细胞凋亡
免疫印迹
标记法
刺激
活力测定
化学
分子生物学
污渍
半胱氨酸蛋白酶3
细胞
男科
内分泌学
程序性细胞死亡
生物
生物化学
医学
基因
作者
Zhefu Hu,Qi‐Zhu Tang,Yuan Liu,Li Jin
出处
期刊:Chinese Journal of Geriatrics
日期:2015-05-14
卷期号:34 (5): 553-556
标识
DOI:10.3760/cma.j.issn.0254-9026.2015.05.026
摘要
Objective
To investigate the effect of lycopene (Lyc) on H9c2 cell apoptosis induced by angiotensin Ⅱ (Ang Ⅱ).
Methods
Using Ang Ⅱ (10 μmol/L) to stimulate H9c2 cells, we observed the protective effect of Lyc on H9c2 cells apoptosis. The H9c2 cells viability induced by different consideration of Lyc or Ang Ⅱ or both was detected by CCK8 assay. The expression levels of Bax and Bcl-2 in H9c2 cells were determined by real-time quantitative reverse transcription polymerase chain reaction (RT-PCR). Western blot was conducted to detect the protein expressions of Bax, Caspase 3, Caspase 9 and Bcl-2 in H9c2 cells. The apoptotic ratio of H9c2 cells was observed by TUNEL assay.
Results
Compared with control group, Ang Ⅱ could decrease the viability of H9c2 cells to (92.87±4.37)%. The result of RT-PCR showed that Ang Ⅱ decreased the expression level of Bcl-2, and Bax level was increased under the stimulation of Ang Ⅱ (P<0.05), while the expression level of Bcl-2 was increased and Bax level was decreased under the co-stimulation of Ang Ⅱ and Lyc in a concentration dependent manner, which indicated that Lyc ameliorated the apoptosis of H9c2 cells. The result of western blot showed that the protein expressions of Bax, Caspase 3 and Caspase 9 were increased, but Bcl-2 was decreased after the stimulation of Ang Ⅱ (P<0.05). While these phenomenon reversed apparently under the co-stimulation of Ang Ⅱ and Lyc. A large number of apoptotic cells were observed under the stimulation of Ang Ⅱ through TUNEL assay. But the number of apoptotic cells reduced significantly under the co-stimulation of Lyc and Ang Ⅱ (P<0.05).
Conclusions
Lyc ameliorates the H9c2 cell apoptosis induced by Ang Ⅱ, which indicates that Lyc may have an important role in the treatment of various cardiovascular diseases.
Key words:
Lycopersicon esculentum; Angiotensin Ⅱ; Myocytes, cardiac; Apoptosis
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