Bellussi Luisa Maria, Vindigni Carla, Cocca Serena, Butorano Marie Aimee Gloria Munezero, Livi Walter, Corallo Giulia, Passali Desiderio
1 Medical Surgical and Neuroscience Department, ENT Clinic, University of Siena, Siena, Italy.
2 Pathology Unit, University Medical School Siena, Italy.
Int J Immunopathol Pharmacol. 2017 Jun;30(2):168-173. doi: 10.1177/0394632017698713. Epub 2017 Mar 15.
High-mobility group box 1 (HMGB1) is a nuclear non-histone protein, playing a critical role as a mediator between innate and acquired immunity; when released extracellularly, it coordinates the cellular stress response (under necrosis, bacterial lipopolysaccharide stimulation) and acts as an inflammatory marker and cytokine. The aim of the study was to demonstrate whether HMGB1 is over-expressed in chronic middle-ear pathologies and whether the entity of expression and the localization are correlated with the degree of the inflammatory reaction, thus suggesting that HMGB1 may play a crucial role in chronic inflammatory disorders of the middle ear, as already demonstrated in other airway diseases. We analyzed 30 samples of middle-ear mucosa in patients affected by chronic suppurative otitis media with ear drum perforation with/without cholesteatoma and otosclerosis as control. The distribution of HMGB1 was evaluated as nuclear, cytoplasmic, and/or extracellular staining. The inflammatory cells observed in the biopsies were mostly lymphocytes and plasmacells. A statistically significant difference in inflammation score between otosclerosis and chronic otitis samples ( P < 0.01; Anova test) and between otosclerosis and cholesteatoma samples ( P < 0.05; Anova test) was observed; the HMGB1 positivity was in accordance with the density of the inflammatory infiltrate. HMGB1 is over-expressed in chronic middle-ear pathologies and may play a role in the progression of the inflammatory process from recurrent acute otitis media to chronic suppurative otitis media.
高迁移率族蛋白B1(HMGB1)是一种核内非组蛋白,作为先天性免疫和获得性免疫之间的介质发挥关键作用;当在细胞外释放时,它协调细胞应激反应(在坏死、细菌脂多糖刺激的情况下),并作为一种炎症标志物和细胞因子发挥作用。本研究的目的是证明HMGB1在慢性中耳疾病中是否过度表达,以及表达量和定位是否与炎症反应程度相关,从而表明HMGB1可能在中耳慢性炎症性疾病中发挥关键作用,正如在其他气道疾病中已得到证实的那样。我们分析了30例患有鼓膜穿孔的慢性化脓性中耳炎患者的中耳黏膜样本,伴有或不伴有胆脂瘤,以耳硬化症作为对照。通过细胞核、细胞质和/或细胞外染色来评估HMGB1的分布。活检中观察到的炎症细胞主要是淋巴细胞和浆细胞。观察到耳硬化症与慢性中耳炎样本之间(P<0.01;方差分析)以及耳硬化症与胆脂瘤样本之间(P<0.05;方差分析)在炎症评分上存在统计学显著差异;HMGB1阳性与炎症浸润密度一致。HMGB1在慢性中耳疾病中过度表达,可能在从复发性急性中耳炎到慢性化脓性中耳炎的炎症过程进展中发挥作用。