ßIV-spectrin as a stalk cell-intrinsic regulator of VEGF signaling.
Nat Commun
; 13(1): 1326, 2022 03 14.
Article
em En
| MEDLINE
| ID: mdl-35288568
ABSTRACT
Defective angiogenesis underlies over 50 malignant, ischemic and inflammatory disorders yet long-term therapeutic applications inevitably fail, thus highlighting the need for greater understanding of the vast crosstalk and compensatory mechanisms. Based on proteomic profiling of angiogenic endothelial components, here we report ßIV-spectrin, a non-erythrocytic cytoskeletal protein, as a critical regulator of sprouting angiogenesis. Early loss of endothelial-specific ßIV-spectrin promotes embryonic lethality in mice due to hypervascularization and hemorrhagic defects whereas neonatal depletion yields higher vascular density and tip cell populations in developing retina. During sprouting, ßIV-spectrin expresses in stalk cells to inhibit their tip cell potential by enhancing VEGFR2 turnover in a manner independent of most cell-fate determining mechanisms. Rather, ßIV-spectrin recruits CaMKII to the plasma membrane to directly phosphorylate VEGFR2 at Ser984, a previously undefined phosphoregulatory site that strongly induces VEGFR2 internalization and degradation. These findings support a distinct spectrin-based mechanism of tip-stalk cell specification during vascular development.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Espectrina
/
Fator A de Crescimento do Endotélio Vascular
Limite:
Animals
Idioma:
En
Ano de publicação:
2022
Tipo de documento:
Article