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微重力介导Notch1信号通路调控巨噬细胞极化影响骨稳态

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目的:探讨微重力介导果蝇双翅边缘缺刻同源基因1(Notch1)信号调控巨噬细胞极化对骨稳态的影响.方法:以尾吊法(HLS)模拟微重力环境构建动物模型.动物分组为Control组、HLS组、HLS+NC组、HLS+si组、HLS+rhNF-κB组,ELISA检测大鼠血清中TNF-α和IL-1β的含量;TUNEL染色检测骨组织的细胞凋亡;免疫荧光检测骨组织中巨噬细胞的极化.以旋转壁式生物反应器模拟微重力环境构建大鼠成骨细胞CP-R091微重力模型;细胞实验分为Control组、HLS组、HLS+NC组、HLS+si组、HLS+rhNF-κB组;CCK-8实验检测各组细胞的增殖活性,AO实验检测各组细胞的凋亡率;PCR检测骨组织和细胞中成骨相关基因的表达;Western blot检测各组骨组织和细胞中Notch1、发状分裂相关增强子-l(HES-1)、Notch通路配体1(Jag-ged1)的表达.结果:与Control组相比,HLS组大鼠血清中TNF-α和IL-1β的含量、细胞凋亡率、M1样巨噬细胞比例明显升高;与HLS组相比,HLS+si组能明显部分逆转上述参数变化趋势,而HLS+rhNF-κB组则使上述参数值变化更显著.与Control组相比,HLS组细胞的增殖活性明显降低,细胞凋亡率明显升高;与HLS组细胞相比,HLS+si组能明显部分逆转上述参数变化趋势,而HLS+rhNF-κB组则使上述参数值更为显著;微重力环境下骨组织和细胞中成骨相关基因Ⅰ型胶原蛋白(COL1)、骨钙素(OCN)以及成骨分化基因Runt相关转录因子2(RUNX2)表达明显降低,而Notch-1、Hes-1和Jagged1的表达明显升高,差异均具有统计学意义(均P<0.05).结论:微重力介导Notch1信号调控巨噬细胞M1/M2样极化,参与骨组织细胞增殖与凋亡,影响骨稳态的进展.
Microgravity-mediated Notch1 signaling pathway affects bone homeostasis by regulating macrophage polarization
Objective:To investigate the effect of microgravity-mediated Notch1 signaling on macrophage polarization on bone homeostasis.Methods:The animal model was constructed by tail-limb suspension(HLS)to simulate the microgravity environment.The animals were grouped into Control group,HLS group,HLS+NC group,HLS+si group,HLS+rhNF-κB group.ELISA was used to detect the content of TNF-α and IL-1β in serum of rats.TUNEL staining was used to detect the apoptosis of bone tissue.Immunofluo-rescence was used to detect the polarization of macrophages in bone tissue.The rat osteoblast CP-R091 microgravity model was con-structed by simulating the microgravity environment with a rotating wall bioreactor.The cell experiments were divided into Control group,HLS group,HLS+NC group,HLS+si group,HLS+rhNF-κB group.CCK-8 test was used to detect the proliferation activity of cells in each group,and AO test was used to test the apoptosis rate of cells in each group.PCR was used to detect the expression of os-teogenesis-related genes in bone tissues and cells.Western blot was used to detect the expression of Notch1,hair division-related en-hancer-1(HES-1),and Notch pathway ligand 1(Jagged1)in bone tissues and cells of each group.Results:Compared with control group,the contents of TNF-α and IL-1β in the serum of the rats in the HLS group,the apoptosis rate,and the proportion of M1 macro-phages were significantly increased.Compared with HLS group,the HLS+si group could obviously partially reverse the change trend of the above parameters,while HLS+rhNF-κB group significantly changed the above parameter values.Compared with control group,the proliferation activity of the cells in the HLS group was significantly reduced,and the apoptosis rate was significantly increased.Com-pared with HLS group,the HLS+si group could obviously partially reverse the change trend of the above parameters,while the HLS+rhNF-κB group made the above parameter values worse.The expressions of the osteogenesis-related genes collagen type Ⅰ(COL1),osteocalcin(OCN)and Runt-related transcription factor 2(RUNX2)in bone tissues and cells in the microgravity environment were significantly decreased,while the expressions of Notch-1,Hes-1 and Jagged1 were significantly increased,and the differences were statistically significant(all P<0.05).Conclusion:Microgravity-mediated Notch1 signaling regulates M1/M2 polarization of macro-phages,participates in cell proliferation and apoptosis in bone tissue,and affects the progress of bone homeostasis.

MicrogravityNotch-1Macrophage polarizationBone homeostasis

许静、郭健、罗永贵、李大星、唐英、娄宝佳、彭淼、郑永

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贵州省骨科医院骨内五病区,贵阳 550000

微重力 果蝇双翅边缘缺刻同源基因1 巨噬细胞极化 骨稳态

贵州省卫生健康委员会项目

gzwkj2022-033

2024

中国免疫学杂志
中国免疫学会,吉林省医学期刊社

中国免疫学杂志

CSTPCD北大核心
影响因子:0.926
ISSN:1000-484X
年,卷(期):2024.40(8)