The development of early human lymphatic vessels as characterized by lymphatic endothelial markers.

Cellular Origin of Lymphatic Endothelial Cells Human Embryos Lymphatic Vessel Development

Journal

The EMBO journal
ISSN: 1460-2075
Titre abrégé: EMBO J
Pays: England
ID NLM: 8208664

Informations de publication

Date de publication:
14 Feb 2024
Historique:
received: 09 11 2023
accepted: 08 01 2024
revised: 02 01 2024
medline: 14 2 2024
pubmed: 14 2 2024
entrez: 14 2 2024
Statut: aheadofprint

Résumé

Lymphatic vessel development studies in mice and zebrafish models have demonstrated that lymphatic endothelial cells (LECs) predominantly differentiate from venous endothelial cells via the expression of the transcription factor Prox1. However, LECs can also be generated from undifferentiated mesoderm, suggesting potential diversity in their precursor cell origins depending on the organ or anatomical location. Despite these advances, recapitulating human lymphatic malformations in animal models has been difficult, and considering lymphatic vasculature function varies widely between species, analysis of development directly in humans is needed. Here, we examined early lymphatic development in humans by analyzing the histology of 31 embryos and three 9-week-old fetuses. We found that human embryonic cardinal veins, which converged to form initial lymph sacs, produce Prox1-expressing LECs. Furthermore, we describe the lymphatic vessel development in various organs and observe organ-specific differences. These characterizations of the early development of human lymphatic vessels should help to better understand the evolution and phylogenetic relationships of lymphatic systems, and their roles in human disease.

Identifiants

pubmed: 38351385
doi: 10.1038/s44318-024-00045-0
pii: 10.1038/s44318-024-00045-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : MEXT | Japan Society for the Promotion of Science (JSPS)
ID : 20K17072
Organisme : MEXT | Japan Society for the Promotion of Science (JSPS)
ID : 23K15949
Organisme : Japan Agency for Medical Research and Development (AMED)
ID : 22jm0610079h0001
Organisme : Mie University (Mie)
ID : Interdisciplinary Collaborative Research Support Project

Informations de copyright

© 2024. The Author(s).

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Auteurs

Shoichiro Yamaguchi (S)

Department of Pathology and Matrix Biology, Graduate School of Medicine, Mie University, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan.

Natsuki Minamide (N)

Department of Pathology and Matrix Biology, Graduate School of Medicine, Mie University, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan.

Hiroshi Imai (H)

Pathology Division, Mie University School of Medicine, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan.

Tomoaki Ikeda (T)

Department of Obstetrics and Gynecology, Mie University School of Medicine, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan.

Masatoshi Watanabe (M)

Department of Oncologic Pathology, Graduate School of Medicine, Mie University, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan.

Kyoko Imanaka-Yoshida (K)

Department of Pathology and Matrix Biology, Graduate School of Medicine, Mie University, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan.

Kazuaki Maruyama (K)

Department of Pathology and Matrix Biology, Graduate School of Medicine, Mie University, 2-174 Edobashi, Tsu, Mie, 514-0001, Japan. k-maruyama0608@med.mie-u.ac.jp.

Classifications MeSH