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(Circulation Research. 2007;100:70.)
© 2007 American Heart Association, Inc.

Molecular Medicine

Critical Role of Endothelial Notch1 Signaling in Postnatal Angiogenesis

Kyosuke Takeshita, Minoru Satoh, Masaaki Ii, Marcy Silver, Florian P. Limbourg, Yasushi Mukai, Yoshiyuki Rikitake, Freddy Radtke, Thomas Gridley, Douglas W. Losordo, James K. Liao

From the Vascular Medicine Research Unit (K.T., M. Satoh, F.P.L., Y.M., Y.R., J.K.L.), Brigham & Women’s Hospital and Harvard Medical School, Boston, Mass; Division of Cardiovascular Research and Medicine (M.I., M. Silver, D.W.L.), St. Elizabeth’s Medical Center, Tufts University School of Medicine, Boston, Mass; Ludwig Institute for Cancer Research (F.R.), Lausanne Branch, University of Lausanne, Epalinges, Switzerland; and The Jackson Laboratory (T.G.), Bar Harbor, Me.

Correspondence to Dr James K. Liao, Brigham & Women’s Hospital, 65 Landsdowne St, Rm 275, Cambridge, MA 02139. E-mail jliao{at}rics.bwh.harvard.edu

Notch receptors are important mediators of cell fate during embryogenesis, but their role in adult physiology, particularly in postnatal angiogenesis, remains unknown. Of the Notch receptors, only Notch1 and Notch4 are expressed in vascular endothelial cells. Here we show that blood flow recovery and postnatal neovascularization in response to hindlimb ischemia in haploinsufficient global or endothelial-specific Notch1^+/– mice, but not Notch4^–/– mice, were impaired compared with wild-type mice. The expression of vascular endothelial growth factor (VEGF) in response to ischemia was comparable between wild-type and Notch mutant mice, suggesting that Notch1 is downstream of VEGF signaling. Treatment of endothelial cells with VEGF increases presenilin proteolytic processing, -secretase activity, Notch1 cleavage, and Hes-1 (hairy enhancer of split homolog-1) expression, all of which were blocked by treating endothelial cells with inhibitors of phosphatidylinositol 3-kinase/protein kinase Akt or infecting endothelial cells with a dominant-negative Akt mutant. Indeed, inhibition of -secretase activity leads to decreased angiogenesis and inhibits VEGF-induced endothelial cell proliferation, migration, and survival. Overexpression of the active Notch1 intercellular domain rescued the inhibitory effects of -secretase inhibitors on VEGF-induced angiogenesis. These findings indicate that the phosphatidylinositol 3-kinase/Akt pathway mediates -secretase and Notch1 activation by VEGF and that Notch1 is critical for VEGF-induced postnatal angiogenesis. These results suggest that Notch1 may be a novel therapeutic target for improving angiogenic response and blood flow recovery in ischemic limbs.

Key Words: angiogenesis • endothelium • ischemia • vasculature

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