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Activation and Immune Regulation Mechanisms of PYHIN Family During Microbial Infection

期刊

FRONTIERS IN MICROBIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.809412

关键词

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

资金

  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

向作者/读者索取更多资源

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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