中华医学美学美容杂志
中華醫學美學美容雜誌
중화의학미학미용잡지
CHINESE JOURNAL OF MEDICAL AESTHETICS AND COSMETOLOGY
2012年
5期
368-371
,共4页
吴文艺%王小影%张丽婷%郑志芳%朱世泽%王朝阳
吳文藝%王小影%張麗婷%鄭誌芳%硃世澤%王朝暘
오문예%왕소영%장려정%정지방%주세택%왕조양
锌指基因217%翻译延伸因子1α%增生性瘢痕%瘢痕疙瘩
鋅指基因217%翻譯延伸因子1α%增生性瘢痕%瘢痕疙瘩
자지기인217%번역연신인자1α%증생성반흔%반흔흘탑
ZNF217%EFlα%Hypertrophic scar%Keloid
目的 探讨锌指基因217(ZNF217)和翻译延伸因子1α(EF1α)在病理性癜痕中的表达及其相互关系,以及它们在瘢痕形成中的作用及机制,为瘢痕防治提供实验依据.方法 利用实时荧光定量聚合酶链式反应(PCR)法、蛋白质免疫印迹(Western印迹)法检测正常皮肤、成熟瘢痕、增生性瘢痕和瘢痕疙瘩组织中ZNF217和EF1α的mRNA、蛋白相对表达水平.结果 正常皮肤、成熟瘢痕、增生性瘢痕和瘢痕疙瘩组织中ZNF217的mRNA及蛋白质相对表达量分别为1.46±0.397、1.45±0.265、4.49±0.999、5.47±0.808;0.276±0.0211、0.299±0.0150、0.743±0.0509、0.747±0.0377.EF1α的mRNA及蛋白质相对表达量分别为1.47±0.469、1.47±0.218、5.10±1.680、5.74±1.920;0.505±0.0371、0.518±0.0153、0.780土0.0369、0.792±0.0290.病理性瘢痕组织中ZNF217的mRNA及蛋白质表达显著高于正常皮肤、成熟瘢痕(P<0.01);病理性瘢痕组织中EF1α的mRNA及蛋白质表达增高,与正常皮肤、成熟瘢痕对照组比较,差异有统计学意义(P<0.01);病理性瘢痕组织中ZNF217的mRNA及蛋白质表达与EF1α的mRNA及蛋白质表达呈正相关.结论 ZNF217在病理性瘢痕组织中表达增高,可能通过调节EF1α等细胞周期调控因子而促进瘢痕组织中细胞的增生,对病理性瘢痕的形成可能起着重要作用.
目的 探討鋅指基因217(ZNF217)和翻譯延伸因子1α(EF1α)在病理性癜痕中的錶達及其相互關繫,以及它們在瘢痕形成中的作用及機製,為瘢痕防治提供實驗依據.方法 利用實時熒光定量聚閤酶鏈式反應(PCR)法、蛋白質免疫印跡(Western印跡)法檢測正常皮膚、成熟瘢痕、增生性瘢痕和瘢痕疙瘩組織中ZNF217和EF1α的mRNA、蛋白相對錶達水平.結果 正常皮膚、成熟瘢痕、增生性瘢痕和瘢痕疙瘩組織中ZNF217的mRNA及蛋白質相對錶達量分彆為1.46±0.397、1.45±0.265、4.49±0.999、5.47±0.808;0.276±0.0211、0.299±0.0150、0.743±0.0509、0.747±0.0377.EF1α的mRNA及蛋白質相對錶達量分彆為1.47±0.469、1.47±0.218、5.10±1.680、5.74±1.920;0.505±0.0371、0.518±0.0153、0.780土0.0369、0.792±0.0290.病理性瘢痕組織中ZNF217的mRNA及蛋白質錶達顯著高于正常皮膚、成熟瘢痕(P<0.01);病理性瘢痕組織中EF1α的mRNA及蛋白質錶達增高,與正常皮膚、成熟瘢痕對照組比較,差異有統計學意義(P<0.01);病理性瘢痕組織中ZNF217的mRNA及蛋白質錶達與EF1α的mRNA及蛋白質錶達呈正相關.結論 ZNF217在病理性瘢痕組織中錶達增高,可能通過調節EF1α等細胞週期調控因子而促進瘢痕組織中細胞的增生,對病理性瘢痕的形成可能起著重要作用.
목적 탐토자지기인217(ZNF217)화번역연신인자1α(EF1α)재병이성전흔중적표체급기상호관계,이급타문재반흔형성중적작용급궤제,위반흔방치제공실험의거.방법 이용실시형광정량취합매련식반응(PCR)법、단백질면역인적(Western인적)법검측정상피부、성숙반흔、증생성반흔화반흔흘탑조직중ZNF217화EF1α적mRNA、단백상대표체수평.결과 정상피부、성숙반흔、증생성반흔화반흔흘탑조직중ZNF217적mRNA급단백질상대표체량분별위1.46±0.397、1.45±0.265、4.49±0.999、5.47±0.808;0.276±0.0211、0.299±0.0150、0.743±0.0509、0.747±0.0377.EF1α적mRNA급단백질상대표체량분별위1.47±0.469、1.47±0.218、5.10±1.680、5.74±1.920;0.505±0.0371、0.518±0.0153、0.780토0.0369、0.792±0.0290.병이성반흔조직중ZNF217적mRNA급단백질표체현저고우정상피부、성숙반흔(P<0.01);병이성반흔조직중EF1α적mRNA급단백질표체증고,여정상피부、성숙반흔대조조비교,차이유통계학의의(P<0.01);병이성반흔조직중ZNF217적mRNA급단백질표체여EF1α적mRNA급단백질표체정정상관.결론 ZNF217재병이성반흔조직중표체증고,가능통과조절EF1α등세포주기조공인자이촉진반흔조직중세포적증생,대병이성반흔적형성가능기착중요작용.
Objective To study the expression of ZNF217 and EF1α gene in the pathological scars and to investigate role and probable mechanism in the pathogenesis of abnormal scar.Methods Quantitative real-time PCR and Western blot were performed to detect the expression and distribution of mRNA and protein of ZNF217 and EF1α in hypertrophic scar (10 cases),keloid (10 cases),normal scar (10 cases),and normal skin (10 cases),and statistics was used to analyze the data.Results The expression of ZNF217 mRNA and protein in the normal skin,normal scar,hypertrophic scar and keloid were 1.46±0.397,1.45±0.265,4.49±0.999,5.47±0.808; 0.276±0.0211,0.299±0.0150,0.743t0.0509 and 0.747±0.0377,respectively.The expression of EF1α mRNA and prorein in the normal skin,normal scar,hypertrophic scar,and keloid were 1.47±0.469,1.47±0.218,5.10±1.68,5.74±1.92; 0.505±0.0371,0.518±0.0153,0.780±0.0369 and 0.792±0.0290,respectively.The positive rate of mRNA and protein of ZNF217 and EF1α was not statistically different between the hypertrophic scar and keloid (P>0.05),while they were all remarkably significant in comparison between normal scar and abnormal scar (P<0.01).In pathological scar mRNA and protein of ZNF217 and EF1α showed a strong positive correlation.Conclusions The expression of ZNF217 and EF1α is increased in pathological scar.Therefore,ZNF217 and EF1α overexpression may play an important role in the proliferation of fibroblasts and in the pathogenesis of pathological scar.