Cardiac-Specific Cre Induces Age-Dependent Dilated Cardiomyopathy (DCM) in Mice

• Published in: Molecules (Basel, Switzerland) Vol. 24; no. 6; p. 1189
• Main Authors: Rehmani, Taha, Salih, Maysoon, Tuana, Balwant S
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26.03.2019; MDPI
• Subjects: Age; Aging; Aging - genetics; Aging - metabolism; Animals; BAX protein; Cardiac function; cardiac-specific-cre; Cardiomyopathy; Cardiomyopathy, Dilated - diagnostic imaging; Cardiomyopathy, Dilated - genetics; Cardiomyopathy, Dilated - metabolism; cardiotoxic; Cre recombinase; cre-lox system; Deoxyribonucleic acid; Dilated cardiomyopathy; Disease Models, Animal; DNA; DNA Damage; Echocardiography; Estrogens; Fibrosis; Gene expression; Gene Expression Regulation; Genes; Genes, Lethal; Genetic engineering; Genetic modification; Genomes; Heart; Histology; Integrases - genetics; Integrases - metabolism; Liquid oxygen; Mammals; Mice; mouse model; Myocytes; Myosin Heavy Chains - genetics; Myosin Heavy Chains - metabolism; p53 Protein; Phenotype; Phenotypes; Stem cells; cre-lox system; cardiotoxic; mouse model; DNA damage; cardiac-specific-cre; dilated cardiomyopathy
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules24061189

The genetic modification of the mouse genome using the cre-lox system has been an invaluable tool in deciphering gene and protein function in a temporal and/or spatial manner. However, it has its pitfalls, as researchers have shown that the unregulated expression of cre recombinase can cause DNA damage, the consequences of which can be very detrimental to mouse health. Previously published literature on the most utilized cardiac-specific cre, αMHC-cre, mouse model exhibited a nonlethal hypertrophic cardiomyopathy (HCM) with aging. However, using the same αMHC-cre mice, we observed a cardiac pathology, resulting in complete lethality by 11 months of age. Echocardiography and histology revealed that the αMHC-cre mice were displaying symptoms of dilated cardiomyopathy (DCM) by seven months of age, which ultimately led to their demise in the absence of any HCM at any age. Molecular analysis showed that this phenotype was associated with the DNA damage response through the downregulation of activated p38 and increased expression of JNK, p53, and Bax, known inducers of myocyte death resulting in fibrosis. Our data urges strong caution when interpreting the phenotypic impact of gene responses using αMHC-cre mice, since a lethal DCM was induced by the cre driver in an age-dependent manner in this commonly utilized model system.