实用医学杂志
實用醫學雜誌
실용의학잡지
THE JOURNAL OF PRACTICAL MEDICINE
2014年
7期
1069-1072
,共4页
郝礼森%张晓岚%任昌镇%李立文%王静%莫艳波%边荣荣%魏月%张家琪%刘玉龄
郝禮森%張曉嵐%任昌鎮%李立文%王靜%莫豔波%邊榮榮%魏月%張傢琪%劉玉齡
학례삼%장효람%임창진%리립문%왕정%막염파%변영영%위월%장가기%류옥령
肝星状细胞%PTEN%Akt%信号转导
肝星狀細胞%PTEN%Akt%信號轉導
간성상세포%PTEN%Akt%신호전도
Hepatic stellate cell%PTEN%Akt%Signaling transduction
目的:探讨过表达的野生型PTEN对体外培养的活化肝星状细胞(HSC)Akt的影响。方法:体外培养活化 HSC,以腺病毒为载体将野生型PTEN基因瞬时转染HSC;Western blot 及实时荧光定量PCR 检测HSC 的PTEN、Akt表达;Western blot检测HSC 的磷酸化Akt[p-Akt (Thr308)]表达。结果:携带野生型PTEN基因的腺病毒成功转染HSC,使活化HSC 的p-Akt (Thr308)表达下调(P<0.01),而对HSC 的总Akt蛋白及 mRNA 表达没有影响(P>0.50)。结论:过表达的野生型 PTEN 通过抑制 Akt 的磷酸化,负性调节活化HSC的PI3K/Akt信号转导。
目的:探討過錶達的野生型PTEN對體外培養的活化肝星狀細胞(HSC)Akt的影響。方法:體外培養活化 HSC,以腺病毒為載體將野生型PTEN基因瞬時轉染HSC;Western blot 及實時熒光定量PCR 檢測HSC 的PTEN、Akt錶達;Western blot檢測HSC 的燐痠化Akt[p-Akt (Thr308)]錶達。結果:攜帶野生型PTEN基因的腺病毒成功轉染HSC,使活化HSC 的p-Akt (Thr308)錶達下調(P<0.01),而對HSC 的總Akt蛋白及 mRNA 錶達沒有影響(P>0.50)。結論:過錶達的野生型 PTEN 通過抑製 Akt 的燐痠化,負性調節活化HSC的PI3K/Akt信號轉導。
목적:탐토과표체적야생형PTEN대체외배양적활화간성상세포(HSC)Akt적영향。방법:체외배양활화 HSC,이선병독위재체장야생형PTEN기인순시전염HSC;Western blot 급실시형광정량PCR 검측HSC 적PTEN、Akt표체;Western blot검측HSC 적린산화Akt[p-Akt (Thr308)]표체。결과:휴대야생형PTEN기인적선병독성공전염HSC,사활화HSC 적p-Akt (Thr308)표체하조(P<0.01),이대HSC 적총Akt단백급 mRNA 표체몰유영향(P>0.50)。결론:과표체적야생형 PTEN 통과억제 Akt 적린산화,부성조절활화HSC적PI3K/Akt신호전도。
Objective Using an adenoviral vector , the wild-type PTEN gene was transduced into activated hepatic stellate cell (HSC) in vitro and the phosphorylation status of Akt were investigated. Methods The wild type PTEN gene was transduced into activated HSC in vitro mediated by adenoviral vector. The expressions of PTEN and total Akt in HSC were measured by Western blot and Real-time fluorescent quantitation PCR. And the expressions of phosphorylated Akt (Thr308) in HSC was determined by Western blot. Results The data showed that exogenous wild type PTEN gene was successfully transduced and expressed in activated HSC in vitro. The over-expression of wild type PTEN resulted in the significant down-regulated expression of phosphorylated Akt (Thr308) in activated HSC (P < 0.01). But no significant defferences were found in the expression of total Akt in activated HSC at both transcriptional and translational levels(P>0.50). Conclusions The overexpression of wild-type PTEN can negatively regulate PI3K/Akt signaling transduction by inhibiting the phosphorylation of Akt in activated HSC in vitro.