Core Concepts
Human embryonic lymphatic vessel development originates from venous endothelial cells, forming diverse patterns across organs.
Abstract
Research on human lymphatic vessel development using 31 embryos and 3 fetuses revealed that Prox1-expressing lymphatic endothelial cells (LECs) originate from cardinal veins. LECs form initial lymph sacs around the veins, with varying rates of development and marker expression in different organs. The study highlights the diversity in lymphatic vessel development across organs and contributes to understanding lymph-related diseases. The emergence of lympho-venous valves between lymph sacs and veins was observed, crucial for normal lymphatic function. The study also explored the development of cardiac, lung, lower jaw, mesentery, intestinal, kidney, and thoracic duct lymphatic vessels at different stages. Notably, the research provides insights into the evolutionarily conserved processes of human lymphatic vessel formation.
Stats
Studies have been conducted for about 120 years on lymphatic vessel development.
Lymphatic endothelial cells predominantly differentiate from venous endothelial cells via Prox1 expression.
LECs can also be generated from undifferentiated mesodermal or hemogenic endothelial cells.
Human embryos produce Prox1-expressing LECs around cardinal veins forming initial lymph sacs.
Different rates of development and marker expression are observed in various organs' lymphatic vessels.
Lympho-venous valves are formed between cardinal veins and emerging lymph sacs.
Quotes
"Lympho-venous valves are formed between lymph sacs and the cardinal veins."
"LECs originate from embryonic veins and form initial lymph sacs."
"Diversity exists in the patterns of human organ-specific lymphatic vessel development."