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线粒体钙离子纳米通道通过调控 mPTP 缓解牙周炎。

Mitochondrial Calcium Ion Nanogluttons Alleviate Periodontitis via Controlling mPTPs.

机构信息

College of Stomatology, Chongqing Medical University, Chongqing, 401147, China.

Stomatological Hospital of Chongqing Medical University, Chongqing, 401147, China.

出版信息

Adv Healthc Mater. 2023 Jun;12(15):e2203106. doi: 10.1002/adhm.202203106. Epub 2023 Mar 22.

Abstract

The mitochondrial permeability transition (mPT) directly affects mitochondrial function in macrophages. Under inflammatory conditions, mitochondrial calcium ion (mitoCa ) overload triggers the persistent opening of mPT pores (mPTPs), further aggravating Ca overload and increasing reactive oxygen species (ROS) to form an adverse cycle. However, there are currently no effective drugs targeting mPTPs to confine or unload excess Ca . It is novelly demonstrated that the initiation of periodontitis and the activation of proinflammatory macrophages depend on the persistent overopening of mPTPs, which is mainly triggered by mitoCa overload and facilitates further mitochondrial ROS leakage into the cytoplasm. To solve the above problems, mitochondrial-targeted "nanogluttons" with PEG-TPP conjugated to the surface of PAMAM and BAPTA-AM encapsulated in the core are designed. These nanogluttons can efficiently "glut" Ca around and inside mitochondria to effectively control the sustained opening of mPTPs. As a result, the nanogluttons significantly inhibit the inflammatory activation of macrophages. Further studies also unexpectedly reveal that the alleviation of local periodontal inflammation in mice is accompanied by diminished osteoclast activity and reduced bone loss. This provides a promising strategy for mitochondria-targeted intervention in inflammatory bone loss in periodontitis and can be extended to treat other chronic inflammatory diseases associated with mitoCa overload.

摘要

线粒体通透性转变(mPT)直接影响巨噬细胞中的线粒体功能。在炎症条件下,线粒体钙离子(mitoCa)超载会触发 mPT 孔(mPTP)的持续开放,进一步加重 Ca 超载并增加活性氧(ROS)形成不良循环。然而,目前还没有针对 mPTP 的有效药物来限制或卸载过多的 Ca。新的研究表明,牙周炎的发生和促炎巨噬细胞的激活依赖于 mPTP 的持续过度开放,这主要是由 mitoCa 超载触发的,并促进进一步的线粒体 ROS 泄漏到细胞质中。为了解决上述问题,设计了表面连接 PEG-TPP 和核心封装 BAPTA-AM 的线粒体靶向“纳米贪吃鬼”。这些纳米贪吃鬼可以有效地“吞噬”线粒体周围和内部的 Ca,有效控制 mPTP 的持续开放。结果,纳米贪吃鬼显著抑制了巨噬细胞的炎症激活。进一步的研究还意外地发现,小鼠局部牙周炎的缓解伴随着破骨细胞活性的降低和骨丢失的减少。这为针对牙周炎中炎症性骨丢失的线粒体靶向干预提供了一种有前途的策略,并可扩展用于治疗其他与 mitoCa 超载相关的慢性炎症性疾病。

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