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Jnk2 缺失通过差异调节 RNA 结合蛋白 HuR 和 CUGBP1 破坏肠道黏膜稳态和成熟。

Jnk2 deletion disrupts intestinal mucosal homeostasis and maturation by differentially modulating RNA-binding proteins HuR and CUGBP1.

机构信息

Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland; Baltimore Veterans Affairs Medical Center, Baltimore, Maryland.

Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Maryland School of Medicine, Baltimore, Maryland;

出版信息

Am J Physiol Cell Physiol. 2014 Jun 15;306(12):C1167-75. doi: 10.1152/ajpcell.00093.2014. Epub 2014 Apr 16.

Abstract

Homeostasis and maturation of the mammalian intestinal epithelium are preserved through strict regulation of cell proliferation, apoptosis, and differentiation, but the exact mechanism underlying this process remains largely unknown. c-Jun NH2-terminal kinase 2 (JNK2) is highly expressed in the intestinal mucosa, and its activation plays an important role in proliferation and also mediates apoptosis in cultured intestinal epithelial cells (IECs). Here, we investigated the in vivo function of JNK2 in the regulation of intestinal epithelial homeostasis and maturation by using a targeted gene deletion approach. Targeted deletion of the jnk2 gene increased cell proliferation within the crypts in the small intestine and disrupted mucosal maturation as indicated by decreases in the height of villi and the villus-to-crypt ratio. JNK2 deletion also decreased susceptibility of the intestinal epithelium to apoptosis. JNK2-deficient intestinal epithelium was associated with an increase in the level of the RNA-binding protein HuR and with a decrease in the abundance of CUG-binding protein 1 (CUGBP1). In studies in vitro, JNK2 silencing protected intestinal epithelial cell-6 (IEC-6) cells against apoptosis and this protection was prevented by inhibiting HuR. Ectopic overexpression of CUGBP1 repressed IEC-6 cell proliferation, whereas CUGBP1 silencing enhanced cell growth. These results indicate that JNK2 is essential for maintenance of normal intestinal epithelial homeostasis and maturation under biological conditions by differentially modulating HuR and CUGBP1.

摘要

哺乳动物肠道上皮细胞的稳态和成熟是通过严格调节细胞增殖、凋亡和分化来维持的,但这一过程的确切机制在很大程度上仍不清楚。c-Jun NH2-末端激酶 2(JNK2)在肠道黏膜中高度表达,其激活在增殖中发挥重要作用,也介导培养的肠上皮细胞(IECs)中的凋亡。在这里,我们通过靶向基因缺失方法研究了 JNK2 在调节肠道上皮细胞稳态和成熟中的体内功能。jnk2 基因的靶向缺失增加了小肠隐窝内的细胞增殖,并破坏了黏膜成熟,表现为绒毛高度和绒毛-隐窝比降低。JNK2 缺失还降低了肠道上皮细胞对凋亡的敏感性。JNK2 缺陷的肠道上皮细胞与 RNA 结合蛋白 HuR 水平升高和 CUG 结合蛋白 1(CUGBP1)丰度降低有关。在体外研究中,JNK2 沉默可保护肠上皮细胞-6(IEC-6)细胞免受凋亡,而 HuR 的抑制可阻止这种保护。CUGBP1 的异位过表达抑制 IEC-6 细胞增殖,而 CUGBP1 沉默增强细胞生长。这些结果表明,JNK2 通过差异调节 HuR 和 CUGBP1,在生物学条件下对维持正常肠道上皮细胞稳态和成熟至关重要。

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