpla3−/− mice displayed similar glucose tolerance and insulin tolerance tests while on regular chow or three different fatty liver–inducing diets. Conclusion: Loss of Pnpla3 does not cause fatty liver, liver enzyme elevation, or insulin resistance in mice. (HEPATOLOGY 2010)</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20648554</pmid><doi>10.1002/hep.23812</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipose Tissue - metabolism Alanine Transaminase - blood Animals Aspartate Aminotransferases - blood Biological and medical sciences Body Composition Body Weight Disease Models, Animal Enzymes Fatty Liver - etiology Fatty Liver - metabolism Gastroenterology. Liver. Pancreas. Abdomen Hepatology Hyperglycemia Insulin Resistance Liver Liver - metabolism Liver diseases Liver. Biliary tract. Portal circulation. Exocrine pancreas Medical sciences Mice Mice, Knockout Obesity - etiology Obesity - metabolism Other diseases. Semiology Phospholipases A2, Calcium-Independent - genetics Phospholipases A2, Calcium-Independent - metabolism Rodents Triglycerides - metabolism |
title | Patatin‐like phospholipase domain‐containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease |
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