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表皮干细胞通过仿生微/纳米纤维支架维持干细胞特性,通过激活 Notch 信号通路促进伤口愈合。

Epidermal stem cells maintain stemness via a biomimetic micro/nanofiber scaffold that promotes wound healing by activating the Notch signaling pathway.

机构信息

Department of Plastic Surgery, Tangdu Hospital, Airforce Military Medical University, Xi'an, 710038, China.

出版信息

Stem Cell Res Ther. 2021 Jun 10;12(1):341. doi: 10.1186/s13287-021-02418-2.

Abstract

BACKGROUND

Epidermal stem cells (EpSCs) play a vital role in wound healing and skin renewal. Although biomaterial scaffolds have been used for transplantation of EpSCs in wound healing, the ex vivo differentiation of EpSCs limits their application.

METHODS

To inhibit the differentiation of EpSCs and maintain their stemness, we developed an electrospun polycaprolactone (PCL)+cellulose acetate (CA) micro/nanofiber for the culture and transplantation of EpSCs. The modulation effect on EpSCs of the scaffold and the underlying mechanism were explored. Liquid chromatography-tandem mass spectrometry for label-free quantitative proteomics was used to analyze proteomic changes in EpSCs cultured on scaffolds. In addition, the role of transplanted undifferentiated EpSCs in wound healing was also studied.

RESULTS

In this study, we found that the PCL+CA micro/nanofiber scaffold can inhibit the differentiation of EpSCs through YAP activation-mediated inhibition of the Notch signaling pathway. Significantly differentially expressed proteomics was observed in EpSCs cultured on scaffolds and IV collagen-coated culture dishes. Importantly, differential expression levels of ribosome-related proteins and metabolic pathway-related proteins were detected. Moreover, undifferentiated EpSCs transplanted with the PCL+CA scaffold can promote wound healing through the activation of the Notch signaling pathway in rat full-thickness skin defect models.

CONCLUSIONS

Overall, our study demonstrated the role of the PCL+CA micro-nanofiber scaffold in maintaining the stemness of EpSCs for wound healing, which can be helpful for the development of EpSCs maintaining scaffolds and exploration of interactions between biomaterials and EpSCs.

摘要

背景

表皮干细胞(EpSCs)在伤口愈合和皮肤更新中起着至关重要的作用。尽管生物材料支架已被用于 EpSCs 在伤口愈合中的移植,但 EpSCs 的体外分化限制了它们的应用。

方法

为了抑制 EpSCs 的分化并维持其干细胞特性,我们开发了一种用于 EpSCs 培养和移植的聚己内酯(PCL)+醋酸纤维素(CA)微/纳米纤维。探讨了支架对 EpSCs 的调制作用及其潜在机制。采用无标记定量蛋白质组学的液相色谱-串联质谱技术分析了支架上培养的 EpSCs 的蛋白质组变化。此外,还研究了移植未分化 EpSCs 在伤口愈合中的作用。

结果

在这项研究中,我们发现 PCL+CA 微/纳米纤维支架可以通过 YAP 激活介导的 Notch 信号通路抑制 EpSCs 的分化。在支架和 IV 型胶原包被培养皿上培养的 EpSCs 中观察到明显的差异表达蛋白质组学。重要的是,检测到核糖体相关蛋白和代谢途径相关蛋白的差异表达水平。此外,用 PCL+CA 支架移植的未分化 EpSCs 通过激活大鼠全层皮肤缺损模型中的 Notch 信号通路促进伤口愈合。

结论

总之,我们的研究表明 PCL+CA 微纳米纤维支架在维持 EpSCs 用于伤口愈合的干细胞特性方面发挥了作用,这有助于开发维持 EpSCs 的支架和探索生物材料与 EpSCs 之间的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d0/8193873/a6ada5a0747e/13287_2021_2418_Fig1_HTML.jpg

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