Adipose-derived stem cell transplantation for therapeutic lymphangiogenesis in a mouse secondary lymphedema model.
Identifieur interne : 000D32 ( PubMed/Curation ); précédent : 000D31; suivant : 000D33Adipose-derived stem cell transplantation for therapeutic lymphangiogenesis in a mouse secondary lymphedema model.
Auteurs : Shuhei Yoshida [Japon] ; Rodrigo Hamuy [Japon] ; Yuuichi Hamada [Japon] ; Hiroshi Yoshimoto [Japon] ; Akiyoshi Hirano [Japon] ; Sadanori Akita [Japon]Source :
- Regenerative medicine [ 1746-076X ] ; 2015.
Descripteurs français
- KwdFr :
- Animaux, Enregistrement sur magnétoscope, Facteur de croissance endothéliale vasculaire de type C (métabolisme), Femelle, Glycoprotéines (métabolisme), Immunohistochimie, Lymphangiogenèse (physiologie), Lymphoedème (), Membre pelvien (anatomopathologie), Modèles animaux de maladie humaine, Mâle, Protéines à fluorescence verte (métabolisme), Rayons infrarouges, Récepteur-3 au facteur croissance endothéliale vasculaire (métabolisme), Régénération, Souris, Souris de lignée C57BL, Technique FISH, Tissu adipeux (cytologie), Transplantation de cellules souches, Vaisseaux lymphatiques (métabolisme).
- MESH :
- anatomopathologie : Membre pelvien.
- cytologie : Tissu adipeux.
- métabolisme : Facteur de croissance endothéliale vasculaire de type C, Glycoprotéines, Protéines à fluorescence verte, Récepteur-3 au facteur croissance endothéliale vasculaire, Vaisseaux lymphatiques.
- physiologie : Lymphangiogenèse.
- Animaux, Enregistrement sur magnétoscope, Femelle, Immunohistochimie, Lymphoedème, Modèles animaux de maladie humaine, Mâle, Rayons infrarouges, Régénération, Souris, Souris de lignée C57BL, Technique FISH, Transplantation de cellules souches.
English descriptors
- KwdEn :
- Adipose Tissue (cytology), Animals, Disease Models, Animal, Female, Glycoproteins (metabolism), Green Fluorescent Proteins (metabolism), Hindlimb (pathology), Immunohistochemistry, In Situ Hybridization, Fluorescence, Infrared Rays, Lymphangiogenesis (physiology), Lymphatic Vessels (metabolism), Lymphedema (therapy), Male, Mice, Mice, Inbred C57BL, Regeneration, Stem Cell Transplantation, Vascular Endothelial Growth Factor C (metabolism), Vascular Endothelial Growth Factor Receptor-3 (metabolism), Video Recording.
- MESH :
- chemical , metabolism : Glycoproteins, Green Fluorescent Proteins, Vascular Endothelial Growth Factor C, Vascular Endothelial Growth Factor Receptor-3.
- cytology : Adipose Tissue.
- metabolism : Lymphatic Vessels.
- pathology : Hindlimb.
- physiology : Lymphangiogenesis.
- therapy : Lymphedema.
- Animals, Disease Models, Animal, Female, Immunohistochemistry, In Situ Hybridization, Fluorescence, Infrared Rays, Male, Mice, Mice, Inbred C57BL, Regeneration, Stem Cell Transplantation, Video Recording.
Abstract
Secondary lymphedema is observed in common after postmalignancy treatment of the breast and the gynecologic organs but effective therapies are not established. Adipose-derived stem cells (ADSCs), which are pluripotent, regenerative in local injection, are tested for murine hindlimb secondary lymphedema by regenerative method.
DOI: 10.2217/rme.15.24
PubMed: 26237700
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pubmed:26237700Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adipose Tissue (cytology)</term>
<term>Animals</term>
<term>Disease Models, Animal</term>
<term>Female</term>
<term>Glycoproteins (metabolism)</term>
<term>Green Fluorescent Proteins (metabolism)</term>
<term>Hindlimb (pathology)</term>
<term>Immunohistochemistry</term>
<term>In Situ Hybridization, Fluorescence</term>
<term>Infrared Rays</term>
<term>Lymphangiogenesis (physiology)</term>
<term>Lymphatic Vessels (metabolism)</term>
<term>Lymphedema (therapy)</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Regeneration</term>
<term>Stem Cell Transplantation</term>
<term>Vascular Endothelial Growth Factor C (metabolism)</term>
<term>Vascular Endothelial Growth Factor Receptor-3 (metabolism)</term>
<term>Video Recording</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Enregistrement sur magnétoscope</term>
<term>Facteur de croissance endothéliale vasculaire de type C (métabolisme)</term>
<term>Femelle</term>
<term>Glycoprotéines (métabolisme)</term>
<term>Immunohistochimie</term>
<term>Lymphangiogenèse (physiologie)</term>
<term>Lymphoedème ()</term>
<term>Membre pelvien (anatomopathologie)</term>
<term>Modèles animaux de maladie humaine</term>
<term>Mâle</term>
<term>Protéines à fluorescence verte (métabolisme)</term>
<term>Rayons infrarouges</term>
<term>Récepteur-3 au facteur croissance endothéliale vasculaire (métabolisme)</term>
<term>Régénération</term>
<term>Souris</term>
<term>Souris de lignée C57BL</term>
<term>Technique FISH</term>
<term>Tissu adipeux (cytologie)</term>
<term>Transplantation de cellules souches</term>
<term>Vaisseaux lymphatiques (métabolisme)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Glycoproteins</term>
<term>Green Fluorescent Proteins</term>
<term>Vascular Endothelial Growth Factor C</term>
<term>Vascular Endothelial Growth Factor Receptor-3</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Membre pelvien</term>
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<keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Adipose Tissue</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Lymphatic Vessels</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Facteur de croissance endothéliale vasculaire de type C</term>
<term>Glycoprotéines</term>
<term>Protéines à fluorescence verte</term>
<term>Récepteur-3 au facteur croissance endothéliale vasculaire</term>
<term>Vaisseaux lymphatiques</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hindlimb</term>
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<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Lymphangiogenèse</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Lymphangiogenesis</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Disease Models, Animal</term>
<term>Female</term>
<term>Immunohistochemistry</term>
<term>In Situ Hybridization, Fluorescence</term>
<term>Infrared Rays</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Regeneration</term>
<term>Stem Cell Transplantation</term>
<term>Video Recording</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Animaux</term>
<term>Enregistrement sur magnétoscope</term>
<term>Femelle</term>
<term>Immunohistochimie</term>
<term>Lymphoedème</term>
<term>Modèles animaux de maladie humaine</term>
<term>Mâle</term>
<term>Rayons infrarouges</term>
<term>Régénération</term>
<term>Souris</term>
<term>Souris de lignée C57BL</term>
<term>Technique FISH</term>
<term>Transplantation de cellules souches</term>
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<front><div type="abstract" xml:lang="en">Secondary lymphedema is observed in common after postmalignancy treatment of the breast and the gynecologic organs but effective therapies are not established. Adipose-derived stem cells (ADSCs), which are pluripotent, regenerative in local injection, are tested for murine hindlimb secondary lymphedema by regenerative method.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26237700</PMID>
<DateCreated><Year>2015</Year>
<Month>08</Month>
<Day>05</Day>
</DateCreated>
<DateCompleted><Year>2016</Year>
<Month>05</Month>
<Day>24</Day>
</DateCompleted>
<DateRevised><Year>2015</Year>
<Month>08</Month>
<Day>05</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1746-076X</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>10</Volume>
<Issue>5</Issue>
<PubDate><Year>2015</Year>
</PubDate>
</JournalIssue>
<Title>Regenerative medicine</Title>
<ISOAbbreviation>Regen Med</ISOAbbreviation>
</Journal>
<ArticleTitle>Adipose-derived stem cell transplantation for therapeutic lymphangiogenesis in a mouse secondary lymphedema model.</ArticleTitle>
<Pagination><MedlinePgn>549-62</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.2217/rme.15.24</ELocationID>
<Abstract><AbstractText Label="AIM" NlmCategory="OBJECTIVE">Secondary lymphedema is observed in common after postmalignancy treatment of the breast and the gynecologic organs but effective therapies are not established. Adipose-derived stem cells (ADSCs), which are pluripotent, regenerative in local injection, are tested for murine hindlimb secondary lymphedema by regenerative method.</AbstractText>
<AbstractText Label="METHODS & RESULTS" NlmCategory="RESULTS">Mice were divided into four groups: no ADSCs, 1 × 10(6) ADSCs, 1 × 10(5) ADSCs and 1 × 10(4) ADSCs (each group, n = 20) in a stringent surgical resection and irradiation. Circumferential measurement, lymphatic flow assessment and quantification of lymphatic vessels were performed.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The numbers of lymphatic vessels by LYVE-1 immunohistochemistry, and VEGF-C- or VEGFR3-expressing cells were significantly increased in transplanted groups (p < 0.05).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">ADSCs can restore the lymphatic vascular network in secondary lymphedema with increased collecting vessels.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Yoshida</LastName>
<ForeName>Shuhei</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Division of Plastic & Reconstructive Surgery, Department of Developmental & Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852 8501, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hamuy</LastName>
<ForeName>Rodrigo</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Division of Plastic & Reconstructive Surgery, Department of Developmental & Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852 8501, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hamada</LastName>
<ForeName>Yuuichi</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>Division of Plastic & Reconstructive Surgery, Oita Sanai Medical Center, 1213 Ichi, Oita 870-1151, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Yoshimoto</LastName>
<ForeName>Hiroshi</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Division of Plastic & Reconstructive Surgery, Department of Developmental & Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852 8501, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hirano</LastName>
<ForeName>Akiyoshi</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Division of Plastic & Reconstructive Surgery, Department of Developmental & Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852 8501, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Akita</LastName>
<ForeName>Sadanori</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Division of Plastic & Reconstructive Surgery, Department of Developmental & Reconstructive Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852 8501, Japan.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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</PublicationTypeList>
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<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Regen Med</MedlineTA>
<NlmUniqueID>101278116</NlmUniqueID>
<ISSNLinking>1746-0751</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D006023">Glycoproteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D042582">Vascular Endothelial Growth Factor C</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C492273">Xlkd1 protein, mouse</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>147336-22-9</RegistryNumber>
<NameOfSubstance UI="D049452">Green Fluorescent Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 2.7.10.1</RegistryNumber>
<NameOfSubstance UI="D040321">Vascular Endothelial Growth Factor Receptor-3</NameOfSubstance>
</Chemical>
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<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000273" MajorTopicYN="N">Adipose Tissue</DescriptorName>
<QualifierName UI="Q000166" MajorTopicYN="Y">cytology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004195" MajorTopicYN="N">Disease Models, Animal</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006023" MajorTopicYN="N">Glycoproteins</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D049452" MajorTopicYN="N">Green Fluorescent Proteins</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006614" MajorTopicYN="N">Hindlimb</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007150" MajorTopicYN="N">Immunohistochemistry</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017404" MajorTopicYN="N">In Situ Hybridization, Fluorescence</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007259" MajorTopicYN="N">Infrared Rays</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D042583" MajorTopicYN="N">Lymphangiogenesis</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D042601" MajorTopicYN="N">Lymphatic Vessels</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008810" MajorTopicYN="N">Mice, Inbred C57BL</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012038" MajorTopicYN="N">Regeneration</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D033581" MajorTopicYN="Y">Stem Cell Transplantation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D042582" MajorTopicYN="N">Vascular Endothelial Growth Factor C</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D040321" MajorTopicYN="N">Vascular Endothelial Growth Factor Receptor-3</DescriptorName>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">VEGF-C</Keyword>
<Keyword MajorTopicYN="N">VEGFR3</Keyword>
<Keyword MajorTopicYN="N">adipose-derived stem cell</Keyword>
<Keyword MajorTopicYN="N">lymphangiogenesis</Keyword>
<Keyword MajorTopicYN="N">mouse</Keyword>
<Keyword MajorTopicYN="N">radiation</Keyword>
<Keyword MajorTopicYN="N">secondary lymphedema</Keyword>
<Keyword MajorTopicYN="N">surgery</Keyword>
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<PubMedPubDate PubStatus="medline"><Year>2016</Year>
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<ArticleIdList><ArticleId IdType="pubmed">26237700</ArticleId>
<ArticleId IdType="doi">10.2217/rme.15.24</ArticleId>
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