Abstract
AbstractLymphatic 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.
Funder
MEXT | Japan Society for the Promotion of Science
SENSHIN Medical Research Foundation
Mochida Memorial Foundation for Medical and Pharmaceutical Research
Japan Agency for Medical Research and Development
Takeda Medical Research Foundation
Terumo Foundation for Life Sciences and Arts
Japan Foundation for Applied Enzymology
Kurozumi Medical Foundation
Mie University
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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1. Lymphatic System Development and Function;Current Cardiology Reports;2024-08-22