重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2014年
12期
1468-1470,1473
,共4页
蔡欣%杨晓玲%杨程%曹成建%王磊%田珏%张焱%姜怡邓
蔡訢%楊曉玲%楊程%曹成建%王磊%田玨%張焱%薑怡鄧
채흔%양효령%양정%조성건%왕뢰%전각%장염%강이산
肝细胞%细胞增殖%同型半胱氨酸%细胞周期素D1%丙氨酸转氨酶%天冬氨酸氨基转移酶
肝細胞%細胞增殖%同型半胱氨痠%細胞週期素D1%丙氨痠轉氨酶%天鼕氨痠氨基轉移酶
간세포%세포증식%동형반광안산%세포주기소D1%병안산전안매%천동안산안기전이매
hepatocytes%cells proliferation%homocysteine%CyclinD1%alanine transaminase%aspartate aminotransferases
目的:探讨同型半胱氨酸(Hcy)对肝细胞增殖及细胞周期素D1(CyclinD1)、丙氨酸氨基转移酶(ALT)和天门冬氨酸氨基转移酶(AST )表达的影响。方法将 HL-7702细胞体外常规培养,分别用0、50、100、200、500μmol/L Hcy刺激细胞,分别于刺激后6、12、24 h采用M T T法检测肝细胞的增殖情况;采用荧光定量 PCR(RT-qPCR)检测CyclinD1 mRNA的表达;采用微板法检测各组细胞培养液中ALT和 AST 的变化。结果不同浓度 Hcy刺激肝细胞不同时间后,细胞的增殖受到抑制,其中100、200、500μmol/L Hcy组与对照组比较差异有统计学意义(P<0.01),24 h作用最明显;不同浓度 Hcy刺激肝细胞24 h后, CyclinD1 mRNA的表达显著下降(P<0.01),细胞培养液中ALT和AST 水平显著升高(P<0.01)。结论 Hcy可以抑制肝细胞增殖,并引起CyclinD1的mRNA表达下降,ALT和AST释放增多。
目的:探討同型半胱氨痠(Hcy)對肝細胞增殖及細胞週期素D1(CyclinD1)、丙氨痠氨基轉移酶(ALT)和天門鼕氨痠氨基轉移酶(AST )錶達的影響。方法將 HL-7702細胞體外常規培養,分彆用0、50、100、200、500μmol/L Hcy刺激細胞,分彆于刺激後6、12、24 h採用M T T法檢測肝細胞的增殖情況;採用熒光定量 PCR(RT-qPCR)檢測CyclinD1 mRNA的錶達;採用微闆法檢測各組細胞培養液中ALT和 AST 的變化。結果不同濃度 Hcy刺激肝細胞不同時間後,細胞的增殖受到抑製,其中100、200、500μmol/L Hcy組與對照組比較差異有統計學意義(P<0.01),24 h作用最明顯;不同濃度 Hcy刺激肝細胞24 h後, CyclinD1 mRNA的錶達顯著下降(P<0.01),細胞培養液中ALT和AST 水平顯著升高(P<0.01)。結論 Hcy可以抑製肝細胞增殖,併引起CyclinD1的mRNA錶達下降,ALT和AST釋放增多。
목적:탐토동형반광안산(Hcy)대간세포증식급세포주기소D1(CyclinD1)、병안산안기전이매(ALT)화천문동안산안기전이매(AST )표체적영향。방법장 HL-7702세포체외상규배양,분별용0、50、100、200、500μmol/L Hcy자격세포,분별우자격후6、12、24 h채용M T T법검측간세포적증식정황;채용형광정량 PCR(RT-qPCR)검측CyclinD1 mRNA적표체;채용미판법검측각조세포배양액중ALT화 AST 적변화。결과불동농도 Hcy자격간세포불동시간후,세포적증식수도억제,기중100、200、500μmol/L Hcy조여대조조비교차이유통계학의의(P<0.01),24 h작용최명현;불동농도 Hcy자격간세포24 h후, CyclinD1 mRNA적표체현저하강(P<0.01),세포배양액중ALT화AST 수평현저승고(P<0.01)。결론 Hcy가이억제간세포증식,병인기CyclinD1적mRNA표체하강,ALT화AST석방증다。
Objective To explore the effects of homoysteine(Hcy) on the proliferation of hepatic cells and the expression of Cy-clinD1 ,ALT and AST .Methods HL-7702 hepatic cells were routinely cultured in vitro and irritated with Hcy at a concentration of 0 ,50 ,100 ,200 ,500μmol/L ,respectively .The proliferation of hepatic cells was measured by MTT at 6 ,12 ,24h after irritation .The expression of CyclinD1 mRNA was detected by quantitative reverse transcription polymerase chain reaction (RT-qPCR) .The chan-ges of ALT and AST in the cells culture medium of each group were determined by the microplate method .Results The prolifera-tion of hepatic cells was inhibited by different concentrations of Hcy ,in which the proliferation rates irritated by Hcy at the concen-trations of 100 ,200 ,500μmol/L were lower than that in control group with statistical difference (P<0 .01) ,and the effect was most markedly at 24h after irritation(P<0 .01);compared with the control group ,when hepatic cells were irritated by Hcy at the concen-trations of 100 ,200 ,500μmol/L for 24h ,the mRNA expression of CyclinD1 was decreased(P<0 .01) ,meanwhile the levels of ALT and AST were significantly increased(P<0 .01) .Conclusion Hcy can inhibit the proliferation of hepatic cells ,cause the decrease of CyclinD1 mRNA expression and result in the increase of ALT and AST release .