Pgc1a is responsible for the sex differences in hepatic Cidec/Fsp27β mRNA expression in hepatic steatosis of mice fed a Western diet
Hepatic fat-specific protein 27 [cell death-inducing DNA fragmentation effector protein C ( )/ ] mRNA levels have been associated with hepatic lipid droplet extent under certain circumstances. To address its hepatic expression under different dietary conditions and in both sexes, apolipoprotein E (...
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creator | Herrera-Marcos, Luis V Sancho-Knapik, Sara Gabás-Rivera, Clara Barranquero, Cristina Gascón, Sonia Romanos, Eduardo Martínez-Beamonte, Roberto Navarro, María A Surra, Joaquín C Arnal, Carmen García-de-Jalón, José A Rodríguez-Yoldi, María J Tena-Sempere, Manuel Sánchez-Ramos, Cristina Monsalve, María Osada, Jesús |
description | Hepatic fat-specific protein 27 [cell death-inducing DNA fragmentation effector protein C (
)/
] mRNA levels have been associated with hepatic lipid droplet extent under certain circumstances. To address its hepatic expression under different dietary conditions and in both sexes, apolipoprotein E (
)
deficient mice were subjected to different experimental conditions for 11 wk to test the influence of cholesterol, Western diet, squalene, oleanolic acid, sex, and surgical castration on
mRNA expression. Dietary cholesterol increased hepatic
expression, an effect that was suppressed when cholesterol was combined with saturated fat as represented by Western diet feeding. Using the latter diet, neither oleanolic acid nor squalene modified its expression. Females showed lower levels of hepatic
expression than males when they were fed Western diets, a result that was translated into a lesser amount of CIDEC/FSP27 protein in lipid droplets and microsomes. This was also confirmed in low-density lipoprotein receptor (
)-deficient mice. Incubation with estradiol resulted in decreased
expression in AML12 cells. Whereas male surgical castration did not modify the expression, ovariectomized females did show increased levels compared with control females. Females also showed increased expression of peroxisome proliferator-activated receptor-γ coactivator 1-α (
), suppressed by ovariectomy, and the values were significantly and inversely associated with those of
. When
-deficient mice were used, the sex differences in
expression disappeared. Therefore, hepatic
expression has a complex regulation influenced by diet and sex hormonal milieu. The mRNA sex differences are controlled by
. |
doi_str_mv | 10.1152/ajpendo.00199.2019 |
format | Article |
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)/
] mRNA levels have been associated with hepatic lipid droplet extent under certain circumstances. To address its hepatic expression under different dietary conditions and in both sexes, apolipoprotein E (
)
deficient mice were subjected to different experimental conditions for 11 wk to test the influence of cholesterol, Western diet, squalene, oleanolic acid, sex, and surgical castration on
mRNA expression. Dietary cholesterol increased hepatic
expression, an effect that was suppressed when cholesterol was combined with saturated fat as represented by Western diet feeding. Using the latter diet, neither oleanolic acid nor squalene modified its expression. Females showed lower levels of hepatic
expression than males when they were fed Western diets, a result that was translated into a lesser amount of CIDEC/FSP27 protein in lipid droplets and microsomes. This was also confirmed in low-density lipoprotein receptor (
)-deficient mice. Incubation with estradiol resulted in decreased
expression in AML12 cells. Whereas male surgical castration did not modify the expression, ovariectomized females did show increased levels compared with control females. Females also showed increased expression of peroxisome proliferator-activated receptor-γ coactivator 1-α (
), suppressed by ovariectomy, and the values were significantly and inversely associated with those of
. When
-deficient mice were used, the sex differences in
expression disappeared. Therefore, hepatic
expression has a complex regulation influenced by diet and sex hormonal milieu. The mRNA sex differences are controlled by
.</description><identifier>ISSN: 0193-1849</identifier><identifier>EISSN: 1522-1555</identifier><identifier>DOI: 10.1152/ajpendo.00199.2019</identifier><identifier>PMID: 31846369</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cell Line ; Cholesterol, Dietary - pharmacology ; Diet, Western - adverse effects ; Female ; Lipid Droplets - metabolism ; Liver - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Non-alcoholic Fatty Liver Disease - genetics ; Non-alcoholic Fatty Liver Disease - metabolism ; Orchiectomy ; Ovariectomy ; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics ; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism ; Proteins - genetics ; Receptors, LDL - genetics ; Receptors, LDL - metabolism ; RNA, Messenger - biosynthesis ; Sex Characteristics</subject><ispartof>American journal of physiology: endocrinology and metabolism, 2020-02, Vol.318 (2), p.E249-E261</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c303t-568595086bcc6615f97c01f319f05246d59058cee0a63ce41c03766b5c18a9e23</citedby><cites>FETCH-LOGICAL-c303t-568595086bcc6615f97c01f319f05246d59058cee0a63ce41c03766b5c18a9e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31846369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Herrera-Marcos, Luis V</creatorcontrib><creatorcontrib>Sancho-Knapik, Sara</creatorcontrib><creatorcontrib>Gabás-Rivera, Clara</creatorcontrib><creatorcontrib>Barranquero, Cristina</creatorcontrib><creatorcontrib>Gascón, Sonia</creatorcontrib><creatorcontrib>Romanos, Eduardo</creatorcontrib><creatorcontrib>Martínez-Beamonte, Roberto</creatorcontrib><creatorcontrib>Navarro, María A</creatorcontrib><creatorcontrib>Surra, Joaquín C</creatorcontrib><creatorcontrib>Arnal, Carmen</creatorcontrib><creatorcontrib>García-de-Jalón, José A</creatorcontrib><creatorcontrib>Rodríguez-Yoldi, María J</creatorcontrib><creatorcontrib>Tena-Sempere, Manuel</creatorcontrib><creatorcontrib>Sánchez-Ramos, Cristina</creatorcontrib><creatorcontrib>Monsalve, María</creatorcontrib><creatorcontrib>Osada, Jesús</creatorcontrib><title>Pgc1a is responsible for the sex differences in hepatic Cidec/Fsp27β mRNA expression in hepatic steatosis of mice fed a Western diet</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol Endocrinol Metab</addtitle><description>Hepatic fat-specific protein 27 [cell death-inducing DNA fragmentation effector protein C (
)/
] mRNA levels have been associated with hepatic lipid droplet extent under certain circumstances. To address its hepatic expression under different dietary conditions and in both sexes, apolipoprotein E (
)
deficient mice were subjected to different experimental conditions for 11 wk to test the influence of cholesterol, Western diet, squalene, oleanolic acid, sex, and surgical castration on
mRNA expression. Dietary cholesterol increased hepatic
expression, an effect that was suppressed when cholesterol was combined with saturated fat as represented by Western diet feeding. Using the latter diet, neither oleanolic acid nor squalene modified its expression. Females showed lower levels of hepatic
expression than males when they were fed Western diets, a result that was translated into a lesser amount of CIDEC/FSP27 protein in lipid droplets and microsomes. This was also confirmed in low-density lipoprotein receptor (
)-deficient mice. Incubation with estradiol resulted in decreased
expression in AML12 cells. Whereas male surgical castration did not modify the expression, ovariectomized females did show increased levels compared with control females. Females also showed increased expression of peroxisome proliferator-activated receptor-γ coactivator 1-α (
), suppressed by ovariectomy, and the values were significantly and inversely associated with those of
. When
-deficient mice were used, the sex differences in
expression disappeared. Therefore, hepatic
expression has a complex regulation influenced by diet and sex hormonal milieu. The mRNA sex differences are controlled by
.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Cholesterol, Dietary - pharmacology</subject><subject>Diet, Western - adverse effects</subject><subject>Female</subject><subject>Lipid Droplets - metabolism</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Non-alcoholic Fatty Liver Disease - genetics</subject><subject>Non-alcoholic Fatty Liver Disease - metabolism</subject><subject>Orchiectomy</subject><subject>Ovariectomy</subject><subject>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics</subject><subject>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism</subject><subject>Proteins - genetics</subject><subject>Receptors, LDL - genetics</subject><subject>Receptors, LDL - metabolism</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Sex Characteristics</subject><issn>0193-1849</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkM9KAzEQh4MotlZfwIPk6GXb_GnSzbEUq0JREcXjkmYnNqW7WZMt1AfwhXwQn8nUVvEyAzO_-RI-hM4p6VMq2EAvG6hL3yeEKtVnqR6gblqwjAohDlE3TXhG86HqoJMYl4SQkRiyY9ThaSi5VF308fBqqMYu4gCx8XV08xVg6wNuF4AjbHDprIUAtYGIXY0X0OjWGTxxJZjBNDZs9PWJq8e7MYZNkyDR-fp_MLagWx_TC97iyplEhxJr_AJpE-rEh_YUHVm9inC27z30PL16mtxks_vr28l4lhlOeJsJmQslSC7nxkhJhVUjQ6jlVFki2FCWQhGRGwCiJTcwpIbwkZRzYWiuFTDeQ5c7bhP82zp9oKhcNLBa6Rr8OhaMs5wngTlJUbaLmuBjDGCLJrhKh_eCkmKrv9jrL370F1v96ehiz1_PKyj_Tn5982-27YLX</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Herrera-Marcos, Luis V</creator><creator>Sancho-Knapik, Sara</creator><creator>Gabás-Rivera, Clara</creator><creator>Barranquero, Cristina</creator><creator>Gascón, Sonia</creator><creator>Romanos, Eduardo</creator><creator>Martínez-Beamonte, Roberto</creator><creator>Navarro, María A</creator><creator>Surra, Joaquín C</creator><creator>Arnal, Carmen</creator><creator>García-de-Jalón, José A</creator><creator>Rodríguez-Yoldi, María J</creator><creator>Tena-Sempere, Manuel</creator><creator>Sánchez-Ramos, Cristina</creator><creator>Monsalve, María</creator><creator>Osada, Jesús</creator><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>20200201</creationdate><title>Pgc1a is responsible for the sex differences in hepatic Cidec/Fsp27β mRNA expression in hepatic steatosis of mice fed a Western diet</title><author>Herrera-Marcos, Luis V ; Sancho-Knapik, Sara ; Gabás-Rivera, Clara ; Barranquero, Cristina ; Gascón, Sonia ; Romanos, Eduardo ; Martínez-Beamonte, Roberto ; Navarro, María A ; Surra, Joaquín C ; Arnal, Carmen ; García-de-Jalón, José A ; Rodríguez-Yoldi, María J ; Tena-Sempere, Manuel ; Sánchez-Ramos, Cristina ; Monsalve, María ; Osada, Jesús</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-568595086bcc6615f97c01f319f05246d59058cee0a63ce41c03766b5c18a9e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Cholesterol, Dietary - pharmacology</topic><topic>Diet, Western - adverse effects</topic><topic>Female</topic><topic>Lipid Droplets - metabolism</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Non-alcoholic Fatty Liver Disease - genetics</topic><topic>Non-alcoholic Fatty Liver Disease - metabolism</topic><topic>Orchiectomy</topic><topic>Ovariectomy</topic><topic>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics</topic><topic>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism</topic><topic>Proteins - genetics</topic><topic>Receptors, LDL - genetics</topic><topic>Receptors, LDL - metabolism</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Sex Characteristics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herrera-Marcos, Luis V</creatorcontrib><creatorcontrib>Sancho-Knapik, Sara</creatorcontrib><creatorcontrib>Gabás-Rivera, Clara</creatorcontrib><creatorcontrib>Barranquero, Cristina</creatorcontrib><creatorcontrib>Gascón, Sonia</creatorcontrib><creatorcontrib>Romanos, Eduardo</creatorcontrib><creatorcontrib>Martínez-Beamonte, Roberto</creatorcontrib><creatorcontrib>Navarro, María A</creatorcontrib><creatorcontrib>Surra, Joaquín C</creatorcontrib><creatorcontrib>Arnal, Carmen</creatorcontrib><creatorcontrib>García-de-Jalón, José A</creatorcontrib><creatorcontrib>Rodríguez-Yoldi, María J</creatorcontrib><creatorcontrib>Tena-Sempere, Manuel</creatorcontrib><creatorcontrib>Sánchez-Ramos, Cristina</creatorcontrib><creatorcontrib>Monsalve, María</creatorcontrib><creatorcontrib>Osada, Jesús</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>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herrera-Marcos, Luis V</au><au>Sancho-Knapik, Sara</au><au>Gabás-Rivera, Clara</au><au>Barranquero, Cristina</au><au>Gascón, Sonia</au><au>Romanos, Eduardo</au><au>Martínez-Beamonte, Roberto</au><au>Navarro, María A</au><au>Surra, Joaquín C</au><au>Arnal, Carmen</au><au>García-de-Jalón, José A</au><au>Rodríguez-Yoldi, María J</au><au>Tena-Sempere, Manuel</au><au>Sánchez-Ramos, Cristina</au><au>Monsalve, María</au><au>Osada, Jesús</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pgc1a is responsible for the sex differences in hepatic Cidec/Fsp27β mRNA expression in hepatic steatosis of mice fed a Western diet</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>318</volume><issue>2</issue><spage>E249</spage><epage>E261</epage><pages>E249-E261</pages><issn>0193-1849</issn><eissn>1522-1555</eissn><abstract>Hepatic fat-specific protein 27 [cell death-inducing DNA fragmentation effector protein C (
)/
] mRNA levels have been associated with hepatic lipid droplet extent under certain circumstances. To address its hepatic expression under different dietary conditions and in both sexes, apolipoprotein E (
)
deficient mice were subjected to different experimental conditions for 11 wk to test the influence of cholesterol, Western diet, squalene, oleanolic acid, sex, and surgical castration on
mRNA expression. Dietary cholesterol increased hepatic
expression, an effect that was suppressed when cholesterol was combined with saturated fat as represented by Western diet feeding. Using the latter diet, neither oleanolic acid nor squalene modified its expression. Females showed lower levels of hepatic
expression than males when they were fed Western diets, a result that was translated into a lesser amount of CIDEC/FSP27 protein in lipid droplets and microsomes. This was also confirmed in low-density lipoprotein receptor (
)-deficient mice. Incubation with estradiol resulted in decreased
expression in AML12 cells. Whereas male surgical castration did not modify the expression, ovariectomized females did show increased levels compared with control females. Females also showed increased expression of peroxisome proliferator-activated receptor-γ coactivator 1-α (
), suppressed by ovariectomy, and the values were significantly and inversely associated with those of
. When
-deficient mice were used, the sex differences in
expression disappeared. Therefore, hepatic
expression has a complex regulation influenced by diet and sex hormonal milieu. The mRNA sex differences are controlled by
.</abstract><cop>United States</cop><pmid>31846369</pmid><doi>10.1152/ajpendo.00199.2019</doi></addata></record> |
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source | MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Cell Line Cholesterol, Dietary - pharmacology Diet, Western - adverse effects Female Lipid Droplets - metabolism Liver - metabolism Male Mice Mice, Inbred C57BL Mice, Knockout Non-alcoholic Fatty Liver Disease - genetics Non-alcoholic Fatty Liver Disease - metabolism Orchiectomy Ovariectomy Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism Proteins - genetics Receptors, LDL - genetics Receptors, LDL - metabolism RNA, Messenger - biosynthesis Sex Characteristics |
title | Pgc1a is responsible for the sex differences in hepatic Cidec/Fsp27β mRNA expression in hepatic steatosis of mice fed a Western diet |
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