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MAPK信号通路介导血管紧张素Ⅱ对人外周血早期内皮祖细胞的功能调节 被引量:2

MAPK pathway mediated angiotensin Ⅱ regulates the function of early endothelial progenitor ceils
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摘要 目的探讨血管紧张素Ⅱ(AngⅡ)对内皮祖细胞(EPCs)增殖、迁移、黏附功能的影响及MAPK信号通路在其中的作用。方法取健康成人外周血分离、培养出EPCs并鉴定。以不同浓度AngⅡ(0.1、1、10、100μmol/L)干预,得出最佳浓度用于后续干预实验。分组:对照组、AngⅡ组、JNK抑制剂SP600125+AngⅡ组、ERKI/2抑制剂A6355+AngII组和p38抑制剂PDl69318+AngⅡ组。检测各组EPCs的增殖、迁移、黏附能力。结果AngII对EPCs增值能力无显著影响;AngⅡ可促进EPCs的迁移、黏附功能,在1μmol/L时达到最大效果。AngII对EPCs迁移功能的促进作用能被JNK抑制剂SP600125(P〈0.01)、ERK1/2抑制剂A6355(P〈0.01)和p38抑制剂PD169318(P〈0.05)抑制。其中,ERK1/2抑制剂A6355的抑制作用最显著。AnsⅡ对EPCs黏附功能的促进作用可被JNK抑制剂SP600125(P〈0.05)、ERK1/2抑制剂A6355(P〈0.01)和p38抑制剂PD169318(P〈0.05)抑制。结论AngⅡ可能通过激活MAPK信号通路促进EPCs的迁移、黏附功能。 Objective To analyze the effects of angiotensin Ⅱ(Ang Ⅱ ) on the proliferation, migration and adhesion of endothelial progenitor cells (EPCs) and the role of MAPK pathway in this process. Methods EPCs were cultured in serum - free EBM - 2 medium for 24 h before incubation with various concentrations of Ang Ⅱ (0.1, 1, 10, 100 μmol/L) for 48h. EPCs proliferation, migration and adhesion capacities were measured. Choose the best concentrations of Ang Ⅱ. The adherent cells were coUected and divided into five groups randomly: control group, AngⅡ group, SP600125 + AngⅡ , A6355 + Ang Ⅱ and PD169318 + Ang Ⅱ group. EPCs proliferation and migration and adhesion were assayed by MTT assay and modified Boyden chamber assay and cell counting respectively. Results Ang Ⅱ significantly increased the migration and adhesive ability of EPCs in a dose - dependent manner, maximum at 1μmol/L (P 〈0.05), but has no effect on proliferative ability. The influence of AngⅡ on EPC migration capacities can be abolished by SP600125 (59.3 ±9.4 vs 113.6 ± 11.2, P 〈0. 01 ), A6355(52.1 ± 10.4 vs 113.6 ± 11.2, P 〈0.01 ) and PD169318(64.6 ± 10.7 vs 113.6± 11. 2, P 〈 0.05 ). Similarly, the adhesive capacities can be inhibited by SP600125 (41.3 ±10.2 vs 67.8 ± 10.3, P〈0.05), A6355(39.6±12.4 vs 67.8 ±10.3, P 〈0.01)and PD169318(42. 1 ± 11.6 vs 67.8 ± 10. 3, P 〈 0. 05 ). Conclusion Ang Ⅱ improves EPC migration and adhesion capacities through activating MAPK pathway.
出处 《中国急救医学》 CAS CSCD 北大核心 2015年第12期1134-1138,I0010,共6页 Chinese Journal of Critical Care Medicine
基金 基金项目:国家自然科学基金青年项目(NSFC81400269) 镇江市社会发展科技支撑项目(SH2014033) 江苏大学临床医学专项基金(JDLCZX012)
关键词 内皮祖细胞(EPCs) 促分裂原活化蛋白激酶(MAPK) 血管紧张素Ⅱ(AngⅡ) Endothelial progenitor cells Mitogen- activated protein kinase (MAPK) Angiotensin Ⅱ ( Ang Ⅱ)
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参考文献15

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二级参考文献63

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