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Vascular Smooth Muscle Cell Behaviors onto Epigallocatechin-3-O-gallate-Blended L-Lactide/ε-Caprolactone Copolymers

机译:血管平滑肌细胞行为在EPIGALLOCATECHIN-3-O-Gallate - 混合L-丙交酯/ε-己内酯共聚物上

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In this study, such behaviors of vascular smooth muscle cells (VSMCs), as proliferation and migration, with serum stimulation were investigated onto (-)-epigallocatechin-3-O-gallate (EGCG)-blended poly(L-lactide-co-ε-caprolactone, PLCL) copolymers (EGCG-b PLCL). VSMCs were primarily cultured from rat aorta, and EGCG-b PLCL films were fabricated by mixing PLCL with EGCG. The proliferation of VSMCs cultured onto EGCG-b PLCL film was significantly suppressed in spite of serum induction. Moreover, recovery of denuded area by VSMCs receiving conditioned media obtained from EGCG-b films was completely inhibited, whereas VSMCs onto intact films migrated into denuded area in response to serum showing essentially complete recovery. These results suggest that inhibition in the behaviors of serum-stimulated VSMCs may be mediated through the anti-proliferative effects of EGCG released from polymer films, and EGCG-b polymers can be applied for fabricating an EGCG-eluting vascular stent.
机译:在该研究中,研究了血管平滑肌细胞(VSMC)的这种行为,作为增殖和迁移,并在( - ) - EPIGALLOCATECHIN-3-O-Gallate(EGCG) - 配聚(L-丙交酯 - 共同)上进行血清刺激ε-己内酯,PLCL)共聚物(EGCG-B PLCL)。 VSMC主要由大鼠主动脉培养,通过将PLCL与EGCG混合来制造EGCG-B PLCL膜。尽管血清诱导,显着抑制了培养到EGCG-B PLCL膜上的VSMC的增殖。此外,通过VSMCS接收从EGCG-B膜获得的调节介质的剥离区域的恢复被完全抑制,而VSMC响应于血清显示基本完全恢复的血清迁移到裸露的区域上。这些结果表明,可以通过从聚合物薄膜释放的EGCG的抗增殖作用介导血清刺激的VSMC的行为中的抑制,并且可以施加EGCG-B聚合物以制造EGCG洗脱血管支架。

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