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家族性地中海热相关吡喃突变抑制 SW982 滑膜肉瘤细胞炎症小体非依赖性白细胞介素-8 分泌的缺陷。

Defect of suppression of inflammasome-independent interleukin-8 secretion from SW982 synovial sarcoma cells by familial Mediterranean fever-derived pyrin mutations.

机构信息

Department of Molecular Pathology, Shinshu University Graduate School of Medicine, Matsumoto, Nagano, 390-8621, Japan.

出版信息

Mol Biol Rep. 2014 Jan;41(1):545-53. doi: 10.1007/s11033-013-2890-y. Epub 2013 Dec 7.

Abstract

Familial Mediterranean fever (FMF) is a recessive inherited autoinflammatory syndrome. Patients with FMF have symptoms such as recurrent fever and abdominal pain, sometimes accompanied by arthralgia. Biopsy specimens have revealed substantial neutrophil infiltration into synovia. FMF patients have a mutation in the Mediterranean fever gene, encoding pyrin, which is known to regulate the inflammasome, a platform for processing interleukin (IL)-1β. FMF patients heterozygous for E148Q mutation, heterozygous for M694I mutation, or combined heterozygous for E148Q and M694I mutations, which were found to be major mutations in an FMF study group in Japan, suffer from arthritis, the severity of which is likely to be lower than in FMF patients with M694V mutations. Expression plasmids of wild-type (WT) pyrin and mutated pyrin, such as E148Q, M694I, M694V, and E148Q+M694I, were constructed, and SW982 synovial sarcoma cells were transfected with these expression plasmids. IL-8 and IL-6 were spontaneously secreted from the culture supernatant of SW982 cells without any stimulation, whereas IL-1β and TNF-α could not be detected even when stimulated with lipopolysaccharide. Notably, two inflammasome components, ASC and caspase-1, could not be detected in SW982 cells by Western blotting. IL-8 but not IL-6 secretion from SW982 cells was largely suppressed by WT pyrin, but less suppressed by mutated pyrin, which appeared to become weaker in the order of E148Q, M694I, E148Q+M694I, and M694V mutations. As for IL-8 and IL-6, similar results were obtained using stable THP-1 cells expressing the WT pyrin or mutated pyrins, such as M694V or E148Q, when stimulated by LPS. In addition, IL-8 secretion from mononuclear cells of FMF patients was significantly higher than that of healthy volunteers when incubated on a culture plate. Thus, our results suggest that IL-8 secretion from SW982 synovial sarcoma cells suppressed by pyrin independently of inflammasome is affected by pyrin mutations, which may reflect the activity in FMF arthritis.

摘要

家族性地中海热(FMF)是一种隐性遗传性自身炎症综合征。FMF 患者有反复发作的发热和腹痛等症状,有时伴有关节炎。活检标本显示滑膜中有大量中性粒细胞浸润。FMF 患者的地中海热基因发生突变,导致 pyrin 编码异常,该基因已知可调节炎症小体,炎症小体是加工白细胞介素(IL)-1β的平台。在日本的 FMF 研究组中发现,E148Q 突变杂合子、M694I 突变杂合子或 E148Q 和 M694I 突变的复合杂合子的 FMF 患者会发生关节炎,其严重程度可能低于 M694V 突变的 FMF 患者。构建了野生型(WT)pyrin 和突变型 pyrin(如 E148Q、M694I、M694V 和 E148Q+M694I)的表达质粒,并将这些表达质粒转染至 SW982 滑膜肉瘤细胞。SW982 细胞在没有任何刺激的情况下,培养上清液中可自发分泌 IL-8 和 IL-6,但即使在脂多糖刺激下,也无法检测到 IL-1β和 TNF-α。值得注意的是,通过 Western blot 无法在 SW982 细胞中检测到两种炎症小体成分 ASC 和 caspase-1。WT pyrin 可显著抑制 SW982 细胞分泌 IL-8,但对突变型 pyrin 的抑制作用较小,其抑制作用按 E148Q、M694I、E148Q+M694I 和 M694V 突变的顺序减弱。对于 IL-8 和 IL-6,当用 LPS 刺激时,在表达 WT pyrin 或突变型 pyrin(如 M694V 或 E148Q)的稳定 THP-1 细胞中也得到了类似的结果。此外,当在培养板上孵育时,FMF 患者的单核细胞分泌的 IL-8 明显高于健康志愿者。因此,我们的研究结果表明,SW982 滑膜肉瘤细胞中炎症小体不依赖 pyrin 抑制的 IL-8 分泌受 pyrin 突变的影响,这可能反映了 FMF 关节炎的活性。

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