Department of Orthopaedic Surgery, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, United States of America.
Department of Orthopaedic Surgery, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, United States of America.
Bone. 2024 Aug;185:117112. doi: 10.1016/j.bone.2024.117112. Epub 2024 May 1.
This review examines the possible role of mitochondria in maintaining calcium and phosphate ion homeostasis and participating in the mineralization of bone, cartilage and other vertebrate hard tissues. The paper builds on the known structural features of mitochondria and the documented observations in these tissues that the organelles contain calcium phosphate granules. Such deposits in mitochondria putatively form to buffer excessively high cytosolic calcium ion concentrations and prevent metabolic deficits and even cell death. While mitochondria protect cytosolic enzyme systems through this buffering capacity, the accumulation of calcium ions by mitochondria promotes the activity of enzymes of the tricarboxylic acid (TCA/Krebs) cycle, increases oxidative phosphorylation and ATP synthesis, and leads to changes in intramitochondrial pH. These pH alterations influence ion solubility and possibly the transitions and composition in the mineral phase structure of the granules. Based on these considerations, mitochondria are proposed to support the mineralization process by providing a mobile store of calcium and phosphate ions, in smaller cluster or larger granule form, while maintaining critical cellular activities. The rise in the mitochondrial calcium level also increases the generation of citrate and other TCA cycle intermediates that contribute to cell function and the development of extracellular mineral. This paper suggests that another key role of the mitochondrion, along with the effects just noted, is to supply phosphate ions, derived from the breakdown of ATP, to endolysosomes and autophagic vesicles originating in the endoplasmic reticulum and Golgi and at the plasma membrane. These many separate but interdependent mitochondrial functions emphasize the critical importance of this organelle in the cellular control of vertebrate mineralization.
这篇综述探讨了线粒体在维持钙和磷酸盐离子稳态以及参与骨、软骨和其他脊椎动物硬组织矿化中的可能作用。本文基于线粒体的已知结构特征和这些组织中细胞器内含有钙磷酸盐颗粒的已有观察结果。这些线粒体中的沉积物推测是为了缓冲过高的细胞质钙离子浓度,防止代谢缺陷甚至细胞死亡。虽然线粒体通过这种缓冲能力保护细胞质酶系统,但线粒体对钙离子的积累会促进三羧酸(TCA/克雷布斯)循环的酶的活性,增加氧化磷酸化和 ATP 合成,并导致线粒体内部 pH 的变化。这些 pH 变化会影响离子的溶解度,并可能影响颗粒中矿物相结构的转变和组成。基于这些考虑,线粒体通过提供较小簇或较大颗粒形式的钙和磷酸盐离子的可移动储存库,同时维持关键的细胞活性,被提出支持矿化过程。线粒体钙离子水平的升高也会增加柠檬酸和其他 TCA 循环中间产物的生成,这些产物有助于细胞功能和细胞外矿物质的发育。本文提出,线粒体的另一个关键作用,除了刚刚提到的作用外,是向源自内质网和高尔基体以及质膜的内溶酶体和自噬小泡提供磷酸根离子,这些磷酸根离子来源于 ATP 的分解。这些许多独立但相互依存的线粒体功能强调了该细胞器在脊椎动物矿化的细胞控制中的关键重要性。