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牙本质细胞中线粒体的稳态:生理学、发病机制和靶向策略。

Mitochondrial homeostasis in odontoblast: Physiology, pathogenesis and targeting strategies.

机构信息

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan 430079, China.

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan 430079, China; Department of Endodontics, School and Hospital of Stomatology, Wuhan University, HongShan District, LuoYu Road No. 237, Wuhan 430079, China.

出版信息

Life Sci. 2024 Sep 1;352:122797. doi: 10.1016/j.lfs.2024.122797. Epub 2024 Jun 23.

DOI:10.1016/j.lfs.2024.122797
PMID:38917871
Abstract

Caries and pulpitis remain a major global disease burden and affect the quality of life of patients. Odontoblasts are key players in the progression of caries and pulpitis, not only secreting and mineralizing to form dentin, but also acting as a wall of defense to initiate immune defenses. Mitochondrion is an information processor for numerous cellular activities, and dysregulation of mitochondrion homeostasis not only affects cellular metabolism but also triggers a wide range of diseases. Elucidating mitochondrial homeostasis in odontoblasts can help deepen scholars' understanding of odontoblast-associated diseases. Articles on mitochondrial homeostasis in odontoblasts were evaluated for information pertinent to include in this narrative review. This narrative review focused on understanding the complex interplay between mitochondrial homeostasis in odontoblasts under physiological and pathological conditions. Furthermore, mitochondria-centered therapeutic strategies (including mitochondrial base editing, targeting platforms, and mitochondrial transplantation) were emphasized by resolving key genes that regulate mitochondrial function. Mitochondria are involved in odontoblast differentiation and function, and act as mitochondrial danger-associated molecular patterns (mtDAMPs) to mediate odontoblast pathological progression. Novel mitochondria-centered therapeutic strategies are particularly attractive as emerging therapeutic approaches for the maintenance of mitochondrial homeostasis. It is expected to probe key events of odontoblast differentiation and advance the clinical resolution of dentin formation and mineralization disorders and odontoblast-related diseases.

摘要

龋病和牙髓炎仍然是全球主要的疾病负担,影响患者的生活质量。成牙本质细胞是龋病和牙髓炎进展的关键参与者,不仅分泌和矿化形成牙本质,还作为防御墙启动免疫防御。线粒体是许多细胞活动的信息处理器,线粒体稳态的失调不仅影响细胞代谢,还会引发广泛的疾病。阐明成牙本质细胞中的线粒体稳态有助于加深学者们对成牙本质细胞相关疾病的理解。评估了有关成牙本质细胞中线粒体稳态的文章,以获取纳入本叙述性综述的相关信息。本叙述性综述重点关注理解生理和病理条件下成牙本质细胞中线粒体稳态的复杂相互作用。此外,通过解决调节线粒体功能的关键基因,强调了以线粒体为中心的治疗策略(包括线粒体基础编辑、靶向平台和线粒体移植)。线粒体参与成牙本质细胞的分化和功能,并作为线粒体危险相关分子模式(mtDAMPs)来介导成牙本质细胞的病理进展。新型以线粒体为中心的治疗策略作为维持线粒体稳态的新兴治疗方法特别有吸引力。预计将探索成牙本质细胞分化的关键事件,并推进牙本质形成和矿化障碍以及与成牙本质细胞相关疾病的临床解决。

相似文献

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Mitochondrial homeostasis in odontoblast: Physiology, pathogenesis and targeting strategies.牙本质细胞中线粒体的稳态:生理学、发病机制和靶向策略。
Life Sci. 2024 Sep 1;352:122797. doi: 10.1016/j.lfs.2024.122797. Epub 2024 Jun 23.
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Mitochondrial DNA leakage induces odontoblast inflammation via the cGAS-STING pathway.线粒体 DNA 渗漏通过 cGAS-STING 通路诱导成牙本质细胞炎症。
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Odontoblast response under carious lesions.龋损下成牙本质细胞的反应。
Proc Finn Dent Soc. 1992;88 Suppl 1:257-74.
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Regulation of reactionary dentin formation by odontoblasts in response to polymicrobial invasion of dentin matrix.成牙本质细胞对牙本质基质多微生物入侵的反应性牙本质形成的调节。
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Odontoblasts: Specialized hard-tissue-forming cells in the dentin-pulp complex.成牙本质细胞:牙本质-牙髓复合体中专门形成硬组织的细胞。
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The role of Mitofusin-1 and Mitofusin-2 in periodontal disease: a comprehensive review.线粒体融合蛋白-1和线粒体融合蛋白-2在牙周病中的作用:综述
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