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组蛋白去乙酰化酶 1 和 2 通过调节肠道上皮细胞分化来抑制肠道炎症反应。

HDAC1 and HDAC2 restrain the intestinal inflammatory response by regulating intestinal epithelial cell differentiation.

机构信息

Département d'anatomie et Biologie Cellulaire, Faculté de Médecine et des Sciences de la Santé, Pavillon de recherche appliquée sur le cancer, Université de Sherbrooke, Sherbrooke, Québec, Canada.

出版信息

PLoS One. 2013 Sep 5;8(9):e73785. doi: 10.1371/journal.pone.0073785. eCollection 2013.

Abstract

Acetylation and deacetylation of histones and other proteins depends on histone acetyltransferases and histone deacetylases (HDACs) activities, leading to either positive or negative gene expression. HDAC inhibitors have uncovered a role for HDACs in proliferation, apoptosis and inflammation. However, little is known of the roles of specific HDACs in intestinal epithelial cells (IEC). We investigated the consequences of ablating both HDAC1 and HDAC2 in murine IECs. Floxed Hdac1 and Hdac2 homozygous mice were crossed with villin-Cre mice. Mice deficient in both IEC HDAC1 and HDAC2 weighed less and survived more than a year. Colon and small intestinal sections were stained with hematoxylin and eosin, or with Alcian blue and Periodic Acid Schiff for goblet cell identification. Tissue sections from mice injected with BrdU for 2 h, 14 h and 48 h were stained with anti-BrdU. To determine intestinal permeability, 4-kDa FITC-labeled dextran was given by gavage for 3 h. Microarray analysis was performed on total colon RNAs. Inflammatory and IEC-specific gene expression was assessed by Western blot or semi-quantitative RT-PCR and qPCR with respectively total colon protein and total colon RNAs. HDAC1 and HDAC2-deficient mice displayed: 1) increased migration and proliferation, with elevated cyclin D1 expression and phosphorylated S6 ribosomal protein, a downstream mTOR target; 2) tissue architecture defects with cell differentiation alterations, correlating with reduction of secretory Paneth and goblet cells in jejunum and goblet cells in colon, increased expression of enterocytic markers such as sucrase-isomaltase in the colon, increased expression of cleaved Notch1 and augmented intestinal permeability; 3) loss of tissue homeostasis, as evidenced by modifications of claudin 3 expression, caspase-3 cleavage and Stat3 phosphorylation; 4) chronic inflammation, as determined by inflammatory molecular expression signatures and altered inflammatory gene expression. Thus, epithelial HDAC1 and HDAC2 restrain the intestinal inflammatory response, by regulating intestinal epithelial cell proliferation and differentiation.

摘要

组蛋白和其他蛋白质的乙酰化和去乙酰化依赖于组蛋白乙酰转移酶和组蛋白去乙酰化酶 (HDACs) 的活性,导致基因表达呈阳性或阴性。HDAC 抑制剂揭示了 HDACs 在增殖、凋亡和炎症中的作用。然而,人们对特定 HDACs 在肠上皮细胞 (IEC) 中的作用知之甚少。我们研究了在鼠 IEC 中消除 HDAC1 和 HDAC2 的后果。Floxed Hdac1 和 Hdac2 纯合子小鼠与 villin-Cre 小鼠交配。缺乏两种 IEC HDAC1 和 HDAC2 的小鼠体重减轻,寿命超过一年。用苏木精和伊红、或用阿尔辛蓝和过碘酸希夫染色法对杯状细胞进行鉴定,对结肠和小肠切片进行染色。用 BrdU 注射 2 h、14 h 和 48 h 的小鼠组织切片用抗 BrdU 染色。用 4-kDa FITC 标记的葡聚糖进行灌胃 3 h 以确定肠道通透性。对总结肠 RNA 进行微阵列分析。通过 Western blot 或半定量 RT-PCR 和 qPCR 分别用总结肠蛋白和总结肠 RNA 评估炎症和 IEC 特异性基因表达。HDAC1 和 HDAC2 缺陷型小鼠表现出:1)迁移和增殖增加,cyclin D1 表达和磷酸化 S6 核糖体蛋白增加,这是下游 mTOR 靶标;2)组织结构缺陷,伴有细胞分化改变,与空肠中分泌型 Paneth 和杯状细胞减少以及结肠中杯状细胞减少、结肠中蔗糖酶-异麦芽糖酶等肠细胞标记物表达增加、Notch1 切割增加和肠道通透性增加相关;3)组织稳态丧失,表现为 Claudin 3 表达、半胱天冬酶-3 切割和 Stat3 磷酸化的改变;4)炎症分子表达谱和炎症基因表达改变表明慢性炎症。因此,上皮细胞 HDAC1 和 HDAC2 通过调节肠上皮细胞增殖和分化来抑制肠道炎症反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d724/3764035/39af3af98688/pone.0073785.g001.jpg

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