Do Neonatal Mouse Hearts Regenerate following Heart Apex Resection?

被引:106
作者
Andersen, Ditte Caroline [1 ,2 ]
Ganesalingam, Suganya [1 ,3 ]
Jensen, Charlotte Harken [1 ]
Sheikh, Soren Paludan [1 ,3 ]
机构
[1] Odense Univ Hosp, Dept Clin Biochem & Pharmacol, Lab Mol & Cellular Cardiol, DK-5000 Odense C, Denmark
[2] Univ Southern Denmark, Inst Clin, DK-5000 Odense C, Denmark
[3] Univ Southern Denmark, Inst Mol Med, DK-5000 Odense C, Denmark
关键词
ADULT; CELLS; MODEL;
D O I
10.1016/j.stemcr.2014.02.008
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
The mammalian heart has generally been considered nonregenerative, but recent progress suggests that neonatal mouse hearts have a genuine capacity to regenerate following apex resection (AR). However, in this study, we performed AR or sham surgery on 400 neonatal mice from inbred and outbred strains and found no evidence of complete regeneration. Ideally, new functional cardiomyocytes, endothelial cells, and vascular smooth muscle cells should be formed in the necrotic area of the damaged heart. Here, damaged hearts were 9.8% shorter and weighed 14% less than sham controls. In addition, the resection border contained a massive fibrotic scar mainly composed of nonmyocytes and collagen disposition. Furthermore, there was a substantial reduction in the number of proliferating cardiomyocytes in AR hearts. Our results thus question the usefulness of the AR model for identifying molecular mechanisms underlying regeneration of the adult heart after damage.
引用
收藏
页码:406 / 413
页数:8
相关论文
共 23 条
[1]
Reprogramming toward Heart Regeneration: Stem Cells and Beyond [J].
Aguirre, Aitor ;
Sancho-Martinez, Ignacio ;
Izpisua Belmonte, Juan Carlos .
CELL STEM CELL, 2013, 12 (03) :275-284
[2]
Genetic Variation and Population Substructure in Outbred CD-1 Mice: Implications for Genome-Wide Association Studies [J].
Aldinger, Kimberly A. ;
Sokoloff, Greta ;
Rosenberg, David M. ;
Palmer, Abraham A. ;
Millen, Kathleen J. .
PLOS ONE, 2009, 4 (03)
[3]
Characterization of DLK1+ Cells Emerging During Skeletal Muscle Remodeling in Response to Myositis, Myopathies, and Acute Injury [J].
Andersen, Ditte C. ;
Petersson, Stine J. ;
Jorgensen, Louise H. ;
Bollen, Peter ;
Jensen, Pernille B. ;
Teisner, Borge ;
Schroeder, Henrik D. ;
Jensen, Charlotte H. .
STEM CELLS, 2009, 27 (04) :898-908
[4]
Limitations of conventional approaches to identify myocyte nuclei in histologic sections of the heart [J].
Ang, Keng-Leong ;
Shenje, Lincoln T. ;
Reuter, Sean ;
Soonpaa, Mark H. ;
Rubart, Michael ;
Field, Loren J. ;
Galinanes, Manuel .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2010, 298 (06) :C1603-C1609
[5]
Compensatory Growth of Healthy Cardiac Cells in the Presence of Diseased Cells Restores Tissue Homeostasis during Heart Development [J].
Drenckhahn, Joerg-Detief ;
Schwarz, Quenten P. ;
Gray, Stephen ;
Laskowski, Adrienne ;
Kiriazis, Helen ;
Mings, Ziqiu ;
Harvey, Richard P. ;
Du, Xiao-Jun ;
Thorburn, David R. ;
Cox, Timothy C. .
DEVELOPMENTAL CELL, 2008, 15 (04) :521-533
[6]
Model Systems for Cardiovascular Regenerative Biology [J].
Garbern, Jessica C. ;
Mummery, Christine L. ;
Lee, Richard T. .
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2013, 3 (04)
[7]
Cardiac Stem Cell Therapy and the Promise of Heart Regeneration [J].
Garbern, Jessica C. ;
Lee, Richard T. .
CELL STEM CELL, 2013, 12 (06) :689-698
[8]
Complete cardiac regeneration in a mouse model of myocardial infarction [J].
Haubner, Bernhard Johannes ;
Adamowicz-Brice, Martyna ;
Khadayate, Sanjay ;
Tiefenthaler, Viktoria ;
Metzler, Bernhard ;
Aitman, Tim ;
Penninger, Josef M. .
AGING-US, 2012, 4 (12) :966-977
[9]
The regenerating mouse ear [J].
Heber-Katz, E .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1999, 10 (04) :415-419
[10]
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data [J].
Hellemans, Jan ;
Mortier, Geert ;
De Paepe, Anne ;
Speleman, Frank ;
Vandesompele, Jo .
GENOME BIOLOGY, 2007, 8 (02)