Karosi Tamás, Jókay István, Kónya József, Szabó László Z, Pytel József, Jóri József, Szalmás Anita, Sziklai István
Department of Otolaryngology/Head & Neck Surgery, University Medical School of Debrecen, Nagyerdei Krt. 98, H-4012 Debrecen, Hungary.
Laryngoscope. 2006 Aug;116(8):1427-33. doi: 10.1097/01.mlg.0000225928.35838.e5.
Otosclerosis is a bone remodeling disorder of the otic capsule causing conductive and sensorineural hearing loss. Persistent measles virus infection of the temporal bone with increased tumor necrosis factor (TNF)-alpha and decreased osteoprotegerin mRNA expression is supposed to be the main etiologic factor in otosclerosis.
Determinants of measles virus infection and reactive inflammation were studied in otosclerosis. The presence of measles virus was shown in otosclerotic patients by reverse transcriptase-polymerase chain reaction (RT-PCR) amplification of the viral RNA. No report is available, however, about the role and interactions of bone-specific cytokines in otosclerosis.
: Nucleic acid was extracted from stapes footplates of clinically otosclerotic patients. Measles virus nucleoprotein RNA was amplified by seminested RT-PCR. TNF-alpha and osteoprotegerin mRNA coexpression was detected by RT-PCR in otosclerotic bone and was correlated to measles virus positivity.
Among 154 clinically stapes fixation otosclerotic patients, 99 stapedes contained measles virus RNA. TNF-alpha mRNA was detectable in 88 virus-positive and in 6 virus-negative stapes footplates. Osteoprotegerin mRNA expression was significantly lower in the TNF-alpha-positive specimens (P < .0001) that was independent from virus positivity.
Detection of TNF-alpha mRNA demonstrates activated osteoclast functions and inflammatory pathways in otosclerotic stapes footplates associated with measles virus presence. Increased expression of TNF-alpha and its action on RANK production inhibits the protective functions of osteoprotegerin on normal bone turnover in the otic capsule.
耳硬化症是一种耳囊的骨重塑紊乱疾病,可导致传导性和感音神经性听力损失。颞骨持续感染麻疹病毒,肿瘤坏死因子(TNF)-α增加而骨保护素mRNA表达降低,被认为是耳硬化症的主要病因。
对耳硬化症中麻疹病毒感染和反应性炎症的决定因素进行了研究。通过逆转录聚合酶链反应(RT-PCR)扩增病毒RNA,在耳硬化症患者中发现了麻疹病毒的存在。然而,关于骨特异性细胞因子在耳硬化症中的作用和相互作用尚无报道。
从临床诊断为耳硬化症患者的镫骨底板中提取核酸。通过半巢式RT-PCR扩增麻疹病毒核蛋白RNA。通过RT-PCR检测耳硬化骨中TNF-α和骨保护素mRNA的共表达,并与麻疹病毒阳性情况相关联。
在154例临床诊断为镫骨固定的耳硬化症患者中,99例镫骨含有麻疹病毒RNA。在88例病毒阳性和6例病毒阴性的镫骨底板中可检测到TNF-α mRNA。骨保护素mRNA表达在TNF-α阳性标本中显著降低(P <.0001),且与病毒阳性无关。
TNF-α mRNA的检测表明,在与麻疹病毒存在相关的耳硬化镫骨底板中,破骨细胞功能和炎症途径被激活。TNF-α表达增加及其对RANK产生的作用抑制了骨保护素对耳囊正常骨转换的保护功能。