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. Author manuscript; available in PMC: 2022 Jul 29.
Published in final edited form as: Immunity. 2022 Jul 12;55(7):1327. doi: 10.1016/j.immuni.2022.06.011

Epithelial STAT6 O-GlcNAcylation drives a concerted anti-helminth alarmin response dependent on tuft cell hyperplasia and Gasdermin C

Ming Zhao, Kaiqun Ren, Xiwen Xiong, Yue Xin, Yujie Zou, Jason C Maynard, Angela Kim, Alexander P Battist, Navya Koneripalli, Yusu Wang, Qianyue Chen, Ruyue Xin, Chenyan Yang, Rong Huang, Jiahui Yu, Zan Huang, Zengdi Zhang, Haiguang Wang, Daoyuan Wang, Yihui Xiao, Oscar C Salgado, Nicholas N Jarjour, Kristin A Hogquist, Xavier S Revelo, Alma L Burlingame, Xiang Gao, Jakob von Moltke, Zhaoyu Lin *, Hai-Bin Ruan *
PMCID: PMC9336012  NIHMSID: NIHMS1822998  PMID: 35830826

In our recent paper entitled “Epithelial STAT6 O-GlcNAcylation drives anti-helminth immunity via a concerted anti-helminth alarmin response dependent on tuft cell hyperplasia and Gasdermin C” (Immunity 55:623–638 2022), we reported the role of GSDMC in serving as a conduit for the release of interleukin-33 from intestinal epithelial cells. We relied on a mouse strain lacking the 4 Gsdmc genes to support our conclusion. Regrettably, we referred incorrectly to a different strain in the STAR Methods and did not include the genetic characterization of the Gsdmc1,2,3,4-flox mouse strain in our article. This information is now accessible as a supplemental file (Methods S1). The authors apologize for any confusion the absence of this information may have created.

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