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Contribution of Mitophagy to Cell‐Mediated Mineralization: Revisiting a 50‐Year‐Old Conundrum

机译:线粒体对细胞介导矿化的贡献:重新审视50年之久的难题

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摘要

Biomineralization in vertebrates is initiated via amorphous calcium phosphate (ACP) precursors. These precursors infiltrate the extracellular collagen matrix where they undergo phase transformation into intrafibrillar carbonated apatite. Although it is well established that ACP precursors are released from intracellular vesicles through exocytosis, an unsolved enigma in this cell‐mediated mineralization process is how ACP precursors, initially produced in the mitochondria, are translocated to the intracellular vesicles. The present study proposes that mitophagy provides the mechanism for transfer of ACP precursors from the dysfunctioned mitochondria to autophagosomes, which, upon fusion with lysosomes, become autolysosomes where the mitochondrial ACP precursors coalesce to form larger intravesicular granules, prior to their release into the extracellular matrix. Apart from endowing the mitochondria with the function of ACP delivery through mitophagy, the present results indicate that mitophagy, triggered upon intramitochondrial ACP accumulation in osteogenic lineage‐committed mesenchymal stem cells, participates in the biomineralization process through the BMP/Smad signaling pathway.
机译:脊椎动物的生物矿化是通过无定形磷酸钙(ACP)前体引发的。这些前体渗透到细胞外胶原基质中,在那里它们经历相转变为原纤维内碳酸磷灰石。尽管已经公认ACP前体是通过胞吐作用从细胞内囊泡中释放出来的,但在细胞介导的矿化过程中尚未解决的谜团就是最初在线粒体中产生的ACP前体如何转移到细胞内囊泡中。本研究提出线粒体提供了将ACP前体从功能异常的线粒体转移至自噬体的机制,自溶体与溶酶体融合后,成为线粒体,线粒体ACP前体在释放入细胞外基质之前会聚结形成较大的囊泡内颗粒。 。除了通过线粒体赋予线粒体ACP功能外,本研究结果还表明线粒体由线粒体内ACP在成骨谱系所致间充质干细胞中的蓄积触发,并通过BMP / Smad信号通路参与生物矿化过程。

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