Nuclear expression of μ-opioid receptors in a human mesothelial cell line

A. Khorram-Manesh, S. Nordlander, A. Novotny, C. Bengtsson, G. Nylund, M. Levin, S. Nordgren, D. S. Delbro
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引用次数: 7

Abstract

1 Possibly acting via μ-opioid receptors (MORs), morphine inhibits the formation of experimentally induced postoperative abdominal adhesions in rats. Mesothelial cells may participate in adhesion formation by secreting mediators that interfere negatively with fibrinolysis. Morphine may prevent adhesions by inhibiting the release of pro-adhesion mediators from mesothelial cells. This study aimed to investigate whether human mesothelial cells express ΜΟR-1; if so, such could constitute a site of action for morphine in adhesion prevention.

2 Cells from Met-5A, a human mesothelial cell line were seeded and prepared for immunocytochemistry and Western blotting.

3 Immunocytochemistry showed MOR-1 expression in mesothelial cells, predominantly in the nuclei. Western blotting showed two bands (c. 35 and 50 kDa) which correspond to those obtained with a control lysate from cells known to express MORs. In addition, we found MOR-1 expression with nuclear and cytoplasmatic localization in biopsies from human abdominal adhesions.

4 The current findings may suggest that morphine could interact directly with mesothelial cells via MOR-1 receptors, and thereby modulate adhesion formation, possibly by interfering with the release of pro-adhesion factors from these cells.

μ-阿片受体在人间皮细胞系中的核表达
1吗啡可能通过μ-阿片受体(MORs)作用,抑制实验性大鼠术后腹腔粘连的形成。间皮细胞可能通过分泌干扰纤维蛋白溶解的介质参与黏附形成。吗啡可能通过抑制间皮细胞中促粘附介质的释放来防止粘连。本研究旨在探讨人间皮细胞是否表达ΜΟR-1;如果是这样,这可能构成吗啡预防粘连的作用部位。2取人间皮细胞系Met-5A细胞进行播种,制备免疫细胞化学和Western blot。3免疫细胞化学显示间皮细胞中有mir -1表达,主要在细胞核中表达。Western blotting显示两个条带(c. 35和50 kDa),对应于从已知表达MORs的细胞中获得的对照裂解物。此外,我们在人腹部粘连的活检中发现了核和细胞质定位的mir -1表达。目前的研究结果可能表明,吗啡可以通过莫尔-1受体直接与间皮细胞相互作用,从而调节粘附形成,可能是通过干扰这些细胞中促粘附因子的释放。
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