Role of Nitric Oxide in the Angiogenic Response In Vitro to Basic Fibroblast Growth Factor

From the Terrence Donnelly Heart Centre, Division of Cardiology, St. Michael's Hospital, Department of Medicine, University of Toronto, Ontario, Canada.

Correspondence to D.J. Stewart, Director, Division of Cardiology, University of Toronto, and Head, Division of Cardiology, St. Michael's Hospital, 30 Bond St, Toronto, Ontario, M5B 1W8, Canada. E-mail stewartd{at}smh.toronto.on.ca

Abstract—Angiogenesis is a complex process that involves the activation of quiescent endothelial cells (ECs) to a proliferative and migratory phenotype and, subsequently, their redifferentiation to form vascular tubes. We hypothesized that NO contributes to angiogenesis by terminating the proliferative action of angiogenic growth factors and initiating a genetic program of EC differentiation. Human umbilical vein ECs (HUVECs) and calf pulmonary artery ECs (CPAECs) were grown directly on plastic dishes or on three-dimensional fibrin matrices. In the absence of fibrin, treatment with NO-donor compounds, such as S-nitroso-N-acetylpenicillamine (SNAP, 0.1 and 0.4 mmol/L), produced a dose-dependent inhibition of proliferation in both cell lines, whereas the inhibition of endogenous NO production using N^G-nitro-L-arginine methyl ester (L-NAME, 1 mmol/L) or N^G-monomethyl-L-arginine (L-NMMA, 1 mmol/L) significantly increased proliferation of the CPAECs. The addition of basic fibroblast growth factor (bFGF, 30 ng/mL) increased the expression of endothelial NO synthase mRNA and the production of NO in both cell types when cultured on three-dimensional fibrin gels and produced profound morphological changes characterized by the appearance of extensive capillary-like vascular structures and the loss of EC monolayers. These changes were quantified by measuring total tube length per low-power field (x100), and a differentiation index was derived using the ratio of tube length over area covered by residual EC monolayer. In the absence of additional angiogenic factors, the differentiation index was low for both HUVECs and CPAECs (control, 1.16±0.19 and 2.07±0.87, respectively). Treatment with bFGF increased the differentiation index significantly in both cell types (10.59±2.03 and 20.02±5.01 for HUVECs and CPAECs, respectively; P<.05 versus control), and the addition of SNAP (0.4 mmol/L) mimicked the angiogenic response to bFGF (8.57±1.34 and 12.20±3.49 for HUVECs and CPAECs, respectively; P<.05 versus control). Moreover, L-NAME inhibited EC tube formation in response to bFGF in a dose-response manner, consistent with a role of endogenous NO production in EC differentiation in this angiogenic model. These findings suggest that NO may act as a crucial signal in the angiogenic response to bFGF, terminating the proliferative actions of angiogenic growth factors and promoting EC differentiation into vascular tubes.

Key Words: nitric oxide • angiogenesis • fibrin gel • proliferation • differentiation

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