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Gasdermin D介导的中性粒细胞焦亡驱动银屑病炎症。

Gasdermin D-mediated neutrophil pyroptosis drives inflammation in psoriasis.

作者信息

Liu Jian, Jiang YuYing, Diao ZiYue, Chen DanDan, Xia RuiYuan, Wang BingWei, Yang Shuo, Yin ZhiQiang

机构信息

Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Immunology, State Key Laboratory of Reproductive Medicine and Offspring Health, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Personalized Cancer Medicine, Gusu School, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi People's Hospital, Wuxi Medical Center, Nanjing Medical University, Nanjing, China.

出版信息

Elife. 2024 Dec 24;13:RP101248. doi: 10.7554/eLife.101248.

Abstract

Psoriasis is a multifactorial immune-mediated inflammatory disease. Its pathogenesis involves abnormal accumulation of neutrophils and T-cell-related abnormalities. Pyroptosis is a type of regulated cell death associated with innate immunity, but its role in psoriasis is unclear. In this study, we found that ) is higher in human psoriatic skin than that in normal skin, and in imiquimod-induced psoriasis-like mouse skin, the expression of was most significantly altered in neutrophils and was also mainly expressed in neutrophils. Immunohistochemical staining of serial sections of skin lesions from psoriasis patients and healthy control also showed that GSDMD expression is higher in psoriasis lesion, especially in neutrophils. deficiency mitigates psoriasis-like inflammation in mice. GSDMD in neutrophils contributes to psoriasis-like inflammation, while depletion in neutrophils attenuates the development of skin inflammation in psoriasis and reduces the release of the inflammatory cytokines. We found that neutrophil pyroptosis is involved in and contributes to psoriasis inflammation, which provides new insights into the treatment of psoriasis by targeting neutrophil pyroptosis.

摘要

银屑病是一种多因素免疫介导的炎症性疾病。其发病机制涉及中性粒细胞的异常聚集和T细胞相关异常。细胞焦亡是一种与固有免疫相关的程序性细胞死亡,但它在银屑病中的作用尚不清楚。在本研究中,我们发现人银屑病皮肤中的(此处原文缺失具体内容)高于正常皮肤,在咪喹莫特诱导的银屑病样小鼠皮肤中,(此处原文缺失具体内容)的表达在中性粒细胞中变化最为显著,且(此处原文缺失具体内容)也主要在中性粒细胞中表达。对银屑病患者和健康对照的皮肤病变连续切片进行免疫组织化学染色也显示,银屑病病变中GSDMD表达较高,尤其是在中性粒细胞中。(此处原文缺失具体内容)缺陷减轻了小鼠的银屑病样炎症。中性粒细胞中的GSDMD促成银屑病样炎症,而中性粒细胞中的(此处原文缺失具体内容)耗竭减弱了银屑病皮肤炎症的发展并减少了炎性细胞因子的释放。我们发现中性粒细胞焦亡参与并促成银屑病炎症,这为通过靶向中性粒细胞焦亡治疗银屑病提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4baa/11668524/b16babc1fb1b/elife-101248-fig1.jpg

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