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 PMID:27629921  

IL-13Rα2 uses TMEM219 in chitinase 3-like-1-induced signalling and effector responses.

Chang-Min Lee | Chuan Hua He | Adel M Nour | Yang Zhou | Bing Ma | Jin Wook Park | Kyung Hee Kim | Charles Dela Cruz | Lokesh Sharma | Mahmoud L Nasr | Yorgo Modis | Chun Geun Lee | Jack A Elias
Nature communications | 2016

Recent studies demonstrated that chitinase 3-like-1 (Chi3l1) binds to and signals via IL-13Rα2. However, the mechanism that IL-13Rα2 uses to mediate the effects of Chi3l1 has not been defined. Here, we demonstrate that the membrane protein, TMEM219, is a binding partner of IL-13Rα2 using yeast two-hybrid, co-immunoprecipitation, co-localization and bimolecular fluorescence complementation assays. Furthermore, fluorescence anisotropy nanodisc assays revealed a direct physical interaction between TMEM219 and IL-13Rα2-Chi3l1 complexes. Null mutations or siRNA silencing of TMEM219 or IL-13Rα2 similarly decreased Chi3l1-stimulated epithelial cell HB-EGF production and macrophage MAPK/Erk and PKB/Akt activation. Null mutations of TMEM219 or IL-13Rα2 also phenocopied one another as regards the ability of Chi3l1 to inhibit oxidant-induced apoptosis and lung injury, promote melanoma metastasis and stimulate TGF-β1. TMEM219 also contributed to the decoy function of IL-13Rα2. These studies demonstrate that TMEM219 plays a critical role in Chi3l1-induced IL-13Rα2 mediated signalling and tissue responses.

Pubmed ID: 27629921

Associated grants

  • Agency: Wellcome Trust, United Kingdom
    Id: 101908/Z/13/Z
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL093017
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001863
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL108638
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL115813
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL126094
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL114501

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