中华放射医学与防护杂志
中華放射醫學與防護雜誌
중화방사의학여방호잡지
Chinese Journal of Radiological Medicine and Protection
2014年
1期
22-25
,共4页
谭伟%尹姣姣%周丽君%黄波%刘晓丹%王豫%顾永清%让蔚清%周平坤
譚偉%尹姣姣%週麗君%黃波%劉曉丹%王豫%顧永清%讓蔚清%週平坤
담위%윤교교%주려군%황파%류효단%왕예%고영청%양위청%주평곤
盐诱导激酶2%电离辐射%基因表达%G2/M期阻滞
鹽誘導激酶2%電離輻射%基因錶達%G2/M期阻滯
염유도격매2%전리복사%기인표체%G2/M기조체
Salt-inducible kinase 2%Ionizing radiation%Gene expression%G2/M arrest
目的 探讨电离辐射对盐诱导激酶2(SIK2)蛋白和mRNA的诱导表达作用及细胞周期相关性.方法 HepG2细胞用60Coγ射线照射,蛋白质印迹法和实时定量PCR法分别检测细胞的SIK2蛋白和mRNA的表达,胸腺嘧啶双阻滞法同步化细胞,流式细胞术测定细胞周期的变化.结果 HepG2细胞2 Gy照射后4、6、10h,SIK2蛋白表达显著增加(t=3.00、3.98、4.17,P<0.05);10 Gy大剂量照射后,SIK2蛋白表达增加的趋势与2 Gy一致,但增加的幅度较前者低.2和10 Gy照射后SIK2基因mRNA均在10 h出现了增加(t=4.54、2.74,P<0.05).照后10 h出现了细胞G2/M阻滞高峰.利用同步化细胞分析表明,细胞周期不同时相中SIK2 mRNA的表达无明显差别.结论 2和10 Gy照射均能诱导SIK2蛋白表达增加,2 Gy的作用更加明显.细胞照射后10 h,SIK2mRNA的表达水平增加,但与辐射诱发细胞G2/M期阻滞引起不同时相细胞的分布变化无关.
目的 探討電離輻射對鹽誘導激酶2(SIK2)蛋白和mRNA的誘導錶達作用及細胞週期相關性.方法 HepG2細胞用60Coγ射線照射,蛋白質印跡法和實時定量PCR法分彆檢測細胞的SIK2蛋白和mRNA的錶達,胸腺嘧啶雙阻滯法同步化細胞,流式細胞術測定細胞週期的變化.結果 HepG2細胞2 Gy照射後4、6、10h,SIK2蛋白錶達顯著增加(t=3.00、3.98、4.17,P<0.05);10 Gy大劑量照射後,SIK2蛋白錶達增加的趨勢與2 Gy一緻,但增加的幅度較前者低.2和10 Gy照射後SIK2基因mRNA均在10 h齣現瞭增加(t=4.54、2.74,P<0.05).照後10 h齣現瞭細胞G2/M阻滯高峰.利用同步化細胞分析錶明,細胞週期不同時相中SIK2 mRNA的錶達無明顯差彆.結論 2和10 Gy照射均能誘導SIK2蛋白錶達增加,2 Gy的作用更加明顯.細胞照射後10 h,SIK2mRNA的錶達水平增加,但與輻射誘髮細胞G2/M期阻滯引起不同時相細胞的分佈變化無關.
목적 탐토전리복사대염유도격매2(SIK2)단백화mRNA적유도표체작용급세포주기상관성.방법 HepG2세포용60Coγ사선조사,단백질인적법화실시정량PCR법분별검측세포적SIK2단백화mRNA적표체,흉선밀정쌍조체법동보화세포,류식세포술측정세포주기적변화.결과 HepG2세포2 Gy조사후4、6、10h,SIK2단백표체현저증가(t=3.00、3.98、4.17,P<0.05);10 Gy대제량조사후,SIK2단백표체증가적추세여2 Gy일치,단증가적폭도교전자저.2화10 Gy조사후SIK2기인mRNA균재10 h출현료증가(t=4.54、2.74,P<0.05).조후10 h출현료세포G2/M조체고봉.이용동보화세포분석표명,세포주기불동시상중SIK2 mRNA적표체무명현차별.결론 2화10 Gy조사균능유도SIK2단백표체증가,2 Gy적작용경가명현.세포조사후10 h,SIK2mRNA적표체수평증가,단여복사유발세포G2/M기조체인기불동시상세포적분포변화무관.
Objective To explore the expression changes of SIK2 in both protein and mRNA levels in response to ionizing radiation and its potential relationship with the cell cycle distribution alteration.Methods HepG2 cells were irradiated with 60Co γ-rays.Western blot and Real-time PCR were used to detect the level of the protein and mRNA,respectively.TdR double-blocking method was used to synchronize cell and the cell cycle distribution was analyzed by flow cytometry.Results The protein level of SIK2 was significantly increased at 4,6,and 10 h (t =3.00,3.98,4.17,P < 0.05) after 2 Gy irradiation.The same increasing tendency of SIK2 protein level was observed in the cells irradiated by 10 Gy of γ-rays,but the increased extent was less than that induced by 2 Gy.A significantly increased mRNA expression of SIK2 was detected at about 10 h after 2 or 10 Gy irradiation (t =4.54,2.74,P <0.05).The G2/M arrest approached to a peak value at 10 h after 2 and 10 Gy irradiation.The result of mRNA level analysis indicated that there was no obvious change among different cell cycle phases of the synchronized cells.Conclusions The level of SIK2 protein can be significantly induced by both 2 Gy and 10 Gy irradiation,and a part of the increased protein level is attributed to the induction of mRNA transcription 10 h post-irradiation.The increased SIK2 mRNA expression is not the consequence of the cell cycle alteration caused by irradiation-induced G2/M arrest.