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S100A8/S100A9及其与软骨和骨的关联。

S100A8/S100A9 and their association with cartilage and bone.

作者信息

Zreiqat H, Howlett C R, Gronthos S, Hume D, Geczy C L

机构信息

Biomaterials and Tissue Engineering Research Unit, Biomedical Engineering, School of AMME, The University of Sydney, Sydney, NSW, Australia.

出版信息

J Mol Histol. 2007 Oct;38(5):381-91. doi: 10.1007/s10735-007-9117-2. Epub 2007 Jul 17.

Abstract

S100A8 and S100A9 are calcium-binding proteins expressed in myeloid cells and are markers of numerous inflammatory diseases in humans. S100A9 has been associated with dystrophic calcification in human atherosclerosis. Here we demonstrate S100A8 and S100A9 expression in murine and human bone and cartilage cells. Only S100A8 was seen in preosteogenic cells whereas osteoblasts had variable, but generally weak expression of both proteins. In keeping with their reported high-mRNA expression, S100A8 and S100A9 were prominent in osteoclasts. S100A8 was expressed in alkaline phosphatase-positive hypertrophic chondrocytes, but not in proliferating chondrocytes within the growth plate where the cartilaginous matrix was calcifying. S100A9 was only evident in the invading vascular osteogenic tissue penetrating the degenerating chondrocytic zone adjacent to the primary spongiosa, where S100A8 was also expressed. Whilst, S100A8 has been shown to be associated with osteoblast differentiation, both S100A8 and S100A9 may contribute to calcification of the cartilage matrix and its replacement with trabecular bone, and to regulation of redox in bone resorption.

摘要

S100A8和S100A9是在髓细胞中表达的钙结合蛋白,是人类多种炎症性疾病的标志物。S100A9与人类动脉粥样硬化中的营养不良性钙化有关。在此,我们证明了S100A8和S100A9在小鼠和人类骨及软骨细胞中的表达。仅在成骨前体细胞中可见S100A8,而成骨细胞中这两种蛋白的表达各不相同,但通常较弱。与报道的高mRNA表达一致,S100A8和S100A9在破骨细胞中很突出。S100A8在碱性磷酸酶阳性的肥大软骨细胞中表达,但在生长板内软骨基质正在钙化的增殖软骨细胞中不表达。S100A9仅在穿透初级海绵体附近退变软骨细胞区的侵入性血管成骨组织中明显,此处也表达S100A8。虽然已表明S100A8与成骨细胞分化有关,但S100A8和S100A9都可能有助于软骨基质的钙化及其被小梁骨替代,并有助于调节骨吸收中的氧化还原反应。

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