Henan Joint International Research Laboratory of Stem Cell Medicine, School of Medical Engineering, Xinxiang Medical University, Xinxiang 453003, China; Lung Stem Cells and Gene Therapy Group, Department of Biomedical Sciences, Advanced Medical and Dental Institute (AMDI), Universiti Sains Malaysia, SAINS@Bertam, 13200 Kepala Batas, Penang, Malaysia; Stem Cells and Biotherapy Engineering Research Center of Henan, National Joint Engineering Laboratory of Stem Cells and Biotherapy, School of Life Science and Technology, Xinxiang Medical University, Xinxiang 453003, China.
Henan Joint International Research Laboratory of Stem Cell Medicine, School of Medical Engineering, Xinxiang Medical University, Xinxiang 453003, China.
Mol Ther. 2023 May 3;31(5):1365-1382. doi: 10.1016/j.ymthe.2023.01.025. Epub 2023 Feb 2.
Mesenchymal stem cells regulate remote intercellular signaling communication via their secreted extracellular vesicles. Here, we report that menstrual blood-derived stem cells alleviate acute lung inflammation and injury via their extracellular vesicle-transmitted miR-671-5p. Disruption of this abundantly expressed miR-671-5p dramatically reduced the ameliorative effect of extracellular vesicles released by menstrual blood-derived stem cells on lipopolysaccharide (LPS)-induced pulmonary inflammatory injury. Mechanistically, miR-671-5p directly targets the kinase AAK1 for post-transcriptional degradation. AAK1 is found to positively regulate the activation of nuclear factor κB (NF-κB) signaling by controlling the stability of the inhibitory protein IκBα. This study identifies a potential molecular basis of how extracellular vesicles derived from mesenchymal stem cells improve pulmonary inflammatory injury and highlights the functional importance of the miR-671-5p/AAK1 axis in the progression of pulmonary inflammatory diseases. More importantly, this study provides a promising cell-based approach for the treatment of pulmonary inflammatory disorders through an extracellular vesicle-dependent pathway.
间充质干细胞通过其分泌的细胞外囊泡调节远程细胞间信号通讯。在这里,我们报告说月经血来源的干细胞通过其细胞外囊泡传递的 miR-671-5p 减轻急性肺炎症和损伤。破坏这种大量表达的 miR-671-5p 可显著降低月经血来源的干细胞释放的细胞外囊泡对脂多糖 (LPS) 诱导的肺炎症性损伤的改善作用。在机制上,miR-671-5p 直接靶向激酶 AAK1 进行转录后降解。发现 AAK1 通过控制抑制蛋白 IκBα 的稳定性,正向调节核因子 κB (NF-κB) 信号的激活。本研究确定了细胞外囊泡衍生自间充质干细胞如何改善肺炎症性损伤的潜在分子基础,并强调了 miR-671-5p/AAK1 轴在肺炎症性疾病进展中的功能重要性。更重要的是,本研究通过细胞外囊泡依赖途径为治疗肺炎症性疾病提供了一种有前途的基于细胞的方法。