Schinke T, McKee M D, Kiviranta R, Karsenty G
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Ann Med. 1998 Dec;30(6):538-41.
Calcification of extracellular matrix (ECM) can be either physiological or pathological. Physiological calcification (or mineralization) of ECM is restricted to bones, teeth and, to a lesser extent, growth plate cartilages. Pathological calcification appears often in the ECM of arteries where it is a frequent complication of atherosclerosis. However, calcification of the ECM of arteries is not restricted to atherosclerosis. Indeed, human diseases have been described that are characterized by calcification of the aortic media in the absence of any atherosclerotic lesions. The existence of these rare diseases, along with several mouse models recently generated and discussed below, indicates that the formation of atherosclerotic lesions and the calcification of the artery ECM are controlled by different genetic pathways. This emerging knowledge has implications for our understanding of ECM calcification beyond atherosclerosis.
细胞外基质(ECM)的钙化可以是生理性的,也可以是病理性的。ECM的生理性钙化(或矿化)仅限于骨骼、牙齿,在较小程度上还包括生长板软骨。病理性钙化常出现在动脉的ECM中,是动脉粥样硬化的常见并发症。然而,动脉ECM的钙化并不局限于动脉粥样硬化。实际上,已有文献描述了一些人类疾病,其特征是在没有任何动脉粥样硬化病变的情况下主动脉中膜钙化。这些罕见疾病的存在,以及最近产生并在下文讨论的几种小鼠模型,表明动脉粥样硬化病变的形成和动脉ECM的钙化受不同的遗传途径控制。这一新兴知识对我们理解动脉粥样硬化以外的ECM钙化具有重要意义。