含生物活性脂质的sco2泡沫复合支架通过上调Hif-1α和增强H型血管形成促进血管化骨再生

Shuang-Fei Li, C. Song, Shengbing Yang, Weijun Yu, Weiqi Zhang, Guohua Zhang, Zhenhao Xi, Eryi Lu
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摘要

骨组织工程在治疗大量骨缺损方面具有巨大的潜力;然而,有效的血管化结合骨再生仍然是该领域的一个挑战。本研究采用超临界二氧化碳(scCO2)发泡技术制备介孔生物活性玻璃(MBGs)颗粒-聚乳酸-羟基乙酸(PLGA)复合支架,该支架具有良好的力学性能和降解性能以及体外生物活性。含有生物活性脂质FTY720的MBG-PLGA支架(指定为FTY/MBG-PLGA)同时表现出生物活性脂质和离子的持续释放。除了为细胞粘附和增殖提供良好的微环境外,FTY/MBG-PLGA支架还能显著促进rBMSCs体外成骨分化,并通过激活Erk1/2通路,显著刺激Hif-1α表达上调,介导rBMSCs成骨和促血管生成作用。此外,FTY/MBG-PLGA提取物诱导HUVECs体外血管生成性能优越。对临界尺寸大鼠颅骨骨缺损的体内评价表明,FTY/MBG-PLGA支架可有效促进血管化骨再生。值得注意的是,在FTY720 /MBG-PLGA组中,新形成的骨组织中H型血管(cd31hiemcnhineo -vessel)的形成显著增强,这强烈提示FTY720和支架释放的治疗性离子协同诱导了更多H型血管的形成,这表明血管生成和成骨的耦合可以有效地实现血管化骨再生。综上所述,研究结果表明,含有生物活性脂质的泡沫多孔MBG-PLGA支架实现了理想的血管耦合骨形成,可能是骨再生医学的一种有前景的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
scCO 2 Foamed Composite Scaffolds Incorporating Bioactive Lipids Promote Vascularized Bone Regeneration Via Hif-1α Upregulation and Enhanced Type H Vessel Formation
Bone tissue engineering has substantial potential for the treatment of massive bone defects; however, efficient vascularization coupled with bone regeneration still remains a challenge in this field. In the current study,supercritical carbon dioxide (scCO2) foaming technique was adopted to fabricate mesoporous bioactive glasses (MBGs) particle-poly (lactic-co-glycolic acid) (PLGA) composite scaffolds with appropriate mechanical and degradation properties as well as in vitro bioactivity. The MBG-PLGA scaffolds incorporating the bioactive lipid FTY720 (designated as FTY/MBG-PLGA) exhibited simultaneously sustained release of thebioactive lipid and ions. In addition to providing a favorable microenvironment for cellular adhesion and proliferation, FTY/MBG-PLGA scaffolds significantly facilitated the in vitro osteogenic differentiation of rBMSCs and also markedly stimulated the up regulation of Hif-1α expression via the activation of the Erk1/2 pathway, which mediated the osteogenic and pro-angiogenic effects on rBMSCs. Furthermore, FTY/MBG-PLGA extracts induced superior in vitro angiogenic performance of HUVECs. In vivo evaluation of critical-sized rat calvarial bone defects indicated that FTY/MBG-PLGA scaffolds potently promoted vascularized bone regeneration. Notably, the significantly enhanced formation of type Hvessels (CD31hiEmcnhineo-vessels) was observed in newly formed bone tissue in FTY/MBG-PLGA group, strongly suggesting that FTY720 and therapeutic ions released from the scaffolds synergistically induced moretype H vessel formation, which indicated the coupling of angiogenesis and osteogenesis to achieve efficiently vascularized bone regeneration. Overall,the results indicated that the foamed porous MBG-PLGA scaffolds incorporating bioactive lipids achieved desirable vascularization-coupled bone formation and could be a promising strategy for bone regenerative medicine.
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