1. Academic Validation
  2. Strongylocentrotus nudus Eggs Polysaccharide Enhances Macrophage Phagocytosis Against E.coli Infection by TLR4/STAT3 Axis

Strongylocentrotus nudus Eggs Polysaccharide Enhances Macrophage Phagocytosis Against E.coli Infection by TLR4/STAT3 Axis

  • Front Pharmacol. 2022 Mar 17;13:807440. doi: 10.3389/fphar.2022.807440.
Xinlei Tian 1 Min Guo 1 Xiaoya Zhang 1 Lingfeng Guo 1 Nan Lan 1 Yaojun Cheng 1 Yannan Han 1 Mingxin Wang 1 Zhonglu Peng 2 Changlin Zhou 1 Hongye Fan 1
Affiliations

Affiliations

  • 1 School of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
  • 2 School of Pharmacy, Xiangnan University, Chenzhou, China.
Abstract

Antibiotics resistance is one of the most significant public health threats globally. Strategies that strengthen host defenses to control pathogen Infection has become a hot research field. Macrophages are part of early host defense mechanisms, and are activated via host Pattern Recognition Receptors (PRRs), such as Toll-like Receptor 4 (TLR4), which then facilitates phagocytosis and elimination of invading pathogens. However, few activators of PRRs have been approved for clinical use because of their toxic effects. This study aimed to investigate whether Strongylocentrotus nudus eggs polysaccharide (SEP), a non-toxic extract from seafood, contributes to host defense against Bacterial infection. Results showed that SEP promoted Bacterial clearance by enhancing phagocytosis by macrophages during E. coli Infection in vitro, but was inhibited by TLR4 specific inhibitor TAK-242, STAT3 Inhibitor Stattic or blockade of CD64. In addition, SEP protected mice from E. coli induced mortality, reduced pulmonary inflammation and inhibited dissemination of bacteria to organs, while TAK-242 retarded the protection of SEP. Overall, SEP strengthened innate host defense and improved the outcome in Bacterial infection, suggesting that SEP could be used as a potential immunomodulator in host-directed therapies.

Keywords

SEP; TLR4; infection; macrophage; phagocytosis.

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