Age-related changes in vascular endothelial growth factor dependency and angiopoietin-1 - Induced plasticity of adult blood vessels

被引:96
作者
Baffert, F
Thurston, G
Rochon-Duck, M
Le, T
Brekken, R
McDonald, DM
机构
[1] Univ Calif San Francisco, Dept Anat, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[3] Univ Texas, SW Med Ctr, Dallas, TX USA
[4] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
关键词
angiogenesis; angiopoietin-1; microvasculature; vascular endothelial growth factor; vascular endothelial growth factor receptor-2;
D O I
10.1161/01.RES.0000125295.43813.1F
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular endothelial growth factor (VEGF) and angiopoietin-1 (Ang1) are essential for vascular development, but this dependency has been assumed not to persist into adult life. In this study, we report that after 10 days of systemic treatment of 4-, 8-, and 16-week-old mice with VEGF-Trap, an inhibitor of VEGF, the number of capillaries in the tracheal mucosa was reduced by 39%, 28%, and 14%, respectively. The magnitude of the reduction decreased with age (r(2)=0.6, P<0.001), but was still significant at 16 weeks. A corresponding age-related decrease in vascular endothelial growth factor receptor-2 (VEGFR-2) immunoreactivity suggests that diminished VEGFR-2 expression may contribute to resistance to VEGF signaling inhibition. VEGF-Trap further reduced VEGFR-2 expression in tracheal capillaries. By comparison, systemic treatment with adenovirus encoding Ang1 led to a significant enlargement of tracheal venules with little age effect (64%, 56%, and 49% increase in diameter at 10 days). When Ang1 was given in combination with VEGF-Trap, tracheal vessels presented the typical response to each factor, showing that the Ang1 effect was not VEGF-mediated, yet Ang1 seems to have a protective effect, as judged by prevention of VEGF-Trap-induced reduction in tracheal capillaries in the oldest group. Together, these findings indicate that VEGF and Ang1 participate in blood vessel survival and plasticity in adult life.
引用
收藏
页码:984 / 992
页数:9
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