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肠道炎症对小鼠回肠中生长抑素受体亚型细胞特异性表达的影响。

Effect of intestinal inflammation on the cell-specific expression of somatostatin receptor subtypes in the murine ileum.

作者信息

Van Op den Bosch J, van Nassauw L, Lantermann K, van Marck E, Timmermans J-P

机构信息

Laboratory of Cell Biology and Histology, Department of Veterinary Sciences, University of Antwerp, Antwerp, Belgium.

出版信息

Neurogastroenterol Motil. 2007 Jul;19(7):596-606. doi: 10.1111/j.1365-2982.2007.00931.x.

Abstract

Despite our knowledge of somatostatin (SOM) in gastrointestinal functions, little information is available on the SOM receptors (SSTRs) mediating these effects. This study focussed on the expression of SSTRs in non-inflamed and Schistosoma mansoni-infected murine ileum using immunocytochemistry, reverse transcriptase (RT)-PCR and quantitative real time RT-PCR (qPCR). In the non-inflamed ileum, SSTRs showed a widespread, cell-type specific expression pattern. For instance, SSTR2A immunoreactivity was detected in a minor population of submucous but not myenteric glial cells. In the inflamed ileum, significant changes in the expression pattern of SSTRs occurred, with SSTR1 and SSTR3 expression on mucosal mast cells (MMCs) and mucosal nerve fibres. SSTR4-immunoreactive nerve fibres were detected in granulomas and the lamina propria. qPCR experiments indicated significantly increased mRNA levels for SOM, SSTR1 and SSTR3 in inflamed ileum. This study reveals that SSTRs are expressed in specific cell types in murine ileum. Expression of SSTR1 and SSTR3 on MMCs and increased density of SOM-expressing nerve fibres in the lamina propria during inflammation, support the hypothesis that SOM is implicated in the physiological control of MMCs during intestinal inflammation. Evidence is provided that in mouse mainly SSTR1, SSTR3 and SSTR4 are involved in the somatostatinergic inflammatory effects during intestinal schistosomiasis.

摘要

尽管我们了解生长抑素(SOM)在胃肠功能中的作用,但关于介导这些效应的生长抑素受体(SSTRs)的信息却很少。本研究利用免疫细胞化学、逆转录(RT)-PCR和定量实时RT-PCR(qPCR),聚焦于SSTRs在未感染曼氏血吸虫的非炎症小鼠回肠以及感染曼氏血吸虫的小鼠回肠中的表达情况。在非炎症回肠中,SSTRs呈现出广泛的、细胞类型特异性的表达模式。例如,在少数黏膜下神经胶质细胞而非肌间神经胶质细胞中检测到了SSTR2A免疫反应性。在炎症回肠中,SSTRs的表达模式发生了显著变化,SSTR1和SSTR3在黏膜肥大细胞(MMCs)和黏膜神经纤维上表达。在肉芽肿和固有层中检测到了SSTR4免疫反应性神经纤维。qPCR实验表明,炎症回肠中SOM、SSTR1和SSTR3的mRNA水平显著升高。本研究揭示,SSTRs在小鼠回肠的特定细胞类型中表达。炎症期间,MMCs上SSTR1和SSTR3的表达以及固有层中表达SOM的神经纤维密度增加,支持了SOM参与肠道炎症期间MMCs生理调控的假说。有证据表明,在小鼠中,主要是SSTR1、SSTR3和SSTR4参与了肠道血吸虫病期间生长抑素能的炎症效应。

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