期刊文献+

心肌样细胞移植对大鼠心肌梗死的疗效观察

Curative effect of transplantion of cardiomyocyte-like cells on myocardial infarction rats
原文传递
导出
摘要 目的观察心肌样细胞(CLC)移植对心肌梗死大鼠的疗效。方法制备大鼠心肌梗死动物模型,4周后超声检测大鼠血流动力学变化;体外分离、纯化大鼠骨髓间充质干细胞(BMSC),15 ng/ml的胰岛素样生长因子1(IGF-1)诱导BMSC分化为CLC 3,7,14和21 d,采用Western blot技术检测心肌标志性蛋白α-SMA,Ttroponin-T和Troponin-I的表达。CLC移植治疗心肌梗死大鼠,实验共分4组:心肌梗死组,生理盐水对照组,BMSC组及CLC组。移植治疗4周,超声检测血流动力学变化后取材大鼠心肌,冰冻切片,HE染色后检测大鼠心肌梗死的面积。统计分析采用单因素方差分析,实验组之间比较采用t检验。结果心肌梗死模型制备4周,模型组大鼠的LVSP数值为(118.74±11.56)mm Hg,低于假手术组(130.42±12.58)mm Hg,模型组大鼠的LVEDP数值为(14.29±7.63)mm Hg,高于假手术组(2.44±1.11)mm Hg,+dp/dt数值为(2645.17±468.16)mm Hg/s低于假手术组(4087.29±525.17)mm Hg/s,-dp/dt数值为(2487.80±348.21)mm Hg/s低于假手术组(3865.81±614.37)mm Hg/s,差异均具有统计学意义(P<0.01)。IGF-1诱导BMSC 3,7,14和21d后均检测到α-SMA、Troponin-T和Troponin-I的表达,与第3天比较P<0.01。移植治疗4周后发现生理盐水对照组大鼠血流动力学没有任何改变,BMSC组及CLC组大鼠的LVEDP数值分别为(9.15±4.54)mm Hg和(4.67±3.46)mm Hg,低于心肌梗死组(14.29±7.63)mm Hg,+dp/dt数值分别为(3245.45±368.76)mm Hg/s和(3612.78±468.54)mm Hg/s,高于心肌梗死组(2645.17±468.16)mm Hg/s,-dp/dt数值分别为(3014.11±412.12)mm Hg/s和(3347.21±398.56)mm Hg/s,高于假手术组(2487.80±348.21)mm Hg/s,同时CLC组大鼠的LVEDP(4.67±3.46)mm Hg低于BMSC组(9.15±4.54)mm Hg,±dp/dt数值分别是(3612.78±468.54)mm Hg/s和(3347.21±398.56)mm Hg/s高于BMSC组(3245.45±368.76)mm Hg/s和(3014.11±412.12)mm Hg/s,差异均具有统计学意义(P<0.01)。BMSC组和CLC组的心梗面积与心肌梗死组比较明显减小,CLC组的梗死面积与BMSC组比较也明显减小,差异均具有统计学意义(P<0.01)。结论 IGF-1诱导BMSC分化为CLC后移植治疗心肌梗死大鼠比单独移植BMSC疗效更好。 Objective To observe the effect of transplanting cardiomyocyte-like cells (CLC) to treat myocardial infarction in rats. Methods Animal models of myocardial infarction were prepared, and hemodynamics changes of rats models were tested by ultrasonic method 4 weeks later. Bone mesenchymal stem cells (BMSC) were isolated and purified in vitro, which were induced to CLCs by 15 ng/ml insulin-like growth factor 1 (IGF-1), and then the expression of myocardial iconic protein α-SMA, Troponin-T and Troponin- I were detected with Western blotting method in 3 d, 7 d, 14 d and 21 d. The experimental rats were randomly assigned into 4 groups (a myocardial infarction group, a normal saline group, a BMSC group and a CLC group). The area of myocardial infarction was detected on rats 4 weeks after transplantation therapy by HE coloring. Data among multiple groups were compared by one-way ANOVA and data between two independent groups were compared by t-test. Results After myocardial infarction models were prepared for 4 weeks, the LVSP ( 118.74± 11.56) mmHg of the model group were significantly lower than those of the sham operation group ( 130.42 ± 12.58) mmHg, the LVEDP ( 14.29 ± 7.63) mmHg of the model group were significantly higher than those of the sham operation group (2.44 ± 1.11 )mmHg, +dp/dt (2645.17 ± 468.16) mmHg/s of the model group were significantly lower than those of the sham group (4087.29 ± 525.17) mmHg/s, and -dp/dt (2487.80 ± 348.21 ) mmHg/s of the model group were also significantly lower than those of the sham group (3865.81 ± 614.37) mmHg/s (P 〈 0.01 ). The expressions of α-SMA, Troponin-T and Troponin- I were detected when BMSCs were induced by IGF-1 on 3 d, 7 d, 14 d and 21 d (P 〈 0.01). There were not any changes in haemodynamics of the normal saline group 4 weeks after transplantation therapy, the LVEDP of the BMSC group (9.15 ± 4.54) mmHg and CLC group (4.67± 3.46) mmHg were significantly lower than those of the myocardial infarction group ( 14.29 ± 7.63 ) mmHg, the +dp/dt of BMSC group (3245.45 ±368.76)mmHg/s and CLC group (3612.78 ± 468.54)mmHg/s were significantly higher than those of the myocardial infarction group (2645.17 ± 468.16) mmHg/s, the -dp/dt of BMSC group (3014.11 ± 412.12) mmHg/s and CLC group (3347.21 ±398.56) mmHg/s were also significantly higher than the sham group (2487.80± 348.21 ) mmHg/s. In the meantime, the LVEDP of the CLC group (4.67 ± 3.46)mmHg was significantly lower than that of the BMSC group (9.15 ± 4.54) mmHg P 〈 0.01, the +dp/dt of the CLC group (3612.78 ± 468.54) mmHg/s were significantly higher than those of the BMSC group (3245.368 ± 468.16), the -dp/dt of the CLC group (3347.21 ±398.56) mmHg/s were also significantly higher than those of the BMSC group ( 3014.11 ± 412.12) mmHg/s. The myocardial infarction area of the BMSC group and CLC group was reduced obviously compared with the myocardial infarction group, and the myocardial infarction area of CLC group was less than that of the BMSC group (P 〈 0.01 ). Conclusion It may be of a better effect that transplanting BMSC induced by IGF-1 into CLC than only transplanting BMSC on myocardial infarction rats.
出处 《中华细胞与干细胞杂志(电子版)》 2017年第4期202-207,共6页 Chinese Journal of Cell and Stem Cell(Electronic Edition)
基金 江苏省生命健康科技专项资金资助项目(BL2012019) 徐州市科技发展项目(XM13B052)
关键词 骨髓 间质干细胞 胰岛素样生长因子I 肌细胞 心脏 心肌梗死 细胞移植 Bone marrow Mesenchymal stem cells Insulin-like growth factor I Myocytes, cardiac Myocardial infarction Cell transplantation
  • 相关文献

参考文献1

二级参考文献19

  • 1Massimiliano Gnecchi,Zhiping Zhang,Aiguo Ni,Victor J. Dzau.Paracrine Mechanisms in Adult Stem Cell Signaling and Therapy[J].Circulation Research.2008(11)
  • 2Amir Abbas Samani,Shoshana Yakar,Derek LeRoith,Pnina Brodt.The Role of the IGF System in Cancer Growth and Metastasis: Overview and Recent Insights[J].Endocrine Reviews.2007(1)
  • 3Oswald J,Boxberger S,Jorgensen B,et al.Mesenchymal stem cells can be differentiated into endothelial cells in vitro. Stem Cells . 2004
  • 4Maeda K,Chung YS,Ogawa Y,et al.Prognostic value of vascular endothelial growth factor expression in gastric carcinoma. Cancer . 1996
  • 5Hui‐TingChen,Mon‐JuanLee,Chung‐HwanChen,Shu‐ChunChuang,Li‐FuChang,Mei‐LingHo,Shao‐HungHung,Yin‐ChihFu,Yan‐HsiungWang,Hsin‐IWang,Gwo‐JawWang,LinKang,Je‐KenChang.Proliferation and differentiation potential of human adipose‐derived mesenchymal stem cells isolated from elderly patients with osteoporotic fractures[J]. Journal of Cellular and Molecular Medicine . 2012 (3)
  • 6Ryang Hwa Lee,Andrey A. Pulin,Min Jeong Seo,Daniel J. Kota,Joni Ylostalo,Benjamin L. Larson,Laura Semprun-Prieto,Patrice Delafontaine,Darwin J. Prockop.Intravenous hMSCs Improve Myocardial Infarction in Mice because Cells Embolized in Lung Are Activated to Secrete the Anti-inflammatory Protein TSG-6[J]. Cell Stem Cell . 2009 (1)
  • 7David Zisa,Arsalan Shabbir,Gen Suzuki,Techung Lee.Vascular endothelial growth factor (VEGF) as a key therapeutic trophic factor in bone marrow mesenchymal stem cell-mediated cardiac repair[J]. Biochemical and Biophysical Research Communications . 2009 (3)
  • 8Paul J. Hauptman,Michael W. Rich,Paul A. Heidenreich,John Chin,Nancy Cummings,Mark E. Dunlap,Michelle L. Edwards,Douglas Gregory,Christopher M. O’Connor,Stephen M. Pezzella,Edward Philbin.The Heart Failure Clinic: A Consensus Statement of the Heart Failure Society of America[J]. Journal of Cardiac Failure . 2008 (10)
  • 9Progression of Left Ventricular Functional Abnormalities in Hypertensive Patients with Heart Failure: An Ultrasonic Two-Dimensional Speckle Tracking Study[J]. Journal of the American Society of Echocardiography . 2008 (12)
  • 10Marzia Leacche,Jorge M. Balaguer,John G. Byrne.Role of cardiac surgery in the post-myocardial infarction patient with heart failure[J]. Current Heart Failure Reports . 2008 (4)

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部