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BMP13转染C_3H_(10)T_(1/2)细胞对改善心梗大鼠心功能的影响 被引量:2

BMP13 on C_3H_(10)T_(1/2) cells to improve cardiac function in myocardial infarction rats
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摘要 目的:探讨在大鼠心肌梗死微环境中骨形态生成蛋白13(Bone morphogenetic protein,BMP13)能否促进C3H10T1/2细胞向心肌样细胞分化并且改善心梗大鼠的心功能。方法:56只SD(Sprague dawley)雄性大鼠随机分成4组:假手术组(SHAM,n=8只),单纯心梗组(Myocardial infarction,MI,n=16只),MI+pAdEasy-GFP重组腺病毒感染干细胞组(MI+GFP,n=16只),MI+pAdEasy-BMP13重组腺病毒感染干细胞组(MI+BMP13,n=16只)。各组体重检测,1次/周;超声心动图检测各组大鼠基线水平及术后4周心功能,比较各组指标变化及差异;Massons’染色比较各组心脏梗死面积差异;免疫荧光检测被植入各组细胞心肌特异性结构蛋白α-MHC及cTnT的表达。结果:重组腺病毒感染C3H10T1/2细胞24 h,每组约80%细胞有绿色荧光表达。术后4周超声心动图显示植入细胞组心功能改善,MI+BMP13组更为明显(P<0.05)。冰冻切片免疫荧光显示MI+GFP组和MI+BMP13组植入细胞处可见α-MHC及cTnT表达。结论:心梗微环境中BMP13可诱导C3H10T1/2细胞向心肌样细胞分化并改善心梗大鼠心功能。 Objective:To investigate whether the bone morphogenetic protein 13(BMP13) can promote C3H10T1/2 cell differentiation into cardiomyocytes in microenvironment and improve the cardiac function of the rats after myocardial infarct(MI).Methods:MI and sham operation were established in sprague dawley(SD) male rats.Totally 56 rats were divided into 4 groups: sham operation group(8 rats),MI group(16 rats),MI+GFP group(16 rats),and MI+BMP13 group(16 rats).Left ventricular(LV) function were assessed by echocardiography on day baseline and 4 weeks after operation.After measuring body weight once a week,on 4 weeks after completion of cardiac function test,rats were sacrificed to take the hearts.Differences in infarct sizes of hearts were compared by Masson's staining.Cardiac-specific structural protein α-MHC and cTnT were implanted in each group and detected by immunofluorescence assay.Results:Each C3H10T1/2 cells had about 80% of cells expressing green fluorescence.On 4 weeks after the experiment,heart function in the groups with cells implanted significantly improved,as compared with MI group,MI+BMP13 group more obvious(P〈0.05).Implanted cells in group MI+GFP and MI+BMP13 had cardiac cell-specific structural protein α-MHC and cTnT expression by immunofluorescence.Conclusion:BMP13 can induce differentiation of C3H10T1/2 cells into myocardial cells and improve cardiac function in myocardial infarction rats.
出处 《重庆医科大学学报》 CAS CSCD 北大核心 2011年第6期677-681,共5页 Journal of Chongqing Medical University
基金 国家自然科学基金资助项目(编号:30772361)
关键词 心肌梗死 左室功能 干细胞 骨形态生成蛋白13 myocardial infarction left ventricular(LV) function stem cell bone morphogenetic protein(BMP13)
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参考文献18

  • 1Miyahara Y,Nagaya N,Kataoka M,et al.Monolayered mesenchy- mal stem cells repair scarred myocardium after myocardial infarction[J]. Nature Medicine, 2006,12 (4) :459-465.
  • 2Becker C,Lacchini S,Muotri A R,et al.Skeletal muscle cells ex- pressing VEGF induce capillary formation and reduce cardiac injury in rats[J].Int J Cardiol, 2006,113 (3) :348-354.
  • 3Kompa A R,Summers R J.Lidocaine and surgical modification reduces mortality in a rat model of cardiac failure induced by coronary artery ligation[J].Journal of Pharmacological and Toxicological Methods, 2000,43(3): 199-203.
  • 4Litwin S E, Katz S E, Morgan J P, et al.Serial echocardiographic assessment of left ventricular geometry and function after large myocardial infarction in the rat[J].Circulation, 1994,89( 1 ):345-354.
  • 5Leobon B,Garcin I,Menasche P,et al.Myoblasts transplanted into rat infarcted myocardium are functionally isolated from their host[J]. Proc Natl Acad Sci USA,2003,100( 13):7808-7811.
  • 6Kehat I,Kenyagin-Karsenti D,Snir M,et al.Human embryonic stem cells can differentiate into myocytes with structural and functional properties of cardiomyocytes[J].J Clin Invest,2001,108(3):407-414.
  • 7Lunde K,Solheim S,Aakhus S,et al.Intracoronary injection of mononuclear bone marrow ceils in acute myocardial infarction[J].N Engl J Med, 2006,355 ( 12):1199-1209.
  • 8Maria E D,Juliana S N,Fabio L N,et al.Rat adipose tissue-derived stem cells transplantation attenuates cardiac dysfunction post infarction and biopolymers enhance cell retention[J].PLoS One, 2010,5 ( 8 ): e 12077.
  • 9Matsuura K, Honda A, Nagai T, et al.Transplantation of cardiac progenitor cells ameliorates cardiac dysfunction after myocardial infarction in mice[J].J Clin Invest, 2009,119 ( 8 ) :2204-2217.
  • 10Kim Y Y, Ku S Y, Janq J,et al.Use of long-term cultured embryoid bodies may enhance cardiomyocyte differentiation by BMP2 [J]. Yonsei Med J,2008,49(5):819-827.

二级参考文献18

  • 1张雷,吴文成,邵素霞,赵春芳.猴左心室乳头肌工作心肌细胞间闰盘的立体结构与发育[J].电子显微学报,2003,22(6):461-462. 被引量:5
  • 2张文,田杰,江德勤,张蕾,朱静,陈沅.骨髓间充质干细胞体外分化为心肌样细胞相关调控基因的时序表达[J].中华心血管病杂志,2004,32(11):1004-1008. 被引量:25
  • 3崔凯,张军,李宝丰,郭国桢.电磁脉冲照射前后大鼠心肌超声背向散射参数变化的研究[J].心脏杂志,2006,18(3):293-295. 被引量:5
  • 4Joong-Yeon Lim,Won Ho Kim,Joon Kim,et al.Involvement of TC F-β 1 signaling in cardiomyocyte differentiation from P19CL6 Cells[J].Mol.Cells,2007,24(3):431-436.
  • 5Waiters M J,Wayman G A,Christian J I,.Bone morphogenetic protein function is required for terminal differentiation of the heart but not for early expression of cardiac marker genes[J].Mech Dev,2001,100(2):263-273.
  • 6Varga A C,Wrana J L.The disparate role of BMP in stem cell biology[J].Oncogene,2005,24(37):5713-5721.
  • 7Makino S,Fukuda K,Miyoshi S,et al.Cardiomyocytes can be generated from marrow sternal cells in vitre[J].J Clin Invest,1999,103(5):697-705.
  • 8Ishida W,Itamamoto T,Kusanagi K,et al.Stood6 is a Smad1/5-induced smad inhibitor.Characterization of bone morphogenetic protein-responsive element in the mouse Smad6 promoter[J].J Biol Chem,2000,275(9):6075-6079.
  • 9GrepinC,Nmer G,Nemer M.Enhanced cardiogenesis in embryonic stem cell overexpressing the GATA-4 transcription factor[J].Development,1997,124(12):2387-2395.
  • 10Davidson SM,Marange M.Hsp25 and the p38 MAPK pathway are involved in differentiation of cardiomyocytes[J].Dev Biol.,2000,218 (2):146-160.

共引文献9

同被引文献13

  • 1顾平,温雅,马芹颖,王彦永,崔冬生,王铭维.骨髓基质细胞条件培养液通过p38信号转导通路诱导中脑神经干细胞分化[J].中国组织工程研究与临床康复,2007,11(37):7329-7332. 被引量:2
  • 2Wang J, Greene SB, Martin JF. BMP signaling in congenital heart disease: new developments and future directions [ J ]. Birth Defects Res A Clin Mol Teratol,2011,91:441 -448.
  • 3Nohe A, Keating E, Knaus P, et al. Signal transduction of bone morphogenetic protein receptors [ J ]. Cell Signal, 2004,16:291 - 299.
  • 4Shibuya H, Iwata H, Masuyama N, et al. Role of TAK1 and TAB1 in BMP signaling in early Xen opus development[ J]. EMBO J, 1998, 17 : 1019 - 1028.
  • 5Elnakish MT, Hassan F, Dakhlallah D, etal. Mesenchymal stem cells for cardiac regeneration: Translation to bedside reality [ J ]. Stem Cells Int, 2012,2012 : 646038. doi : 10.1155/2012/646038.
  • 6Miyazono K, Kamiya Y, Morikawa M. Bone morphogenetic protein receptors and signal transduction [ J ]. J Biochem, 2010,147:35 - 51.
  • 7Barruet E, Hadadeh O, Peiretti F, et al. P38 mitogen activa- ted protein kinase controls two successive-steps during the early mesodermal commitment of embryonic stem cells [ J ]. Stem Cells Dev,2011,20 : 1233 - 1246.
  • 8Aouadi M, Bost F, Caron L,et al. P38 mitogen activated protein kinase activity commits embryonic stem cells to ei- ther neurogenesis or cardiomyogenesis [ J ]. Stem Cells, 2006,24 : 1399 - 1406.
  • 9Wu J, Kubota J, Hirayama J, et al. P38 Mitogen-activated protein kinase controls a switch between cardiomyocyte and neuronal commitment of murine embryonic stem cells by activating myocyte enhancer factor 2C-dependent bone morphogenetic protein 2 transcription [ J ]. Stem Cells Dev,2010,19 : 1723 - 1734.
  • 10谭金童,陈沅,向平.BMP_9对C_3H10T_(1/2)干细胞向心肌样细胞分化的影响[J].重庆医科大学学报,2009,34(6):672-676. 被引量:10

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