イシイ　ヤスオ   石井　泰雄    所属   統合教育学修センター 統合教育学修センター    職種   講師
論文種別	原著
言語種別	英語
査読の有無	査読あり
表題	VEGF family members regulate myocardial tubulogenesis and coronary artery formation in the embryo.
掲載誌名	正式名：Circulation research 略　 称：Circ Res ISSNコード：(1524-4571)0009-7330(Linking)
掲載区分	国外
巻・号・頁	98(7),pp.947-53
著者・共著者	Tomanek Robert J, Ishii Yasuo, Holifield Jennifer S, Sjogren Christina L, Hansen Heidi K, Mikawa Takashi
担当区分	2nd著者
発行年月	2006/04
概要	This study tested the hypothesis that coronary tubulogenesis and coronary artery formation require VEGF family members. Quail embryos were injected with soluble vascular endothelial growth factor (VEGF) receptors R1 (Flt-1), R2 (Flk-1), R3 (Flt-4), VEGF-Trap (a chimera of R1 and R2), or neutralizing antibodies to VEGF-A, VEGF-B, or fibroblast growth factor (FGF)-2. Our data document that tubulogenesis is temporally dependent on multiple VEGF family members, because the early stage of tubulogenesis was markedly inhibited by VEGF-Trap and to a lesser extent by soluble VEGFR-1. Some inhibition of tubulogenesis was documented when anti-FGF-2, but not anti-VEGF-A, antibodies were injected at embryonic day 6 (E6). Most importantly, we found that VEGF-Trap injected at either E6 or E7 prevented the formation of coronary arteries. Soluble VEGFR-1 and soluble VEGFR-2 modified the formation of coronary arteries, whereas soluble VEGFR-3 was without effect. Antibodies to VEGF-B, but not VEGF-A, had a strong inhibitory effect on coronary artery development. The absence of coronary artery stems, and thus a functional coronary circulation, in the embryos injected with VEGF-Trap caused an accumulation of erythrocytes in the subepicardium and muscular interventricular septum. Using retroviral cell tagging, we showed that some of the erythrocytes in blood islands and small vascular tubes were progeny of the proepicardium. Thus, another salient finding of this study is the first definitive documentation of proepicardially derived hemangioblasts, which can differentiate into erythrocytes.
DOI	10.1161/01.RES.0000216974.75994.da
PMID	16527987