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Angiopoietin—1基因修饰的骨髓间充质干细胞(MSC)的蛋白质组学方法分析

Proteomics Analysis of Angiopoietin-1 Modified Mesenchymal Stem Cell
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摘要 Angiopoietin (Ang),as a cytokine found in recent years that can promote angiogenesis,belongs to a growth factor family including Ang 1,Ang 2,Ang 3 and Ang 4.Most research focus on Ang 1 and its receptor Tie 2.Different from vascular endothelial growth factor,Ang 1/Tie 2 affect the end of angiogenesis,induce cell migration and maintain survive of endothelial cell and play an important role in angiogenesis and maintenance of the stability of the neoformative capillary network.Ang 1 is composed of 498 amino acids.The homology between human and mouse is 96.7%.Ang 1 is extensively distributed in tissues containing rich blood vessels such as muscle,prostate,ovary,uterus,but little is in tissues which have no or a few blood vessel.Adenovirus vector is able to transfect effectively Ang 1 gene to MSC.Previous studies have demonstrated that MSCAng 1 cell can highly express and secrete Ang 1 protein.MSCAng 1 could survive in the cardiac muscle tissue of acute myocardial infarction rat,and express exogenous Ang 1 protein for a period time.In acute myocardial infarction,MSCAng 1 cell have more potent effect on prompting angiogenesis than MSC cell.Moreover,MSCAng 1 cell could further reduce infarct size,increase thickness of cardiac ventricle wall,and improve cardiac muscle reconstitution.This study aim to find differential expressed protein related with Ang 1 using proteomic technologies.Protein spots showing significant difference by gel image analysis and statistics analysis were selected for identification using ESI MS/MS.We hope this work can provide new clues for the study on mechanism of action of Ang 1. Angiopoietin (Ang),as a cytokine found in recent years that can promote angiogenesis,belongs to a growth factor family including Ang 1,Ang 2,Ang 3 and Ang 4.Most research focus on Ang 1 and its receptor Tie 2.Different from vascular endothelial growth factor,Ang 1/Tie 2 affect the end of angiogenesis,induce cell migration and maintain survive of endothelial cell and play an important role in angiogenesis and maintenance of the stability of the neoformative capillary network.Ang 1 is composed of 498 amino acids.The homology between human and mouse is 96.7%.Ang 1 is extensively distributed in tissues containing rich blood vessels such as muscle,prostate,ovary,uterus,but little is in tissues which have no or a few blood vessel.Adenovirus vector is able to transfect effectively Ang 1 gene to MSC.Previous studies have demonstrated that MSCAng 1 cell can highly express and secrete Ang 1 protein.MSCAng 1 could survive in the cardiac muscle tissue of acute myocardial infarction rat,and express exogenous Ang 1 protein for a period time.In acute myocardial infarction,MSCAng 1 cell have more potent effect on prompting angiogenesis than MSC cell.Moreover,MSCAng 1 cell could further reduce infarct size,increase thickness of cardiac ventricle wall,and improve cardiac muscle reconstitution.This study aim to find differential expressed protein related with Ang 1 using proteomic technologies.Protein spots showing significant difference by gel image analysis and statistics analysis were selected for identification using ESI MS/MS.We hope this work can provide new clues for the study on mechanism of action of Ang 1.
出处 《分析测试学报》 CAS CSCD 北大核心 2007年第z1期47-49,共3页 Journal of Instrumental Analysis
基金 国家自然科学基金资助项目(30371562)
关键词 PROTEOMICS ANGIOPOIETIN-1 Mesenchymal stem cell Proteomics Angiopoietin-1 Mesenchymal stem cell
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参考文献4

  • 1[1]DAVIS S,ALDRICH T H,JONES P F,et al.Isolation of angiopoietin-1,a ligand for the TIE 2 receptor,by secretion -trap expression cloning[J].Cell,1996,87:1161-1169.
  • 2[2]SURI C,JONES PF,PATAN S,et al.Requisite role of angiopoietin-1,a ligand for the tie2 receptor,during embryonic angiogenesis[J].Cell,1996,87(7):1171-1180.
  • 3[3]LI J J,HUANG Y Q,BASCH R,et al.Thrombin induces the release of angiopoietin-1 from platelets[J].Thromb-Haemost,2001,85(2):204-206.
  • 4[4]DAVIS S,ALDRICH T H,JONES P F,et al.[J].Cell,1996,8:1161-1169.

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