中国比较医学杂志
中國比較醫學雜誌
중국비교의학잡지
CHINESE JOURNAL OF COMPARATIVE MEDICINE
2014年
9期
5-8,13
,共5页
李微%张涛%解现星%孟威%刘慧芳%肖霖力%李春风%刘源
李微%張濤%解現星%孟威%劉慧芳%肖霖力%李春風%劉源
리미%장도%해현성%맹위%류혜방%초림력%리춘풍%류원
Alpha-亚麻酸%脂肪酸合成%基因表达
Alpha-亞痳痠%脂肪痠閤成%基因錶達
Alpha-아마산%지방산합성%기인표체
Alpha-Linolenic acid%Fatty acid synthesis%Gene expression
目的:探讨不同剂量Alpha-亚麻酸( ALA)对硬脂酸培养后的HepG2细胞脂肪酸合成基因表达的影响。方法 HepG2细胞分为对照组(NC)以及含有0.5 mmol/L硬脂酸的培养液培养高脂组(HF),培养36 h后应用实时定量PCR检测脂肪酸合成关键基因SREBP1C、FAS及ACC表达;基因表达存在显著差异后分别用10%、20%、50%、70%、100%ALA替代硬脂酸培养36 h,实时定量PCR和免疫印迹法检测上述基因mRNA水平及蛋白表达。结果硬脂酸处理后HepG2细胞SREBP1C、FAS及ACC基因显著升高(P <0.001),ALA替代组SREBP1C基因mRNA表达水平均显著低于高脂组( P <0.001),0.5 mmol/L ALA组及0.35 mmol/L ALA组FAS显著低于高脂组( P <0.001),各替代组ACC基因mRNA水平与高脂组无统计学差异;替代组SREBP1C及FAS蛋白表达水平显著低于高脂组,而ACC蛋白表达量与高脂组无明显差异。结论硬脂酸促进HepG2细胞脂肪酸合成,ALA通过抑制SREBP1C及FAS基因表达来减弱脂肪酸合成。
目的:探討不同劑量Alpha-亞痳痠( ALA)對硬脂痠培養後的HepG2細胞脂肪痠閤成基因錶達的影響。方法 HepG2細胞分為對照組(NC)以及含有0.5 mmol/L硬脂痠的培養液培養高脂組(HF),培養36 h後應用實時定量PCR檢測脂肪痠閤成關鍵基因SREBP1C、FAS及ACC錶達;基因錶達存在顯著差異後分彆用10%、20%、50%、70%、100%ALA替代硬脂痠培養36 h,實時定量PCR和免疫印跡法檢測上述基因mRNA水平及蛋白錶達。結果硬脂痠處理後HepG2細胞SREBP1C、FAS及ACC基因顯著升高(P <0.001),ALA替代組SREBP1C基因mRNA錶達水平均顯著低于高脂組( P <0.001),0.5 mmol/L ALA組及0.35 mmol/L ALA組FAS顯著低于高脂組( P <0.001),各替代組ACC基因mRNA水平與高脂組無統計學差異;替代組SREBP1C及FAS蛋白錶達水平顯著低于高脂組,而ACC蛋白錶達量與高脂組無明顯差異。結論硬脂痠促進HepG2細胞脂肪痠閤成,ALA通過抑製SREBP1C及FAS基因錶達來減弱脂肪痠閤成。
목적:탐토불동제량Alpha-아마산( ALA)대경지산배양후적HepG2세포지방산합성기인표체적영향。방법 HepG2세포분위대조조(NC)이급함유0.5 mmol/L경지산적배양액배양고지조(HF),배양36 h후응용실시정량PCR검측지방산합성관건기인SREBP1C、FAS급ACC표체;기인표체존재현저차이후분별용10%、20%、50%、70%、100%ALA체대경지산배양36 h,실시정량PCR화면역인적법검측상술기인mRNA수평급단백표체。결과경지산처리후HepG2세포SREBP1C、FAS급ACC기인현저승고(P <0.001),ALA체대조SREBP1C기인mRNA표체수평균현저저우고지조( P <0.001),0.5 mmol/L ALA조급0.35 mmol/L ALA조FAS현저저우고지조( P <0.001),각체대조ACC기인mRNA수평여고지조무통계학차이;체대조SREBP1C급FAS단백표체수평현저저우고지조,이ACC단백표체량여고지조무명현차이。결론경지산촉진HepG2세포지방산합성,ALA통과억제SREBP1C급FAS기인표체래감약지방산합성。
Objective To investigate the effects of different doses Alpha-Linolenic acid ( ALA ) on the expressions of fatty acid synthesis-related genes in HepG2 cells.Methods HepG2 cells were divided into two groups, normal control group (NC) and high fat group (HF) in which cells were firstly cultured for 36h in the medium contained 0.5mmol/L stearic acid.Real-time quantitative PCR was taken to detect mRNA expression of genes SREBP1C, FAS and ACC which are related to fatty synthesis.While there are significant differences in fatty synthesis, 10%, 20%, 50%, 70% and 100%ALA took the place of stearic acid, 36h later, real-time quantitative PCR and Western blotting were taken to detect mRNA and protein expression of genes related to fatty synthesis.Results SREBP1C mRNA expression of ALA substitution groups were significantly lower than the high-fat group ( P <0.001) .The FAS of 0.5 mmol/L ALA group and 0.35 mmol/L ALA group were significantly lower than the high-fat group (P <0.001).ACC genes mRNA level was not significantly different from high-fat group.SREBP1C and FAS protein expression were significantly lower than the high-fat group, but ACC showed no significant difference.Conclusions Saturated fatty acids promote hepatocyte fatty acid synthesis, ALA abates fatty acid synthesis by inhibiting FAS and SREBP1C gene expression.