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芳烃受体激活通过转录诱导抗菌肽α-防御素1,从而导致肠道微生物群失调和结肠炎的逆转。

AhR Activation Transcriptionally Induces Anti-Microbial Peptide Alpha-Defensin 1 Leading to Reversal of Gut Microbiota Dysbiosis and Colitis.

作者信息

Palrasu Manikandan, Kakar Khadija, Marudamuthu Amarnath, Hamida Hamida, Thada Shruthi, Zhong Yin, Staley Shanieka, Busbee Philip Brandon, Li Jie, Garcia-Buitrago Monica, Nagarkatti Mitzi, Nagarkatti Prakash

机构信息

Department of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, South Carolina, USA.

Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.

出版信息

Gut Microbes. 2025 Dec;17(1):2460538. doi: 10.1080/19490976.2025.2460538. Epub 2025 Feb 2.

Abstract

Alpha-defensin 1 is a small antimicrobial peptide that acts as the first line of defense against pathogens. It is induced following microbial cues and inflammatory signals in neutrophils and Paneth cells in the small intestine, which suggests that it plays a role in microbial homeostasis in the gut. The gut microbial products also serve as ligands for the aryl hydrocarbon receptor (AhR), an environmental sensor. In the current study, we investigated if there is any crosstalk between AhR and alpha-defensin 1. Interestingly, we found a positive correlation between AhR and alpha-defensin 1 protein levels in ileal tissues from active Crohn's' (CD) patients and epithelial cells (IECs) from multiple models of murine colitis. downregulation of AhR led to inhibition of α-defensin 1, while activation of AhR induced α-defensin 1 in IECs. AhR directly targeted the dioxin response element 3 (DRE3) region on the α-defensin 1 promoter in IECs. AhR-mediated induction of α-defensin 1 in colitis mice reversed the gut microbial dysbiosis and alleviated colitis. Our data identify a novel signaling pathway in which AhR acts as a transcription factor for α-defensin 1, leading to regulation of homeostasis between gut microbiota, intestinal mucosa, and mucosal immunity.

摘要

α-防御素1是一种小抗菌肽,作为抵御病原体的第一道防线。它在小肠中的中性粒细胞和潘氏细胞中,受微生物信号和炎症信号诱导产生,这表明它在肠道微生物稳态中发挥作用。肠道微生物产物也是环境传感器芳烃受体(AhR)的配体。在本研究中,我们调查了AhR与α-防御素1之间是否存在相互作用。有趣的是,我们发现活动性克罗恩病(CD)患者回肠组织以及多种小鼠结肠炎模型的上皮细胞(IECs)中,AhR与α-防御素1蛋白水平呈正相关。AhR的下调导致α-防御素1受到抑制,而AhR的激活则在IECs中诱导α-防御素1的产生。AhR直接靶向IECs中α-防御素1启动子上的二噁英反应元件3(DRE3)区域。AhR介导的结肠炎小鼠α-防御素1的诱导逆转了肠道微生物失调并减轻了结肠炎。我们的数据确定了一条新的信号通路,其中AhR作为α-防御素1的转录因子,导致肠道微生物群、肠黏膜和黏膜免疫之间的稳态调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e78/11792800/50ba3f867973/KGMI_A_2460538_F0001_OC.jpg

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