Integration of vascular progenitors into functional blood vessels represents a distinct mechanism of vascular growth.
Integration of vascular progenitors into functional blood vessels represents a distinct mechanism of vascular growth.
复制标题
血管祖细胞整合到功能性血管中代表了血管生长的独特机制。
DOI:
10.1016/j.devcel.2022.02.015
复制
发表时间:
2022-03-28
影响因子:
11.8
通讯作者:
Sumanas, Saulius
中科院分区:
文献类型:
--
作者:
Metikala, Sanjeeva;Warkala, Michael;Chetty, Satish Casie;Chestnut, Brendan;Florat, Diandra Rufin;Plender, Elizabeth;Nester, Olivia;Koenig, Andrew L.;Astrof, Sophie;Sumanas, Saulius
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 (termed 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 vascular progenitor marker etv2 / etsrp function 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 of how new vascular progenitors incorporate into established vasculature. Metikala et al describe new late-forming vascular progenitor cells which incorporate into established blood vessels in zebrafish embryos. These cells can partially regenerate embryonic vasculature when all other endothelial cells are ablated. The authors identify their transcriptional profile and provide evidence for the presence of similar cells in mammalian embryos.
登录
查看更多内容
影响因子:
56.9
作者:
Asahara, T;Murohara, T;Isner, JM
通讯作者:
Isner, JM
影响因子:
9.8
作者:
Craig MP;Sumanas S
通讯作者:
Sumanas S
影响因子:
7
作者:
Auer TO;Duroure K;De Cian A;Concordet JP;Del Bene F
通讯作者:
Del Bene F
影响因子:
2.7
作者:
Dooley, KA;Davidson, AJ;Zon, LI
通讯作者:
Zon, LI
影响因子:
2.7
作者:
Davison, Jon M.;Akitake, Courtney M.;Parsons, Michael J.
通讯作者:
Parsons, Michael J.