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编号:10871603
尾加压素Ⅱ对乳鼠心肌成纤维细胞增殖的影响及细胞内信号转导机制
http://www.100md.com 《第四军医大学学报》 2004年第6期
细胞分裂,,大鼠;尾加压素Ⅱ;心肌;成纤维细胞;,细胞分裂,0引言,1材料和方法,2结果,3讨论,【参考文献】
     Effect of urotensin Ⅱ on the proliferation of cardiac myofibroblasts and its intracellular signaling mechanism in newborn SD rats

    YANG JingXiao, ZHAO LianYou, ZHENG QiangSun, SHANG FuJun, YU XinYa, LI AiGuo

    Department of Cardiology, Tangdu Hospital, Fourth Military Medical University, Xian 710038, China

    【Abstract】 AIM: To explore the effects of urotensinⅡ (UⅡ) on the proliferation of the cardiac fibroblasts (CFs) and its intracellular signaling mechanism in newborn SD rats. METHODS: CFs from newborn SD rats were isolated and cultured. Cell number was observed by MTT assay. Cell cycle was evaluated by flow cytometry (FCM). RESULTS: With the treatment of 10-10, 10-9, 10-8 mol/L UⅡ, the cell number, S phase cell percentage and the proliferation index (PI), were significantly higher than those of control group. G0/G1 phase cell percentage was significantly lower than that in control group (P<0.01), but the indices in the 10-7 mol/L UⅡ group were not significantly different from those of control(P>0.05). The OD values in 10-6 mol/L Che+10-8 mol/L UⅡ, 10-5 mol/L PD98059+10-8 mol/L UⅡ and 5 mg/L CsA+10-8 mol/L UⅡ groups increased significantly compared with those in control group (P<0.05), but decreased compared with those in 10-8 mol/L UⅡ group (P<0.05). Compared with those in control group, S phase cell percentage and PI increased, but G0/G1 phase cell percentage decreased in 10-6 mol/L Che+10-8 mol/L UⅡ and 5 mg/L CsA+10-8 mol/L UⅡ groups (P<0.05). No difference was found between 10-5 mol/L PD98059+10-8 mol/L UⅡ and control groups (P>0.05). Compared with those in 10-8 mol/L UⅡ group, S phase cell percentage and the PI declined significantly (P<0.01), while G0/G1 phase cell percentage rose remarkably in 10-6 mol/L Che+10-8 mol/L UⅡ, 10-5 mol/L PD98059+10-8 mol/L UⅡ and 5 mg/L CsA+10-8 mol/L UⅡ groups (P<0.01). CONCLUSION: UⅡ can stimulate the proliferation of CFs in newborn SD rats and the UⅡinduced proliferation of CFs is probably mediated by PKC/MAPK/CaN. ......

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