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Expansion of microvascular networks in vivo by phthalimide neovascular factor 1 (PNF1)

机译:邻苯二甲酰亚胺新血管因子1(PNF1)扩大体内微血管网络

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摘要

Phthalimide neovascular factor (PNF1, formerly SC-3-149) is a potent stimulator of proangiogenic signaling pathways in endothelial cells. In this study, we evaluated the in vivo effects of sustained PNF1 release to promote ingrowth and expansion of microvascular networks surrounding biomaterial implants. The dorsal skinfold window chamber was used to evaluate the structural remodeling response of the local microvasculature. PNF1 was released from poly(lactic-co-glycolic acid) (PLAGA) films, and a transport model was utilized to predict PNF1 penetration into the surrounding tissue. PNF1 significantly expanded microvascular networks within a 2 mm radius from implants after 3 and 7 days by increasing microvessel length density and lumenal diameter of local arterioles and venules. Staining of histological sections with CD11b showed enhanced recruitment of circulating white blood cells, including monocytes, which are critical for the process of vessel enlargement through arteriogenesis. As PNF1 has been shown to modulate MT1-MMP, a facilitator of CCL2 dependent leukocyte transmigration, aspects of window chamber experiments were repeated in CCR2−/− (CCL2 receptor) mouse chimeras to more fully explore the critical nature of monocyte recruitment on the therapeutic benefits of PNF1 function in vivo.
机译:邻苯二甲酰亚胺新血管因子(PNF1,以前为SC-3-149)是内皮细胞促血管生成信号通路的有效刺激剂。在这项研究中,我们评估了PNF1持续释放的体内效应,以促进生物材料植入物周围的微血管网络向内生长和扩展。背部皮褶窗室用于评估局部微脉管系统的结构重塑反应。从聚乳酸-乙醇酸(PLAGA)薄膜中释放出PNF1,并利用转运模型预测PNF1渗透到周围组织中。通过增加微血管的长度密度和局部小动脉和小静脉的管腔直径,PNF1可以在3天和7天后从植入物半径2 mm处显着扩展微血管网络。用CD11b染色的组织学切片显示循环白细胞(包括单核细胞)的募集增强,这对通过动脉生成的血管扩张过程至关重要。由于已显示PNF1调节MT1-MMP(CCL2依赖性白细胞迁移的促进剂),因此在CCR2 -/-(CCL2受体)小鼠嵌合体中重复了窗室实验的各个方面,以更充分地探索关键单核细胞募集的性质对体内PNF1功能的治疗益处有帮助。

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