Nox1 regulates apoptosis and potentially stimulates branching morphogenesis in sinusoidal endothelial cells

S Kobayashi, Y Nojima, M Shibuya, Y Maru - Experimental cell research, 2004 - Elsevier
S Kobayashi, Y Nojima, M Shibuya, Y Maru
Experimental cell research, 2004Elsevier
Tubulogenic transformation of a nontubulogenic endothelial cell line NP31 by a
constitutively activated form of the Flt-1 kinase (NP31/kinase) was accompanied by an
increased expression of Nox1 by sixfold over NP31. Overexpression of Nox1 in NP31 cells
(NP31/Nox1) stimulated branching morphogenesis in Matrigel but surprisingly cords lacked
a lumen. The branching morphogenesis by NP31/kinase and NP31/Nox1 cells was blocked
either by N-acetyl-l-cysteine (NAC) or Tiron. Vascular endothelial growth factor (VEGF) …
Tubulogenic transformation of a nontubulogenic endothelial cell line NP31 by a constitutively activated form of the Flt-1 kinase (NP31/kinase) was accompanied by an increased expression of Nox1 by sixfold over NP31. Overexpression of Nox1 in NP31 cells (NP31/Nox1) stimulated branching morphogenesis in Matrigel but surprisingly cords lacked a lumen. The branching morphogenesis by NP31/kinase and NP31/Nox1 cells was blocked either by N-acetyl-l-cysteine (NAC) or Tiron. Vascular endothelial growth factor (VEGF)-dependent sinusoidal endothelial cells (SEC) in primary culture showed fivefold increase in Nox1 expression 4 days after VEGF stimulation. Interestingly, VEGF-resistant apoptosis in SEC at day 7 was inhibited by NAC or by anti-Nox1 siRNA. These results suggest that Nox1 regulates apoptosis in SEC and can potentially stimulate branching morphogenesis in SEC-derived NP 31 cells.
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