Regulation of Macrophage Polarization Through Periodic Photo‐Thermal Treatment to Facilitate Osteogenesis

Abstract The richened reactive oxygen species (ROS) and their derived excessive inflammation at bone injured sites hinder osteogenesis of endosseous Ti‐based implants. Herein, anti‐oxidized polydopamine (PDA) is deposited on hydrothermal growth formed hydroxyapatite (HA) nanorods on Ti to form a core‐shell structural nanorod‐like array with HA as a core and PDA as an amorphous shell (PDA@HA), showing not only ROS scavenging ability but also near‐infrared (NIR) light derived photo‐thermal effects. PDA@HA suppresses inflammation based on its ROS scavenging ability to a certain extent, while periodic photo‐thermal treatment (PTT) at a mild temperature (41 ± 1 °C) further accelerates the transition of the macrophages (MΦs) adhered to PDA@HA from the pro‐inflammatory (M1) phenotype to the anti‐inflammatory (M2) phenotype in vitro and in vivo. Transcriptomic analysis reveals that the activation of the PI3K‐Akt1 signaling pathway is responsible for the periodic PTT induced acceleration of the M1‐to‐M2 transition of MΦs. Acting on mesenchymal stem cells (MSCs) with paracrine cytokines of M2 macrophages, PDA@HA with mild PTT greatly promote the osteogenetic functions of MSCs and thus osteogenesis. This work paves a way of employing mildly periodic PTT to induce a favorable immunomodulatory microenvironment for osteogenesis and provides insights into its underlying immunomodulation mechanism.