首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Infiltration of plasma rich in growth factors enhances in vivo angiogenesis and improves reperfusion and tissue remodeling after severe hind limb ischemia
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Infiltration of plasma rich in growth factors enhances in vivo angiogenesis and improves reperfusion and tissue remodeling after severe hind limb ischemia

机译:严重后肢缺血后,富含生长因子的血浆浸润增强了体内血管生成,并改善了再灌注和组织重塑

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摘要

PRGF is a platelet concentrate within a plasma suspension that forms an in situ-generated fibrin-matrix delivery system, releasing multiple growth factors and other bioactive molecules that play key roles in tissue regeneration. This study was aimed at exploring the angiogenic and myogenic effects of PRGF on in vitro endothelial cells (HUVEC) and skeletal myoblasts (hSkMb) as well as on in vivo mouse subcutaneously implanted matrigel and on limb muscles after a severe ischemia. Human PRGF was prepared and characterized. Both proliferative and anti-apoptotic responses to PRGF were assessed in vitro in HUVEC and hSkMb. In vivo murine matrigel plug assay was conducted to determine the angiogenic capacity of PRGF, whereas in vivo ischemic hind limb model was carried out to demonstrate PRGF-driven vascular and myogenic regeneration. Primary HUVEC and hSkMb incubated with PRGF showed a dose dependent proliferative and anti-apoptotic effect and the PRGF matrigel plugs triggered an early and significant sustained angiogenesis compared with the control group. Moreover, mice treated with PRGF intramuscular infiltrations displayed a substantial reperfusion enhancement at day 28 associated with a fibrotic tissue reduction. These findings suggest that PRGF-induced angiogenesis is functionally effective at expanding the perfusion capacity of the new vasculature and attenuating the endogenous tissue fibrosis after a severe-induced skeletal muscle ischemia. (C) 2015 Elsevier B.V. All rights reserved.
机译:PRGF是血浆悬浮液中的血小板浓缩液,可形成原位生成的纤维蛋白基质递送系统,释放多种生长因子和其他在组织再生中起关键作用的生物活性分子。这项研究旨在探讨PRGF对体外内皮细胞(HUVEC)和骨骼肌成肌细胞(hSkMb)以及体内小鼠皮下植入基质胶和严重缺血后肢体肌肉的血管生成和肌源性作用。制备并表征了人PRGF。在体外HUVEC和hSkMb中评估了PRGF的增殖和抗凋亡反应。进行体内鼠matrigel塞测定法以确定PRGF的血管生成能力,而进行体内缺血后肢模型以证明PRGF驱动的血管和肌原性再生。与PRGF孵育的原发性HUVEC和hSkMb表现出剂量依赖性的增殖和抗凋亡作用,与对照组相比,PRGF matrigel栓触发了早期且显着的持续血管生成。此外,用PRGF肌内浸润处理的小鼠在第28天显示出明显的再灌注增强,与纤维化组织减少有关。这些发现表明,在严重诱导的骨骼肌缺血后,PRGF诱导的血管生成在功能上有效地扩展了新脉管系统的灌注能力并减轻了内源性组织纤维化。 (C)2015 Elsevier B.V.保留所有权利。

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