Xie Qing, Li Guang-ming, Zhou Xia-qiu, Liao Dan, Yu Hong, Guo Qing
Department of Infectious Diseases, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China.
Zhonghua Gan Zang Bing Za Zhi. 2003 May;11(5):298-301.
To investigate the effect of Tauroursodeoxycholic acid (TUDCA) on Taurodeoxycholic acid (TDCA)-induced HepG2 cell apoptosis and to clarify the molecular mechanism of its anti-apoptosis effect of TUDCA.
Morphologic evaluation of apoptotic cells was performed by Hoechst 33258 staining and electron microscope. DNA fragment was detected by electrophoresis on 1.5% agarose gels. Apoptosis rate was measured by flow cytometry using PI dye. Following incubation of HepG2 cells either with TDCA alone, or coincubation with TUDCA and TDCA, the releasing level of cytochrome c from mitochondria into cytosol was determined by western blot, also the activity of caspase-3, 8, 9.
Incubating the cells with 400 micromol/L TDCA for 12 h induced the cells apoptosis significantly. The apoptotic rate decreased from 50.35% +/- 2.20% to 13.78% +/- 0.84% after coincubation with TUDCA, and this anti-apoptotic effect of TUDCA was confirmed by morphological and DNA ladder detection. TUDCA significantly inhibited the release of cytochrome C from mitochondria into cytosol, and the activity of caspase-9, 3 (t > or = 13.00, P < 0.01), especially at 12 h, caspase-3 activity decreased by 54.9% (t = 16.88, P < 0.01) and 52.5%, however it had no obvious effect on the activity of caspase-8 (t = 1.94, P > 0.05).
TUDCA prevents HepG2 cells apoptosis induced by TDCA through modulating mitochondrial membrane stability, inhibiting the release of cytochrome c and the activation of procaspase-9 and 3. Anti-apoptotic mechanism of TUDCA may be considered to be one of the most important reasons that TUDCA exerts significant efficacy in the treatment of cholestatic liver diseases.
研究牛磺熊去氧胆酸(TUDCA)对牛磺脱氧胆酸(TDCA)诱导的HepG2细胞凋亡的影响,并阐明其抗凋亡作用的分子机制。
采用Hoechst 33258染色和电子显微镜对凋亡细胞进行形态学评估。通过1.5%琼脂糖凝胶电泳检测DNA片段。使用PI染料通过流式细胞术测量凋亡率。将HepG2细胞单独用TDCA孵育,或与TUDCA和TDCA共同孵育后,通过蛋白质免疫印迹法测定细胞色素c从线粒体释放到细胞质中的水平,以及半胱天冬酶-3、8、9的活性。
用400微摩尔/升TDCA孵育细胞12小时可显著诱导细胞凋亡。与TUDCA共同孵育后,凋亡率从50.35%±2.20%降至13.78%±0.84%,TUDCA的这种抗凋亡作用通过形态学和DNA梯状条带检测得到证实。TUDCA显著抑制细胞色素C从线粒体释放到细胞质中,以及半胱天冬酶-9、3的活性(t≥13.00,P<0.01),尤其是在12小时时,半胱天冬酶-3活性降低了54.9%(t=16.88,P<0.01)和52.5%,然而它对半胱天冬酶-8的活性没有明显影响(t=1.94,P>0.05)。
TUDCA通过调节线粒体膜稳定性、抑制细胞色素c释放以及procaspase-9和3的激活来防止TDCA诱导的HepG2细胞凋亡。TUDCA的抗凋亡机制可能被认为是其在胆汁淤积性肝病治疗中发挥显著疗效的最重要原因之一。