Fatty acid binding protein-4 is expressed in the mouse placental labyrinth, yet is dispensable for placental triglyceride accumulation and fetal growth.
Identifieur interne : 001914 ( PubMed/Curation ); précédent : 001913; suivant : 001915Fatty acid binding protein-4 is expressed in the mouse placental labyrinth, yet is dispensable for placental triglyceride accumulation and fetal growth.
Auteurs : A. Makkar [États-Unis] ; T. Mishima [États-Unis] ; G. Chang [République populaire de Chine] ; C. Scifres [États-Unis] ; Y. Sadovsky [États-Unis]Source :
- Placenta [ 1532-3102 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Protéines de liaison aux acides gras.
- métabolisme : Placenta, Protéines de liaison aux acides gras, Triglycéride, Trophoblastes.
- physiologie : Développement foetal.
- Animaux, Femelle, Grossesse, Souris, Souris knockout.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Fatty Acid-Binding Proteins.
- chemical , metabolism : Fatty Acid-Binding Proteins, Triglycerides.
- metabolism : Placenta, Trophoblasts.
- physiology : Fetal Development.
- Animals, Female, Mice, Mice, Knockout, Pregnancy.
Abstract
Fatty Acid Binding Protein-4 (FABP4) is a member of a family of FABP proteins that regulate intracellular lipid trafficking in diverse tissues. We recently showed that FABP4 regulates triglyceride accumulation in primary human trophoblasts. To assess the function of placental FABP4 in vivo, we tested the hypothesis that FABP4 is expressed in the murine placenta, and regulates placenta triglyceride accumulation.
DOI: 10.1016/j.placenta.2014.07.008
PubMed: 25096952
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pubmed:25096952Le document en format XML
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<term>Female</term>
<term>Fetal Development (physiology)</term>
<term>Mice</term>
<term>Mice, Knockout</term>
<term>Placenta (metabolism)</term>
<term>Pregnancy</term>
<term>Triglycerides (metabolism)</term>
<term>Trophoblasts (metabolism)</term>
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<term>Développement foetal (physiologie)</term>
<term>Femelle</term>
<term>Grossesse</term>
<term>Placenta (métabolisme)</term>
<term>Protéines de liaison aux acides gras (génétique)</term>
<term>Protéines de liaison aux acides gras (métabolisme)</term>
<term>Souris</term>
<term>Souris knockout</term>
<term>Triglycéride (métabolisme)</term>
<term>Trophoblastes (métabolisme)</term>
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<front><div type="abstract" xml:lang="en">Fatty Acid Binding Protein-4 (FABP4) is a member of a family of FABP proteins that regulate intracellular lipid trafficking in diverse tissues. We recently showed that FABP4 regulates triglyceride accumulation in primary human trophoblasts. To assess the function of placental FABP4 in vivo, we tested the hypothesis that FABP4 is expressed in the murine placenta, and regulates placenta triglyceride accumulation.</div>
</front>
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<Month>09</Month>
<Day>02</Day>
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<JournalIssue CitedMedium="Internet"><Volume>35</Volume>
<Issue>10</Issue>
<PubDate><Year>2014</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Placenta</Title>
<ISOAbbreviation>Placenta</ISOAbbreviation>
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<ArticleTitle>Fatty acid binding protein-4 is expressed in the mouse placental labyrinth, yet is dispensable for placental triglyceride accumulation and fetal growth.</ArticleTitle>
<Pagination><MedlinePgn>802-7</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.placenta.2014.07.008</ELocationID>
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<Abstract><AbstractText Label="INTRODUCTION" NlmCategory="BACKGROUND">Fatty Acid Binding Protein-4 (FABP4) is a member of a family of FABP proteins that regulate intracellular lipid trafficking in diverse tissues. We recently showed that FABP4 regulates triglyceride accumulation in primary human trophoblasts. To assess the function of placental FABP4 in vivo, we tested the hypothesis that FABP4 is expressed in the murine placenta, and regulates placenta triglyceride accumulation.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">C57Bl/6 wild type or Fabp4-null mice were time-bred, and fetuses and placentas harvested at different time points during pregnancy. Placental FABP4 expression was assessed at different gestational ages, using quantitative PCR, immunohistochemistry, immunofluorescence and western immunoblotting. FABPs expression was examined by RT-qPCR. Placental lipids were extracted using the Folch method and triglyceride levels determined using a colorimetric quantification kit.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Using immunohistochemistry, we found that FABP4 was expressed in the placental labyrinthine layer, predominantly in endothelial cells in association with CD31 positive fetal capillaries. The level of placental FABP4 mRNA and protein increased from E12.5 to E16.5 and slightly decreased at E18.5. Breeding of Fabp4 heterozygous mice resulted in embryonic genotypes that followed a Mendelian distribution and exhibited normal weight and morphology, triglyceride content, and expression of other FABP family members. Exposure to hypoxia (O2 = 12%) between E12.5-E18.5 did not uncover a difference between wild type and Fabp4-null mice.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">FABP4 is expressed in the mouse placental labyrinth, with highest expression at E16.5. FABP4 is dispensable for feto-placental growth and placental lipid accumulation.</AbstractText>
<CopyrightInformation>Copyright © 2014 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Makkar</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA; Department of Pediatrics, University of Pittsburgh, USA.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Mishima</LastName>
<ForeName>T</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Chang</LastName>
<ForeName>G</ForeName>
<Initials>G</Initials>
<AffiliationInfo><Affiliation>Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA; Tsinghua University School of Medicine Education Program, Beijing, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Scifres</LastName>
<ForeName>C</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sadovsky</LastName>
<ForeName>Y</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA; Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: rideoutl@mwri.magee.edu.</Affiliation>
</AffiliationInfo>
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<Grant><GrantID>R01 HD045675</GrantID>
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<MedlineTA>Placenta</MedlineTA>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
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