First Department of Internal Medicine, Democritus University of Thrace, Alexandroupolis, Greece.
Hum Immunol. 2011 Feb;72(2):135-8. doi: 10.1016/j.humimm.2010.11.006. Epub 2010 Dec 7.
Familial Mediterranean fever (FMF) inflammatory attacks are often triggered by metabolic or physical stress. mTOR signaling and autophagy modulate cellular responses to metabolic danger signals. In this study, we investigated the implication of mTOR inhibition and autophagy in FMF pathophysiology. mTOR inhibition induced MEFV gene expression in polymorphonuclear cells (PMNs) from healthy individuals, whereas it had no effect on PMNs from attack-free FMF patients. A significant reduction in pyrin levels in PMNs from FMF patients after mTOR inhibition was also observed. Pyrin levels in control PMNs remained unaffected. Moreover, the basal autophagic status in PMNs from FMF patients was reduced, as indicated by the lower LC3B-II/I ratio and ATG mRNA expression levels. However, mTOR inhibition had similar effects on the induction of autophagy in the two groups. The differential pyrin expression after metabolic stress induction and the impaired basal autophagy suggest a potential role in the triggering of FMF attacks.
家族性地中海热(FMF)炎症发作通常由代谢或物理应激引发。mTOR 信号和自噬调节细胞对代谢危险信号的反应。在这项研究中,我们研究了 mTOR 抑制和自噬在 FMF 病理生理学中的作用。mTOR 抑制诱导健康个体中性粒细胞(PMN)中 MEFV 基因表达,而对无攻击 FMF 患者的 PMN 无影响。mTOR 抑制后还观察到 FMF 患者 PMN 中 pyrin 水平显著降低。对照 PMN 中的 pyrin 水平不受影响。此外,FMF 患者 PMN 的基础自噬状态降低,表现为 LC3B-II/I 比值和 ATG mRNA 表达水平较低。然而,mTOR 抑制对两组自噬的诱导具有相似的作用。代谢应激诱导后 pyrin 表达的差异和基础自噬受损表明其在触发 FMF 攻击中具有潜在作用。