4.6 Review

COPs and POPs: Modulators of inflammasome activity

Journal

JOURNAL OF IMMUNOLOGY
Volume 179, Issue 12, Pages 7993-7998

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.179.12.7993

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Funding

  1. NIAID NIH HHS [R03AI067806, R21 AI067680-02, R03 AI067806, R21AI067680, R21 AI067680, R03 AI067806-02] Funding Source: Medline
  2. NIGMS NIH HHS [1R01GM071723, R01 GM071723-01A2, R01 GM071723] Funding Source: Medline

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Inflammasomes represent(12) molecular platforms for the activation of inflammatory caspases and are essential for processing and secretion of the inflammatory cytokines IL-1 beta and IL-18. Multiple key proteins of inflammasomes contain caspase recruitment domains (CARDs) or pyrin domains (PYDs). Dissecting CARD- and PYD-mediated interactions substantially improved our understanding of the mechanisms by which these protein platforms are activated and emphasized their essential role during the inflammatory cytokine response. However, their precise regulation is still poorly understood. A family of small proteins that are composed of either a CARD or a PYD only emerged as important inflammasome regulators. These CARD-only proteins (COPs) and PYD-only proteins (POPs) function as endogenous dominant negative proteins that modulate the activity of inflammasomes in response to pathogen infection and tissue destruction. In this review we will summarize the most recent advances in the regulation of inflammasomes and highlight their importance for immunity and inflammatory disease.

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