实用医学杂志
實用醫學雜誌
실용의학잡지
The Journal of Practical Medicine
2015年
20期
3340-3342
,共3页
李春艳%贾丽萍%石蕾%周贤
李春豔%賈麗萍%石蕾%週賢
리춘염%가려평%석뢰%주현
奥曲肽%人肝星状细胞%凋亡%Bcl-2%Bax
奧麯肽%人肝星狀細胞%凋亡%Bcl-2%Bax
오곡태%인간성상세포%조망%Bcl-2%Bax
Octreotide%Hepatic stellate cells%Apoptosis%Bcl-2%Bax
目的:观察奥曲肽对活化人肝星状细胞凋亡和凋亡相关蛋白Bcl-2/Bax 表达的影响,探讨奥曲肽抗肝纤维化可能的作用机制。方法:不同浓度的奥曲肽作用于传代的人肝星状细胞株(HSC-LX2)24 h、48 h后,应用FITC-TUNEL检测各组细胞凋亡,应用免疫细胞化学法检测HSC-LX2中Bcl-2、Bax蛋白表达,应用Western-blot法检测HSC-LX2中Bcl-2蛋白表达。结果:奥曲肽可促进HSC-LX2细胞调亡,细胞凋亡率随奥曲肽浓度增加而增高(P <0.05);与24 h比较,相同浓度奥曲肽作用于HSC-LX248 h细胞凋亡率均明显增高(P <0.05);免疫细胞化学结果显示:与对照组相比,奥曲肽明显降低HSC-LX2中Bcl-2蛋白表达,而增加Bax蛋白表达(P <0.05);Western-blot结果表明:与对照组相比,奥曲肽可明显降低HSC-LX2中Bcl-2蛋白表达(P <0.05)。结论:奥曲肽可呈剂量和时间依赖性促进人肝星状细胞凋亡,其机制可能与奥曲肽诱发人肝星状细胞Bcl-2蛋白表达下调,Bax蛋白表达上调有关。
目的:觀察奧麯肽對活化人肝星狀細胞凋亡和凋亡相關蛋白Bcl-2/Bax 錶達的影響,探討奧麯肽抗肝纖維化可能的作用機製。方法:不同濃度的奧麯肽作用于傳代的人肝星狀細胞株(HSC-LX2)24 h、48 h後,應用FITC-TUNEL檢測各組細胞凋亡,應用免疫細胞化學法檢測HSC-LX2中Bcl-2、Bax蛋白錶達,應用Western-blot法檢測HSC-LX2中Bcl-2蛋白錶達。結果:奧麯肽可促進HSC-LX2細胞調亡,細胞凋亡率隨奧麯肽濃度增加而增高(P <0.05);與24 h比較,相同濃度奧麯肽作用于HSC-LX248 h細胞凋亡率均明顯增高(P <0.05);免疫細胞化學結果顯示:與對照組相比,奧麯肽明顯降低HSC-LX2中Bcl-2蛋白錶達,而增加Bax蛋白錶達(P <0.05);Western-blot結果錶明:與對照組相比,奧麯肽可明顯降低HSC-LX2中Bcl-2蛋白錶達(P <0.05)。結論:奧麯肽可呈劑量和時間依賴性促進人肝星狀細胞凋亡,其機製可能與奧麯肽誘髮人肝星狀細胞Bcl-2蛋白錶達下調,Bax蛋白錶達上調有關。
목적:관찰오곡태대활화인간성상세포조망화조망상관단백Bcl-2/Bax 표체적영향,탐토오곡태항간섬유화가능적작용궤제。방법:불동농도적오곡태작용우전대적인간성상세포주(HSC-LX2)24 h、48 h후,응용FITC-TUNEL검측각조세포조망,응용면역세포화학법검측HSC-LX2중Bcl-2、Bax단백표체,응용Western-blot법검측HSC-LX2중Bcl-2단백표체。결과:오곡태가촉진HSC-LX2세포조망,세포조망솔수오곡태농도증가이증고(P <0.05);여24 h비교,상동농도오곡태작용우HSC-LX248 h세포조망솔균명현증고(P <0.05);면역세포화학결과현시:여대조조상비,오곡태명현강저HSC-LX2중Bcl-2단백표체,이증가Bax단백표체(P <0.05);Western-blot결과표명:여대조조상비,오곡태가명현강저HSC-LX2중Bcl-2단백표체(P <0.05)。결론:오곡태가정제량화시간의뢰성촉진인간성상세포조망,기궤제가능여오곡태유발인간성상세포Bcl-2단백표체하조,Bax단백표체상조유관。
Objective To investigate the effects of octreotide on the apoptosis of human hepatic stellate cells (HSCs) and expression of Bcl-2/Bax in HSCs,and to reveal the mechanism underlying octreotide against hepatic fibrosis. Methods HSCs lines (HSC-LX2) were incubated with different concentrations of octreotide for 24 and 48 hours. Cell apoptosis was evaluated by Fitc-tunel fluorescence staining. Bcl-2 and Bax protein exoression in HSC-LX2 was detected by immunocytochemistry. Meanwhile, Bcl-2 protein of HSC-LX2 were detected by Western blot assay. Results Octreotide could promote the apoptosis of HSC-LX2, and the apoptosis rate was significantly increased with the concentration of octreotide(P < 0.05). The HSC-LX2 were incubated with the same concentration of octreotide for 24 and 48 hours, the cell apoptosis rate of 48-hour octreotide treatment was significantly higher than that of 24-hour octreotide treatment (P < 0.05). The immunocytochemistry result indicated that octreotide could significantly decrease Bcl-2 expression and increase Bax expression in HSC-LX2 (P<0.05); Western blot assay showed that octreotide could also significantly inhibit Bcl-2 expression in HSC-LX2 (P<0.05). Conclusions Octreotide could induce the apoptosis of HSCs in a dose-and time-dependent manner, the mechanism of octreotide inducing HSCs apoptosis might be associated with down-regulation of Bcl-2 and upregulation of Bax in HSC.