Group 2 innate lymphoid cells protect lung endothelial cells from pyroptosis in sepsis

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作者
Dengming Lai
Jing Tang
Linsong Chen
Erica K. Fan
Melanie J. Scott
Yuehua Li
Timothy R. Billiar
Mark A. Wilson
Xiangming Fang
Qiang Shu
Jie Fan
机构
[1] The Children’s Hospital of Zhejiang University School of Medicine,Department of Thoracic and Cardiovascular Surgery
[2] University of Pittsburgh School of Medicine,Department of Surgery
[3] Southern Medical University,Department of Anesthesiology, Nanfang Hospital
[4] Tongji University School of Medicine,Department of Thoracic Surgery, Shanghai Pulmonary Hospital
[5] University of Pittsburgh School of Arts and Science,Research and Development
[6] Veterans Affairs Pittsburgh Healthcare System,McGowan Institute for Regenerative Medicine
[7] University of Pittsburgh,Department of Anesthesiology and Intensive Care Unit, The First Affiliated Hospital
[8] Zhejiang University School of Medicine,undefined
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摘要
Group 2 innate lymphoid cells (ILC2) are one of three subgroups of innate lymphoid cells (ILC1, ILC2, and ILC3), and the major ILC population detected in the lungs. The function of ILC2 in the regulation of lung inflammation remains unclear. In the current study, we explored an important role of ILC2 in protecting lung endothelial cell (EC) from pyroptosis in sepsis-induced acute lung inflammation and the underlying mechanism. Using a cecal ligation and puncture (CLP) mouse sepsis model, we demonstrated that IL-33, which is released in response to sepsis, acting through its receptor ST2 mediates ILC2 expansion in the lungs. We further showed that the increased ILC2 in the lungs secrete IL-9, which in turn prevents lung EC from undergoing pyroptosis, a pro-inflammatory cell death form, by attenuating caspase-1 activation. These findings suggest a previously unidentified innate pathway that negatively regulates lung inflammation following sepsis.
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