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机构地区:[1]上海交通大学附属第九人民医院老年病科,上海市200011
出 处:《老年医学与保健》2011年第1期25-29,共5页Geriatrics & Health Care
基 金:上海市教委课题(06BZ016)
摘 要:目的研究信号蛋白Smad3在TGF-β1促大鼠骨髓间充质干细胞分化成平滑肌样细胞中的作用。方法运用免疫细胞化学、RT—PCR证实BMSC中存在TGF-β1/smad3信号传导通路的基础上,运用反义Smad3进行干预。实验分三组:反义Smad3组(反义Smad3腺病毒转染大鼠BMSC),空载对照组(空载腺病毒转染大鼠BMSC)及未转染组;一组均予10ng/mL浓度的TGF-β1诱导1W。通过免疫细胞化学和实时定量PCR比较反义Smad3干预后各组SMut=actin的表达变化。结果经免疫细胞化学法、RT-PCR检测证明BMSC中存在TGF-β1/smad3表达。运用针对靶基因Smad3的反义技术干预后,经10ng/mLTGF-β1诱导,相比未转染组及空载组,反义smad3腺病毒转染组SMα-actin阳性细胞表达数明显减少。实时定量PCR也显示反义smad3组SMα-actinmRNA的相对含量明显低于未转染组(O.460±0.259VS2.932±0.375,P〈0.01),而空载组与未转染组相比无明显统计学差异。结论TGF-β1促BMSC成平滑肌样细胞分化的过程中受Smad3选择性调节,Smad3可能是TGF-β1促BMSC分化成平滑肌样细胞的细胞内信号途径。Objective To observe the role of Smad3 signal transduction in TGF-β1 action. Methods TGF-β1/smad3 expression was confirmed in bone marrow mesenchymal stem cell (BMSC) by RT-PCR and immunocytochemistry. BMSC was divided into three groups: non-transfected group, experimental group (BMSC transfected with antisense Smad3 adenovirus vector) and blank group (BMSC transfected with empty adenovirus vector). One week after 10ng/ml TGF-β1 induction, SM -actin and the rate of differentiation were measured by immunocytochemistry and real-time quantitative PCR identification. Results After 7 days induction by TGF-β1 (10ng/ml), SMα-actin-positive cells were significantly reduced, and the SM ct-actin mRNA expression was significantly lower than the relative content of non-transfected group (0.460 0.259 vs 2.932 0.375, P 〈0.01), while the blank group and non-transfected group had no significant statistical difference. Conclusion The differentiation of BMSC into smooth muscle-like cell could be partly inhibited by antisense Smad3 via block- ing the TGF-β1/Smad3 pathway.
关 键 词:骨髓间充质干细胞 TGF-Β1 平滑肌样细胞 反义Smad3
分 类 号:R543[医药卫生—心血管疾病]
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