hUC-MSC-exosomes deliver Let-7b/7f-5p to dermal papilla cells for a multi-target synergistic treatment of androgenetic alopecia

毛囊 旁分泌信号 微泡 雄激素受体 细胞生物学 毛乳头 化学 癌症研究 脱发 细胞凋亡 间充质干细胞 斑秃 信号转导 外体 生物 细胞生长 男性型秃发 内科学 内分泌学 干细胞 药理学 碱性磷酸酶 再生医学 头发周期 机械转化 刺猬信号通路 PTEN公司 小RNA 受体 连环素
作者
Qimei Chen,Xueer Wang,Y Zhang,Fengting Liang,Haitao Zhang,Chipeng Guo,黄棉波,Jie Yang,X G Wang,Yong Miao,Li Zhang,Min Zhang
出处
期刊:Journal of Nanobiotechnology [BioMed Central]
标识
DOI:10.1186/s12951-026-04752-0
摘要

BACKGROUND: Exosomes play pivotal roles in immunomodulation, tissue regeneration, and the treatment of diseases. However, their specific mechanisms of action remain unclear. Therefore, this study aimed to elucidate the therapeutic mechanisms of human umbilical cord mesenchymal stem cell-derived exosomes (hUC-MSC-exosomes) in androgenic alopecia (AGA). We established a modified AGA mouse model and found that hUC-MSC-Exosomes could be taken up by dermal papilla cells (DPCs), promoted the transition of hair follicles from telogen to anagen, ameliorated hair follicle miniaturization, and enhanced hair regeneration and thickening. RESULTS: Cytological experiments revealed that exosomes inhibited aging and apoptosis of DPCs, promoted their proliferation and migration, increased alkaline phosphatase (ALP) levels, stimulated the secretion of paracrine cytokines, and reduced the expression level of the androgen receptor (AR). Exosomal miRNA sequencing analysis revealed that the top 10 miRNAs were primarily from the Let-7 family. GO and Reactome functional enrichment analyses and dual-luciferase reporter experiments revealed that hUC-MSC-exosomes delivered Let-7b-5p to target the deubiquitinating enzyme USP12, thereby inhibiting AR deubiquitination and promoting AR ubiquitination and degradation. This process further activates the Wnt/β-catenin pathway and suppresses the TGF-β/Smad pathway. CONCLUSIONS: In summary, this study provides insights into the underlying mechanisms of action of hUC-MSC-exosomes in AGA, indicating their therapeutic potential. In-depth analysis revealed that Let-7b-5p simultaneously targets DKK3 to activate the Wnt/β-catenin pathway in multiple dimensions. Moreover, hUC-MSC-exosomes delivered Let-7f-5p to target Smad2, synergizing with Let-7b to inhibit the TGF-β/Smad pathway and suppress DHT-induced DPC apoptosis. Further exploratory clinical trial showed that hUC-MSC-exosomes increased hair density and average hair diameter in patients with AGA.
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