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免疫染色质阅读器 SP140 调节微生物群并增加炎症性肠病风险。

Immune chromatin reader SP140 regulates microbiota and risk for inflammatory bowel disease.

机构信息

Center for the Study of Inflammatory Bowel Disease, Division of Gastroenterology, Department of Medicine, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA; Program in Immunology, Harvard Medical School, Boston, MA 02115, USA.

Center for the Study of Inflammatory Bowel Disease, Division of Gastroenterology, Department of Medicine, Massachusetts General Hospital Research Institute, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.

出版信息

Cell Host Microbe. 2022 Oct 12;30(10):1370-1381.e5. doi: 10.1016/j.chom.2022.08.018. Epub 2022 Sep 20.

Abstract

Inflammatory bowel disease (IBD) is driven by host genetics and environmental factors, including commensal microorganisms. Speckled Protein 140 (SP140) is an immune-restricted chromatin "reader" that is associated with Crohn's disease (CD), multiple sclerosis (MS), and chronic lymphocytic leukemia (CLL). However, the disease-causing mechanisms of SP140 remain undefined. Here, we identify an immune-intrinsic role for SP140 in regulating phagocytic defense responses to prevent the expansion of inflammatory bacteria. Mice harboring altered microbiota due to hematopoietic Sp140 deficiency exhibited severe colitis that was transmissible upon cohousing and ameliorated with antibiotics. Loss of SP140 results in blooms of Proteobacteria, including Helicobacter in Sp140 mice and Enterobacteriaceae in humans bearing the CD-associated SP140 loss-of-function variant. Phagocytes from patients with the SP140 loss-of-function variant and Sp140 mice exhibited altered antimicrobial defense programs required for control of pathobionts. Thus, mutations within this epigenetic reader may constitute a predisposing event in human diseases provoked by microbiota.

摘要

炎症性肠病 (IBD) 由宿主遗传学和环境因素驱动,包括共生微生物。斑点蛋白 140(SP140)是一种免疫受限的染色质“阅读器”,与克罗恩病(CD)、多发性硬化症(MS)和慢性淋巴细胞白血病(CLL)有关。然而,SP140 的致病机制仍未确定。在这里,我们确定了 SP140 在调节吞噬防御反应中的免疫内在作用,以防止炎症细菌的扩张。由于造血 Sp140 缺乏导致微生物群改变的小鼠表现出严重的结肠炎,在共同饲养时可传播,并通过抗生素改善。SP140 的缺失导致变形菌的大量繁殖,包括 Sp140 小鼠中的幽门螺杆菌和携带与 CD 相关的 SP140 功能丧失变异的人类中的肠杆菌科。携带 SP140 功能丧失变异的患者和 Sp140 小鼠的吞噬细胞表现出改变的抗菌防御程序,这是控制病原体所必需的。因此,这个表观遗传读取器中的突变可能构成由微生物引发的人类疾病的易患事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/10266544/8e9c12c0d62e/nihms-1837217-f0001.jpg

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