Reinhold Ann Kristin, Schwabe Joachim, Lux Thomas J, Salvador Ellaine, Rittner Heike L
Department of Anaesthesiology, University Hospitals Würzburg, Wüerzburg, Germany.
Front Neurosci. 2018 Dec 18;12:936. doi: 10.3389/fnins.2018.00936. eCollection 2018.
Peripheral neuropathy is accompanied by changes in the neuronal environment. The blood-nerve barrier (BNB) is crucial in protecting the neural homeostasis: Tight junctions (TJ) seal paracellular spaces and thus prevent external stimuli from entering. In different models of neuropathic pain, the BNB is impaired, thus contributing to local damage, immune cell invasion and, ultimately, the development of neuropathy with its symptoms. In this study, we examined changes in expression and microstructural localization of two key tight junction proteins (TJP), claudin-1 and the cytoplasmic anchoring ZO-1, in the sciatic nerve of mice subjected to chronic constriction injury (CCI). Via qPCR and analysis of fluorescence immunohistochemistry, a marked downregulation of mRNA as well as decreased fluorescence intensity were observed in the nerve for both proteins. Moreover, a distinct zig-zag structure for both proteins located at cell-cell contacts, indicative of the localization of TJs, was observed in the perineurial compartment of sham-operated animals. This microstructural location in cell-cell-contacts was lost in neuropathy as semiquantified via computational analysis, based on a novel algorithm. In summary, we provide evidence that peripheral neuropathy is not only associated with decrease in relevant TJPs but also exhibits alterations in TJP arrangement and loss in barrier tightness, presumably due to internalization. Specifically, semiquantification of TJP in cell-cell-contacts of microcompartments could be used in the future for routine clinical samples of patients with neuropathy.
周围神经病变伴随着神经元环境的变化。血-神经屏障(BNB)对于保护神经内环境稳定至关重要:紧密连接(TJ)封闭细胞旁间隙,从而防止外部刺激进入。在不同的神经性疼痛模型中,血-神经屏障受损,进而导致局部损伤、免疫细胞浸润,并最终引发伴有症状的神经病变。在本研究中,我们检测了慢性压迫损伤(CCI)小鼠坐骨神经中两种关键紧密连接蛋白(TJP),即闭合蛋白-1和细胞质锚定蛋白ZO-1的表达变化及微观结构定位。通过定量聚合酶链反应(qPCR)和荧光免疫组织化学分析,观察到两种蛋白在神经中的mRNA显著下调以及荧光强度降低。此外,在假手术动物的神经束膜区,观察到两种蛋白位于细胞间接触部位呈现独特的锯齿状结构,这表明紧密连接的定位。基于一种新算法,通过计算分析半定量显示,在神经病变中这种细胞间接触部位的微观结构定位丧失。总之,我们提供的证据表明,周围神经病变不仅与相关紧密连接蛋白的减少有关,而且还表现出紧密连接蛋白排列的改变和屏障紧密性的丧失,推测是由于内化作用。具体而言,未来可将微区室细胞间接触部位紧密连接蛋白的半定量用于神经病变患者的常规临床样本检测。