Isolation and Culture of Neonatal Mouse Cardiomyocytes

被引:154
作者
Ehler, Elisabeth [1 ,2 ]
Moore-Morris, Thomas [3 ]
Lange, Stephan [3 ]
机构
[1] Kings Coll London, Randall Div, London WC2R 2LS, England
[2] Kings Coll London, Div Cardiovasc, London WC2R 2LS, England
[3] Univ Calif San Diego, Sch Med, Div Cardiol, La Jolla, CA 92093 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2013年 / 79期
关键词
Cellular Biology; Issue; 79; Biomedical Engineering; Bioengineering; Molecular Biology; Cell Culture Techniques; Primary Cell Culture; Disease Models; Animal; Models; Cardiovascular; Cell Biology; neonatal mouse; cardiomyocytes; isolation; culture; primary cells; NMC; heart cells; animal model;
D O I
10.3791/50154
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Cultured neonatal cardiomyocytes have long been used to study myofibrillogenesis and myofibrillar functions. Cultured cardiomyocytes allow for easy investigation and manipulation of biochemical pathways, and their effect on the biomechanical properties of spontaneously beating cardiomyocytes. The following 2-day protocol describes the isolation and culture of neonatal mouse cardiomyocytes. We show how to easily dissect hearts from neonates, dissociate the cardiac tissue and enrich cardiomyocytes from the cardiac cell-population. We discuss the usage of different enzyme mixes for cell-dissociation, and their effects on cell-viability. The isolated cardiomyocytes can be subsequently used for a variety of morphological, electrophysiological, biochemical, cell-biological or biomechanical assays. We optimized the protocol for robustness and reproducibility, by using only commercially available solutions and enzyme mixes that show little lot-to-lot variability. We also address common problems associated with the isolation and culture of cardiomyocytes, and offer a variety of options for the optimization of isolation and culture conditions.
引用
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页数:10
相关论文
共 47 条
[1]
Sequential myofibrillar breakdown accompanies mitotic division of mammalian cardiomyocytes [J].
Ahuja, P ;
Perriard, E ;
Perriard, JC ;
Ehler, E .
JOURNAL OF CELL SCIENCE, 2004, 117 (15) :3295-3306
[2]
THE EFFECT OF A CHEMICAL PHOSPHATASE ON SINGLE CALCIUM CHANNELS AND THE INACTIVATION OF WHOLE-CELL CALCIUM CURRENT FROM ISOLATED GUINEA-PIG VENTRICULAR MYOCYTES [J].
ALLEN, TJA ;
CHAPMAN, RA .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1995, 430 (01) :68-80
[3]
[Anonymous], 2010, CULTURE ANIMAL CELLS
[4]
MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure [J].
Arber, S ;
Hunter, JJ ;
Ross, J ;
Hongo, M ;
Sansig, G ;
Borg, J ;
Perriard, JC ;
Chien, KR ;
Caroni, P .
CELL, 1997, 88 (03) :393-403
[5]
Formation of cardiac fibers in Matrigel matrix [J].
Bakunts, Karina ;
Gillum, Nikki ;
Karabekian, Zaruhi ;
Sarvazyan, Narine .
BIOTECHNIQUES, 2008, 44 (03) :341-+
[6]
Bashor M M, 1979, Methods Enzymol, V58, P119
[7]
CULTURE OF THE TERMINALLY DIFFERENTIATED ADULT CARDIAC-MUSCLE CELL - A LIGHT AND SCANNING ELECTRON-MICROSCOPE STUDY .9. [J].
CLAYCOMB, WC ;
PALAZZO, MC .
DEVELOPMENTAL BIOLOGY, 1980, 80 (02) :466-482
[8]
Long-term culture of embryonic rat cardiomyocytes on an organosilane surface in a serum-free medium [J].
Das, M ;
Molnar, P ;
Gregory, C ;
Riedel, L ;
Jamshidi, A ;
Hickman, JJ .
BIOMATERIALS, 2004, 25 (25) :5643-5647
[9]
Simple and High Yielding Method for Preparing Tissue Specific Extracellular Matrix Coatings for Cell Culture [J].
DeQuach, Jessica A. ;
Mezzano, Valeria ;
Miglani, Amar ;
Lange, Stephan ;
Keller, Gordon M. ;
Sheikh, Farah ;
Christman, Karen L. .
PLOS ONE, 2010, 5 (09)
[10]
Comparison of nonviral transfection and adeno-associated viral transduction on cardiomyocytes [J].
Djurovic, S ;
Iversen, N ;
Jeansson, S ;
Hoover, F ;
Christensen, G .
MOLECULAR BIOTECHNOLOGY, 2004, 28 (01) :21-31