首页|MCC950调控巨噬细胞极化改善放射性肺损伤

MCC950调控巨噬细胞极化改善放射性肺损伤

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探讨NLRP3特异性抑制剂MCC950对放射性肺损伤的改善作用及其可能机制.将36只7周雌性C57BL/6J小鼠随机分成对照组、辐照组和辐照+MCC950组.辐照组和辐照+MCC950组小鼠接受单次20 Gy剂量全胸廓辐照,对照组小鼠接受0 Gy剂量辐照.辐照+MCC950组小鼠辐照后第二天给予MCC950药物干预,对照组及辐照组小鼠给予生理盐水.辐照后12周检测小鼠肺系数以及肺干湿比.苏木精-伊红染色法检测小鼠肺损伤程度.蛋白免疫印迹检测巨噬细胞极化标记物、NLRP3炎性小体和炎症因子等分子蛋白表达变化.结果显示:与对照组相比,辐照组小鼠肺系数、肺干湿比以及肺损伤指标均显著升高,巨噬细胞M1型极化态标记物CD86表达明显增加,M2型极化态标记物CD163表达明显减少,NLRP3炎性小体(NLRP3、ASC和Caspase-1)和炎症因子(Pro-IL-1β、IL-1β、IL-18和TNF-a)表达均显著增加;而与辐照组小鼠相比,辐照+MCC950组小鼠肺系数、肺干湿比和肺组织炎性损伤均明显降低,CD86表达减少,CD163表达明显增加,NLRP3、ASC、Caspase-1、Pro-IL-1β、IL-1β、IL-18和TNF-a表达均明显减少.结果提示,MCC950可能是通过调控巨噬细胞极化进而改善放射性肺损伤,其有望成为放射性肺损伤的防治干预药物.
MCC950 ameliorates radiation induced lung injury through modulating macrophage polarization
To investigate the beneficial effect of NLRP3 inflammasome specific inhibitor MCC950 on radiation induced lung injury(RILI)and its potential mechanism in mice.A total of 36 female C57BL/6J mice aged 7 weeks were randomly assigned to the control group,the irradiation group,and the irradiation plus MCC950 group.The irradiation group and irradiation plus MCC950 group mice were exposed to whole-thorax radiation at a single 20 Gy dose.The control group mice were provided with an irradiation dose of 0 Gy.The irradiation plus MCC950 group mice were treated with MCC950 following irradiation.The mice in control group and irradiation group were treated with the same amount of normal saline.After 12 weeks,the body weight and the dry and wet lung weight of the three groups mice were measured to assess the lung coefficient(the ratio of the lung wet weigh to the body weight of each mouse)and the wet-to-dry lung weight ratio(weight of the wet lung/weight of the dry lung).The degree of lung tissue injury was assessed using hematoxylin eosin staining.Western blotting was performed to evaluate the expression of macrophage polarization markers,NLRP3 inflammasome,and inflammatory factors.The experimental results indicated that compared with the control group mice,the lung coefficient,wet-to-dry lung weight ratio,the lung tissue injury score,and the protein expression of M1 macrophage markers(CD86),NLRP3 inflammasome(NLRP3,ASC,and Caspase-1),and inflammatory cytokines(Pro-IL-1β,IL-1β,IL-18,and TNF-a)of the irradiation group mice were dramatically enhanced,whereas the protein expression of M2 macrophage markers(CD163)was significantly decreased.Compared with the irradiation group mice,irradiation plus MCC950 group mice had higher protein expression of CD163,and remarkably reduced the lung coefficient,wet-to-dry lung weight ratio,the lung tissue injury score,and the protein expression of CD86,NLRP3,ASC,Caspase-1,Pro-IL-1β,IL-1β,IL-18,and TNF-a.The above results demonstrated that MCC950 ameliorates RILI through modulating macrophage polarization,and it promises to be an intervention agent against RILI.

MCC950NLRP3 inflammasomeMacrophage PolarizationInflammatory factorRadiation induced lung injury

王贞、路素丽、何贵成、杨惠、乃爱桃、曾慧

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湖南环境生物职业技术学院解剖教研室 衡阳 421001

南华大学附属第一医院肿瘤科 衡阳 421001

南华大学附属第一医院病理科 衡阳 421001

南华大学附属第一医院超声科 衡阳 421001

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MCC950 NLRP3炎性小体 巨噬细胞极化 炎症因子 放射性肺损伤

湖南省自然科学基金项目湖南省自然科学基金项目湖南省自然科学基金项目湖南省自然科学基金项目

2021JJ401852021JJ405032023JJ405912023JJ40583

2024

辐射研究与辐射工艺学报
中国科学院上海应用物理研究所

辐射研究与辐射工艺学报

CSTPCD
影响因子:0.527
ISSN:1000-3436
年,卷(期):2024.42(5)
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