Bone immune responses based on macrophages are critical in the osteogenesis of bone abnormalities.In general,M2 macrophage facilitate the promotion of osteogenesis,as well,M1 macrophage play an important role in early...Bone immune responses based on macrophages are critical in the osteogenesis of bone abnormalities.In general,M2 macrophage facilitate the promotion of osteogenesis,as well,M1 macrophage play an important role in early bone healing,as confirmed by previous studies.However,it is not clear how M1 macrophage are involved in the bone immune response.MiR-21a-5p is a highly expressed microRNA in M1 macrophage in contrast to M2.Therefore,the current work sought to ascertain the influence of M1 macrophage on bone healing via exosomal miR-21a-5p and the probable mechanism.We discovered that injecting M1 macrophage exosomes overexpressing miR-21a-5p into bone defect locations enhanced bone regeneration in vivo.Furthermore,by directly targeting GATA2,miR-21a-5p accelerated MC3T3-E1 osteogenic differentiation.Our findings showed that exosomal miR-21a-5p from M1 macrophage may be transported to osteoblasts and target GATA2 to enhance bone defect healing.展开更多
基金supported by the Science Foundation of Shandong Province of China(Grant Nos ZR2021MH026,ZR2022MH075,ZR2020MH100)Shandong Province Medical and Health Science and Technology Development Plan(2018WS426)+1 种基金Liaocheng Key Research and Development Plan of Shandong Province of China(Grant Nos 2022YDSF16,2022YDSF21)Liaocheng People’s Hospital Youth Fund Project(Grant No.LYQN201914).
文摘Bone immune responses based on macrophages are critical in the osteogenesis of bone abnormalities.In general,M2 macrophage facilitate the promotion of osteogenesis,as well,M1 macrophage play an important role in early bone healing,as confirmed by previous studies.However,it is not clear how M1 macrophage are involved in the bone immune response.MiR-21a-5p is a highly expressed microRNA in M1 macrophage in contrast to M2.Therefore,the current work sought to ascertain the influence of M1 macrophage on bone healing via exosomal miR-21a-5p and the probable mechanism.We discovered that injecting M1 macrophage exosomes overexpressing miR-21a-5p into bone defect locations enhanced bone regeneration in vivo.Furthermore,by directly targeting GATA2,miR-21a-5p accelerated MC3T3-E1 osteogenic differentiation.Our findings showed that exosomal miR-21a-5p from M1 macrophage may be transported to osteoblasts and target GATA2 to enhance bone defect healing.
