Division of Cardiovascular Diseases, Department of Biochemistry and Molecular Biology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.
Arterioscler Thromb Vasc Biol. 2012 Mar;32(3):704-11. doi: 10.1161/ATVBAHA.111.243733. Epub 2012 Jan 5.
Tissue factor pathway inhibitor (TFPI) is the primary regulator of the tissue factor (TF) coagulation pathway. As such, TFPI may regulate the proangiogenic effects of TF. TFPI may also affect angiogenesis independently of TF, through sequences within its polybasic carboxyl terminus (TFPI C terminus [TFPIct]). We aimed to determine the effects of TFPI on angiogenesis and the role of TFPIct.
Transgenic overexpression of TFPI attenuated angiogenesis in the murine hindlimb ischemia model and an aortic sprout assay. In vitro, TFPI inhibited endothelial cell migration. Peptides within the human TFPIct inhibited endothelial cell cord formation and migration in response to vascular endothelial growth factor (VEGF) 165 but not VEGF121. Furthermore, exposure to human TFPIct inhibited the phosphorylation of VEGF receptor 2 at residue Lys951, a residue known to be critical for endothelial cell migration. Finally, systemic delivery of a murine TFPIct peptide inhibited angiogenesis in the hindlimb model.
These data demonstrate an inhibitory role for TFPI in angiogenesis that is, in part, mediated through peptides within its carboxyl terminus. In addition to its known role as a TF antagonist, TFPI, via its carboxyl terminus, may regulate angiogenesis by directly blocking VEGF receptor 2 activation and attenuating the migratory capacity of endothelial cells.
组织因子途径抑制剂(TFPI)是组织因子(TF)凝血途径的主要调节剂。因此,TFPI 可能调节 TF 的促血管生成作用。TFPI 也可能通过其多碱性羧基末端(TFPI C 末端 [TFPIct])内的序列独立于 TF 影响血管生成。我们旨在确定 TFPI 对血管生成的影响及其 TFPIct 的作用。
TFPI 的转基因过表达减弱了小鼠后肢缺血模型和主动脉芽检测中的血管生成。在体外,TFPI 抑制内皮细胞迁移。人 TFPIct 内的肽抑制内皮细胞索形成和迁移对血管内皮生长因子(VEGF)165 的反应,但不抑制 VEGF121。此外,暴露于人 TFPIct 抑制了 VEGF 受体 2 残基 Lys951 的磷酸化,该残基对于内皮细胞迁移至关重要。最后,系统递送鼠 TFPIct 肽抑制了后肢模型中的血管生成。
这些数据表明 TFPI 在血管生成中具有抑制作用,部分是通过其羧基末端内的肽介导的。除了其作为 TF 拮抗剂的已知作用外,TFPI 通过其羧基末端可能通过直接阻断 VEGF 受体 2 的激活和减弱内皮细胞的迁移能力来调节血管生成。