Rab11FIP2 controls NLRP3 inflammasome activation through Rab11b

Abstract

Membrane trafficking through the trans-Golgi network has recently been shown to guide activation of the NLRP3 inflammasome. The GTPases Rab11a and Rab11b, and their effector molecule Rab11-FIP2, are regulators of endosome trafficking and retrograde transport. Rab11-FIP2 binds phosphatidylinositol species including PI4P, enriched in the trans-Golgi network and peripheral endosomes following NLRP3 inflammasome activation. We here demonstrate that Rab11-FIP2 and Rab11b, but not Rab11a, control caspase-1 mediated cleavage of pro-IL-1{beta} and GSDMD, and pyroptotic cell death in human macrophages. Rab11-FIP2 also controlled LPS stimulated IKK{beta} activation by TAK1 and IKK{beta} mediated NLRP3 translocation to the trans-Golgi network. Furthermore, we show that NLRP3 bound Rab11-FIP2 via its KMKK motif and that Rab11-FIP2 interacts with NLRP3 via its N-terminal C2-domain. The formation of PI4P positive endosomes and ASC-specks were also controlled by Rab11-FIP2. Collectively our results demonstrate that Rab11-FIP2 and Rab11b control NLRP3 inflammasome activation on early endosomes in human macrophages.