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|本期目录/Table of Contents|

骨髓间充质干细胞体外对H2O2损伤大鼠心肌细胞的保护

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2010年第1期
页码:
33-36
栏目:
基础研究
出版日期:
2010-01-04

文章信息/Info

Title:
Role of bone mesenchymal stem cells in protection of cardiomyocyte apoptosis by H2O2
作者:
曹青王飞林继先陈书艳
上海交通大学医学院附属新华医院心内科,上海 200092
Author(s):
CAO Qing WANG Fei LIN Ji-xian CHEN Shu-yan
Department of Cardiology, Xinhua Hospital, Medical School, Shanghai Jiaotong University, Shanghai 200092, China
关键词:
骨髓间充质干细胞凋亡缺血/再灌注损伤氧自由基大鼠
Keywords:
bone marrow mesenchymal stem cell ischemia-reperfusion injury apoptosis oxygen-derived free radicals rat
分类号:
Q25;R457.7
DOI:
-
文献标识码:
A
摘要:
目的: 观察骨髓间充质干细胞(bone mesenchymal stem cells,BMSC)对过氧化氢(H2O2)诱导乳鼠心肌细胞凋亡蛋白Bcl-2家族的影响。方法: 培养新生大鼠的心肌细胞,分为3组,即对照组、模型组和BMSC处理组。用Transwell小室建立心肌细胞与BMSC共培养体系,分别于培养12、24和48 h,采用MTT比色法检测单孔细胞的存活率;用Western blot法检测凋亡蛋白Bcl-2和Bax的表达。结果: 模型组细胞和BMSC处理组细胞在H2O2的诱导下出现细胞凋亡。造模12 h后,模型组细胞的存活率明显低于对照组(P<0.05);BMSC处理组细胞的存活率与模型组相比无明显差异。造模24 h和48 h后,BMSC处理组细胞的存活率与模型组差异明显(P<0.05)。造模12 h后,Bax和Bcl-2蛋白的表达无明显变化。造模24 h后,BMSC处理组细胞中Bax蛋白的表达明显低于模型组(P<0.05),Bcl-2蛋白的表达虽有变化,但无统计学意义。结论: BMSC可调控心肌细胞线粒体凋亡途径,减轻氧自由基对心肌细胞的损伤,其抑制凋亡的作用可能是通过下调Bax蛋白的表达而实现的。
Abstract:
AIM: To observe the influence of cell apoptosis-related protein Bcl-2 family on H2O2-treated cardiac myocytes from neonatal rats by bone mesenchymal stem cells (BMSC). METHODS: Cardiac myocytes from neonatal rats were cultured and divided into three groups: control group, model group and BMSC-treated group. Transwell inserts were used for setting up co-culture system between cardiac myocytes and BMSC. MTT colorimetry was used to detect the cellular survival rate separately at 12, 24 and 48 h. Expression of cell apoptosis protein including Bcl-2 and Bax was examined by Western blot. RESULTS: Twelve hours after H2O2 treatment, the cell survival rate in model group was lower than in control group (P<0.05). There was no difference between model group and BMSC-treated group. Cellular survival rates of model group and BMSC-treated group were significantly different at 24 and 48 h. Twelve hours after H2O2 treatment, no difference was found in the expression level of Bax and Bcl-2 among the three groups. Bax expression in BMSC-treated group was significantly down-regulated at 24 h compared with model group (P<0.05). Although Bcl-2 expression was altered, there was no statistically significant difference. CONCLUSION: BMSC decrease myocyte apoptosis after damage from oxygen-derived free radicals, which may result from the down-regulation of Bax expression.

参考文献/References

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备注/Memo

备注/Memo:
收稿日期:2008-9-8.通讯作者:陈书艳,主任医师,主要从事干细胞移植治疗心血管疾病的研究Email:sychen_doctor@hotmail.com 作者简介:曹青,硕士生Email:mcngc@tom.com
更新日期/Last Update: 2010-01-05