Osteopontin and cardiovascular system
- 30 November 2006
- journal article
- review article
- Published by Springer Nature in Molecular and Cellular Biochemistry
- Vol. 300 (1-2) , 1-7
- https://doi.org/10.1007/s11010-006-9368-3
Abstract
A matricellular protein, osteopontin (OPN), is expressed in response to mechanical stress and similar stimuli in the heart, integrates the inter-ECM signal transduction network of component cells, and maintains efficient contractility through quantitative and qualitative control of extracellular matrix (ECM) proteins. In particular, OPN is re-expressed in the process of tissue damage; combines with other cell growth factors, cytokines, chemokines, and proteases as a cytokine itself or as an adhesion molecule; and controls the differentiation and growth of cells involved in re-storation of tissues by controlling inter-cellular signal transduction and production of ECM proteins through regulation of expression levels and activity. A study using mice lacking a functional OPN gene indicated that tissue restoration fails and collagen deposition is inhibited through matrix metalloproteinases (MMPs) in mice lacking OPN. Thus, while OPN accelerates the cardiovascular remodeling process, it also regulates the balance of various inter-cellular activities. In addition, OPN not only promotes arteriosclerosis but is also closely associated with angiogenesis. With the roles of OPN expected to be clinically elucidated, the clinical use of OPN for control of cardiovascular remodeling may be feasible. Points (1) Osteopontin (OPN) efficiently propagates contraction in the heart as a matricellular protein and thereby controls ECM proteins both quantitatively and qualitatively. (2) The quantitative and qualitative control of ECM proteins is involved in interaction with OPN receptors including those of the integrin family, CD44, and others. (3) OPN promotes myocardial remodeling through TGFβ and MMPs. (4) OPN not only promotes arteriosclerosis but is also closely associated with arteriosteogenesis. (5) In animals lacking OPN, tissue remodeling process is inhibited, especially in terms of fibrosis after myocardial infarction. (6) While the significance of OPN as an immune system molecule is still unclear in detail, the significance of OPN in the regenerative immune system has begun to be determined.Keywords
This publication has 37 references indexed in Scilit:
- Osteopontin Modulates Myocardial Hypertrophy in Response to Chronic Pressure Overload in MiceHypertension, 2004
- Role of Osteopontin in Cardiac Fibrosis and Remodeling in Angiotensin II-Induced Cardiac HypertrophyHypertension, 2004
- ERK1/2 and JNKs, but not p38 kinase, are involved in reactive oxygen species‐mediated induction of osteopontin gene expression by angiotensin II and interleukin‐1β in adult rat cardiac fibroblastsJournal of Cellular Physiology, 2003
- Inactivation of the Osteopontin Gene Enhances Vascular Calcification of Matrix Gla Protein–deficient MiceThe Journal of Experimental Medicine, 2002
- Anoikis mechanismsCurrent Opinion in Cell Biology, 2001
- Altered wound healing in mice lacking a functional osteopontin gene (spp1).Journal of Clinical Investigation, 1998
- Neutralizing Antibodies Directed Against Osteopontin Inhibit Rat Carotid Neointimal Thickening After Endothelial DenudationArteriosclerosis, Thrombosis, and Vascular Biology, 1997
- Site‐directed mutagenesis of the arginine‐glycine‐aspartic acid sequence in osteopontin destroys cell adhesion and migration functionsJournal of Cellular Biochemistry, 1995
- Osteopontin mRNA is expressed by smooth muscle-derived foam cells in human atherosclerotic lesions of the aorta.Journal of Clinical Investigation, 1993
- Multiple forms of SppI (secreted phosphoprotein, osteopontin) synthesized by normal and transformed rat bone cell populations: Regulation by TGF-βBiochemical and Biophysical Research Communications, 1989