NLRP3 ablation enhances tolerance in heat stroke pathology by inhibiting IL-1β-mediated neuroinflammation

• Published in: Journal of neuroinflammation 2021-06, Vol.18 (1), p.128-128, Article 128
• Main Authors: Zhang, Zi-Teng, Gu, Xiao-Lei, Zhao, Xin, He, Xian, Shi, Hao-Wei, Zhang, Kun, Zhang, Yi-Ming, Su, Yi-Nan, Zhu, Jiang-Bo, Li, Zhi-Wei, Li, Guo-Bao
• Format: Article
• Language: English
• Subjects: Animals; Antibodies; Antibodies, Neutralizing - therapeutic use; Body temperature; Brain - metabolism; Brain - pathology; Cytokines; Disease Models, Animal; Experiments; Heat; Heat Stroke - complications; Heat Stroke - drug therapy; Heat Stroke - pathology; Heat Stroke - physiopathology; Heat tolerance; Heat treatments; Heatstroke; Humidity; Hyperthermia; Hypothalamus; IL-1β; Immunological tolerance; Infections; Inflammasomes; Inflammasomes - metabolism; Inflammation; Injection; Interleukin-1beta - immunology; Interleukin-1beta - metabolism; Laboratory animals; Lipopolysaccharides; Lipoteichoic acid; Male; Medical research; Mice; Mice, Inbred C57BL; Mice, Knockout; Neuroinflammation; Neuroinflammatory Diseases - complications; Neuroinflammatory Diseases - metabolism; NLR Family, Pyrin Domain-Containing 3 Protein - deficiency; NLR Family, Pyrin Domain-Containing 3 Protein - genetics; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism; NLRP3 inflammasome; Proteins; Signal Transduction; Stroke; Survival; Teichoic Acids; Thermotolerance; Tumor necrosis factor-TNF
• ISSN: 1742-2094; 1742-2094
• DOI: 10.1186/s12974-021-02179-y

Patients with prior illness are more vulnerable to heat stroke-induced injury, but the underlying mechanism is unknown. Recent studies suggested that NLRP3 inflammasome played an important role in the pathophysiology of heat stroke. In this study, we used a classic animal heat stroke model. Prior infection was mimicked by using lipopolysaccharide (LPS) or lipoteichoic acid (LTA) injection before heat stroke (LPS/LTA 1 mg/kg). Mice survival analysis curve and core temperature (T ) elevation curve were produced. NLRP3 inflammasome activation was measured by using real-time PCR and Western blot. Mice hypothalamus was dissected and neuroinflammation level was measured. To further demonstrate the role of NLRP3 inflammasome, Nlrp3 knockout mice were used. In addition, IL-1β neutralizing antibody was injected to test potential therapeutic effect on heat stroke. Prior infection simulated by LPS/LTA injection resulted in latent inflammation status presented by high levels of cytokines in peripheral serum. However, LPS/LTA failed to cause any change in animal survival rate or body temperature. In the absence of LPS/LTA, heat treatment induced heat stroke and animal death without significant systemic or neuroinflammation. Despite a decreased level of IL-1β in hypothalamus, Nlrp3 knockout mice demonstrated no survival advantage under mere heat exposure. In animals with prior infection, their heat tolerance was severely impaired and NLRP3 inflammasome induced neuroinflammation was detected. The use of Nlrp3 knockout mice enhanced heat tolerance and alleviated heat stroke-induced death by reducing mice hypothalamus IL-1β production with prior infection condition. Furthermore, IL-1β neutralizing antibody injection significantly extended endotoxemic mice survival under heat stroke. Based on the above results, NLRP3/IL-1β induced neuroinflammation might be an important mechanistic factor in heat stroke pathology, especially with prior infection. IL-1β may serve as a biomarker for heat stroke severity and potential therapeutic method.