炎症
生物
干扰素
神经科学
细胞生物学
信号转导
免疫学
作者
Patrycja M. Forster,Manuel O. Jakob,Dilmurat Yusuf,Marvin Bubeck,Heidi Limberger,Yanjiang Luo,Paula Thieme,Alexandra Polici,Nele Sterczyk,Sotiria Boulekou,Laura P. Bartel,Catalina Cosovanu,Mario Witkowski,Miguel González-Acera,Anja A. Kühl,Carl Weidinger,Imke Atreya,Raja Atreya,Petra Bacher,Christoph Becker
出处
期刊:Neuron
[Cell Press]
日期:2025-03-17
卷期号:113 (9): 1333-1351.e7
被引量:16
标识
DOI:10.1016/j.neuron.2025.02.018
摘要
Enteric infections often cause long-term sequelae, including persistent gastrointestinal symptoms, such as pain, discomfort, or irritable bowel syndrome. The plethora of sensory symptoms indicates that gut-innervating neurons might be directly affected by inflammation. However, sequencing studies of neurons in the gastrointestinal tract are hampered by difficulties in purifying neurons, especially during inflammation. Activating a nuclear GFP tag selectively in neurons enabled sort purification of intrinsic and extrinsic neurons of the gastrointestinal tract in models of intestinal inflammation. Using bulk and single-nucleus RNA sequencing, we mapped the whole transcriptomic landscape and identified a conserved neuronal response to inflammation, which included the interferon signaling and ferroptosis pathway. Deletion of the interferon receptor 1 in neurons regulated ferroptosis, neuronal loss, and consequently gut-transit time. Collectively, this study offers a resource documenting neuronal adaptation to inflammatory conditions and exposes the interferon and ferroptosis pathways as signaling cascades activated in neurons during inflammation.
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