George Annette, Buehl Achim, Sommer Claudia
Neurologische Klinik der Universität, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Exp Neurol. 2005 Mar;192(1):163-6. doi: 10.1016/j.expneurol.2004.11.002.
The pro-inflammatory cytokine tumor necrosis factor-alpha (TNF) is involved in injury-induced peripheral nerve pathology and in the generation of neuropathic pain. Here, we investigated local protein levels of the two known TNF receptors, TNF receptor 1 and 2 (TNFR1, TNFR2), on days 0, 1, 3, 7, 14, and 28 after unilateral crush or chronic constriction injury (CCI) of mouse sciatic nerves using enzyme-linked immunoassay. Both receptors were detectable at a low level in nerve homogenates from naive mice. After crush or CCI, TNFR1 increased by 2-fold on days 3 and day 7. Unlike TNFR1, TNFR2 was markedly upregulated already on day 1 after crush or CCI. TNFR2 increased by 7-fold on days 3 and 7, and remained elevated at a lower level until day 28 after both CCI and crush injury. These data indicate that endoneurial TNFR1 and TNFR2 proteins are differentially regulated during Wallerian degeneration.
促炎细胞因子肿瘤坏死因子-α(TNF)参与损伤诱导的周围神经病理过程以及神经性疼痛的产生。在此,我们使用酶联免疫吸附测定法,研究了小鼠坐骨神经单侧挤压或慢性压迫损伤(CCI)后第0、1、3、7、14和28天,两种已知TNF受体即TNF受体1和2(TNFR1、TNFR2)的局部蛋白水平。在未处理小鼠的神经匀浆中可检测到低水平的两种受体。挤压或CCI后,TNFR1在第3天和第7天增加了2倍。与TNFR1不同,TNFR2在挤压或CCI后的第1天就已显著上调。TNFR2在第3天和第7天增加了7倍,并且在CCI和挤压损伤后的第28天之前一直保持在较低水平升高。这些数据表明,在华勒氏变性过程中,神经内膜TNFR1和TNFR2蛋白受到不同的调节。