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首页> 外文期刊>Acta biomaterialia >Kidney regeneration with biomimetic vascular scaffolds based on vascular corrosion casts
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Kidney regeneration with biomimetic vascular scaffolds based on vascular corrosion casts

机译:基于血管腐蚀铸造的肾脏再生与仿生血管支架

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We have developed a biomimetic renal vascular scaffold based on a vascular corrosion casting technique. This study evaluated the feasibility of using this novel biomimetic scaffold for kidney regeneration in a rat kidney cortical defect model. Vascular corrosion casts were prepared from normal rat kidneys by perfusion with 10% polycaprolactone (PCL) solution, followed by tissue digestion. The corrosion PCL cast was coated with collagen, and PCL was removed from within the collagen coating, leaving only a hollow collagen-based biomimetic vascular scaffold. The fabricated scaffolds were pre-vascularized with MS1 endothelial cell coating, incorporated into 3D renal constructs, and subsequently implanted either with or without human renal cells in the renal cortex of nude rats. The implanted collagen-based vascular scaffold was easily identified and integrated into native kidney tissue. The biomimetic vascular scaffold coated with endothelial cells (MS1) showed significantly enhanced vascularization, as compared to the uncoated scaffold and hydrogel only groups (P < 0.001). Along with the improved vascularization effects, the MS1-coated scaffolds showed a significant renal cell infiltration from the neighboring host tissue, as compared to the other groups (P < 0.05). Moreover, addition of human renal cells to the MS1-coated scaffold resulted in further enhancement of vascularization and tubular structure regeneration within the implanted constructs. The biomimetic collagen vascular scaffolds coated with endothelial cells are able to enhance vascularization and facilitate the formation of renal tubules after 14 days when combined with human renal cells. This study shows the feasibility of bioengineering vascularized functional renal tissues for kidney regeneration.
机译:我们基于血管腐蚀铸造技术开发了一种仿生肾血管支架。该研究评估了在大鼠肾皮质缺陷模型中使用这种新型仿生支架进行肾再生的可行性。通过灌注10%聚己内酯(PCL)溶液,从正常大鼠肾脏中制备血管腐蚀施用,然后用组织消化。腐蚀PCL铸件涂有胶原蛋白,并从胶原涂层中除去PCL,只留下胶原基的基础血管血管支架。用MS1内皮细胞涂层预先血管化的支架,其掺入3D肾构建体中,随后在裸鼠的肾皮层中有或没有人肾细胞植入。容易鉴定植入的基于胶原基血管支架并整合到天然肾组织中。涂有内皮细胞(MS1)的仿生血管支架显示出显着增强的血管化,与未涂覆的支架和水凝胶仅相比(P <0.001)相比。随着改善的血管化效果,MS1涂覆的支架与其他基团相比,MS1涂覆的支架显示出从相邻宿主组织的显着肾细胞浸润(P <0.05)。此外,向MS1涂覆的支架中添加人肾细胞,得到植入构建体内的血管化和管状结构再生的进一步增强。涂有内皮细胞的仿生胶原血管支架能够增强血管化并促进在与人肾细胞结合14天后形成肾小管。本研究表明,生物工程化血管化功能肾组织的可行性肾再生。

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