CAJ | 학술논문

目的探讨EGR1在调控肝再生过程中的功能地位.方法使用RT-PCR法测定部分切肝和假手术后不同时间点野生小鼠静止和再生肝组织EGR-1 mRNA水平;使用western blot检测部分切肝后48和72 h野生小鼠和EGR1基因敲出鼠的全肝组织裂解液中EGR1蛋白质的表达水平并对其进行比较.结果肝再生过程中EGR1基因的诱导表达开始于部分切肝后6～12 h,继而下降,但于48 h表达再次增高;而EGR1蛋白质表达在部分切肝后12～48 h均可检测到.因此,肝再生过程中EGR1蛋白质表达的时段恰好对应于肝细胞的有丝分裂进程.结论正常肝再生的有效进程中EGR1基因的表达是必需的.肝再生过程中,EGR1参与了肝细胞有丝分裂周期的调控.
목적탐토EGR1재조공간재생과정중적공능지위.방법사용RT-PCR법측정부분절간화가수술후불동시간점야생소서정지화재생간조직EGR-1 mRNA수평;사용western blot검측부분절간후48화72 h야생소서화EGR1기인고출서적전간조직렬해액중EGR1단백질적표체수평병대기진행비교.결과간재생과정중EGR1기인적유도표체개시우부분절간후6～12 h,계이하강,단우48 h표체재차증고;이EGR1단백질표체재부분절간후12～48 h균가검측도.인차,간재생과정중EGR1단백질표체적시단흡호대응우간세포적유사분렬진정.결론정상간재생적유효진정중EGR1기인적표체시필수적.간재생과정중,EGR1삼여료간세포유사분렬주기적조공.
Objective: To investigate the functional importance of EGR-1 gene in regulating liver regeneration. Methods: EGR-1 mRNA levels were quantified in quiescent and regenerating liver derived from replicate wildtype mice at serial time-points after partial hepatectomy or sham surgery by using real time RTPCR. EGR-1 protein in whole cell lysate derived from wildtype and EGR-1 null mouse liver at 48 and 72hours after partial hepatectomy were compared and menitored by Western blot. Results: The data showed that during liver regeneration induction of EGR-1 gene expression occur 6～12 hours after partial hepatectomy,then declines, and increases again at 48 hours after partial hepatectomy, and that EGR-1 protein expression was detectable 12～48 hours after surgery. Thus the EGR-1 protein was present in regenerating liver at the time corresponding to hepatocellular mitotic progression. Conclusions: EGR-1 is indeed necessary for normal liver regeneration to proceed efficiently. The functional role of EGR-1 during liver regeneration involves modulation of mitotic cell cycle progression.