骨骼和牙齿组织矿化:内质网/高尔基复合体、内溶酶体和自噬运输系统的潜在作用。

Bone Pub Date : 2025-01-13 DOI:10.1016/j.bone.2025.117390
Irving M Shapiro, Makarand V Risbud, Tengteng Tang, William J Landis
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引用次数: 0

摘要

本文综述了内质网/高尔基复合体和细胞内囊泡在介导导致或与脊椎动物组织矿化相关的事件中的潜在作用。钙离子在内质网和高尔基体的小管和腔隙中积累的观察表明,这些细胞器在这一过程中可能具有重要作用。类似水平的钙离子(接近毫摩尔)存在于由核内体、溶酶体和自噬体产生的囊泡中。这些细胞器中磷酸离子的细胞水平也很高(毫摩尔)。虽然这些离子形成矿物质的来源尚未确定,但有充分的理由认为它们可能是在ATP的合成代谢过程中从线粒体中释放出来的,可能与基质合成有关。已发表的研究表明,上文提到的细胞内细胞器内的钙和磷酸盐离子或它们的簇状物作为货物导致细胞外矿物质的形成。封存在线粒体中的矿物质已被证明是一种无定形的磷酸钙。含有离子、离子簇或矿物的囊泡以质膜泡、分泌性溶酶体或可能的腔内囊泡的形式离开细胞。这种细胞调控的过程为离子或矿物颗粒快速运输到骨骼和牙齿组织的矿化前沿提供了一种手段。在细胞外基质中,离子或矿物质可能结合形成更大的聚集体和潜在的矿物核,它们可能与胶原蛋白和其他蛋白质结合。硬组织细胞是如何在运输矿化细胞外基质所需的大量离子的同时,执行其内务管理和其他生物合成功能的,目前尚不清楚。解决这一问题以及本综述中提出的相关问题,为进一步研究促进骨骼和牙齿组织矿化的细胞内过程提供了指导方针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Skeletal and dental tissue mineralization: The potential role of the endoplasmic reticulum/Golgi complex and the endolysosomal and autophagic transport systems.

This paper presents a review of the potential role of the endoplasmic reticulum/Golgi complex and intracellular vesicles in mediating events leading to or associated with vertebrate tissue mineralization. The possible importance of these organelles in this process is suggested by observations that calcium ions accumulate in the tubules and lacunae of the endoplasmic reticulum and Golgi. Similar levels of calcium ions (approaching millimolar) are present in vesicles derived from endosomes, lysosomes and autophagosomes. The cellular level of phosphate ions in these organelles is also high (millimolar). While the source of these ions for mineral formation has not been identified, there are sound reasons for considering that they may be liberated from mitochondria during the utilization of ATP for anabolic purposes, perhaps linked to matrix synthesis. Published studies indicate that calcium and phosphate ions or their clusters contained as cargo within the intracellular organelles noted above lead to formation of extracellular mineral. The mineral sequestered in mitochondria has been documented as an amorphous calcium phosphate. The ion-, ion cluster- or mineral- containing vesicles exit the cell in plasma membrane blebs, secretory lysosomes or possibly intraluminal vesicles. Such a cell-regulated process provides a means for the rapid transport of ions or mineral particles to the mineralization front of skeletal and dental tissues. Within the extracellular matrix, the ions or mineral may associate to form larger aggregates and potential mineral nuclei, and they may bind to collagen and other proteins. How cells of hard tissues perform their housekeeping and other biosynthetic functions while transporting the very large volumes of ions required for mineralization of the extracellular matrix is far from clear. Addressing this and related questions raised in this review suggests guidelines for further investigations of the intracellular processes promoting the mineralization of the skeletal and dental tissues.

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