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骨桥蛋白与心血管系统。

Osteopontin and cardiovascular system.

作者信息

Okamoto Hiroshi

机构信息

Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine, Kita-Ku, Kita-14, Nishi-5, Sapporo 060-8638, Japan.

出版信息

Mol Cell Biochem. 2007 Jun;300(1-2):1-7. doi: 10.1007/s11010-006-9368-3. Epub 2006 Nov 30.

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 restoration 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 TGFbeta 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.

摘要

基质细胞蛋白骨桥蛋白(OPN)在心脏中响应机械应力和类似刺激而表达,整合组成细胞的细胞外基质(ECM)信号转导网络,并通过对细胞外基质(ECM)蛋白进行定量和定性控制来维持有效的收缩力。特别是,OPN在组织损伤过程中重新表达;作为细胞因子本身或作为粘附分子与其他细胞生长因子、细胞因子、趋化因子和蛋白酶结合;并通过调节表达水平和活性来控制细胞间信号转导和ECM蛋白的产生,从而控制参与组织修复的细胞的分化和生长。一项使用缺乏功能性OPN基因的小鼠的研究表明,缺乏OPN的小鼠的组织修复失败,并且通过基质金属蛋白酶(MMP)抑制胶原蛋白沉积。因此,虽然OPN加速心血管重塑过程,但它也调节各种细胞间活动的平衡。此外,OPN不仅促进动脉粥样硬化,还与血管生成密切相关。随着OPN的作用有望在临床上得到阐明,将OPN用于控制心血管重塑的临床应用可能是可行的。要点:(1)骨桥蛋白(OPN)作为一种基质细胞蛋白在心脏中有效地传播收缩,从而在数量和质量上控制ECM蛋白。(2)ECM蛋白的定量和定性控制涉及与包括整合素家族、CD44等在内的OPN受体的相互作用。(3)OPN通过TGFβ和MMP促进心肌重塑。(4)OPN不仅促进动脉粥样硬化,还与动脉生成密切相关。(5)在缺乏OPN的动物中组织重塑过程受到抑制,尤其是在心肌梗死后的纤维化方面。(6)虽然OPN作为免疫系统分子的意义仍不清楚,但OPN在再生免疫系统中的意义已开始得到确定。

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