MiR146a-loaded engineered exosomes released from silk fibroin patch promote diabetic wound healing by targeting IRAK1

• Published in: Signal transduction and targeted therapy 2023-02, Vol.8 (1), p.62-62, Article 62
• Main Authors: Li, Qiankun, Hu, Wenzhi, Huang, Qilin, Yang, Jie, Li, Bingmin, Ma, Kui, Wei, Qian, Wang, Yaxi, Su, Jianlong, Sun, Mengli, Cui, Shengnan, Yang, Rungong, Li, Haihong, Fu, Xiaobing, Zhang, Cuiping
• Format: Article
• Language: English
• Subjects: 631/61/2296; 631/61/391; 631/61/54; Biomaterials; Cancer Research; Cell Biology; Collagen; Diabetes; Diabetes Mellitus; Exosomes; Exosomes - genetics; Exosomes - metabolism; Fibroins - genetics; Fibroins - metabolism; Fibroins - pharmacology; Fusion protein; Humans; Inflammation; Interleukin-1 Receptor-Associated Kinases - genetics; Interleukin-1 Receptor-Associated Kinases - metabolism; Internal Medicine; IRAK protein; Medicine; Medicine & Public Health; Mesenchymal Stem Cells; Mesenchyme; miRNA; Oncology; Pathology; Phage display; Regenerative medicine; Silk; Stem cells; Tissue engineering; Transcriptomics; Vascularization; Wound healing; Wound Healing - genetics
• ISSN: 2059-3635; 2095-9907; 2059-3635
• DOI: 10.1038/s41392-022-01263-w

Unhealable diabetic wounds need to be addressed with the help of newer, more efficacious strategies. Exosomes combined with biomaterials for sustained delivery of therapeutic agents are expected to bring new hope for chronic wound treatment. Here, the engineered exosomes modified for efficiently loading miR146a and attaching to silk fibroin patch (SFP) were demonstrated to promote diabetic wound healing. Silk fibroin binding peptide (SFBP) was screened through phage display, and SFBP-Gluc-MS2 (SGM) and pac-miR146a-pac fusion protein were constructed. The designed exosomes (SGM-Exos, miR146a-Exos, and SGM-miR146a-Exos) were isolated from the engineered placental mesenchymal stem cells (PMSCs) transduced with SGM or/and pac-miR146a-pac protein. Gluc signals indicated SGM-Exo@SFP markedly increased the binding rate and the stability of SGM-Exo. Moreover, the loading efficiency of miR146a in SGM-miR146a-Exos was ten-fold higher than that in miR146a-Exos. Superior to untreated, SGM-miR146a-Exo-only treated, and SFP-only treated groups, SGM-miR146a-Exo@SFP drived wound healing associated with less inflammation, collagen deposition, and neovascularization. The transcriptomics analysis suggested anti-inflammatory and regenerative effects with SGM-miR146a-Exo@SFP treatment. Here, we show efficient exosome@biomaterial-based miRNA delivery systems for regenerative medicine and tissue engineering.