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基质小泡介导的矿化与破骨细胞对骨矿化的调节。

Matrix Vesicle-Mediated Mineralization and Osteocytic Regulation of Bone Mineralization.

机构信息

Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Faculty of Dental Medicine, Hokkaido University, Sapporo 060-8586, Japan.

Northern Army Medical Unit, Camp Makomanai, Japan Ground Self-Defense Forces, Sapporo 005-8543, Japan.

出版信息

Int J Mol Sci. 2022 Sep 1;23(17):9941. doi: 10.3390/ijms23179941.

Abstract

Bone mineralization entails two mineralization phases: primary and secondary mineralization. Primary mineralization is achieved when matrix vesicles are secreted by osteoblasts, and thereafter, bone mineral density gradually increases during secondary mineralization. Nearby extracellular phosphate ions (PO) flow into the vesicles via membrane transporters and enzymes located on the vesicles' membranes, while calcium ions (Ca), abundant in the tissue fluid, are also transported into the vesicles. The accumulation of Ca and PO in the matrix vesicles induces crystal nucleation and growth. The calcium phosphate crystals grow radially within the vesicle, penetrate the vesicle's membrane, and continue to grow outside the vesicle, ultimately forming mineralized nodules. The mineralized nodules then attach to collagen fibrils, mineralizing them from the contact sites (i.e., collagen mineralization). Afterward, the bone mineral density gradually increases during the secondary mineralization process. The mechanisms of this phenomenon remain unclear, but osteocytes may play a key role; it is assumed that osteocytes enable the transport of Ca and PO through the canaliculi of the osteocyte network, as well as regulate the mineralization of the surrounding bone matrix via the Phex/SIBLINGs axis. Thus, bone mineralization is biologically regulated by osteoblasts and osteocytes.

摘要

骨矿化包括两个矿化阶段

原发性矿化和继发性矿化。当成骨细胞分泌基质小泡时,即可实现原发性矿化,此后,在继发性矿化过程中,骨矿物质密度逐渐增加。附近的细胞外磷酸盐离子 (PO) 通过位于小泡膜上的膜转运蛋白和酶流入小泡,而组织液中丰富的钙离子 (Ca) 也被转运到小泡内。基质小泡中 Ca 和 PO 的积累诱导晶体成核和生长。磷酸钙晶体在小泡内呈放射状生长,穿透小泡膜,并在小泡外继续生长,最终形成矿化结节。矿化结节随后附着在胶原纤维上,从接触部位开始矿化(即,胶原矿化)。然后,在继发性矿化过程中,骨矿物质密度逐渐增加。这一现象的机制尚不清楚,但成骨细胞可能发挥关键作用;据推测,成骨细胞能够通过骨细胞网络的小管来运输 Ca 和 PO,并通过 Phex/SIBLINGs 轴来调节周围骨基质的矿化。因此,骨矿化是由成骨细胞和骨细胞进行生物学调控的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f77/9456179/df3dae26c91c/ijms-23-09941-g001.jpg

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