School of Materials Engineering, Shanghai University of Engineering Science, Shanghai 201620, China.
School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Colloids Surf B Biointerfaces. 2022 Jan;209(Pt 2):112218. doi: 10.1016/j.colsurfb.2021.112218. Epub 2021 Nov 15.
Regeneration of urethral defects has been difficult in the clinic. To address it, the collagen/ poly (L-lactide-co-caprolactone) (P(LLA-CL)) nanoyarn scaffold delivering adipose-derived stem cells' exosomes (ADSC-exos) was fabricated. The multipotential differentiation potential of ADSCs were confirmed by Adipogenic, osteogenic, and chondrogenic differentiation. The 3-(4,5-dimethylthiazol-2-yl)- 2,5-diphenyltetrazolium bromide assay shows that 50% concentration of ADSC-exos nanoyarn scaffold dramatically enhanced the cell viability of fibroblasts. The ADSC-exos nanoyarn scaffold for human foreskin fibroblasts (HFFs) and human urethral scar fibroblasts (HSFs) shows good biocompatibility: theproduction of inflammatory factors IL-6 and Col 1A1 was less, indicating that ADSC-exos had the minimal inflammatory effect of cells. Besides, the cells on the ADSC-exos nanoyarn scaffold did not appear to contribute to DNA damage in the same way as the normal cell's growth did. The HFFs seeding on the ADSC-exos nanoyarn scaffold shows a typical morphology of extending outwards. Urethral repair with ADSC-exos nanoyarn scaffold did not lead to either a sign of urethral stricture or scar formation after 4 weeks post-surgery. The deposition of collagen was less and the epithelial cells formed multiple layer epithelium. The treatment of ADSC-exos stimulated epithelization and vascularization. And the transition from an inflammatory state to a regenerative state was promoted. The ADSC-exos-treated group did not promote the over-proliferation of fibroblasts and the expression of Collagen I. Therefore, the ADSC-exos nanoyarn scaffold has evident, positive effects on wound healing and tissue fibrosis inhibition.
尿道缺损的再生在临床上一直难以解决。为了解决这个问题,我们制备了一种递送脂肪来源干细胞外泌体(ADSC-exos)的胶原/聚(L-丙交酯-co-己内酯)(P(LLA-CL))纳米纤维支架。ADSCs 的多能分化潜能通过脂肪分化、成骨分化和软骨分化得到证实。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐测定法显示,ADSC-exos 纳米纤维支架 50%浓度可显著提高成纤维细胞的细胞活力。ADSC-exos 纳米纤维支架对人包皮成纤维细胞(HFFs)和人尿道瘢痕成纤维细胞(HSFs)表现出良好的生物相容性:促炎因子 IL-6 和 Col 1A1 的产生较少,表明 ADSC-exos 对细胞的炎症作用最小。此外,与正常细胞的生长方式不同,细胞在 ADSC-exos 纳米纤维支架上生长不会导致 DNA 损伤。在 ADSC-exos 纳米纤维支架上接种的 HFFs 向外伸展的典型形态。尿道修复后 4 周,ADSC-exos 纳米纤维支架治疗未导致尿道狭窄或瘢痕形成的迹象。胶原沉积较少,上皮细胞形成多层上皮。ADSC-exos 的治疗刺激了上皮化和血管生成。并促进了从炎症状态向再生状态的转变。ADSC-exos 处理组不会促进成纤维细胞过度增殖和胶原 I 的表达。因此,ADSC-exos 纳米纤维支架对伤口愈合和组织纤维化抑制具有明显的积极作用。