中国修复重建外科杂志
中國脩複重建外科雜誌
중국수복중건외과잡지
CHINESE JOURNAL OF REPARATIVE AND RECONSTRUCTIVE SURGERY
2007年
7期
702-706
,共5页
肖志波%郝立君%任立宏%滕雯
肖誌波%郝立君%任立宏%滕雯
초지파%학립군%임립굉%등문
wt-P53蛋白%端粒酶活性%瘢痕疙瘩%成纤维细胞
wt-P53蛋白%耑粒酶活性%瘢痕疙瘩%成纖維細胞
wt-P53단백%단립매활성%반흔흘탑%성섬유세포
wt-P53 protein%Telomerase activity%Keloid%Fibroblasts
目的 探讨wt-P53蛋白对人瘢痕疙瘩成纤维细胞(keloid fibroblasts,KFBs)端粒酶活性的影响;明确在人KFBs中wt-P53蛋白与端粒酶活性之间的相互关系.方法 将来源于人瘢痕疙瘩组织的KFBs随机分成两组,转染组采用腺病毒介导法将野生型wt-p53基因转染至人KFBs;非转染组KFBs未进行野生型wt-p53基因转染.转染48 h后,采用间接免疫荧光法和Western blotting法检测KFBs wt-P53蛋白的表达;并于转染后1~7 d,采用TRAP-ELISA法检测KFBs端粒酶活性.结果 两组均有wt-P53蛋白表达,转染组wt-P53蛋白表达明显高于非转染组;转染后1~7 d,转染组端粒酶活性均明显低于非转染组(P<0.05).结论 wt-P53蛋白能够抑制人KFBs端粒酶活性.
目的 探討wt-P53蛋白對人瘢痕疙瘩成纖維細胞(keloid fibroblasts,KFBs)耑粒酶活性的影響;明確在人KFBs中wt-P53蛋白與耑粒酶活性之間的相互關繫.方法 將來源于人瘢痕疙瘩組織的KFBs隨機分成兩組,轉染組採用腺病毒介導法將野生型wt-p53基因轉染至人KFBs;非轉染組KFBs未進行野生型wt-p53基因轉染.轉染48 h後,採用間接免疫熒光法和Western blotting法檢測KFBs wt-P53蛋白的錶達;併于轉染後1~7 d,採用TRAP-ELISA法檢測KFBs耑粒酶活性.結果 兩組均有wt-P53蛋白錶達,轉染組wt-P53蛋白錶達明顯高于非轉染組;轉染後1~7 d,轉染組耑粒酶活性均明顯低于非轉染組(P<0.05).結論 wt-P53蛋白能夠抑製人KFBs耑粒酶活性.
목적 탐토wt-P53단백대인반흔흘탑성섬유세포(keloid fibroblasts,KFBs)단립매활성적영향;명학재인KFBs중wt-P53단백여단립매활성지간적상호관계.방법 장래원우인반흔흘탑조직적KFBs수궤분성량조,전염조채용선병독개도법장야생형wt-p53기인전염지인KFBs;비전염조KFBs미진행야생형wt-p53기인전염.전염48 h후,채용간접면역형광법화Western blotting법검측KFBs wt-P53단백적표체;병우전염후1~7 d,채용TRAP-ELISA법검측KFBs단립매활성.결과 량조균유wt-P53단백표체,전염조wt-P53단백표체명현고우비전염조;전염후1~7 d,전염조단립매활성균명현저우비전염조(P<0.05).결론 wt-P53단백능구억제인KFBs단립매활성.
Objective To evaluated the role of wt-P53 protein in telomerase regulation in keloid fibroblasts(KFBs). Methods The fibroblasts were derived from human keloid tissue which was proved by pathological diagnosis. KFBs were divided into 2 groups, the transfection group and the untransfection group. wt-p53 gene was transfected into the fibroblasts by adenovirus vectors in the transfection group. The KFBs untransfected with wt-p53 gene served as control (untransfection group). After 48 hours of transfection, the expression of wt-P53 protein was analyzed by both Western blotting and immunofluorescence method, respectively. The telomerase activity was evaluated by TRAP-ELISA after 1-7 days of transfection.Results All the KFBs from 2 groups expressed wt-P53 protein. But the expression level of wt-P53 protein in the transfection group was significantly higher than that in the untransfection group. At the same time of high expression of wt-P53 protein, the telomerase activity of KFBs in transfection group was significantly lower than that in the untransfection group( P<0.05). Conclusion High level expression of wt-P53 protein can transiently inhibit the telomerase activity of KFBs.