Generation of specialized blood vessels via lymphatic transdifferentiation

转分化 生物 淋巴系统 斑马鱼 细胞生物学 再生(生物学) 重编程 淋巴管内皮 细胞命运测定 谱系(遗传) 淋巴管 细胞 解剖 干细胞 免疫学 遗传学 基因 转录因子 癌症 转移
作者
Rudra Nayan Das,Yaara Tevet,Stav Refael Safriel,Yanchao Han,Noga Moshe,Giuseppina Lambiase,Ivan Bassi,Julian Nicenboim,Matthias Brückner,Dana Hirsch,Raya Eilam-Altstädter,Wiebke Herzog,Roi Avraham,Kenneth D. Poss,Karina Yaniv
出处
期刊:Nature [Springer Nature]
卷期号:606 (7914): 570-575 被引量:22
标识
DOI:10.1038/s41586-022-04766-2
摘要

The lineage and developmental trajectory of a cell are key determinants of cellular identity. In the vascular system, endothelial cells (ECs) of blood and lymphatic vessels differentiate and specialize to cater to the unique physiological demands of each organ1,2. Although lymphatic vessels were shown to derive from multiple cellular origins, lymphatic ECs (LECs) are not known to generate other cell types3,4. Here we use recurrent imaging and lineage-tracing of ECs in zebrafish anal fins, from early development to adulthood, to uncover a mechanism of specialized blood vessel formation through the transdifferentiation of LECs. Moreover, we demonstrate that deriving anal-fin vessels from lymphatic versus blood ECs results in functional differences in the adult organism, uncovering a link between cell ontogeny and functionality. We further use single-cell RNA-sequencing analysis to characterize the different cellular populations and transition states involved in the transdifferentiation process. Finally, we show that, similar to normal development, the vasculature is rederived from lymphatics during anal-fin regeneration, demonstrating that LECs in adult fish retain both potency and plasticity for generating blood ECs. Overall, our research highlights an innate mechanism of blood vessel formation through LEC transdifferentiation, and provides in vivo evidence for a link between cell ontogeny and functionality in ECs.
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