泛素-蛋白酶体抑制剂MG132上调Wnt/β-catenin信号通路改善骨质疏松的实验研究
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作者Author单位AddressE-Mail
邵荣学 SHAO Rong-xue 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China shaorongxue@163.com 
张亮 ZHANG Liang 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China  
杨贺杰 YANG He-jie 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China  
张志敬 ZHANG Zhi-jing 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China  
乐军 YUE Jun 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China  
潘浩 PAN Hao 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China  
周辉 ZHOU Hui 杭州市中医院, 浙江 杭州 310007 Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou 310007, Zhejiang, China  
全仁夫 QUAN Ren-fu 浙江中医药大学附属江南医院, 浙江 杭州 311201  
期刊信息:《中国骨伤》2022年,第35卷,第1期,第59-64页
DOI:10.12200/j.issn.1003-0034.2022.01.012
基金项目:杭州市卫生计生科技计划项目(编号:2018A60)
中文摘要:

目的:探讨泛素-蛋白酶体抑制剂MG132改善骨质疏松的机制。

方法:32只雌性SD大鼠,体质量220~250 g,8周龄,分为4组(n=8)。A组和B组大鼠采用去卵巢法制备骨质疏松症模型,造模成功后分别给予蛋白酶体抑制剂MG132和二甲基亚砜(dimethyl sulfoxide,DMSO)干预;C组为假手术对照组,D组为正常组,C组及D组均给予MG132干预。分别于给药后6、12周分批处死动物,于股骨颈组织取材,行病理形态学观察,Micro-CT分析,检测组织中20S蛋白酶体活性,Wnt和β-catenin的表达。

结果:形态学观察显示:A组,骨小梁轻度变细,呈网状,偶有中断;B组,骨小梁明显变细、变薄,不连续;C组与D组相似,骨小梁形态结构完整,排列呈网状。骨密度(bone mineral density,BMD),骨表面积(bone surface,BS),骨体积分数(bone volume/total volume,BV/TV)及骨小梁厚度(trabecular thickness,Tb.Th)的分析结果显示:不同时间点,B组的参数比较均差于其他各组(P<0.05),A组的BS差于C组和D组(P<0.05),C组和D组所有参数差异无统计学意义。20S蛋白酶体的RFU值检测结果显示:B组显著高于其他各组(P<0.05);Western blot检测结果显示,A组Wnt蛋白和β-catenin蛋白的灰度值显著高于其他各组(P<0.05)。

结论:泛素-蛋白酶体抑制剂MG-132可抑制β-catenin蛋白的降解,从而调控Wnt/β-catenin信号通路,延缓骨质疏松的发生和发展。
【关键词】蛋白酶体抑制剂  Wnt/β-catenin  信号通路  骨质疏松
 
Experimental study of proteasome inhibitor MG132 up-regulates Wnt/β-catenin signaling pathway to improve osteoporosis
ABSTRACT  

Objective To explore the mechanism of proteasome inhibitor MG132 in improving osteoporosis.

Methods: Total of 32 female SD rats,weighing 220 to 250 g and 8 weeks old,were selected. They were randomly divided into 4 groups(n=8). Rats of group A and group B were cut off ovaris on both sides to make model of osteoporosis,and then they were given proteasome inhibitors MG132 and dimethyl sufoxide (DMSO) respectively. Group C was a sham group and rats were given MG132. Group D was a normal group and rats were given MG132 too. The rats were killed in batches at 6 and 12 weeks after administration,and the femoral neck tissues were obtained. Relevant data were analyzed,such as pathomorphological observation,micro-CT analysis,detection of 20S proteasome activity in tissues,and expression of Wnt and β-catenin.

Results: Morphological observation showed that the trabecular were slightly thinner,reticulated,and occasionally interrupted in group A,while the trabecular were obviously thinner and discontinuous in group B. And the trabecular were intact and arranged reticulated in group C and D. The analysis results of bone mineral density(BMD),bone surface(BS),bone volume/total volume(BV/TV) and trabecular thickness(Tb.Th) showed that group B was worse than other groups in all parameters at different time points(P<0.05),and group A was worse than group C and group D in BS(P<0.05),there was no significant difference in all parameters between group C and group D. RFU value of 20S proteasome in group B was significantly higher than that in other groups(P<0.05). According to the results of Western blot,the gray values of Wnt protein and β-catenin protein in group A were significantly higher than those in other groups (P<0.05).

Conclusion: MG-132,a ubiquitin proteasome inhibitor,can regulate Wnt/β-catenin signaling pathway by inhibiting the degradation of β-catenin protein,and delaying the occurrence and development of osteoporosis.
KEY WORDS  Proteasome inhibitor  Wnt/β-catenin  Signaling pathway  Osteoporosis
 
引用本文,请按以下格式著录参考文献:
中文格式:邵荣学,张亮,杨贺杰,张志敬,乐军,潘浩,周辉,全仁夫.泛素-蛋白酶体抑制剂MG132上调Wnt/β-catenin信号通路改善骨质疏松的实验研究[J].中国骨伤,2022,35(1):59~64
英文格式:SHAO Rong-xue,ZHANG Liang,YANG He-jie,ZHANG Zhi-jing,YUE Jun,PAN Hao,ZHOU Hui,QUAN Ren-fu.Experimental study of proteasome inhibitor MG132 up-regulates Wnt/β-catenin signaling pathway to improve osteoporosis[J].zhongguo gu shang / China J Orthop Trauma ,2022,35(1):59~64
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