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March 10, 2026Journal of Nanobiotechnology1 citationsOpen Access

Photothermal reprogramming of synovial M1 macrophages reshapes the pro-inflammatory microenvironment to reverse temporomandibular joint osteoarthritis

YWYanyi WangStomatology HospitalJRJiangyan RenStomatology HospitalTRTingyu RenHebei University of Technology

Key Points

  • The aim is to investigate the effects of photothermal reprogramming on synovial M1 macrophages in temporomandibular joint osteoarthritis.
  • Applied mild hyperthermia to reprogram synovial M1 macrophages.
  • Suppressed NF-κB pathway to modify macrophage secretome.
  • Engineered folic acid-conjugated Y8 nanocomposites for targeted therapy.
  • Utilized 808 nm irradiation for localized treatment in an animal model.
  • Attenuation of chondrocyte catabolism and promotion of chondrocyte anabolism observed.
  • Localized photothermal reprogramming significantly reduced cartilage degradation in TMJOA mice.
  • Engineered nanocomposites successfully targeted M1 macrophages.

Abstract

Temporomandibular joint osteoarthritis (TMJOA) involves progressive synovial inflammation-driven cartilage degeneration. While thermotherapy empirically alleviates symptoms, its immunomodulatory mechanism remains elucidated. Here, we revealed that targeted mild hyperthermia reprogramed synovial M1 macrophages via NF-κB pathway suppression, shifting their secretome to attenuate chondrocyte catabolism while enhancing anabolism. This thermally-modified macrophage conditioned medium concurrently promoted osteogenic mineralization. Capitalizing on this, we engineered folic acid-conjugated Y8 nanocomposites (FA-Y8 NPs) for precision M1-targeting photothermal therapy. Under 808 nm irradiation, FA-Y8 NPs achieved localized photothermal reprogramming of synovial M1 macrophages and attenuating cartilage degradation in CFA-induced TMJOA mice. This study reveals thermal immunomodulation of synovial macrophages as a potential mechanism for TMJOA remission and establishes a targeted nanoplatform for spatial control of joint inflammation.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/69af953870916d39fea4c978https://doi.org/10.1186/s12951-026-04258-9
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