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Activation and Immune Regulation Mechanisms of PYHIN Family During Microbial Infection

Journal

FRONTIERS IN MICROBIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.809412

Keywords

innate immunity; PRR; PAMP; PYHIN family; AIM2; IFI16; p202; p204

Categories

Funding

  1. National Natural Science Fund for Young Scholars [31800639]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB29030104]
  3. National Natural Science Foundation of China [32071213, 31870731, 31971129]
  4. Fundamental Research Funds for the Central Universities
  5. Shaanxi Provincial Scientific and Technological Activities Funding Project [2020001]
  6. Young Talent Program of Xi'an Jiaotong University

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This article summarizes the recent advances in understanding the activation and immune regulation mechanisms of the PYHIN family during microbial infection, and provides accurate insights into the signaling mechanisms of PYHIN family receptors through structural characterizations of AIM2, IFI16, p202, and p204.
The innate immune system defenses against pathogen infections via patten-recognition receptors (PRRs). PRRs initiate immune responses by recognizing pathogen-associated molecular patterns (PAMPs), including peptidoglycan, lipopolysaccharide, and nucleic acids. Several nucleic acid sensors or families have been identified, such as RIG-I-like receptors (RLRs), Toll-like receptors (TLRs), cyclic GMP-AMP synthase (cGAS), and PYHIN family receptors. In recent years, the PYHIN family cytosolic DNA receptors have increased attention because of their important roles in initiating innate immune responses. The family members in humans include Absent in melanoma 2 (AIM2), IFN-gamma inducible protein 16 (IFI16), interferon-inducible protein X (IFIX), and myeloid cell nuclear differentiation antigen (MNDA). The PYHIN family members are also identified in mice, including AIM2, p202, p203, p204, and p205. Herein, we summarize recent advances in understanding the activation and immune regulation mechanisms of the PYHIN family during microbial infection. Furthermore, structural characterizations of AIM2, IFI16, p202, and p204 provide more accurate insights into the signaling mechanisms of PYHIN family receptors. Overall, the molecular details will facilitate the development of reagents to defense against viral infections.

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