4.6 Review

The NLRP6 inflammasome

Journal

IMMUNOLOGY
Volume 162, Issue 3, Pages 281-289

Publisher

WILEY
DOI: 10.1111/imm.13293

Keywords

caspase; inflammasome; innate immune receptors; microbiome; NLRP6; pattern recognition receptors

Categories

Funding

  1. European Crohn's and Colitis Organization (ECCO) Fellowship
  2. Ke Lin Program of the First Affiliated Hospital, Sun Yat-sen University
  3. Walter Benjamin fellowship from Deutsche Forschungsgemeinschaft (DFG)

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NLRP6, a member of the NOD-like receptor family, acts as a cytosolic innate immune sensor recognizing microbial patterns. It can form an inflammasome to mediate the maturation and secretion of pro-inflammatory cytokines, but also exerts functions independently of the inflammasome, playing a critical role in maintaining tissue homeostasis.
The NOD-like receptor family pyrin domain containing 6 (NLRP6), a member of the NOD-like receptor (NLR) family, acts as a cytosolic innate immune sensor that recognizes microbe-associated molecular patterns. In some circumstances upon activation, NLRP6 recruits the adaptor apoptosis-associated speck-like protein (ASC) and the inflammatory caspase-1 or caspase-11 to form an inflammasome, which mediates the maturation and secretion of the pro-inflammatory cytokines IL-18 and IL-1 beta. In other contexts, NLRP6 can exert its function in an inflammasome-independent manner. Tight regulation of the NLRP6 inflammasome is critical in maintaining tissue homeostasis, while improper inflammasome activation may contribute to the development of multiple diseases. In intestinal epithelial cells, the NLRP6 inflammasome is suggested to play a role in regulating gut microbiome composition, goblet cell function and related susceptibility to gastrointestinal inflammatory, infectious and neoplastic diseases. Additionally, NLRP6 may regulate extra-intestinal diseases. In this review, we summarize current knowledge on the NLRP6 inflammasome and its activation and regulation patterns, as well as its effector functions contributing to disease modulation. We discuss current challenges in NLRP6 research and future prospects in harnessing its function into potential human interventions.

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