Mouse cardiac surgery: comprehensive techniques for the generation of mouse models of human diseases and their application for genomic studies
- 13 February 2004
- journal article
- Published by American Physiological Society in Physiological Genomics
- Vol. 16 (3) , 349-360
- https://doi.org/10.1152/physiolgenomics.00041.2003
Abstract
Mouse models mimicking human diseases are important tools in trying to understand the underlying mechanisms of many disease states. Several surgical models have been described that mimic human myocardial infarction (MI) and pressure-overload-induced cardiac hypertrophy. However, there are very few detailed descriptions for performing these surgical techniques in mice. Consequently, the number of laboratories that are proficient in performing cardiac surgical procedures in mice has been limited. Microarray technologies measure the expression of thousands of genes simultaneously, allowing for the identification of genes and pathways that may potentially be involved in the disease process. The statistical analysis of microarray experiments is highly influenced by the amount of variability in the experiment. To keep the number of required independent biological replicates and the associated costs of the study to a minimum, it is critical to minimize experimental variability by optimizing the surgical procedures. The aim of this publication was to provide a detailed description of techniques required to perform mouse cardiac surgery, such that these models can be utilized for genomic studies. A description of three major surgical procedures has been provided: 1) aortic constriction, 2) pulmonary artery banding, 3) MI (including ischemia-reperfusion). Emphasis has been placed on technical procedures with the inclusion of thorough descriptions of all equipment and devices employed in surgery, as well as the application of such techniques for expression profiling studies. The cardiac surgical techniques described have been, and will continue to be, important for elucidating the molecular mechanisms of cardiac hypertrophy and failure with high-throughput technology.Keywords
This publication has 30 references indexed in Scilit:
- Minimally invasive aortic banding in mice: effects of altered cardiomyocyte insulin signaling during pressure overloadAmerican Journal of Physiology-Heart and Circulatory Physiology, 2003
- Protective effect of melatonin on myocardial infarctionAmerican Journal of Physiology-Heart and Circulatory Physiology, 2003
- Fundamentals of experimental design for cDNA microarraysNature Genetics, 2002
- Lower Risk of Postinfarct Rupture in Mouse Heart Overexpressing β2-Adrenergic Receptors: Importance of Collagen ContentJournal of Cardiovascular Pharmacology, 2002
- Determination of minimum sample size and discriminatory expression patterns in microarray dataBioinformatics, 2002
- Application of C1-Esterase Inhibitor During Reperfusion of Ischemic MyocardiumCirculation, 2001
- Left-Ventricular Structural and Functional Remodeling in the Mouse after Myocardial Infarction: Assessment with the Isovolumetrically-contracting Langendorff HeartJournal of Molecular and Cellular Cardiology, 1998
- Myocyte apoptosis during acute myocardial infarction in the mouse localizes to hypoxic regions but occurs independently of p53.Journal of Clinical Investigation, 1997
- Intracoronary Application of C1 Esterase Inhibitor Improves Cardiac Function and Reduces Myocardial Necrosis in an Experimental Model of Ischemia and ReperfusionCirculation, 1997
- Heart and lung disease in engineered miceNature Medicine, 1995