Volumetric imaging reveals VEGF-C-dependent formation of hepatic lymph vessels in mice.

3D reconstruction VEGF-C liver lymphatic endothelial cells lymphatic vessel portal tracts portal vein whole mount imaging

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2022
Historique:
received: 21 05 2022
accepted: 19 07 2022
entrez: 2 9 2022
pubmed: 3 9 2022
medline: 3 9 2022
Statut: epublish

Résumé

The liver is a major biosynthetic and detoxifying organ in vertebrates, but also generates 25%-50% of the lymph passing through the thoracic duct and is thereby the organ with the highest contribution to lymph flow. In contrast to its metabolic function, the role of the liver for lymph generation and composition is presently severely understudied. We took a rigorous, volume imaging-based approach to describe the microarchitecture and spatial composition of the hepatic lymphatic vasculature with cellular resolution in whole mount immune stained specimen ranging from thick sections up to entire mouse liver lobes. Here, we describe that in healthy adult livers, lymphatic vessels were exclusively located within the portal tracts, where they formed a unique, highly ramified tree. Ragged, spiky initials enmeshed the portal veins along their entire length and communicated with long lymphatic vessels that followed the path of the portal vein in close association with bile ducts. Together these lymphatic vessels formed a uniquely shaped vascular bed with a delicate architecture highly adapted to the histological structure of the liver. Unexpectedly, with the exception of short collector stretches at the porta hepatis, which we identified as exit point of the liver lymph vessels, the entire hepatic lymph vessel system was comprised of capillary lymphatic endothelial cells only. Functional experiments confirmed the space of Disse as the origin of the hepatic lymph and flow

Identifiants

pubmed: 36051444
doi: 10.3389/fcell.2022.949896
pii: 949896
pmc: PMC9424489
doi:

Types de publication

Journal Article

Langues

eng

Pagination

949896

Informations de copyright

Copyright © 2022 Bobe, Beckmann, Klump, Dierkes, Kirschnick, Redder, Bauer, Schäfers, Erapaneedi, Risse, van de Pavert and Kiefer.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Stefanie Bobe (S)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.
Gerhard-Domagk-Institute of Pathology, University Hospital Münster, Münster, Germany.

Daniel Beckmann (D)

Institute for Geoinformatics, University of Münster, Münster, Germany.

Dorothee Maria Klump (DM)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Cathrin Dierkes (C)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Nils Kirschnick (N)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Esther Redder (E)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Nadine Bauer (N)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Michael Schäfers (M)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Raghu Erapaneedi (R)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Benjamin Risse (B)

Institute for Geoinformatics, University of Münster, Münster, Germany.

Serge A van de Pavert (SA)

Centre National de la Recherche Scientifique (CNRS), National Institute for Health and Medical Research (INSERM), Centre d'Immunologie de Marseille-Luminy (CIML), Aix-Marseille University, Marseille, France.

Friedemann Kiefer (F)

European Institute for Molecular Imaging, University of Münster, Münster, Germany.

Classifications MeSH