中国动物传染病学报
中國動物傳染病學報
중국동물전염병학보
CHINESE JOURNAL OF VETERINARY PARASITOLOGY
2014年
2期
13-19
,共7页
曲昱蓉%詹媛%仇旭升%谭磊%孙英杰%宋翠萍%丁铲
麯昱蓉%詹媛%仇旭升%譚磊%孫英傑%宋翠萍%丁鏟
곡욱용%첨원%구욱승%담뢰%손영걸%송취평%정산
新城疫病毒%泛素-蛋白酶体系统%蛋白酶体抑制剂%复制
新城疫病毒%汎素-蛋白酶體繫統%蛋白酶體抑製劑%複製
신성역병독%범소-단백매체계통%단백매체억제제%복제
Newcastle disease virus%ubiquitin-proteasome system%proteasome inhibitor%replication
本文主要对细胞的泛素-蛋白酶体系统是否参与新城疫病毒(Newcastle disease virus,NDV)的复制过程进行了研究。用NDV感染HeLa细胞,对细胞样品进行Western blot实验,并检测细胞26S蛋白酶体的三种蛋白水解活性变化。同时使用多种泛素-蛋白酶体系统相关的抑制剂处理细胞并做NDV感染,测定细胞上清中病毒TCID50值,比较药物处理与DMSO处理对病毒增殖的影响。结果表明,HeLa细胞在感染NDV后,细胞内泛素化蛋白水平降低,而26S蛋白酶体的三种蛋白水解活性都显著升高;使用泛素-蛋白酶体系统抑制剂后NDV的增殖受到了明显的抑制,证明NDV在HeLa细胞内的增殖与细胞自身的泛素-蛋白酶体系统关系密切。
本文主要對細胞的汎素-蛋白酶體繫統是否參與新城疫病毒(Newcastle disease virus,NDV)的複製過程進行瞭研究。用NDV感染HeLa細胞,對細胞樣品進行Western blot實驗,併檢測細胞26S蛋白酶體的三種蛋白水解活性變化。同時使用多種汎素-蛋白酶體繫統相關的抑製劑處理細胞併做NDV感染,測定細胞上清中病毒TCID50值,比較藥物處理與DMSO處理對病毒增殖的影響。結果錶明,HeLa細胞在感染NDV後,細胞內汎素化蛋白水平降低,而26S蛋白酶體的三種蛋白水解活性都顯著升高;使用汎素-蛋白酶體繫統抑製劑後NDV的增殖受到瞭明顯的抑製,證明NDV在HeLa細胞內的增殖與細胞自身的汎素-蛋白酶體繫統關繫密切。
본문주요대세포적범소-단백매체계통시부삼여신성역병독(Newcastle disease virus,NDV)적복제과정진행료연구。용NDV감염HeLa세포,대세포양품진행Western blot실험,병검측세포26S단백매체적삼충단백수해활성변화。동시사용다충범소-단백매체계통상관적억제제처리세포병주NDV감염,측정세포상청중병독TCID50치,비교약물처리여DMSO처리대병독증식적영향。결과표명,HeLa세포재감염NDV후,세포내범소화단백수평강저,이26S단백매체적삼충단백수해활성도현저승고;사용범소-단백매체계통억제제후NDV적증식수도료명현적억제,증명NDV재HeLa세포내적증식여세포자신적범소-단백매체계통관계밀절。
The objective of the present study was to examine the effect of cellular ubiquitin-proteasome system on Newcastle disease virus (NDV) replication in Hela cells. To determine whether ubiquitin-proteasome system was activated in NDV infected HeLa cells, cellular samples were taken at indicated times for Western blot and for measurement of chymotrypsin-, trypsin-and caspase-like activities. Additionally, NDV infected HeLa cells were treated with different inhibitors of ubiquitin-proteasome system and virus titers (TCID50) in culture supernatants were determined. A significant increase in 26S proteasome activity was observed after NDV infection while ubiquitinated proteins decreased. The application of inhibitors significantly reduced NDV production and delayed viral propagation. In conclusion, ubiquitin-proteasome system plays a critical role in NDV replication in HeLa cells.