Establishment of an Acquired Lymphedema Model in the Mouse Hindlimb: Technical Refinement and Molecular Characteristics.
Identifieur interne : 008B59 ( Ncbi/Merge ); précédent : 008B58; suivant : 008B60Establishment of an Acquired Lymphedema Model in the Mouse Hindlimb: Technical Refinement and Molecular Characteristics.
Auteurs : Daisuke Iwasaki ; Yuhei Yamamoto ; Naoki Murao ; Akihiko Oyama ; Emi Funayama ; Hiroshi FurukawaSource :
- Plastic and reconstructive surgery [ 1529-4242 ] ; 2017.
Descripteurs français
- KwdFr :
- ARN (analyse), ARN messager (analyse), Animaux, Facteur de croissance endothéliale vasculaire de type A (analyse), Facteur de croissance endothéliale vasculaire de type C (analyse), Immunohistochimie, Lymphe (physiologie), Lymphoedème (anatomopathologie), Lymphoedème (étiologie), Lymphographie, Membre pelvien, Modèles animaux de maladie humaine, Mâle, Noeuds lymphatiques (), Protéines suppresseurs de tumeurs (analyse), Protéines à homéodomaine (analyse), Réaction de polymérisation en chaine en temps réel, Récepteur-3 au facteur croissance endothéliale vasculaire (analyse), Souris, Souris de lignée C57BL, Système lymphatique (physiologie), Vert indocyanine.
- MESH :
- analyse : ARN, ARN messager, Facteur de croissance endothéliale vasculaire de type A, Facteur de croissance endothéliale vasculaire de type C, Protéines suppresseurs de tumeurs, Protéines à homéodomaine, Récepteur-3 au facteur croissance endothéliale vasculaire.
- anatomopathologie : Lymphoedème.
- physiologie : Lymphe, Système lymphatique.
- étiologie : Lymphoedème.
- Animaux, Immunohistochimie, Lymphographie, Membre pelvien, Modèles animaux de maladie humaine, Mâle, Noeuds lymphatiques, Réaction de polymérisation en chaine en temps réel, Souris, Souris de lignée C57BL, Vert indocyanine.
English descriptors
- KwdEn :
- Animals, Disease Models, Animal, Hindlimb, Homeodomain Proteins (analysis), Immunohistochemistry, Indocyanine Green, Lymph (physiology), Lymph Nodes (surgery), Lymphatic System (physiology), Lymphedema (etiology), Lymphedema (pathology), Lymphography, Male, Mice, Mice, Inbred C57BL, RNA (analysis), RNA, Messenger (analysis), Real-Time Polymerase Chain Reaction, Tumor Suppressor Proteins (analysis), Vascular Endothelial Growth Factor A (analysis), Vascular Endothelial Growth Factor C (analysis), Vascular Endothelial Growth Factor Receptor-3 (analysis).
- MESH :
- chemical , analysis : Homeodomain Proteins, RNA, RNA, Messenger, Tumor Suppressor Proteins, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factor C, Vascular Endothelial Growth Factor Receptor-3.
- etiology : Lymphedema.
- pathology : Lymphedema.
- physiology : Lymph, Lymphatic System.
- surgery : Lymph Nodes.
- Animals, Disease Models, Animal, Hindlimb, Immunohistochemistry, Indocyanine Green, Lymphography, Male, Mice, Mice, Inbred C57BL, Real-Time Polymerase Chain Reaction.
Abstract
The pathophysiology of secondary lymphedema remains poorly understood. This study aimed to establish a consistent mouse hindlimb lymphedema model for further investigation of the mechanism and treatment of lymphedema.
DOI: 10.1097/PRS.0000000000002887
PubMed: 28027235
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pubmed:28027235Le document en format XML
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Oyama</name></author><author><name sortKey="Funayama, Emi" sort="Funayama, Emi" uniqKey="Funayama E" first="Emi" last="Funayama">Emi Funayama</name></author><author><name sortKey="Furukawa, Hiroshi" sort="Furukawa, Hiroshi" uniqKey="Furukawa H" first="Hiroshi" last="Furukawa">Hiroshi Furukawa</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2017">2017</date><idno type="RBID">pubmed:28027235</idno><idno type="pmid">28027235</idno><idno type="doi">10.1097/PRS.0000000000002887</idno><idno type="wicri:Area/PubMed/Corpus">000439</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000439</idno><idno type="wicri:Area/PubMed/Curation">000439</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000439</idno><idno type="wicri:Area/PubMed/Checkpoint">000439</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000439</idno><idno 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uniqKey="Oyama A" first="Akihiko" last="Oyama">Akihiko Oyama</name></author><author><name sortKey="Funayama, Emi" sort="Funayama, Emi" uniqKey="Funayama E" first="Emi" last="Funayama">Emi Funayama</name></author><author><name sortKey="Furukawa, Hiroshi" sort="Furukawa, Hiroshi" uniqKey="Furukawa H" first="Hiroshi" last="Furukawa">Hiroshi Furukawa</name></author></analytic><series><title level="j">Plastic and reconstructive surgery</title><idno type="eISSN">1529-4242</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Disease Models, Animal</term><term>Hindlimb</term><term>Homeodomain Proteins (analysis)</term><term>Immunohistochemistry</term><term>Indocyanine Green</term><term>Lymph (physiology)</term><term>Lymph Nodes (surgery)</term><term>Lymphatic System (physiology)</term><term>Lymphedema (etiology)</term><term>Lymphedema (pathology)</term><term>Lymphography</term><term>Male</term><term>Mice</term><term>Mice, Inbred C57BL</term><term>RNA (analysis)</term><term>RNA, Messenger (analysis)</term><term>Real-Time Polymerase Chain Reaction</term><term>Tumor Suppressor Proteins (analysis)</term><term>Vascular Endothelial Growth Factor A (analysis)</term><term>Vascular Endothelial Growth Factor C (analysis)</term><term>Vascular Endothelial Growth Factor Receptor-3 (analysis)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>ARN (analyse)</term><term>ARN messager (analyse)</term><term>Animaux</term><term>Facteur de croissance endothéliale vasculaire de type A (analyse)</term><term>Facteur de croissance endothéliale vasculaire de type C (analyse)</term><term>Immunohistochimie</term><term>Lymphe (physiologie)</term><term>Lymphoedème (anatomopathologie)</term><term>Lymphoedème (étiologie)</term><term>Lymphographie</term><term>Membre pelvien</term><term>Modèles animaux de maladie humaine</term><term>Mâle</term><term>Noeuds lymphatiques ()</term><term>Protéines suppresseurs de tumeurs (analyse)</term><term>Protéines à homéodomaine (analyse)</term><term>Réaction de polymérisation en chaine en temps réel</term><term>Récepteur-3 au facteur croissance endothéliale vasculaire (analyse)</term><term>Souris</term><term>Souris de lignée C57BL</term><term>Système lymphatique (physiologie)</term><term>Vert indocyanine</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Homeodomain Proteins</term><term>RNA</term><term>RNA, Messenger</term><term>Tumor Suppressor Proteins</term><term>Vascular Endothelial Growth Factor A</term><term>Vascular Endothelial Growth Factor C</term><term>Vascular Endothelial Growth Factor Receptor-3</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>ARN</term><term>ARN messager</term><term>Facteur de croissance endothéliale vasculaire de type A</term><term>Facteur de croissance endothéliale vasculaire de type C</term><term>Protéines suppresseurs de tumeurs</term><term>Protéines à homéodomaine</term><term>Récepteur-3 au facteur croissance endothéliale vasculaire</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphoedème</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Lymphe</term><term>Système lymphatique</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Lymph</term><term>Lymphatic System</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Lymph Nodes</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphoedème</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Disease Models, Animal</term><term>Hindlimb</term><term>Immunohistochemistry</term><term>Indocyanine Green</term><term>Lymphography</term><term>Male</term><term>Mice</term><term>Mice, Inbred C57BL</term><term>Real-Time Polymerase Chain Reaction</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Immunohistochimie</term><term>Lymphographie</term><term>Membre pelvien</term><term>Modèles animaux de maladie humaine</term><term>Mâle</term><term>Noeuds lymphatiques</term><term>Réaction de polymérisation en chaine en temps réel</term><term>Souris</term><term>Souris de lignée C57BL</term><term>Vert indocyanine</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The pathophysiology of secondary lymphedema remains poorly understood. This study aimed to establish a consistent mouse hindlimb lymphedema model for further investigation of the mechanism and treatment of lymphedema.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">28027235</PMID><DateCreated><Year>2016</Year><Month>12</Month><Day>27</Day></DateCreated><DateCompleted><Year>2017</Year><Month>06</Month><Day>01</Day></DateCompleted><DateRevised><Year>2017</Year><Month>08</Month><Day>17</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1529-4242</ISSN><JournalIssue CitedMedium="Internet"><Volume>139</Volume><Issue>1</Issue><PubDate><Year>2017</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Plastic and reconstructive surgery</Title><ISOAbbreviation>Plast. Reconstr. Surg.</ISOAbbreviation></Journal><ArticleTitle>Establishment of an Acquired Lymphedema Model in the Mouse Hindlimb: Technical Refinement and Molecular Characteristics.</ArticleTitle><Pagination><MedlinePgn>67e-78e</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1097/PRS.0000000000002887</ELocationID><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The pathophysiology of secondary lymphedema remains poorly understood. This study aimed to establish a consistent mouse hindlimb lymphedema model for further investigation of the mechanism and treatment of lymphedema.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">The authors developed a novel postsurgical lymphedema model in the mouse hindlimb by modifying previously described methods. Lymphedema in the hindlimb was created by removing both the inguinal and popliteal lymph nodes together with the surrounding fat pads, followed by silicone splint placement in the inguinal region. Using this modified mouse model, the authors analyzed lymphatic function, histologic changes, and the expression of lymphangiogenic factors including vascular endothelial growth factor C at various time points.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">The splinted lymphedema model showed a significant increase of edema formation in the hindlimb compared with the sham surgery control animals. Indocyanine green lymphography revealed lymphatic drainage impairment shown by dermal backflow and rerouting of lymph flow in the lymphedema model. Histopathologic and immunohistochemical examinations showed a significant increase of skin thickness and abnormally dilated lymphatics in the lymphedema model. The expression of lymphangiogenic factors in lymphedematous tissues of the splinted lymphedema model was significantly increased compared with controls, depending on the degree of lymphedema.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">This splinted lymphedema model closely simulates the volume response, histopathology, and lymphography characteristics of human acquired lymphedema. Given these similarities to human lymphedema, this refinement of a mouse hindlimb model of acquired lymphedema represents a promising platform for the study of lymphatic vascular insufficiency and for the evaluation of new therapeutic modalities.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Iwasaki</LastName><ForeName>Daisuke</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Sapporo, Hokkaido, Japan From the Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, University of Hokkaido.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yamamoto</LastName><ForeName>Yuhei</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Murao</LastName><ForeName>Naoki</ForeName><Initials>N</Initials></Author><Author ValidYN="Y"><LastName>Oyama</LastName><ForeName>Akihiko</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Funayama</LastName><ForeName>Emi</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Furukawa</LastName><ForeName>Hiroshi</ForeName><Initials>H</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Plast Reconstr Surg</MedlineTA><NlmUniqueID>1306050</NlmUniqueID><ISSNLinking>0032-1052</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018398">Homeodomain Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D025521">Tumor Suppressor Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D042461">Vascular Endothelial Growth Factor A</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D042582">Vascular Endothelial Growth Factor C</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C102225">prospero-related homeobox 1 protein</NameOfSubstance></Chemical><Chemical><RegistryNumber>63231-63-0</RegistryNumber><NameOfSubstance UI="D012313">RNA</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.7.10.1</RegistryNumber><NameOfSubstance UI="D040321">Vascular Endothelial Growth Factor Receptor-3</NameOfSubstance></Chemical><Chemical><RegistryNumber>IX6J1063HV</RegistryNumber><NameOfSubstance UI="D007208">Indocyanine Green</NameOfSubstance></Chemical></ChemicalList><CitationSubset>AIM</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004195" MajorTopicYN="Y">Disease Models, Animal</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006614" MajorTopicYN="Y">Hindlimb</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018398" MajorTopicYN="N">Homeodomain Proteins</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007150" MajorTopicYN="N">Immunohistochemistry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007208" MajorTopicYN="N">Indocyanine Green</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008196" MajorTopicYN="N">Lymph</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008198" MajorTopicYN="N">Lymph Nodes</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008208" MajorTopicYN="N">Lymphatic System</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="Y">Lymphedema</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008220" MajorTopicYN="N">Lymphography</DescriptorName></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="D012313" MajorTopicYN="N">RNA</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D060888" MajorTopicYN="N">Real-Time Polymerase Chain Reaction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D025521" MajorTopicYN="N">Tumor Suppressor Proteins</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D042461" MajorTopicYN="N">Vascular Endothelial Growth Factor A</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D042582" MajorTopicYN="N">Vascular Endothelial Growth Factor C</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D040321" MajorTopicYN="N">Vascular Endothelial Growth Factor Receptor-3</DescriptorName><QualifierName UI="Q000032" 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uniqKey="Furukawa H" first="Hiroshi" last="Furukawa">Hiroshi Furukawa</name><name sortKey="Iwasaki, Daisuke" sort="Iwasaki, Daisuke" uniqKey="Iwasaki D" first="Daisuke" last="Iwasaki">Daisuke Iwasaki</name><name sortKey="Murao, Naoki" sort="Murao, Naoki" uniqKey="Murao N" first="Naoki" last="Murao">Naoki Murao</name><name sortKey="Oyama, Akihiko" sort="Oyama, Akihiko" uniqKey="Oyama A" first="Akihiko" last="Oyama">Akihiko Oyama</name><name sortKey="Yamamoto, Yuhei" sort="Yamamoto, Yuhei" uniqKey="Yamamoto Y" first="Yuhei" last="Yamamoto">Yuhei Yamamoto</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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