The Role of Macrophage Efferocytosis in the Pathogenesis of Apical Periodontitis.

Int J Mol Sci

Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an 710004, China.

Published: March 2024

AI Article Synopsis

  • Macrophages (Mφs) are vital for maintaining immune balance in the area around tooth roots during bacterial infections, specifically in cases of apical periodontitis (AP).
  • This study investigates the role of Mφ efferocytosis (the process of macrophages clearing dead cells) in AP, utilizing both clinical specimens and specific laboratory models.
  • Results indicate that enhancing Mφ efferocytosis promotes Mφ polarization towards the beneficial M2 type, potentially offering a new therapeutic approach for improving AP outcomes.

Article Abstract

Macrophages (Mφs) play a crucial role in the homeostasis of the periapical immune micro-environment caused by bacterial infection. Mφ efferocytosis has been demonstrated to promote the resolution of multiple infected diseases via accelerating Mφ polarization into M2 type. However, the Mφ efferocytosis-apical periodontitis (AP) relationship has not been elucidated yet. This study aimed to explore the role of Mφ efferocytosis in the pathogenesis of AP. Clinical specimens were collected to determine the involvement of Mφ efferocytosis in the periapical region via immunohistochemical and immunofluorescence staining. For a further understanding of the moderator effect of Mφ efferocytosis in the pathogenesis of AP, both an in vitro AP model and in vivo AP model were treated with ARA290, a Mφ efferocytosis agonist. Histological staining, micro-ct, flow cytometry, RT-PCR and Western blot analysis were performed to detect the inflammatory status, alveolar bone loss and related markers in AP models. The data showed that Mφ efferocytosis is observed in the periapical tissues and enhancing the Mφ efferocytosis ability could effectively promote AP resolution via facilitating M2 Mφ polarization. Collectively, our study demonstrates the functional importance of Mφ efferocytosis in AP pathology and highlights that accelerating Mφ efferocytosis via ARA290 could serve as an adjuvant therapeutic strategy for AP.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11011522PMC
http://dx.doi.org/10.3390/ijms25073854DOI Listing

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