Cardioprotective molecules are enriched in beating cardiomyocytes derived from human embryonic stem cells

被引:9
作者
Chae, Jung-Il [1 ,2 ]
Kim, Jumi [3 ]
Son, Mi-Young [4 ]
Jeon, Young-Joo [1 ,2 ]
Kim, Dong-Wook [1 ,2 ]
Kim, Hye Eun [3 ]
Lee, Min Ji [3 ]
Ryu, Joohyun [5 ]
Park, Byoung Chul [5 ]
Lee, Dong-Seok [6 ]
Seo, Kang Seok [7 ]
Lee, Hak Kyo [8 ]
Choi, Nag-Jin [9 ]
Kang, Yong-Kook [4 ]
Chung, Hyung Min [3 ,10 ]
机构
[1] Chonbuk Natl Univ, Sch Dent, Dept Oral Pharmacol, Jeonju, South Korea
[2] Chonbuk Natl Univ, Project BK21, Inst Oral Biosci, Jeonju, South Korea
[3] CHA Bio & Diostech Co Ltd, Seoul 135907, South Korea
[4] KRIBB, Dev & Differentiat Res Ctr, Taejon 305806, South Korea
[5] KRIBB, Med Prote Res Ctr, Taejon 305806, South Korea
[6] Kyungpook Natl Univ, Coll Nat Sci, Taegu 702701, South Korea
[7] Sunchon Natl Univ, Dept Anim Sci & Technol, Sunchon 540742, South Korea
[8] Hankyong Natl Univ, Genom Informat Ctr, Ansung City 456749, Kyeonggi Do, South Korea
[9] Chonbuk Natl Univ, Coll Agr & Life Sci, Dept Anim Sci, Jeonju, South Korea
[10] CHA Univ, Coll Med, CHA Stem Cell Inst, Grad Sch Life Sci, Seoul 135907, South Korea
关键词
Human embryonic stem cell; Embryonic body; Cardiomyocytes; Proteomic analysis; RAT CARDIAC MYOCYTES; HEAT-SHOCK PROTEINS; INTERMEDIATE-FILAMENTS; PROTEOMIC ANALYSIS; OXIDATIVE STRESS; THERAPEUTIC STEM; TRANSPLANTATION; ANNEXINS; TISSUE; MOUSE;
D O I
10.1016/j.ijcard.2012.07.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cardiomyocytes derived from human embryonic stem cells (hESC-CMs) have attracted attention because of their cardiac regenerative potential in vivo. Differentiated CMs can be distinguished into two different phenotypic populations: beating and non-beating CMs. A thorough understanding of the different molecular conditions of beating and non-beating CMs would provide valuable information for other potential applications and cell therapy. Methods: In this study, we generated a comparative protein profiles using proteomic analysis and western blotting, to compare the specific protein expression patterns of beating and non-beating hESC-CMs. Results: Abundantly 72 upregulated proteins are involved in different biological processes such as stimulus response, cellular catabolism and cell motility. Among these proteins, such as HSPs and other antioxidant molecules, are known to be proteins that potentially play an important role in cardioprotection through the enhancement of cell survival in hypoxic and ischemic conditions present in the injured heart. Conclusion: As a first step toward understanding the different molecular conditions of beating and non-beating hESC-CMs, we sought to study their differential expression patterns and discuss their relevance to in vivo functioning in cardiac injury repair. Thus, the results of this study could provide further evidence supporting a cardiac regenerative approach using an optimized cell source derived from hESCs. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:341 / 354
页数:14
相关论文
共 67 条
[31]   Stem Cell Therapy for Vascular Regeneration Adult, Embryonic, and Induced Pluripotent Stem Cells [J].
Leeper, Nicholas J. ;
Hunter, Arwen L. ;
Cooke, John P. .
CIRCULATION, 2010, 122 (05) :517-526
[32]   Control of plasma glucose with alpha-glucosidase inhibitor attenuates oxidative stress and slows the progression of heart failure in mice [J].
Liao, YL ;
Takashima, S ;
Zhao, H ;
Asano, Y ;
Shintani, Y ;
Minamino, T ;
Kim, J ;
Fujita, M ;
Hori, M ;
Kitakaze, M .
CARDIOVASCULAR RESEARCH, 2006, 70 (01) :107-116
[33]   HSP60 in heart failure: abnormal distribution and role in cardiac myocyte apoptosis [J].
Lin, Li ;
Kim, S. C. ;
Wang, Yin ;
Gupta, S. ;
Davis, B. ;
Simon, S. I. ;
Torre-Amione, G. ;
Knowlton, A. A. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 293 (04) :H2238-H2247
[34]   Heat shock protein 27 regulates oxidative stress-induced apoptosis in cardiomyocytes: mechanisms via reactive oxygen species generation and Akt activation [J].
Liu Li ;
Zhang Xiao-jin ;
Jiang Su-rong ;
Ding Zheng-nian ;
Ding Guo-xian ;
Huang Jun ;
Cheng Yun-lin .
CHINESE MEDICAL JOURNAL, 2007, 120 (24) :2271-2277
[35]   High-throughput comparative proteome analysis using a quantitative cysteinyl-peptide enrichment technology [J].
Liu, T ;
Qian, WJ ;
Strittmatter, EF ;
Camp, DG ;
Anderson, GA ;
Thrall, BD ;
Smith, RD .
ANALYTICAL CHEMISTRY, 2004, 76 (18) :5345-5353
[36]   Chronic heart failure induced by coronary artery ligation in Lewis inbred rats [J].
Liu, YH ;
Yang, XP ;
Nass, O ;
Sabbah, HN ;
Peterson, E ;
Carretero, OA .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (02) :H722-H727
[37]   Optimizing Cardiac Fatty Acid and Glucose Metabolism as an Approach to Treating Heart Failure [J].
Lopaschuk, Gary D. .
SEMINARS IN CARDIOTHORACIC AND VASCULAR ANESTHESIA, 2006, 10 (03) :228-230
[38]   Transplantation of low dose CD34+Kdr+ cells promotes vascular and muscular regeneration in ischemic limbs [J].
Madeddu, P ;
Emanueli, C ;
Pelosi, E ;
Salis, MB ;
Cerio, AM ;
Bonanno, G ;
Patti, M ;
Stassi, G ;
Condorelli, G ;
Peschle, C .
FASEB JOURNAL, 2004, 18 (12) :1737-+
[39]   Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy [J].
Manilal, S ;
Sewry, CA ;
Pereboev, A ;
Man, NT ;
Gobbi, P ;
Hawkes, S ;
Love, DR ;
Morris, GE .
HUMAN MOLECULAR GENETICS, 1999, 8 (02) :353-359
[40]   Heart failure [J].
McMurray, JJV ;
Pfeffer, MA .
LANCET, 2005, 365 (9474) :1877-1889