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鞘氨醇-1-磷酸受体 2(S1PR2)在维持肠道屏障和诱导溃疡性结肠炎中的作用。

The function of Sphingosine-1-phosphate receptor 2 (S1PR2) in maintaining intestinal barrier and inducing ulcerative colitis.

机构信息

The Department of Gastroenterology and Hepatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, People's Republic of China.

Surgery, The First Affiliated Hospital of Wenzhou Medical UniversityThe Department of Hepato-Pancreato-Biliary, Wenzhou, People's Republic of China.

出版信息

Bioengineered. 2022 May;13(5):13703-13717. doi: 10.1080/21655979.2022.2076500.

Abstract

Sphingosine-1-phosphate receptor 2 (S1PR2) was highly expressed in intestinal epithelial cells (IECs) and facilitated the proliferation of IECs. However, the specific function of S1PR2 in intestinal diseases, such as ulcerative colitis (UC), remains unclear. Accordingly, the current study set out to investigate the function of S1PR2 in maintaining intestinal barrier and inducing UC. S1PR2-overexpressed and knockdown Caco-2 cells were established to explore the function of S1PR2 on the permeability of IECs barrier. The UC-like mouse model in which UC is induced by dextran sulfate sodium (DSS) was established and utilized to investigate the role for S1PR2. The results showed that S1PR2 functioned as a maintainer of IECs permeability and a pathogenic factor for UC. A series of in vitro and in vivo experiments were conducted, and it was found that S1PR2 played an important role in intestinal epithelial cell proliferation and maintenance of intestinal epithelial cell barrier, possibly by the regulation on the expression level of SphK2, HDAC1, HDAC2, and ERK1/2 signaling pathway. The expression of S1PR2 was upregulated in UC mice and the colonic pathological damage in UC mice could be alleviated by the inhibition of S1PR2. Collectively, these results suggest that S1PR2 functions as a maintainer of IECs permeability and a pathogenic factor for UC. The research suggests S1PR2 may be an effective target for developing therapeutic strategies against UC. S1PR2, Sphingosine-1-phosphate receptor 2; UC, ulcerative colitis; IECs, intestinal epithelial cells; DSS, dextran sulfate sodium; IBD, inflammation bowel disease; CD, Crohn's disease; S1P, sphingosin-1-phosphate; SphK, sphingosine kinase; HIECs, human IECs; siRNA, small interfering RNA; CCK-8, cell counting kit-8; TEER, transepithelial electrical resistance; TEM, transmission electron microscope; RT-PCR, real-time reverse transcriptase polymerase-chain reaction; ELISA, enzyme-linked immunosorbent assay; HE, hematoxylin and eosin.

摘要

Sphingosine-1-phosphate receptor 2 (S1PR2) 在肠道上皮细胞 (IECs) 中高度表达,促进 IECs 的增殖。然而,S1PR2 在肠道疾病(如溃疡性结肠炎 (UC))中的具体功能尚不清楚。因此,本研究旨在探讨 S1PR2 在维持肠道屏障和诱导 UC 中的作用。通过建立 S1PR2 过表达和敲低 Caco-2 细胞来研究 S1PR2 对 IECs 屏障通透性的影响。通过葡聚糖硫酸钠 (DSS) 诱导 UC 的 UC 样小鼠模型来研究 S1PR2 的作用。结果表明,S1PR2 是 IECs 通透性的维持因子和 UC 的致病因子。通过一系列体内外实验发现,S1PR2 通过调节 SphK2、HDAC1、HDAC2 和 ERK1/2 信号通路的表达水平,在肠道上皮细胞增殖和维持肠道上皮细胞屏障中发挥重要作用。S1PR2 在 UC 小鼠中表达上调,抑制 S1PR2 可减轻 UC 小鼠的结肠病理损伤。综上所述,S1PR2 是 IECs 通透性的维持因子和 UC 的致病因子。研究表明,S1PR2 可能是治疗 UC 的有效靶点。S1PR2,Sphingosine-1-phosphate receptor 2;UC,溃疡性结肠炎;IECs,肠道上皮细胞;DSS,葡聚糖硫酸钠;IBD,炎症性肠病;CD,克罗恩病;S1P,Sphingosine-1-phosphate;SphK,Sphingosine kinase;HIECs,人 IECs;siRNA,小干扰 RNA;CCK-8,细胞计数试剂盒-8;TEER,跨上皮电阻;TEM,透射电子显微镜;RT-PCR,实时逆转录聚合酶链反应;ELISA,酶联免疫吸附测定;HE,苏木精和伊红。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3c1/9276026/cd9695b0893a/KBIE_A_2076500_UF0001_OC.jpg

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