Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice
In the present study, we performed a metabolomics analysis to evaluate a MODY5/RCAD mouse mutant line as a potential model for HNF1B-associated diseases. Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue s...
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Veröffentlicht in: | Journal of proteome research 2018-07, Vol.17 (7), p.2293-2306 |
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creator | Torell, Frida Bennett, Kate Cereghini, Silvia Fabre, Mélanie Rännar, Stefan Lundstedt-Enkel, Katrin Moritz, Thomas Haumaitre, Cécile Trygg, Johan Lundstedt, Torbjörn |
description | In the present study, we performed a metabolomics analysis to evaluate a MODY5/RCAD mouse mutant line as a potential model for HNF1B-associated diseases. Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue specific metabolite distribution. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to identify the differences between MODY5/RCAD and wild-type mice in each of the tissues. The differences included, for example, increased levels of amino acids in the kidneys and reduced levels of fatty acids in the muscles of the MODY5/RCAD mice. Interestingly, campesterol was found in higher concentrations in the MODY5/RCAD mice, with a four-fold and three-fold increase in kidneys and pancreas, respectively. As expected, the MODY5/RCAD mice displayed signs of impaired renal function in addition to disturbed liver lipid metabolism, with increased lipid and fatty acid accumulation in the liver. From a metabolomics perspective, the MODY5/RCAD model was proven to display a metabolic pattern similar to what would be suspected in HNF1B-associated diseases. These findings were in line with the presumed outcome of the mutation based on the different anatomy and function of the tissues as well as the effect of the mutation on development. |
doi_str_mv | 10.1021/acs.jproteome.7b00821 |
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Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue specific metabolite distribution. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to identify the differences between MODY5/RCAD and wild-type mice in each of the tissues. The differences included, for example, increased levels of amino acids in the kidneys and reduced levels of fatty acids in the muscles of the MODY5/RCAD mice. Interestingly, campesterol was found in higher concentrations in the MODY5/RCAD mice, with a four-fold and three-fold increase in kidneys and pancreas, respectively. As expected, the MODY5/RCAD mice displayed signs of impaired renal function in addition to disturbed liver lipid metabolism, with increased lipid and fatty acid accumulation in the liver. From a metabolomics perspective, the MODY5/RCAD model was proven to display a metabolic pattern similar to what would be suspected in HNF1B-associated diseases. These findings were in line with the presumed outcome of the mutation based on the different anatomy and function of the tissues as well as the effect of the mutation on development.</description><identifier>ISSN: 1535-3893</identifier><identifier>ISSN: 1535-3907</identifier><identifier>EISSN: 1535-3907</identifier><identifier>DOI: 10.1021/acs.jproteome.7b00821</identifier><identifier>PMID: 29873499</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>amino acids ; Bioinformatics and Systems Biology ; Bioinformatik och systembiologi ; campesterol ; discriminant analysis ; fatty acids ; gas chromatography ; HNF1B-associated diseases ; kidneys ; lipid metabolism ; liver ; mass spectrometry ; metabolites ; metabolomics ; mice ; MODY5 ; mouse model ; multiorgan samples ; muscles ; mutants ; mutation ; OPLS-DA ; pancreas ; proteome ; RCAD ; renal function ; tissues</subject><ispartof>Journal of proteome research, 2018-07, Vol.17 (7), p.2293-2306</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a497t-50cc06e6d3af850d1a13a8c7d3f705c1c616352ffc08e8f6c247f3c294802b903</citedby><cites>FETCH-LOGICAL-a497t-50cc06e6d3af850d1a13a8c7d3f705c1c616352ffc08e8f6c247f3c294802b903</cites><orcidid>0000-0002-6294-7844 ; 0000-0003-3799-6094</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.jproteome.7b00821$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.jproteome.7b00821$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,776,780,881,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29873499$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-150378$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-361549$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://res.slu.se/id/publ/96388$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Torell, Frida</creatorcontrib><creatorcontrib>Bennett, Kate</creatorcontrib><creatorcontrib>Cereghini, Silvia</creatorcontrib><creatorcontrib>Fabre, Mélanie</creatorcontrib><creatorcontrib>Rännar, Stefan</creatorcontrib><creatorcontrib>Lundstedt-Enkel, Katrin</creatorcontrib><creatorcontrib>Moritz, Thomas</creatorcontrib><creatorcontrib>Haumaitre, Cécile</creatorcontrib><creatorcontrib>Trygg, Johan</creatorcontrib><creatorcontrib>Lundstedt, Torbjörn</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><title>Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice</title><title>Journal of proteome research</title><addtitle>J. Proteome Res</addtitle><description>In the present study, we performed a metabolomics analysis to evaluate a MODY5/RCAD mouse mutant line as a potential model for HNF1B-associated diseases. Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue specific metabolite distribution. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to identify the differences between MODY5/RCAD and wild-type mice in each of the tissues. The differences included, for example, increased levels of amino acids in the kidneys and reduced levels of fatty acids in the muscles of the MODY5/RCAD mice. Interestingly, campesterol was found in higher concentrations in the MODY5/RCAD mice, with a four-fold and three-fold increase in kidneys and pancreas, respectively. As expected, the MODY5/RCAD mice displayed signs of impaired renal function in addition to disturbed liver lipid metabolism, with increased lipid and fatty acid accumulation in the liver. From a metabolomics perspective, the MODY5/RCAD model was proven to display a metabolic pattern similar to what would be suspected in HNF1B-associated diseases. These findings were in line with the presumed outcome of the mutation based on the different anatomy and function of the tissues as well as the effect of the mutation on development.</description><subject>amino acids</subject><subject>Bioinformatics and Systems Biology</subject><subject>Bioinformatik och systembiologi</subject><subject>campesterol</subject><subject>discriminant analysis</subject><subject>fatty acids</subject><subject>gas chromatography</subject><subject>HNF1B-associated diseases</subject><subject>kidneys</subject><subject>lipid metabolism</subject><subject>liver</subject><subject>mass spectrometry</subject><subject>metabolites</subject><subject>metabolomics</subject><subject>mice</subject><subject>MODY5</subject><subject>mouse model</subject><subject>multiorgan samples</subject><subject>muscles</subject><subject>mutants</subject><subject>mutation</subject><subject>OPLS-DA</subject><subject>pancreas</subject><subject>proteome</subject><subject>RCAD</subject><subject>renal function</subject><subject>tissues</subject><issn>1535-3893</issn><issn>1535-3907</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqNkktvEzEUhS0Eog_4CaBZsmDS6_H4xS5KWkBqFMRLYmV5HLuayjNO7TGIf4_TpGHFY3Ut6zvHvjoHoRcYZhgafKFNmt1uY5hsGOyMdwCiwY_QKaaE1kQCf_xwFpKcoLOUbgEw5UCeopNGCk5aKU_RemUn3QXfm-pDDK73_XhTBVetsp_6EG_0WH3Sw9bb9Ka6_K591uV6vCfWy2_04uNivizwpMepWvXGPkNPnPbJPj_Mc_Tl6vLz4l19vX77fjG_rnUr-VRTMAaYZRuinaCwwRoTLQzfEMeBGmwYZoQ2zhkQVjhmmpY7YhrZCmg6CeQc1Xvf9MNuc6e2sR90_KmC7lXyudNxN1SySjIiROFf_5Ff9l_nquyqclaEYdrKv9r_xoesMAXCd_av9nxJ5C7bNKmhT8Z6r0cbclJNiYJh0Yr_QIFiYJLT3ZJ0j5oYUorWHf-BQe1aoEoL1LEF6tCCont5eCJ3g90cVQ-xFwDvgXt9yHEsWf3D9Bct6cHf</recordid><startdate>20180706</startdate><enddate>20180706</enddate><creator>Torell, Frida</creator><creator>Bennett, Kate</creator><creator>Cereghini, Silvia</creator><creator>Fabre, Mélanie</creator><creator>Rännar, Stefan</creator><creator>Lundstedt-Enkel, Katrin</creator><creator>Moritz, Thomas</creator><creator>Haumaitre, Cécile</creator><creator>Trygg, Johan</creator><creator>Lundstedt, Torbjörn</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D93</scope><scope>DF2</scope><orcidid>https://orcid.org/0000-0002-6294-7844</orcidid><orcidid>https://orcid.org/0000-0003-3799-6094</orcidid></search><sort><creationdate>20180706</creationdate><title>Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice</title><author>Torell, Frida ; Bennett, Kate ; Cereghini, Silvia ; Fabre, Mélanie ; Rännar, Stefan ; Lundstedt-Enkel, Katrin ; Moritz, Thomas ; Haumaitre, Cécile ; Trygg, Johan ; Lundstedt, Torbjörn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a497t-50cc06e6d3af850d1a13a8c7d3f705c1c616352ffc08e8f6c247f3c294802b903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>amino acids</topic><topic>Bioinformatics and Systems Biology</topic><topic>Bioinformatik och systembiologi</topic><topic>campesterol</topic><topic>discriminant analysis</topic><topic>fatty acids</topic><topic>gas chromatography</topic><topic>HNF1B-associated diseases</topic><topic>kidneys</topic><topic>lipid metabolism</topic><topic>liver</topic><topic>mass spectrometry</topic><topic>metabolites</topic><topic>metabolomics</topic><topic>mice</topic><topic>MODY5</topic><topic>mouse model</topic><topic>multiorgan samples</topic><topic>muscles</topic><topic>mutants</topic><topic>mutation</topic><topic>OPLS-DA</topic><topic>pancreas</topic><topic>proteome</topic><topic>RCAD</topic><topic>renal function</topic><topic>tissues</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Torell, Frida</creatorcontrib><creatorcontrib>Bennett, Kate</creatorcontrib><creatorcontrib>Cereghini, Silvia</creatorcontrib><creatorcontrib>Fabre, Mélanie</creatorcontrib><creatorcontrib>Rännar, Stefan</creatorcontrib><creatorcontrib>Lundstedt-Enkel, Katrin</creatorcontrib><creatorcontrib>Moritz, Thomas</creatorcontrib><creatorcontrib>Haumaitre, Cécile</creatorcontrib><creatorcontrib>Trygg, Johan</creatorcontrib><creatorcontrib>Lundstedt, Torbjörn</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Umeå universitet</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Torell, Frida</au><au>Bennett, Kate</au><au>Cereghini, Silvia</au><au>Fabre, Mélanie</au><au>Rännar, Stefan</au><au>Lundstedt-Enkel, Katrin</au><au>Moritz, Thomas</au><au>Haumaitre, Cécile</au><au>Trygg, Johan</au><au>Lundstedt, Torbjörn</au><aucorp>Sveriges lantbruksuniversitet</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2018-07-06</date><risdate>2018</risdate><volume>17</volume><issue>7</issue><spage>2293</spage><epage>2306</epage><pages>2293-2306</pages><issn>1535-3893</issn><issn>1535-3907</issn><eissn>1535-3907</eissn><abstract>In the present study, we performed a metabolomics analysis to evaluate a MODY5/RCAD mouse mutant line as a potential model for HNF1B-associated diseases. Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue specific metabolite distribution. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to identify the differences between MODY5/RCAD and wild-type mice in each of the tissues. The differences included, for example, increased levels of amino acids in the kidneys and reduced levels of fatty acids in the muscles of the MODY5/RCAD mice. Interestingly, campesterol was found in higher concentrations in the MODY5/RCAD mice, with a four-fold and three-fold increase in kidneys and pancreas, respectively. As expected, the MODY5/RCAD mice displayed signs of impaired renal function in addition to disturbed liver lipid metabolism, with increased lipid and fatty acid accumulation in the liver. From a metabolomics perspective, the MODY5/RCAD model was proven to display a metabolic pattern similar to what would be suspected in HNF1B-associated diseases. These findings were in line with the presumed outcome of the mutation based on the different anatomy and function of the tissues as well as the effect of the mutation on development.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29873499</pmid><doi>10.1021/acs.jproteome.7b00821</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6294-7844</orcidid><orcidid>https://orcid.org/0000-0003-3799-6094</orcidid></addata></record> |
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subjects | amino acids Bioinformatics and Systems Biology Bioinformatik och systembiologi campesterol discriminant analysis fatty acids gas chromatography HNF1B-associated diseases kidneys lipid metabolism liver mass spectrometry metabolites metabolomics mice MODY5 mouse model multiorgan samples muscles mutants mutation OPLS-DA pancreas proteome RCAD renal function tissues |
title | Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice |
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