Human umbilical cord mesenchymal stem cell-derived nanovesicles ameliorate acute lung injury by hsa-let-7g-5p inhibition of NF-κB/NLRP3 pathway
Yilin Huang , Yan Zeng , Ailin Wu , Yang Chen , Yuanhao Zhou , Youni Zhang , Hai Zou , Weijiao Fan , Xiaoyi Chen , Jinyang Chen , Jie Wang , Xianghong Yang , Xiaoru Chang , Xiaozhou Mou , Yuexing Tu
Extracellular Vesicles and Circulating Nucleic Acids ›› 2026, Vol. 7 ›› Issue (2) : 465 -89.
Aim: Acute lung injury (ALI), marked by vigorous inflammatory reactions and elevated incidence, is a grave clinical issue for which efficacious pharmaceutical interventions are still lacking. This research delves into the anti-inflammatory actions and the associated pathways of nanovesicles originating from human umbilical cord mesenchymal stem cells (UCMSC-NVs) within a model of ALI induced by lipopolysaccharide (LPS).
Methods: UCMSC-NVs were prepared via serial extrusion and characterized using transmission electron microscopy and dynamic light scattering. Their effects on pulmonary inflammation and injury were evaluated in an LPS-induced ALI mouse model. Anti-inflammatory effects were analyzed using Western blot, enzyme-linked immunosorbent assay (ELISA), and immunofluorescence, focusing on the role of hsa-let-7g-5p in regulating the nuclear factor κB (NF-κB)/NOD-like receptor protein 3 (NLRP3) pathway.
Results: The UCMSC-NVs acquired through serial extrusion displayed bilayer vesicle structures, with a mean diameter of around 100 nm. Moreover, these vesicles exhibited elevated expression levels of CD9, CD63, and CD81. Administration of UCMSC-NVs significantly alleviated lung damage, accompanied by a reduction in alveolar leakage and neutrophil infiltration. Furthermore, it significantly downregulated the expression of pro-inflammatory cytokines, such as interleukin (IL)-6, IL-1β, and tumor necrosis factor-α (TNF-α). UCMSC-NVs reduced macrophage infiltration in the lungs of ALI mice by inhibiting the NF-κB/NLRP3 signaling, leading to a shift in macrophage polarization, with decreased M1 and increased M2 polarization. Our findings demonstrated a novel therapeutic mechanism wherein hsa-let-7g-5p encapsulated within UCMSC-NVs alleviates inflammation by inhibiting NF-κB/NLRP3 expression, thereby mitigating ALI.
Conclusion: These results provide a foundation for the development of novel cell-free therapies with clinical potential for treating inflammatory lung diseases such as ALI and acute respiratory distress syndrome (ARDS).
Umbilical cord mesenchymal stem cell-derived nanovesicles / acute lung injury / inflammation / microRNA / NF-κB/NLRP3 inflammasome pathway
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