G protein subunit Gγ13-mediated signaling pathway is critical to the inflammation resolution and functional recovery of severely injured lungs
Yi-Hong Li,
Yi-Sen Yang,
Yan-Bo Xue,
Hao Lei,
Sai-Sai Zhang,
Junbin Qian,
Yushi Yao,
Ruhong Zhou,
Liquan Huang
Affiliations
Yi-Hong Li
College of Life Sciences, Zhejiang University, Hangzhou, China
Yi-Sen Yang
College of Life Sciences, Zhejiang University, Hangzhou, China
Yan-Bo Xue
College of Life Sciences, Zhejiang University, Hangzhou, China
Hao Lei
College of Life Sciences, Zhejiang University, Hangzhou, China
Sai-Sai Zhang
College of Life Sciences, Zhejiang University, Hangzhou, China
Junbin Qian
Zhejiang Provincial Key Laboratory of Precision Diagnosis and Therapy for Major Gynecological Diseases, Women’s Hospital, Zhejiang University School of Medicine, Hangzhou, China; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, China; Cancer Center, Zhejiang University, Hangzhou, China
Yushi Yao
Institute of Immunology and Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
Ruhong Zhou
College of Life Sciences, Zhejiang University, Hangzhou, China; Zhejiang University Shanghai Institute for Advanced Study, Shanghai, Shanghai, China
College of Life Sciences, Zhejiang University, Hangzhou, China; Zhejiang University Shanghai Institute for Advanced Study, Shanghai, Shanghai, China; Monell Chemical Senses Center, Philadelphia, United States
Tuft cells are a group of rare epithelial cells that can detect pathogenic microbes and parasites. Many of these cells express signaling proteins initially found in taste buds. It is, however, not well understood how these taste signaling proteins contribute to the response to the invading pathogens or to the recovery of injured tissues. In this study, we conditionally nullified the signaling G protein subunit Gγ13 and found that the number of ectopic tuft cells in the injured lung was reduced following the infection of the influenza virus H1N1. Furthermore, the infected mutant mice exhibited significantly larger areas of lung injury, increased macrophage infiltration, severer pulmonary epithelial leakage, augmented pyroptosis and cell death, greater bodyweight loss, slower recovery, worsened fibrosis and increased fatality. Our data demonstrate that the Gγ13-mediated signal transduction pathway is critical to tuft cells-mediated inflammation resolution and functional repair of the damaged lungs.To our best knowledge, it is the first report indicating subtype-specific contributions of tuft cells to the resolution and recovery.