Endometrial pinopode biomarkers: Molecules and microRNAs.
Identifieur interne : 000270 ( Main/Exploration ); précédent : 000269; suivant : 000271Endometrial pinopode biomarkers: Molecules and microRNAs.
Auteurs : Fahimeh Zamani Rarani [Iran] ; Fatemeh Borhani [Iran] ; Bahman Rashidi [Iran]Source :
- Journal of cellular physiology [ 1097-4652 ] ; 2018.
Descripteurs français
- KwdFr :
- Animaux (MeSH), Appareil de Golgi (génétique), Appareil de Golgi (ultrastructure), Facteur inhibiteur de la leucémie (génétique), Femelle (MeSH), Humains (MeSH), Marqueurs biologiques (métabolisme), Protéines à homéodomaine (génétique), Rats (MeSH), Réticulum endoplasmique rugueux (génétique), Réticulum endoplasmique rugueux (ultrastructure), Souris (MeSH), Sélectine L (génétique), Utérus (métabolisme), Utérus (ultrastructure), microARN (génétique), Épithélium (métabolisme), Épithélium (ultrastructure).
- MESH :
- génétique : Appareil de Golgi, Facteur inhibiteur de la leucémie, Protéines à homéodomaine, Réticulum endoplasmique rugueux, Sélectine L, microARN.
- métabolisme : Marqueurs biologiques, Utérus, Épithélium.
- ultrastructure : Animaux, Appareil de Golgi, Femelle, Humains, Rats, Réticulum endoplasmique rugueux, Souris, Utérus, Épithélium.
English descriptors
- KwdEn :
- Animals (MeSH), Biomarkers (metabolism), Endoplasmic Reticulum, Rough (genetics), Endoplasmic Reticulum, Rough (ultrastructure), Epithelium (metabolism), Epithelium (ultrastructure), Female (MeSH), Golgi Apparatus (genetics), Golgi Apparatus (ultrastructure), Homeobox A10 Proteins (MeSH), Homeodomain Proteins (genetics), Humans (MeSH), L-Selectin (genetics), Leukemia Inhibitory Factor (genetics), Mice (MeSH), MicroRNAs (genetics), Rats (MeSH), Uterus (metabolism), Uterus (ultrastructure).
- MESH :
- chemical , genetics : Homeodomain Proteins, L-Selectin, Leukemia Inhibitory Factor, MicroRNAs.
- chemical , metabolism : Biomarkers.
- genetics : Endoplasmic Reticulum, Rough, Golgi Apparatus.
- metabolism : Epithelium, Uterus.
- ultrastructure : Endoplasmic Reticulum, Rough, Epithelium, Golgi Apparatus, Uterus.
- Animals, Female, Homeobox A10 Proteins, Humans, Mice, Rats.
Abstract
Ultrastructural changes on the apical surface of the luminal epithelium of the uterus are known as pinopodes. Their morphology in species and in special species is associated with different results about size, duration, and percentage of surface area covered by pinopodes. The content of pinopodes is different in rodents and humans. In mice and rats pinopodes have many vacuoles and no organelle that extends to the actin stalk above the microvilli. Human pinopodes do not have a large vacuole and contain the golgi complex, a rough endoplasmic reticulum, secretory vesicles, and mitochondria that extend from the entire cell surface. It has been suggested that pinopodes are good markers of endometrial receptivity and implantation window. There are several molecular markers related to the presence of pinopodes, including integrins, leukemia inhibiting factor (LIF), l-selectin, HOXA10, glutaredoxin, glycodelinA, heparin-binding epidermal growth factor, mucins, and microRNAs (miRNAs). Multiple lines of evidence have indicated that miRNAs could affect the expression of LIF and pinopodes in the endometrium and these molecules play key roles in implantation window processes. Here, we have summarized the morphology and function of pinopodes. Moreover, we have highlighted several molecules in relation to pinopodes that could be used as biomarkers.
DOI: 10.1002/jcp.26852
PubMed: 29968908
Affiliations:
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Iran.</nlm:affiliation><country xml:lang="fr">Iran</country><wicri:regionArea>Department of Basic Sciences, Faculty of Medicine, Gonabad University of Medical Sciences, Gonabad</wicri:regionArea><wicri:noRegion>Gonabad</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:affiliation>Department of Basic Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</nlm:affiliation><country xml:lang="fr">Iran</country><wicri:regionArea>Department of Basic Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran</wicri:regionArea><wicri:noRegion>Tehran</wicri:noRegion></affiliation></author><author><name sortKey="Rashidi, Bahman" sort="Rashidi, Bahman" uniqKey="Rashidi B" first="Bahman" last="Rashidi">Bahman Rashidi</name><affiliation wicri:level="1"><nlm:affiliation>Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</nlm:affiliation><country 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uniqKey="Rarani F" first="Fahimeh Zamani" last="Rarani">Fahimeh Zamani Rarani</name><affiliation wicri:level="1"><nlm:affiliation>Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</nlm:affiliation><country xml:lang="fr">Iran</country><wicri:regionArea>Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan</wicri:regionArea><wicri:noRegion>Isfahan</wicri:noRegion></affiliation></author><author><name sortKey="Borhani, Fatemeh" sort="Borhani, Fatemeh" uniqKey="Borhani F" first="Fatemeh" last="Borhani">Fatemeh Borhani</name><affiliation wicri:level="1"><nlm:affiliation>Department of Basic Sciences, Faculty of Medicine, Gonabad University of Medical Sciences, Gonabad, Iran.</nlm:affiliation><country xml:lang="fr">Iran</country><wicri:regionArea>Department of Basic Sciences, Faculty of Medicine, Gonabad University of Medical Sciences, 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Isfahan</wicri:regionArea><wicri:noRegion>Isfahan</wicri:noRegion></affiliation></author></analytic><series><title level="j">Journal of cellular physiology</title><idno type="eISSN">1097-4652</idno><imprint><date when="2018" type="published">2018</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals (MeSH)</term><term>Biomarkers (metabolism)</term><term>Endoplasmic Reticulum, Rough (genetics)</term><term>Endoplasmic Reticulum, Rough (ultrastructure)</term><term>Epithelium (metabolism)</term><term>Epithelium (ultrastructure)</term><term>Female (MeSH)</term><term>Golgi Apparatus (genetics)</term><term>Golgi Apparatus (ultrastructure)</term><term>Homeobox A10 Proteins (MeSH)</term><term>Homeodomain Proteins (genetics)</term><term>Humans (MeSH)</term><term>L-Selectin (genetics)</term><term>Leukemia Inhibitory Factor (genetics)</term><term>Mice (MeSH)</term><term>MicroRNAs (genetics)</term><term>Rats (MeSH)</term><term>Uterus (metabolism)</term><term>Uterus (ultrastructure)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux (MeSH)</term><term>Appareil de Golgi (génétique)</term><term>Appareil de Golgi (ultrastructure)</term><term>Facteur inhibiteur de la leucémie (génétique)</term><term>Femelle (MeSH)</term><term>Humains (MeSH)</term><term>Marqueurs biologiques (métabolisme)</term><term>Protéines à homéodomaine (génétique)</term><term>Rats (MeSH)</term><term>Réticulum endoplasmique rugueux (génétique)</term><term>Réticulum endoplasmique rugueux (ultrastructure)</term><term>Souris (MeSH)</term><term>Sélectine L (génétique)</term><term>Utérus (métabolisme)</term><term>Utérus (ultrastructure)</term><term>microARN (génétique)</term><term>Épithélium (métabolisme)</term><term>Épithélium (ultrastructure)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Homeodomain Proteins</term><term>L-Selectin</term><term>Leukemia Inhibitory Factor</term><term>MicroRNAs</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Biomarkers</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Endoplasmic Reticulum, Rough</term><term>Golgi Apparatus</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Appareil de Golgi</term><term>Facteur inhibiteur de la leucémie</term><term>Protéines à homéodomaine</term><term>Réticulum endoplasmique rugueux</term><term>Sélectine L</term><term>microARN</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Epithelium</term><term>Uterus</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Marqueurs biologiques</term><term>Utérus</term><term>Épithélium</term></keywords><keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en"><term>Endoplasmic Reticulum, Rough</term><term>Epithelium</term><term>Golgi Apparatus</term><term>Uterus</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Female</term><term>Homeobox A10 Proteins</term><term>Humans</term><term>Mice</term><term>Rats</term></keywords><keywords scheme="MESH" qualifier="ultrastructure" xml:lang="fr"><term>Animaux</term><term>Appareil de Golgi</term><term>Femelle</term><term>Humains</term><term>Rats</term><term>Réticulum endoplasmique rugueux</term><term>Souris</term><term>Utérus</term><term>Épithélium</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Ultrastructural changes on the apical surface of the luminal epithelium of the uterus are known as pinopodes. Their morphology in species and in special species is associated with different results about size, duration, and percentage of surface area covered by pinopodes. The content of pinopodes is different in rodents and humans. In mice and rats pinopodes have many vacuoles and no organelle that extends to the actin stalk above the microvilli. Human pinopodes do not have a large vacuole and contain the golgi complex, a rough endoplasmic reticulum, secretory vesicles, and mitochondria that extend from the entire cell surface. It has been suggested that pinopodes are good markers of endometrial receptivity and implantation window. There are several molecular markers related to the presence of pinopodes, including integrins, leukemia inhibiting factor (LIF), l-selectin, HOXA10, glutaredoxin, glycodelinA, heparin-binding epidermal growth factor, mucins, and microRNAs (miRNAs). Multiple lines of evidence have indicated that miRNAs could affect the expression of LIF and pinopodes in the endometrium and these molecules play key roles in implantation window processes. Here, we have summarized the morphology and function of pinopodes. Moreover, we have highlighted several molecules in relation to pinopodes that could be used as biomarkers.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">29968908</PMID><DateCompleted><Year>2019</Year><Month>09</Month><Day>25</Day></DateCompleted><DateRevised><Year>2019</Year><Month>12</Month><Day>10</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1097-4652</ISSN><JournalIssue CitedMedium="Internet"><Volume>233</Volume><Issue>12</Issue><PubDate><Year>2018</Year><Month>12</Month></PubDate></JournalIssue><Title>Journal of cellular physiology</Title><ISOAbbreviation>J Cell Physiol</ISOAbbreviation></Journal><ArticleTitle>Endometrial pinopode biomarkers: Molecules and microRNAs.</ArticleTitle><Pagination><MedlinePgn>9145-9158</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1002/jcp.26852</ELocationID><Abstract><AbstractText>Ultrastructural changes on the apical surface of the luminal epithelium of the uterus are known as pinopodes. Their morphology in species and in special species is associated with different results about size, duration, and percentage of surface area covered by pinopodes. The content of pinopodes is different in rodents and humans. In mice and rats pinopodes have many vacuoles and no organelle that extends to the actin stalk above the microvilli. Human pinopodes do not have a large vacuole and contain the golgi complex, a rough endoplasmic reticulum, secretory vesicles, and mitochondria that extend from the entire cell surface. It has been suggested that pinopodes are good markers of endometrial receptivity and implantation window. There are several molecular markers related to the presence of pinopodes, including integrins, leukemia inhibiting factor (LIF), l-selectin, HOXA10, glutaredoxin, glycodelinA, heparin-binding epidermal growth factor, mucins, and microRNAs (miRNAs). Multiple lines of evidence have indicated that miRNAs could affect the expression of LIF and pinopodes in the endometrium and these molecules play key roles in implantation window processes. Here, we have summarized the morphology and function of pinopodes. Moreover, we have highlighted several molecules in relation to pinopodes that could be used as biomarkers.</AbstractText><CopyrightInformation>© 2018 Wiley Periodicals, Inc.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Rarani</LastName><ForeName>Fahimeh Zamani</ForeName><Initials>FZ</Initials><AffiliationInfo><Affiliation>Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Borhani</LastName><ForeName>Fatemeh</ForeName><Initials>F</Initials><AffiliationInfo><Affiliation>Department of Basic Sciences, Faculty of Medicine, Gonabad University of Medical Sciences, Gonabad, Iran.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Department of Basic Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Rashidi</LastName><ForeName>Bahman</ForeName><Initials>B</Initials><Identifier Source="ORCID">0000-0003-1133-9571</Identifier><AffiliationInfo><Affiliation>Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2018</Year><Month>07</Month><Day>03</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Cell Physiol</MedlineTA><NlmUniqueID>0050222</NlmUniqueID><ISSNLinking>0021-9541</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015415">Biomarkers</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000080905">Homeobox A10 Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018398">Homeodomain Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D053605">Leukemia Inhibitory Factor</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D035683">MicroRNAs</NameOfSubstance></Chemical><Chemical><RegistryNumber>126880-86-2</RegistryNumber><NameOfSubstance UI="D019041">L-Selectin</NameOfSubstance></Chemical><Chemical><RegistryNumber>140441-81-2</RegistryNumber><NameOfSubstance UI="C069634">HOXA10 protein, human</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015415" MajorTopicYN="N">Biomarkers</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018870" MajorTopicYN="N">Endoplasmic Reticulum, Rough</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004848" MajorTopicYN="N">Epithelium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="Y">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006056" MajorTopicYN="N">Golgi Apparatus</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000080905" MajorTopicYN="N">Homeobox A10 Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018398" MajorTopicYN="N">Homeodomain Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019041" MajorTopicYN="N">L-Selectin</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D053605" MajorTopicYN="N">Leukemia Inhibitory Factor</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D035683" MajorTopicYN="N">MicroRNAs</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051381" MajorTopicYN="N">Rats</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014599" MajorTopicYN="N">Uterus</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="Y">ultrastructure</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">endometrium</Keyword><Keyword MajorTopicYN="Y">implantation window</Keyword><Keyword MajorTopicYN="Y">microRNA</Keyword><Keyword MajorTopicYN="Y">molecule</Keyword><Keyword MajorTopicYN="Y">pinopodes</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2018</Year><Month>03</Month><Day>04</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2018</Year><Month>05</Month><Day>10</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2018</Year><Month>7</Month><Day>4</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2019</Year><Month>9</Month><Day>26</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2018</Year><Month>7</Month><Day>4</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">29968908</ArticleId><ArticleId IdType="doi">10.1002/jcp.26852</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Iran</li></country></list><tree><country name="Iran"><noRegion><name sortKey="Rarani, Fahimeh Zamani" sort="Rarani, Fahimeh Zamani" uniqKey="Rarani F" first="Fahimeh Zamani" last="Rarani">Fahimeh Zamani Rarani</name></noRegion><name sortKey="Borhani, Fatemeh" sort="Borhani, Fatemeh" uniqKey="Borhani F" first="Fatemeh" last="Borhani">Fatemeh Borhani</name><name sortKey="Borhani, Fatemeh" sort="Borhani, Fatemeh" uniqKey="Borhani F" first="Fatemeh" last="Borhani">Fatemeh Borhani</name><name sortKey="Rashidi, Bahman" sort="Rashidi, Bahman" uniqKey="Rashidi B" first="Bahman" last="Rashidi">Bahman Rashidi</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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