Yuan Zhou, Zheng Qi, Huang Xin-yu, Fan Jia
Department of General Surgery, the Sixth People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai 200233, China.
Zhonghua Wai Ke Za Zhi. 2007 Oct 1;45(19):1350-3.
To study the role of inhibition FAK expression by FAK siRNA in liver cancer cell (MHCC97-H) adhesion, invasion and cytoskeleton rearrangement.
FAK siRNA was transfected into MHCC97-H cell by Lipofectamine 2000; then, FAK expression was detected by Western blot analysis. The change of cell adhesive and invasive ability after RNAi was checked by cell adhesive assay and cell invasive assay respectively. Meanwhile, matrix metalloproteinase-2 secretion was checked by gelatin zymography. Cytoskeleton rearrangement labeled by immunofluorescence antibody was examined by confocal laser scanning microscope.
FAK expression in MHCC97-H cell was obviously inhibited by specific FAK siRNA; However, it was not inhibited by negative siRNA. Adhesion rate between MHCC97-H cell and extracellular matrix decreased from 57.3% to 35.8% after RNA interference (P < 0.05). Compared with untreated group, the number of cell penetrating matrigel also decreased from 31.3 +/- 2.6 to 14.5 +/- 3.1 after transfection (P < 0.05). Besides, matrix metalloproteinase-2 secretion was significantly reduced for FAK expression inhibited by FAK siRNA. FAK inhibition influenced Vinculin rearrangement, blocked the formation of lamellipodium, delayed the time of focal adhesion formation.
Down-regulation the expression of FAK can reduce adhesive rate and invasive number of MHCC97-H cell by influencing cytoskeleton rearrangement and decreasing matrix metalloproteinase-2 secretion.
研究FAK小干扰RNA(siRNA)抑制FAK表达在肝癌细胞(MHCC97-H)黏附、侵袭及细胞骨架重排中的作用。
采用脂质体2000将FAK siRNA转染至MHCC97-H细胞;随后,通过蛋白质免疫印迹分析检测FAK表达。分别采用细胞黏附实验和细胞侵袭实验检测RNA干扰后细胞黏附及侵袭能力的变化。同时,采用明胶酶谱法检测基质金属蛋白酶-2的分泌情况。通过共聚焦激光扫描显微镜观察免疫荧光抗体标记的细胞骨架重排情况。
特异性FAK siRNA可明显抑制MHCC97-H细胞中FAK的表达;而阴性siRNA则无此抑制作用。RNA干扰后,MHCC97-H细胞与细胞外基质之间的黏附率从57.3%降至35.8%(P<0.05)。转染后,与未处理组相比,穿透基质胶的细胞数量也从31.3±2.6降至14.5±3.1(P<0.05)。此外,FAK siRNA抑制FAK表达后,基质金属蛋白酶-2的分泌显著减少。FAK的抑制影响了纽蛋白的重排,阻碍了片状伪足的形成,延迟了黏着斑形成的时间。
下调FAK表达可通过影响细胞骨架重排和减少基质金属蛋白酶-2的分泌,降低MHCC97-H细胞的黏附率和侵袭数量。