泛素特异性蛋白酶42调节人脂肪干细胞成骨向分化  

Ubiquitin-specific protease 42 regulates osteogenic differentiation of human adipose-derived stem cells

作　　者：潘媛 顾航 肖涵 赵笠君 汤祎熳 葛雯姝[1] PAN Yuan;GU Hang;XIAO Han;ZHAO Lijun;TANG Yiman;GE Wenshu(Department of General DentistryⅡ,Peking University School and Hospital of Stomatology&National Center for Stomatology&National Clinical Research Center for Oral Diseases&National Engineering Research Center of Oral Biomate-rials and Digital Medical Devices,Beijing 100081,China;Fourth Clinical Division,Peking University School and Hospital of Stomatology,Beijing 100025,China)

机构地区：[1]北京大学口腔医学院·口腔医院综合二科,国家口腔医学中心,国家口腔疾病临床医学研究中心,口腔生物材料和数字诊疗装备国家工程研究中心,北京100081 [2]北京大学口腔医学院·口腔医院第四门诊部,北京100025

出　　处：《北京大学学报（医学版）》2024年第1期9-16,共8页Journal of Peking University:Health Sciences

基　　金：国家自然科学基金(82071089、82001013)。

摘　　要：目的:探索泛素特异性蛋白酶42(ubiquitin-specific protease 42,USP42)在人脂肪干细胞(human adipose-derived stem cells,hASCs)体内外成骨向分化中的作用。方法:用慢病毒转染hASCs,构建敲低和过表达USP42的稳定转染细胞系,通过碱性磷酸酶(alkaline phosphatase,ALP)染色及活性定量、茜素红S矿化结节染色及定量,检测实验组(敲低组和过表达组)及对照组在成骨诱导下hASCs成骨向分化能力的差异,通过定量逆转录聚合酶链反应(quantitative reverse transcription polymerase chain reaction,qRT-PCR)检测实验组及对照组成骨相关基因的表达水平,通过蛋白免疫印迹实验检测实验组及对照组成骨相关蛋白的表达水平,通过裸鼠异位成骨实验评价USP42在hASCs体内成骨向分化中的作用。结果:敲低组USP42的mRNA和蛋白表达显著低于对照组,过表达组显著高于对照组。成骨诱导7 d后,敲低组的ALP活性显著高于对照组,过表达组显著低于对照组;成骨诱导14 d后,敲低组茜素红S染色显著深于对照组,过表达组显著浅于对照组。qRT-PCR结果显示,成骨诱导14 d时,敲低组ALP、成骨细胞特异性转录因子(osterix,OSX)和Ⅰ型胶原(collagen typeⅠ,COLⅠ)的mRNA表达水平显著高于对照组,过表达组显著低于对照组。蛋白免疫印迹实验结果显示,成骨诱导14 d时敲低组runt相关转录因子2(runt-related transcription factor 2,RUNX2)、OSX和COLⅠ蛋白表达水平显著高于对照组,过表达组显著低于对照组。裸鼠皮下移植物苏木精-伊红染色结果显示,敲低组类骨组织百分比较对照组显著增高。结论:敲低USP42显著促进hASCs的体内外成骨向分化,过表达USP42显著抑制hASCs的体内成骨向分化,USP42可作为骨组织工程学潜在治疗靶点。Objective:To explore the effect of ubiquitin-specific protease 42(USP42)on osteogenic differentiation of human adipose-derived stem cells(hASCs)in vivo and in vitro.Methods:A combination of experiments was carried out with genetic depletion of USP42 using a lentiviral strategy.Alkaline phosphatase(ALP)staining and quantification,alizarin red S(ARS)staining and quantification were used to determine the osteogenic differentiation ability of hASCs under osteogenic induction between the experimental group(knockdown group and overexpression group)and the control group.Quantitative reverse transcription PCR(qRT-PCR)was used to detect the expression levels of osteogenesis related genes in the experimental group and control group,and Western blotting was used to detect the expression levels of osteogenesis related proteins in the experimental group and control group.Nude mice ectopic implantation experiment was used to evaluate the effect of USP42 on the osteogenic differentiation of hASCs in vivo.Results:The mRNA and protein expressions of USP42 in knockdown group were significantly lower than those in control group,and those in overexpression group were significantly higher than those in control group.After 7 days of osteogenic induction,the ALP activity in the knockdown group was significantly higher than that in the control group,and ALP activity in overexpression group was significantly lower than that in control group.After 14 days of osteogenic induction,ARS staining was significantly deeper in the knockdown group than in the control group,and significantly lighter in overexpression group than in the control group.The results of qRT-PCR showed that the mRNA expression levels of ALP,osterix(OSX)and collagen typeⅠ(COLⅠ)in the knockdown group were significantly higher than those in the control group after 14 days of osteogenic induction,and those in overexpression group were significantly lower than those in control group.The results of Western blotting showed that the expression levels of runt-related transcript

关 键 词：泛素特异性蛋白酶类 人脂肪干细胞 细胞分化 骨和骨组织 再生医学 

分 类 号：R318[医药卫生—生物医学工程]