Age-dependent changes in myocardial matrix metalloproteinase/tissue inhibitor of metalloproteinase profiles and fibroblast function

• Published in: Cardiovascular research 2005-05, Vol.66 (2), p.410-419
• Main Authors: Lindsey, Merry L, Goshorn, Danielle K, Squires, Christina E, Escobar, G Patricia, Hendrick, Jennifer W, Mingoia, Joseph T, Sweterlitsch, Sarah E, Spinale, Francis G
• Format: Article
• Language: English
• Subjects: Aging - physiology; Animals; Cell Proliferation; Collagen - metabolism; Electrocardiography; Female; Fibroblasts - cytology; Immunoblotting; Male; Matrix Metalloproteinase 3 - analysis; Matrix Metalloproteinase 8 - analysis; Matrix Metalloproteinase 9 - analysis; Matrix Metalloproteinases - analysis; Matrix Metalloproteinases - metabolism; Matrix Metalloproteinases, Membrane-Associated; Metalloendopeptidases - analysis; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Myocardium - cytology; Myocardium - enzymology; Tissue Inhibitor of Metalloproteinase-3 - analysis; Tissue Inhibitor of Metalloproteinase-4; Tissue Inhibitor of Metalloproteinases - analysis; Tissue Inhibitor of Metalloproteinases - metabolism; Ventricular Function, Left - physiology
• ISSN: 0008-6363
• DOI: 10.1016/j.cardiores.2004.11.029

To evaluate the effects of aging on left ventricular (LV) geometry, collagen levels, matrix metalloproteinase (MMP) and tissue inhibitor of metalloproteinase (TIMP) abundance, and myocardial fibroblast function. Young (3-month-old; n=28), middle-aged (MA; 15-month-old; n=17), and old (23-month-old; n=16) CB6F1 mice of both sexes were used in this study. Echocardiographic parameters were measured; collagen, MMP, and TIMP levels were determined for both the soluble and insoluble protein fractions; and fibroblast function was evaluated. LV end-diastolic dimensions and wall thickness increased in both MA and old mice, accompanied by increased soluble protein and decreased insoluble collagen. Immunoblotting revealed differential MMP/TIMP profiles. Compared to MA levels, MMP-3, MMP-8, MMP-9, MMP-12, and MMP-14 increased, and TIMP-3 and TIMP-4 decreased in the insoluble fraction of old mice, suggesting increased extracellular matrix (ECM) degradative capacity. Fibroblast proliferation was blunted with age. This study, for the first time, identified specific differences in cellular and extracellular processes that likely contribute to age-dependent ECM remodeling.