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Lymph node transplantation results in spontaneous lymphatic reconnection and restoration of lymphatic flow.

Identifieur interne : 001708 ( PubMed/Corpus ); précédent : 001707; suivant : 001709

Lymph node transplantation results in spontaneous lymphatic reconnection and restoration of lymphatic flow.

Auteurs : Seth Z. Aschen ; Gina Farias-Eisner ; Daniel A. Cuzzone ; Nicholas J. Albano ; Swapna Ghanta ; Evan S. Weitman ; Sagrario Ortega ; Babak J. Mehrara

Source :

RBID : pubmed:24469165

English descriptors

Abstract

Although lymph node transplantation has been shown to improve lymphatic function, the mechanisms regulating lymphatic vessel reconnection and functional status of lymph nodes remains poorly understood.

DOI: 10.1097/01.prs.0000436840.69752.7e
PubMed: 24469165

Links to Exploration step

pubmed:24469165

Le document en format XML

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<title xml:lang="en">Lymph node transplantation results in spontaneous lymphatic reconnection and restoration of lymphatic flow.</title>
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<name sortKey="Aschen, Seth Z" sort="Aschen, Seth Z" uniqKey="Aschen S" first="Seth Z" last="Aschen">Seth Z. Aschen</name>
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<nlm:affiliation>New York, N.Y.; and Madrid, Spain From the Division of Plastic and Reconstructive Surgery, Memorial Sloan-Kettering Cancer Center; and the Biotechnology Programme, Spanish National Cancer Research Centre.</nlm:affiliation>
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<author>
<name sortKey="Farias Eisner, Gina" sort="Farias Eisner, Gina" uniqKey="Farias Eisner G" first="Gina" last="Farias-Eisner">Gina Farias-Eisner</name>
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<name sortKey="Cuzzone, Daniel A" sort="Cuzzone, Daniel A" uniqKey="Cuzzone D" first="Daniel A" last="Cuzzone">Daniel A. Cuzzone</name>
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<name sortKey="Albano, Nicholas J" sort="Albano, Nicholas J" uniqKey="Albano N" first="Nicholas J" last="Albano">Nicholas J. Albano</name>
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<name sortKey="Ghanta, Swapna" sort="Ghanta, Swapna" uniqKey="Ghanta S" first="Swapna" last="Ghanta">Swapna Ghanta</name>
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<name sortKey="Weitman, Evan S" sort="Weitman, Evan S" uniqKey="Weitman E" first="Evan S" last="Weitman">Evan S. Weitman</name>
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<name sortKey="Ortega, Sagrario" sort="Ortega, Sagrario" uniqKey="Ortega S" first="Sagrario" last="Ortega">Sagrario Ortega</name>
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<name sortKey="Mehrara, Babak J" sort="Mehrara, Babak J" uniqKey="Mehrara B" first="Babak J" last="Mehrara">Babak J. Mehrara</name>
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<nlm:affiliation>New York, N.Y.; and Madrid, Spain From the Division of Plastic and Reconstructive Surgery, Memorial Sloan-Kettering Cancer Center; and the Biotechnology Programme, Spanish National Cancer Research Centre.</nlm:affiliation>
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<name sortKey="Cuzzone, Daniel A" sort="Cuzzone, Daniel A" uniqKey="Cuzzone D" first="Daniel A" last="Cuzzone">Daniel A. Cuzzone</name>
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<title level="j">Plastic and reconstructive surgery</title>
<idno type="eISSN">1529-4242</idno>
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<term>Animals</term>
<term>Lymph Nodes (physiology)</term>
<term>Lymph Nodes (transplantation)</term>
<term>Lymphatic Vessels (physiology)</term>
<term>Lymphatic Vessels (surgery)</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
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<term>Lymph Nodes</term>
<term>Lymphatic Vessels</term>
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<term>Lymphatic Vessels</term>
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<term>Lymph Nodes</term>
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<term>Animals</term>
<term>Male</term>
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<front>
<div type="abstract" xml:lang="en">Although lymph node transplantation has been shown to improve lymphatic function, the mechanisms regulating lymphatic vessel reconnection and functional status of lymph nodes remains poorly understood.</div>
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<Month>01</Month>
<Day>28</Day>
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<DateCompleted>
<Year>2014</Year>
<Month>03</Month>
<Day>24</Day>
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<DateRevised>
<Year>2016</Year>
<Month>10</Month>
<Day>19</Day>
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<ISSN IssnType="Electronic">1529-4242</ISSN>
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<Volume>133</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2014</Year>
<Month>Feb</Month>
</PubDate>
</JournalIssue>
<Title>Plastic and reconstructive surgery</Title>
<ISOAbbreviation>Plast. Reconstr. Surg.</ISOAbbreviation>
</Journal>
<ArticleTitle>Lymph node transplantation results in spontaneous lymphatic reconnection and restoration of lymphatic flow.</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Although lymph node transplantation has been shown to improve lymphatic function, the mechanisms regulating lymphatic vessel reconnection and functional status of lymph nodes remains poorly understood.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The authors developed and used LacZ lymphatic reporter mice to examine the lineage of lymphatic vessels infiltrating transferred lymph nodes. In addition, the authors analyzed lymphatic function, expression of vascular endothelial growth factor (VEGF)-C, maintenance of T- and B-cell zone, and anatomical localization of lymphatics and high endothelial venules.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Reporter mice were specific and highly sensitive in identifying lymphatic vessels. Lymph node transfer was associated with rapid return of lymphatic function and clearance of technetium-99 secondary to a massive infiltration of recipient mouse lymphatics and putative connections to donor lymphatics. T- and B-cell populations in the lymph node were maintained. These changes correlated with marked increases in the expression of VEGF-C in the perinodal fat and infiltrating lymphatics. Newly formed lymphatic channels in transferred lymph nodes were in close anatomical proximity to high endothelial venules.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Transferred lymph nodes have rapid infiltration of functional host lymphatic vessels and maintain T- and B-cell populations. This process correlates with increased endogenous expression of VEGF-C in the perinodal fat and infiltrating lymphatics. Anatomical proximity of newly formed lymphatics and high endothelial venules supports the hypothesis that lymph node transfer can improve lymphedema by exchanges with the systemic circulation.</AbstractText>
</Abstract>
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<LastName>Aschen</LastName>
<ForeName>Seth Z</ForeName>
<Initials>SZ</Initials>
<AffiliationInfo>
<Affiliation>New York, N.Y.; and Madrid, Spain From the Division of Plastic and Reconstructive Surgery, Memorial Sloan-Kettering Cancer Center; and the Biotechnology Programme, Spanish National Cancer Research Centre.</Affiliation>
</AffiliationInfo>
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<LastName>Cuzzone</LastName>
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<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>R01 HL111130</GrantID>
<Acronym>HL</Acronym>
<Agency>NHLBI NIH HHS</Agency>
<Country>United States</Country>
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<Grant>
<GrantID>T32 CA009501</GrantID>
<Acronym>CA</Acronym>
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<CommentsCorrectionsList>
<CommentsCorrections RefType="Cites">
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</CommentsCorrections>
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