Nur77 as a novel regulator of Paneth cell differentiation and function

IF 7.9 2区 医学 Q1 IMMUNOLOGY Mucosal Immunology Pub Date : 2024-08-01 DOI:10.1016/j.mucimm.2023.09.001
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Abstract

Serving as a part of intestinal innate immunity, Paneth cells play an important role in intestinal homeostasis maintenance via their multiple functions. However, the regulation of Paneth cells has been proven to be complex and diverse. Here, we identified nuclear receptor Nur77 as a novel regulator of Paneth cell differentiation and function. Nur77 deficiency led to the loss of Paneth cells in murine ileal crypts. Intestinal tissues or organoids with Nur77 deficiency exhibited the impaired intestinal stem cell niche and failed to enhance antimicrobial peptide expression after Paneth cell degranulation. The defects in Paneth cells and antimicrobial peptides in Nur7−/− mice led to intestinal microbiota disorders. Nur77 deficiency rendered postnatal mice susceptible to necrotizing enterocolitis. Mechanistically, Nur77 transcriptionally inhibited Dact1 expression to activate Wnt signaling activity, thus promoting Paneth cell differentiation and function. Taken together, our data suggest the regulatory role of Nur77 in Paneth cell differentiation and function and reveal a novel Dact1-mediated Wnt inhibition mechanism in Paneth cell development.

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Nur77是Paneth细胞分化和功能的新型调节因子
作为肠道先天性免疫的一部分,Paneth 细胞通过其多种功能在维持肠道平衡方面发挥着重要作用。然而,事实证明对 Paneth 细胞的调控是复杂多样的。在这里,我们发现核受体Nur77是Paneth细胞分化和功能的新型调控因子。Nur77 缺乏会导致小鼠回肠隐窝中 Paneth 细胞的丧失。缺乏Nur77的肠组织或器官组织显示出受损的肠干细胞龛位,并且在Paneth细胞脱颗粒后不能增强抗菌肽的表达。Nur7-/-小鼠Paneth细胞和抗菌肽的缺陷导致肠道微生物群紊乱。缺乏Nur77会使出生后的小鼠易患坏死性小肠结肠炎。从机制上讲,Nur77通过转录抑制Dact1的表达来激活Wnt信号活性,从而促进Paneth细胞的分化和功能。综上所述,我们的数据表明了Nur77在Paneth细胞分化和功能中的调控作用,并揭示了在Paneth细胞发育过程中Dact1介导的新型Wnt抑制机制。
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来源期刊
Mucosal Immunology
Mucosal Immunology 医学-免疫学
CiteScore
16.60
自引率
3.80%
发文量
100
审稿时长
12 days
期刊介绍: Mucosal Immunology, the official publication of the Society of Mucosal Immunology (SMI), serves as a forum for both basic and clinical scientists to discuss immunity and inflammation involving mucosal tissues. It covers gastrointestinal, pulmonary, nasopharyngeal, oral, ocular, and genitourinary immunology through original research articles, scholarly reviews, commentaries, editorials, and letters. The journal gives equal consideration to basic, translational, and clinical studies and also serves as a primary communication channel for the SMI governing board and its members, featuring society news, meeting announcements, policy discussions, and job/training opportunities advertisements.
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