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gasdermin D依赖性中性粒细胞胞外陷阱加剧细胞因子风暴,促进坏疽性脓皮病的发病机制。

Gasdermin D-dependent neutrophil extracellular traps exacerbate cytokine storm contributing to pyoderma gangrenosum pathogenesis.

作者信息

Li Sheng, Ying Shuni, Fang Hong, Qiao Jianjun

机构信息

Department of Dermatology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

出版信息

iScience. 2025 Jan 30;28(3):111925. doi: 10.1016/j.isci.2025.111925. eCollection 2025 Mar 21.

Abstract

Pyoderma gangrenosum (PG) is characterized by the agonizing necrotizing ulcers with non-infectious neutrophil infiltration. Neutrophil extracellular traps (NETs) represent one of the mechanisms of neutrophils activation, and gasdermin D (GSDMD) plays a regulatory role in NETs. In this study, we discovered that the serum levels of NETs were elevated in PG patients compared to healthy controls. Injection of serum from PG patients into the dorsal skin of wild-type mice led to the formation of localized cutaneous ulcers. Furthermore, subsequent modeling demonstrated a significant increase of NETs and GSDMD in skin lesions and peripheral blood serum of wild-type mice. In mice, the severity of skin ulcers after modeling was significantly diminished. Overall, our findings shed light on the role of GSDMD in regulating the production of NETs by neutrophils and the release of inflammatory factors in the pathogenesis of PG and establish an animal model for studying PG.

摘要

坏疽性脓皮病(PG)的特征是伴有非感染性中性粒细胞浸润的剧痛性坏死性溃疡。中性粒细胞胞外陷阱(NETs)是中性粒细胞活化的机制之一,而gasdermin D(GSDMD)在NETs中起调节作用。在本研究中,我们发现与健康对照相比,PG患者血清中NETs水平升高。将PG患者的血清注射到野生型小鼠的背部皮肤会导致局部皮肤溃疡的形成。此外,后续建模显示野生型小鼠皮肤损伤和外周血血清中NETs和GSDMD显著增加。在基因敲除小鼠中,建模后皮肤溃疡的严重程度显著减轻。总体而言,我们的研究结果揭示了GSDMD在调节中性粒细胞产生NETs以及PG发病机制中炎症因子释放方面的作用,并建立了用于研究PG的动物模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11872606/ea8474faa3a0/fx1.jpg

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