Objective In this study, human umbilical cord mesenchymal stem cells (hUC-MSCs) were stimulated with tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) to obtain preconditioned exosomes (Exos). Comparative miRNA profiling was performed between cytokine-primed Exos and conventionally cultured counterparts to identify differentially expressed miRNAs. Functional validation of candidate miRNAs will elucidate their mechanistic roles in promoting cutaneous repair, thereby advancing the clinical translation of Exos-based regenerative therapies. Methods We successfully extracted and characterized hUC-MSCs derived Exos (hUCMSCs-Exos) and classified them into Exos obtained under normal culture conditions (Con-Exos) and those stimulated by TNF-α+IL-1β obtained Exos (TNF-α+IL-1β-Exos). The wound healing rate was observed and counted by establishing a mouse whole skin defect wound model in vivo . In vitro , human umbilical vein endothelial cells (HUVECs) were stimulated with two groups of hUCMSCs-Exos to observe the tube formation of HUVECs and the results of 5-ethynyl-2’-deoxyuridine (EdU) assay.Then, the differential miRNAs in the two groups of hUCMSCs-Exos were detected and validated to identify the candidate effector miRNAs, which were then analyzed by databases and searched and screened for common target genes. Results TNF-α+IL-1β-Exos accelerated wound healing more than Con-Exos, mainly by increasing collagen deposition and expression of the angiogenic marker CD31. Sequencing and bioinformatics analyses revealed that the key miRNA for both co-actions was miR-215-5p. Cellular experiments showed that miR-215-5p mimics promoted HUVECs tubulogenesis and proliferation, whereas the inhibitor effect was not significant. In animal experiments, miR-215-5p mimics also significantly accelerated wound healing in mice. Conclusion TNF-α+IL-1β-Exos demonstrated superior wound healing efficacy compared to Con-Exos. This enhanced therapeutic effect may be attributed to the elevated expression of miR-215-5p in TNF-α+IL-1β-Exos. Mechanistically, miR-215-5p activates the WNK1 / p-Smad3 / VEGF-A signaling axis, promoting angiogenesis and accelerating cutaneous wound repair.
Zhou et al. (2026) studied this question.