肿瘤药学
腫瘤藥學
종류약학
ANTI-TUMOR PHARMACY
2014年
6期
415-418
,共4页
刘应兰%杨静%曹仁贤%姜孝新
劉應蘭%楊靜%曹仁賢%薑孝新
류응란%양정%조인현%강효신
乙醛脱氢酶%aldefluor%β细胞%增殖%胰腺部分切除术
乙醛脫氫酶%aldefluor%β細胞%增殖%胰腺部分切除術
을철탈경매%aldefluor%β세포%증식%이선부분절제술
ALDH%Aldefluor%Beta cell proliferation%Partial pancreatectomy
目的:探讨肿瘤干细胞标志物乙醛脱氢酶(ALDH)在小鼠胰腺β细胞增殖模型中的表达情况。方法通过胰腺部分切除术构建小鼠胰腺β细胞增殖的模型,采用流式细胞术和免疫荧光检测其胰腺β细胞中ALDH的表达,采用Western blot检测细胞周期相关蛋白CyclinD1、CDK2及CDK4的表达。结果胰腺部分切除术后2周的胰岛细胞中aldefluor+细胞明显增多,Ki-67+β细胞比例明显升高,且aldefluor+细胞CyclinD1、CyclinD2和CDK4蛋白表达水平均明显高于aldefluor-细胞。胰腺部分切除术后小鼠胰腺中的ALDH+细胞绝大部分均为β细胞。结论胰腺部分切除术诱导的增殖胰岛β细胞具有较高的ALDH活性,aldefluor荧光标记可能作为筛选增殖β细胞的标记物。
目的:探討腫瘤榦細胞標誌物乙醛脫氫酶(ALDH)在小鼠胰腺β細胞增殖模型中的錶達情況。方法通過胰腺部分切除術構建小鼠胰腺β細胞增殖的模型,採用流式細胞術和免疫熒光檢測其胰腺β細胞中ALDH的錶達,採用Western blot檢測細胞週期相關蛋白CyclinD1、CDK2及CDK4的錶達。結果胰腺部分切除術後2週的胰島細胞中aldefluor+細胞明顯增多,Ki-67+β細胞比例明顯升高,且aldefluor+細胞CyclinD1、CyclinD2和CDK4蛋白錶達水平均明顯高于aldefluor-細胞。胰腺部分切除術後小鼠胰腺中的ALDH+細胞絕大部分均為β細胞。結論胰腺部分切除術誘導的增殖胰島β細胞具有較高的ALDH活性,aldefluor熒光標記可能作為篩選增殖β細胞的標記物。
목적:탐토종류간세포표지물을철탈경매(ALDH)재소서이선β세포증식모형중적표체정황。방법통과이선부분절제술구건소서이선β세포증식적모형,채용류식세포술화면역형광검측기이선β세포중ALDH적표체,채용Western blot검측세포주기상관단백CyclinD1、CDK2급CDK4적표체。결과이선부분절제술후2주적이도세포중aldefluor+세포명현증다,Ki-67+β세포비례명현승고,차aldefluor+세포CyclinD1、CyclinD2화CDK4단백표체수평균명현고우aldefluor-세포。이선부분절제술후소서이선중적ALDH+세포절대부분균위β세포。결론이선부분절제술유도적증식이도β세포구유교고적ALDH활성,aldefluor형광표기가능작위사선증식β세포적표기물。
Objective To investigate the expression of aldehyde dehydrogenase (ALDH) in the beta-cell proliferation model. Methods The presence of aldefluor+beta cells was detected by flow cytometry (FCM) and immunofluorescence in partial pancrea-tectomy (PPX) model. The expression of cell-cycle activators CDK2, CyclinD1 and CDK4 were detected by Western blot. Results The aldefluor+beta cells are essentially all positive for Ki-67 in PPX model, and expressed high levels of cell-cycle activators Cy-clinD1, CyclinD2 and CDK4. Conclusion Our data thus revealed that the proliferating beta cells induced by partial pancreatectomy showed a high ALDH activity. Moreover, our data also suggest that aldefluor lineage-tracing might be a marker for screening prolif-erating beta cells.