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静电纺丝纳米纤维和脂肪来源干细胞的外泌体用于尿道再生:体内外评估。

Electrospun nanoyarn and exosomes of adipose-derived stem cells for urethral regeneration: Evaluations in vitro and in vivo.

机构信息

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.

出版信息

Colloids Surf B Biointerfaces. 2022 Jan;209(Pt 2):112218. doi: 10.1016/j.colsurfb.2021.112218. Epub 2021 Nov 15.

Abstract

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.

摘要

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。

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