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Native extracellular matrix/fibroin hydrogels for adipose tissue engineering with enhanced vascularization

机译:用于脂肪组织工程的天然细胞外基质/纤维素水凝胶,具有增强的血管化

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Adipose tissue engineering is a promising field for regeneration of soft tissue defects. However, vascularization is needed since nutrients and oxygen cannot reach cells in thick implants by diffusion. Obtaining a biocompatible scaffold with good mechanical properties is another problem. In this study, we aimed to develop thick and vascularized adipose tissue constructs supporting cell viability and adipose tissue regeneration. Hydrogels were prepared by mixing rat decellularized adipose tissue (DAT) and silk fibroin (Fib) at different v/v ratios (3:1, 1:1 and 1:3) and vortexing. Gelation times decreased with increasing fibroin ratio Among hydrogel groups 1:3-DAT: Fib ratio group showed similar mechanical properties with adipose tissue. Both pre-adipocytes and pre-endothelial cells, pre-differentiated from adipose derived stem cells (ASCs), were encapsulated in hydrogels at a 1:3 ratio. In vitro analyses showed that hydrogels with 1:3 (v/v) DAT: Fib ratio supported better cell viability. Pre-adipocytes had lipid vesicles, and pre-endothelial cells formed tubular structures inside hydrogels only after 3 days in vitro. When endothelial and adipogenic pre-differentiated ASCs (for 7 days before encapsulation) were encapsulated together into 1:3-DAT: Fib hydrogels both cell types continued to differentiate into the committed cell lineage. Vascularization process in the hydrogels implanted with adipogenic and endothelial pre-differentiated ASCs took place between the first and second week after implantation which was faster than observed in the empty hydrogels. ASCs pre-differentiated towards adipogenic lineage inside hydrogels had begun to accumulate lipid vesicles after 1 week of subcutaneous implantation Based on these results, we suggest that 1:3-DAT: Fib hydrogels with enhanced vascularization hold promise for adipose tissue engineering.
机译:脂肪组织工程是用于再生软组织缺陷的有希望的领域。然而,需要血管化,因为营养和氧气不能通过扩散到达厚植入物中的细胞。获得具有良好机械性能的生物相容性支架是另一个问题。在这项研究中,我们的目标是开发厚血管化的脂肪组织构建体支持细胞活力和脂肪组织再生。通过在不同V / V比率(3:1,1:1和1:3)和涡旋中,通过将大鼠脱细胞化脂肪组织(DAT)和丝素蛋白(FIB)混合来制备水凝胶。随着水凝胶基团中的纤维素比例增加,凝胶化时间减少了1:3-DAT:FIB比率组与脂肪组织显示出类似的机械性能。从脂肪衍生的干细胞(ASCS)预分化的前脂肪细胞和预介质细胞均在1:3的比例下包封在水凝胶中。体外分析显示,具有1:3(v / v)DAT的水凝胶:FIB比率支持更好的细胞活力。前脂肪细胞具有脂质囊泡,并且仅在体外3天后仅在水凝胶内形成管状结构。当内皮和脂肪发生的预分化ASC(封装前7天)被包封成1:3-DAT:FIB水凝胶,两种细胞类型继续分化为犯下的细胞谱系。在植入后的第一周和第二周之间植入含有脂肪发生和内皮预分化ASC的水凝胶中的血管化过程在植入后的第一周和第二周之间比在空的水凝胶中观察到。基于这些结果,在水凝胶内部朝向水凝胶内部倾向于脂肪酸谱系的ascs已经开始积累脂质囊泡,我们建议1:3-dat:Fib水凝胶,具有增强的血管化组织工程的承诺。

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