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A genetic Xenopus laevis tadpole model to study lymphangiogenesis.

Identifieur interne : 003956 ( PubMed/Checkpoint ); précédent : 003955; suivant : 003957

A genetic Xenopus laevis tadpole model to study lymphangiogenesis.

Auteurs : Annelii Ny [Belgique] ; Marta Koch ; Martin Schneider ; Elke Neven ; Ricky T. Tong ; Sunit Maity ; Christian Fischer ; Stephane Plaisance ; Diether Lambrechts ; Christophe Héligon ; Sven Terclavers ; Malgorzata Ciesiolka ; Roland K Lin ; Wing Yan Man ; Irena Senn ; Sabine Wyns ; Florea Lupu ; André Br Ndli ; Kris Vleminckx ; Désiré Collen ; Mieke Dewerchin ; Edward M. Conway ; Lieve Moons ; Rakesh K. Jain ; Peter Carmeliet

Source :

RBID : pubmed:16116431

Descripteurs français

English descriptors

Abstract

Lymph vessels control fluid homeostasis, immunity and metastasis. Unraveling the molecular basis of lymphangiogenesis has been hampered by the lack of a small animal model that can be genetically manipulated. Here, we show that Xenopus tadpoles develop lymph vessels from lymphangioblasts or, through transdifferentiation, from venous endothelial cells. Lymphangiography showed that these lymph vessels drain lymph, through the lymph heart, to the venous circulation. Morpholino-mediated knockdown of the lymphangiogenic factor Prox1 caused lymph vessel defects and lymphedema by impairing lymphatic commitment. Knockdown of vascular endothelial growth factor C (VEGF-C) also induced lymph vessel defects and lymphedema, but primarily by affecting migration of lymphatic endothelial cells. Knockdown of VEGF-C also resulted in aberrant blood vessel formation in tadpoles. This tadpole model offers opportunities for the discovery of new regulators of lymphangiogenesis.

DOI: 10.1038/nm1285
PubMed: 16116431


Affiliations:


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pubmed:16116431

Le document en format XML

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<div type="abstract" xml:lang="en">Lymph vessels control fluid homeostasis, immunity and metastasis. Unraveling the molecular basis of lymphangiogenesis has been hampered by the lack of a small animal model that can be genetically manipulated. Here, we show that Xenopus tadpoles develop lymph vessels from lymphangioblasts or, through transdifferentiation, from venous endothelial cells. Lymphangiography showed that these lymph vessels drain lymph, through the lymph heart, to the venous circulation. Morpholino-mediated knockdown of the lymphangiogenic factor Prox1 caused lymph vessel defects and lymphedema by impairing lymphatic commitment. Knockdown of vascular endothelial growth factor C (VEGF-C) also induced lymph vessel defects and lymphedema, but primarily by affecting migration of lymphatic endothelial cells. Knockdown of VEGF-C also resulted in aberrant blood vessel formation in tadpoles. This tadpole model offers opportunities for the discovery of new regulators of lymphangiogenesis.</div>
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<AbstractText>Lymph vessels control fluid homeostasis, immunity and metastasis. Unraveling the molecular basis of lymphangiogenesis has been hampered by the lack of a small animal model that can be genetically manipulated. Here, we show that Xenopus tadpoles develop lymph vessels from lymphangioblasts or, through transdifferentiation, from venous endothelial cells. Lymphangiography showed that these lymph vessels drain lymph, through the lymph heart, to the venous circulation. Morpholino-mediated knockdown of the lymphangiogenic factor Prox1 caused lymph vessel defects and lymphedema by impairing lymphatic commitment. Knockdown of vascular endothelial growth factor C (VEGF-C) also induced lymph vessel defects and lymphedema, but primarily by affecting migration of lymphatic endothelial cells. Knockdown of VEGF-C also resulted in aberrant blood vessel formation in tadpoles. This tadpole model offers opportunities for the discovery of new regulators of lymphangiogenesis.</AbstractText>
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<DescriptorName UI="D042583" MajorTopicYN="N">Lymphangiogenesis</DescriptorName>
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<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008208" MajorTopicYN="N">Lymphatic System</DescriptorName>
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<QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D025521" MajorTopicYN="N">Tumor Suppressor Proteins</DescriptorName>
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<DescriptorName UI="D014982" MajorTopicYN="N">Xenopus laevis</DescriptorName>
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<Year>2005</Year>
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<PublicationStatus>ppublish</PublicationStatus>
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<ArticleId IdType="pii">nm1285</ArticleId>
<ArticleId IdType="doi">10.1038/nm1285</ArticleId>
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<name sortKey="Koch, Marta" sort="Koch, Marta" uniqKey="Koch M" first="Marta" last="Koch">Marta Koch</name>
<name sortKey="Lambrechts, Diether" sort="Lambrechts, Diether" uniqKey="Lambrechts D" first="Diether" last="Lambrechts">Diether Lambrechts</name>
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<name sortKey="Maity, Sunit" sort="Maity, Sunit" uniqKey="Maity S" first="Sunit" last="Maity">Sunit Maity</name>
<name sortKey="Man, Wing Yan" sort="Man, Wing Yan" uniqKey="Man W" first="Wing Yan" last="Man">Wing Yan Man</name>
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<name sortKey="Neven, Elke" sort="Neven, Elke" uniqKey="Neven E" first="Elke" last="Neven">Elke Neven</name>
<name sortKey="Plaisance, Stephane" sort="Plaisance, Stephane" uniqKey="Plaisance S" first="Stephane" last="Plaisance">Stephane Plaisance</name>
<name sortKey="Schneider, Martin" sort="Schneider, Martin" uniqKey="Schneider M" first="Martin" last="Schneider">Martin Schneider</name>
<name sortKey="Senn, Irena" sort="Senn, Irena" uniqKey="Senn I" first="Irena" last="Senn">Irena Senn</name>
<name sortKey="Terclavers, Sven" sort="Terclavers, Sven" uniqKey="Terclavers S" first="Sven" last="Terclavers">Sven Terclavers</name>
<name sortKey="Tong, Ricky T" sort="Tong, Ricky T" uniqKey="Tong R" first="Ricky T" last="Tong">Ricky T. Tong</name>
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