The role of trophoblastic microRNAs in placental viral infection.
Identifieur interne : 000F06 ( PubMed/Checkpoint ); précédent : 000F05; suivant : 000F07The role of trophoblastic microRNAs in placental viral infection.
Auteurs : Jean-Francois Mouillet [États-Unis] ; Yingshi Ouyang ; Avraham Bayer ; Carolyn B. Coyne ; Yoel SadovskySource :
- The International journal of developmental biology [ 1696-3547 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- cytologie : Trophoblastes.
- génétique : Exosomes, microARN.
- métabolisme : Placenta.
- physiologie : Trophoblastes.
- virologie : Placenta.
- Animaux, Femelle, Grossesse, Humains, Régulation de l'expression des gènes.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : MicroRNAs.
- cytology : Trophoblasts.
- genetics : Exosomes.
- metabolism : Placenta.
- physiology : Trophoblasts.
- virology : Placenta.
- Animals, Female, Gene Expression Regulation, Humans, Pregnancy.
Abstract
During the past decade, various types of small non-coding RNAs were found to be expressed in all kingdoms and phyla of life. Intense research efforts have begun to shed light on their biological functions, although much remains to be determined in order to fully characterize their scope of biological action. Typically, small RNAs provide sequence specificity to a protein complex that is driven to silence a long target RNA. MicroRNAs (miRNAs) are small RNAs that are coded in the genome of most eukaryotes, and contribute to the cellular identity by regulating cell-specific gene networks by translational repression or degradation of mRNA. These effects commonly fine-tune gene expression associated with developmental or environmental cues. Different cell types can be characterized by their distinctive cellular miRNA landscape. The human placenta expresses a unique set of miRNAs, a high proportion of which is derived from a large cluster located on chromosome 19, (termed chromosome 19 miRNA cluster, or C19MC). Interestingly, a fraction of these placenta-enriched miRNAs are released to the extracellular environment through exosomes that were recently found to induce an antiviral immunity. In this review, we explore relevant placental viral infections and discuss the antiviral role of exosome-packaged placental C19MC miRNAs in this context.
DOI: 10.1387/ijdb.130349ys
PubMed: 25023694
Affiliations:
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Coyne</name></author><author><name sortKey="Sadovsky, Yoel" sort="Sadovsky, Yoel" uniqKey="Sadovsky Y" first="Yoel" last="Sadovsky">Yoel Sadovsky</name></author></analytic><series><title level="j">The International journal of developmental biology</title><idno type="eISSN">1696-3547</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Exosomes (genetics)</term><term>Female</term><term>Gene Expression Regulation</term><term>Humans</term><term>MicroRNAs (genetics)</term><term>Placenta (metabolism)</term><term>Placenta (virology)</term><term>Pregnancy</term><term>Trophoblasts (cytology)</term><term>Trophoblasts (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term><term>Exosomes (génétique)</term><term>Femelle</term><term>Grossesse</term><term>Humains</term><term>Placenta (métabolisme)</term><term>Placenta (virologie)</term><term>Régulation de l'expression des gènes</term><term>Trophoblastes (cytologie)</term><term>Trophoblastes (physiologie)</term><term>microARN (génétique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>MicroRNAs</term></keywords><keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Trophoblastes</term></keywords><keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Trophoblasts</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Exosomes</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Exosomes</term><term>microARN</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Placenta</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Placenta</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Trophoblastes</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Trophoblasts</term></keywords><keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Placenta</term></keywords><keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Placenta</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Female</term><term>Gene Expression Regulation</term><term>Humans</term><term>Pregnancy</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Femelle</term><term>Grossesse</term><term>Humains</term><term>Régulation de l'expression des gènes</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">During the past decade, various types of small non-coding RNAs were found to be expressed in all kingdoms and phyla of life. Intense research efforts have begun to shed light on their biological functions, although much remains to be determined in order to fully characterize their scope of biological action. Typically, small RNAs provide sequence specificity to a protein complex that is driven to silence a long target RNA. MicroRNAs (miRNAs) are small RNAs that are coded in the genome of most eukaryotes, and contribute to the cellular identity by regulating cell-specific gene networks by translational repression or degradation of mRNA. These effects commonly fine-tune gene expression associated with developmental or environmental cues. Different cell types can be characterized by their distinctive cellular miRNA landscape. The human placenta expresses a unique set of miRNAs, a high proportion of which is derived from a large cluster located on chromosome 19, (termed chromosome 19 miRNA cluster, or C19MC). Interestingly, a fraction of these placenta-enriched miRNAs are released to the extracellular environment through exosomes that were recently found to induce an antiviral immunity. In this review, we explore relevant placental viral infections and discuss the antiviral role of exosome-packaged placental C19MC miRNAs in this context.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25023694</PMID><DateCreated><Year>2014</Year><Month>07</Month><Day>15</Day></DateCreated><DateCompleted><Year>2015</Year><Month>03</Month><Day>06</Day></DateCompleted><DateRevised><Year>2016</Year><Month>10</Month><Day>19</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1696-3547</ISSN><JournalIssue CitedMedium="Internet"><Volume>58</Volume><Issue>2-4</Issue><PubDate><Year>2014</Year></PubDate></JournalIssue><Title>The International journal of developmental biology</Title><ISOAbbreviation>Int. J. Dev. Biol.</ISOAbbreviation></Journal><ArticleTitle>The role of trophoblastic microRNAs in placental viral infection.</ArticleTitle><Pagination><MedlinePgn>281-9</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1387/ijdb.130349ys</ELocationID><Abstract><AbstractText>During the past decade, various types of small non-coding RNAs were found to be expressed in all kingdoms and phyla of life. Intense research efforts have begun to shed light on their biological functions, although much remains to be determined in order to fully characterize their scope of biological action. Typically, small RNAs provide sequence specificity to a protein complex that is driven to silence a long target RNA. MicroRNAs (miRNAs) are small RNAs that are coded in the genome of most eukaryotes, and contribute to the cellular identity by regulating cell-specific gene networks by translational repression or degradation of mRNA. These effects commonly fine-tune gene expression associated with developmental or environmental cues. Different cell types can be characterized by their distinctive cellular miRNA landscape. The human placenta expresses a unique set of miRNAs, a high proportion of which is derived from a large cluster located on chromosome 19, (termed chromosome 19 miRNA cluster, or C19MC). Interestingly, a fraction of these placenta-enriched miRNAs are released to the extracellular environment through exosomes that were recently found to induce an antiviral immunity. In this review, we explore relevant placental viral infections and discuss the antiviral role of exosome-packaged placental C19MC miRNAs in this context.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mouillet</LastName><ForeName>Jean-Francois</ForeName><Initials>JF</Initials><AffiliationInfo><Affiliation>Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ouyang</LastName><ForeName>Yingshi</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Bayer</LastName><ForeName>Avraham</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Coyne</LastName><ForeName>Carolyn B</ForeName><Initials>CB</Initials></Author><Author ValidYN="Y"><LastName>Sadovsky</LastName><ForeName>Yoel</ForeName><Initials>Y</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>UL1 TR000005</GrantID><Acronym>TR</Acronym><Agency>NCATS NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 AI081759</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01HD065893</GrantID><Acronym>HD</Acronym><Agency>NICHD NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 HD065893</GrantID><Acronym>HD</Acronym><Agency>NICHD NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>UL1 RR024153</GrantID><Acronym>RR</Acronym><Agency>NCRR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 HD075665</GrantID><Acronym>HD</Acronym><Agency>NICHD NIH HHS</Agency><Country>United 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MajorTopicYN="N">Exosomes</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005786" MajorTopicYN="Y">Gene Expression Regulation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D035683" MajorTopicYN="N">MicroRNAs</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010920" MajorTopicYN="N">Placenta</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011247" MajorTopicYN="N">Pregnancy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014327" MajorTopicYN="N">Trophoblasts</DescriptorName><QualifierName UI="Q000166" MajorTopicYN="N">cytology</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading></MeshHeadingList><OtherID Source="NLM">NIHMS670811</OtherID><OtherID Source="NLM">PMC4377297</OtherID></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>7</Month><Day>16</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>7</Month><Day>16</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2015</Year><Month>3</Month><Day>7</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">25023694</ArticleId><ArticleId IdType="pii">130349ys</ArticleId><ArticleId IdType="doi">10.1387/ijdb.130349ys</ArticleId><ArticleId IdType="pmc">PMC4377297</ArticleId><ArticleId IdType="mid">NIHMS670811</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Pennsylvanie</li></region><settlement><li>Pittsburgh</li></settlement><orgName><li>Université de Pittsburgh</li></orgName></list><tree><noCountry><name sortKey="Bayer, Avraham" sort="Bayer, Avraham" uniqKey="Bayer A" first="Avraham" last="Bayer">Avraham Bayer</name><name sortKey="Coyne, Carolyn B" sort="Coyne, Carolyn B" uniqKey="Coyne C" first="Carolyn B" last="Coyne">Carolyn B. Coyne</name><name sortKey="Ouyang, Yingshi" sort="Ouyang, Yingshi" uniqKey="Ouyang Y" first="Yingshi" last="Ouyang">Yingshi Ouyang</name><name sortKey="Sadovsky, Yoel" sort="Sadovsky, Yoel" uniqKey="Sadovsky Y" first="Yoel" last="Sadovsky">Yoel Sadovsky</name></noCountry><country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Mouillet, Jean Francois" sort="Mouillet, Jean Francois" uniqKey="Mouillet J" first="Jean-Francois" last="Mouillet">Jean-Francois Mouillet</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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