IL-4诱导中央巨细胞病变中多核巨细胞的形成和β5整合素的表达

A. Aghbali, Sona Rafieyan, Leila Mohamed-Khosroshahi, B. Baradaran, D. Shanehbandi, M. Kouhsoltani
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Isolated monocytes were then cultured in the absence or presence of IL-4 (10 and 20 ng/mL), and following RNA extraction and cDNA synthesis, Real-time PCR was performed to determine the level of β5 integrin expression. The formation of CGCGs and morphological analyses were done under light microscopy. For confirmation of CGCGs, immunocytochemistry technique was also carried out by anti-RANK (receptor-activator of NF-κB ligand) antibody. Results In both patient and control groups, β5 levels were significantly enhanced by increasing the IL-4 dose from 10 to 20 ng/mL. In addition, these differences were significant between patient and control groups without IL-4 treatment. On the other hand, the number of cells which expressed RANK and therefore the number of giant cells were significantly higher in the patient group in comparison to controls, as assessed by immunohistochemistry evaluations. 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引用次数: 8

摘要

目前已经确定,IL-4通过诱导单核细胞表面整合素的表达,在单核细胞向多核巨细胞(MGCs)的发育过程中起着核心作用。本研究的目的是探讨IL-4在巨细胞肉芽肿患者外周血样品中诱导β5整合素表达的潜在作用。材料与方法采用人单核细胞分离试剂盒ⅱ从中枢性巨细胞肉芽肿(CGCG)患者和正常人外周血中分离单核细胞。将分离的单核细胞在IL-4(10和20 ng/mL)缺失或存在的情况下进行培养,提取RNA和合成cDNA后,采用Real-time PCR检测β5整合素的表达水平。光镜下观察ccggs的形成和形态分析。通过免疫细胞化学技术检测NF-κB配体受体激活物(receptor-activator of NF-κB ligand)抗体,确认cgcg的存在。结果IL-4剂量从10 ~ 20 ng/mL均可显著提高患者和对照组β5水平。此外,这些差异在未接受IL-4治疗的患者和对照组之间具有显著性。另一方面,通过免疫组织化学评估,与对照组相比,患者组中表达RANK的细胞数量和巨细胞数量明显更高。在本研究中,我们发现在IL-4刺激下β5整合素的表达水平升高。研究表明,这种整合素在巨噬细胞与巨噬细胞融合和巨细胞发育过程中起着重要的调节作用。关键词:β5整合素,巨细胞,Il-4,单核细胞,等级
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IL-4 induces the formation of multinucleated giant cells and expression of β5 integrin in central giant cell lesion
Background It is now well established that IL-4 has a central role in the development of monocytes to multinucleated giant cells (MGCs) by inducing the expression of integrins on the surface of monocytes. The aim of this study was to investigate the potential role of IL-4 in induction of β5 integrin expression in the peripheral blood samples of patients with giant cell granuloma. Material and Methods Monocytes were isolated from peripheral blood samples of patients with central giant cell granuloma (CGCG) and healthy controls using human Monocyte Isolation Kit II. Isolated monocytes were then cultured in the absence or presence of IL-4 (10 and 20 ng/mL), and following RNA extraction and cDNA synthesis, Real-time PCR was performed to determine the level of β5 integrin expression. The formation of CGCGs and morphological analyses were done under light microscopy. For confirmation of CGCGs, immunocytochemistry technique was also carried out by anti-RANK (receptor-activator of NF-κB ligand) antibody. Results In both patient and control groups, β5 levels were significantly enhanced by increasing the IL-4 dose from 10 to 20 ng/mL. In addition, these differences were significant between patient and control groups without IL-4 treatment. On the other hand, the number of cells which expressed RANK and therefore the number of giant cells were significantly higher in the patient group in comparison to controls, as assessed by immunohistochemistry evaluations. Conclusions In this study, we showed an elevation in the expression levels of β5 integrin when stimulated by IL-4. It is strongly indicated that this integrin acts as an important mediator during macrophage to macrophage fusion and development of giant cells. Key words:β5 integrin, giant cell, Il-4, monocyte, rank.
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