A macrophage cell membrane-coated cascade-targeting photothermal nanosystem for combating intracellular bacterial
Jingdi Xiong1, Haiqin Tang2, Lizhong Sun1
1State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.
Abstract:
Current antibacterial interventions encounter formidable challenges when confronting intracellular bacteria, attributable to their clustering within phagocytes, particularly macrophages, evading host immunity and resisting antibiotics. Herein, we have developed an intelligent cell membrane-based nanosystem, denoted as MM@DAu NPs, which seamlessly integrates cascade-targeting capabilities with controllable antibacterial functions for the precise elimination of intracellular bacteria. MM@DAu NPs feature a core comprising D-alanine-functionalized gold nanoparticles (DAu NPs) enveloped by a macrophage cell membrane (MM) coating. Upon administration, MM@DAu NPs harness the intrinsic homologous targeting ability of their macrophage membrane to infiltrate bacteria-infected macrophages. Upon internalization within these host cells, exposed DAu NPs from MM@DAu NPs selectively bind to intracellular bacteria through the bacteria-targeting agent, D-alanine present on DAu NPs. This intricate process establishes a cascade mechanism that efficiently targets intracellular bacteria. Upon exposure to near-infrared irradiation, the accumulated DAu NPs surrounding intracellular bacteria induce local hyperthermia, enabling precise clearance of intracellular bacteria. Further validation in animal models infected with the typical intracellular bacteria, Staphylococcus aureus, substantiates the exceptional cascade-targeting efficacy and photothermal antibacterial potential of MM@DAu NPs in vivo. Therefore, this integrated cell membrane-based cascade-targeting photothermal nanosystem offers a promising approach for conquering persistent intracellular infections without drug resistance risks. STATEMENT OF SIGNIFICANCE: Intracellular bacterial infections lead to treatment failures and relapses because intracellular bacteria could cluster within phagocytes, especially macrophages, evading the host immune system and resisting antibiotics. Herein, we have developed an intelligent cell membrane-based nanosystem MM@DAu NPs, which is designed to precisely eliminate intracellular bacteria through a controllable cascade-targeting photothermal antibacterial approach. MM@DAu NPs combine D-alanine-functionalized gold nanoparticles with a macrophage cell membrane coating. Upon administration, MM@DAu NPs harness the homologous targeting ability of macrophage membrane to infiltrate bacteria-infected macrophages. Upon internalization, exposed DAu NPs from MM@DAu NPs selectively bind to intracellular bacteria through the bacteria-targeting agent, enabling precise clearance of intracellular bacteria through local hyperthermia. This integrated cell membrane-based cascade-targeting photothermal nanosystem offers a promising avenue for conquering persistent intracellular infections without drug resistance risks.
Insights
This study introduces MM@DAu NPs, a novel nanosystem targeting intracellular bacteria within macrophages. It uses a cascade approach and photothermal therapy for effective bacterial elimination, overcoming antibiotic resistance challenges.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Infectious Diseases
Background:
- Intracellular bacteria pose treatment challenges due to evasion of host immunity within phagocytes.
- Current antibiotics are often ineffective against bacteria residing inside host cells, leading to persistent infections.
- Macrophage-mediated infections require specialized therapeutic strategies.
Purpose of the Study:
- To develop an intelligent nanosystem for precise elimination of intracellular bacteria.
- To create a cell membrane-based system with cascade-targeting and photothermal antibacterial functions.
- To overcome limitations of conventional antibacterial treatments for intracellular pathogens.
Main Methods:
- Fabrication of MM@DAu NPs using D-alanine-functionalized gold nanoparticles and macrophage cell membrane coating.
- Utilizing homologous targeting of the macrophage membrane for infiltration into infected macrophages.
- Employing D-alanine for selective binding to intracellular bacteria and near-infrared irradiation for photothermal therapy.
- In vivo validation in Staphylococcus aureus-infected animal models.
Main Results:
- MM@DAu NPs demonstrated effective homologous targeting and infiltration into infected macrophages.
- The cascade-targeting mechanism successfully localized D-alanine-functionalized gold nanoparticles to intracellular bacteria.
- Photothermal therapy induced by near-infrared irradiation achieved precise clearance of intracellular bacteria.
- In vivo studies confirmed the efficacy of MM@DAu NPs against Staphylococcus aureus infections.
Conclusions:
- The developed MM@DAu NPs nanosystem offers a promising strategy for treating persistent intracellular bacterial infections.
- This approach combines cell membrane biomimicry, cascade targeting, and photothermal therapy for enhanced antibacterial efficacy.
- The nanosystem shows potential for overcoming drug resistance and improving treatment outcomes for challenging infections.
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