Human NLRP1 is a sensor for double-stranded RNA

Author:

Bauernfried Stefan1ORCID,Scherr Matthias J.2ORCID,Pichlmair Andreas34ORCID,Duderstadt Karl E.25ORCID,Hornung Veit12ORCID

Affiliation:

1. Gene Center and Department of Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.

2. Max-Planck Institute of Biochemistry, Martinsried, Germany.

3. Institute of Virology, Technical University of Munich, School of Medicine, Munich, Germany.

4. German Center for Infection Research (DZIF), Munich, Germany.

5. Physics Department, Technical University of Munich, Garching, Germany.

Abstract

A dsRNA detector in the immune toolkit Nod-like receptor (NLR) proteins recognize pathogen-associated molecular patterns within cells, which triggers the formation of signaling complexes called inflammasomes. These complexes then initiate pyroptosis, a highly inflammatory form of cell death. Recent work has shown that a rhinovirus protease can activate the human NLRP1 inflammasome, but it was unclear whether this is the only pathogen-derived trigger for NLRP1. Bauernfried et al. report that long, double-stranded RNA (dsRNA) generated in the course of Semliki Forest virus infection binds and activates NLRP1 in epithelial cells. dsRNA binding triggered NLRP1 to acquire adenosine triphosphatase (ATPase) activity, a common feature of activated NLR proteins. Thus, in addition to its ability to recognize viral protease activity, human NLRP1 can act as a genuine sensor of virus-associated nucleic acids. Science , this issue p. eabd0811

Funder

European Research Council

Deutsche Forschungsgemeinschaft

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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