Journal article
Integration of vascular progenitors into functional blood vessels represents a distinct mechanism of vascular growth
Developmental cell, Vol.57(6), pp.767-782.e6
03/28/2022
DOI: 10.1016/j.devcel.2022.02.015
PMCID: PMC9365108
PMID: 35276066
Abstract
During embryogenesis, the initial vascular network forms by the process of vasculogenesis, or the specification of vascular progenitors de novo. In contrast, the majority of later-forming vessels arise by angiogenesis from the already established vasculature. Here, we show that new vascular progenitors in zebrafish embryos emerge from a distinct site along the yolk extension, or secondary vascular field (SVF), incorporate into the posterior cardinal vein, and contribute to subintestinal vasculature even after blood circulation has been initiated. We further demonstrate that SVF cells participate in vascular recovery after chemical ablation of vascular endothelial cells. Inducible inhibition of the function of vascular progenitor marker etv2/etsrp prevented SVF cell differentiation and resulted in the defective formation of subintestinal vasculature. Similar late-forming etv2+ progenitors were also observed in mouse embryos, suggesting that SVF cells are evolutionarily conserved. Our results characterize a distinct mechanism by which new vascular progenitors incorporate into established vasculature.
Details
- Title: Subtitle
- Integration of vascular progenitors into functional blood vessels represents a distinct mechanism of vascular growth
- Creators
- Sanjeeva MetikalaMichael Warkala - Rutgers HealthSatish Casie ChettyBrendan Chestnut - Cincinnati Children's Hospital Medical CenterDiandra Rufin Florat - University of South FloridaElizabeth Plender - Cincinnati Children's Hospital Medical CenterOlivia Nester - Cincinnati Children's Hospital Medical CenterAndrew L KoenigSophie Astrof - Rutgers HealthSaulius Sumanas
- Resource Type
- Journal article
- Publication Details
- Developmental cell, Vol.57(6), pp.767-782.e6
- DOI
- 10.1016/j.devcel.2022.02.015
- PMID
- 35276066
- PMCID
- PMC9365108
- NLM abbreviation
- Dev Cell
- ISSN
- 1534-5807
- eISSN
- 1878-1551
- Grant note
- R01 HL103920 / NHLBI NIH HHS R01 HL134935 / NHLBI NIH HHS R21 AI128445 / NIAID NIH HHS R01 HL153005 / NHLBI NIH HHS F31 HL135986 / NHLBI NIH HHS R01 HL158049 / NHLBI NIH HHS
- Language
- English
- Date published
- 03/28/2022
- Academic Unit
- Stead Family Department of Pediatrics
- Record Identifier
- 9985161355502771
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