Mitochondrion: an emerging platform critical for host antiviral signaling

Abstract

Introduction: Toll-like receptors (TLRs) and cytoplasmic retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs) are the two major receptor systems for detecting RNA viruses. RLRs play essential roles within the cytosol of various cell types. The signaling pathways converge at the mitochondrial antiviral signalling protein (MAVS) on the outer membrane of mitochondria. Recent research has surprisingly shown that many mitochondrial intrinsic factors play novel functions in RLR signaling, conferring a new perspective of therapeutic drug design to inhibit viral infection.

Areas covered: This review covers the literature of the past 6 years and summarizes the components, regulation and mechanisms of RLR signaling, highlighting the function and regulation of mitochondrial proteins, such as MAVS and translocase of outer membrane (Tom)70 in this process. The authors attempt to delineate the complicated cross-talk among subcellular organelles in the context of intracellular antiviral signaling.

Expert opinion: It is imperative to elucidate the specific roles and mechanisms of post-translational modifications in MAVS signaling. The sub-cellular dynamics of regulatory proteins should be correlated with their multiple functions. Animal models are needed to further probe the integration of mitochondria with innate immunity evolutionarily; they will be instrumental for identifying novel antiviral targets and, ultimately, for developing specific clinical drugs.

Keywords::

• antiviral signal transduction
• IKK
• inflammation
• innate immunity
• IRF3
• MAVS/IPS-1/Cardif/VISA
• mitochondria
• NF-κB
• RIG-I
• TBK1
• Tom70

Acknowledgements

We apologize for our colleagues for the works that are not cited because of the lack of space. We thank X Liu and Y Huang (Shanhai Institute for Biological Sciences) for critical reading of this manuscript.

Notes

This box summarizes key points contained in the article.