Department of Immunology, Medical College of Qingdao University, Qingdao, China.
Department of Biochemistry and Molecular Biology, Medical College of Qingdao University, Qingdao, China.
Scand J Immunol. 2020 Aug;92(2):e12896. doi: 10.1111/sji.12896. Epub 2020 Jun 17.
Sciatic nerve injury affects quality of life. Many immune cells and inflammatory cytokines have been reported to be involved in sciatic nerve injury, but little is known about the ligands and receptors that trigger inflammatory responses. By using a modified sciatic nerve clamp injury method, we found that the recruitment of Schwann cells and the inflammatory response were enhanced after sciatic nerve injury. Toll-like receptor 4 (TLR4), one of the major members of the TLR family, is highly expressed in Schwann cells. Under certain conditions, myeloid differentiation protein 2 (MD2) binds to TLR4 on the membrane and plays important roles in the inflammatory response. The reductions in the recruitment of Schwann cells and the inflammatory response induced by the blockade of TLR4 or MD2 suggest that TLR4 and MD2 are involved in sciatic nerve injury. What are the endogenous signals that activate the inflammatory response? A large number of free saturated fatty acids (SFAs) are released from Schwann cells, adipocytes and the blood after sciatic nerve injury. Liang et al reported that Schwann cells can be stimulated by palmitic acid (PA). Here, we found that the expression and secretion of TNF-α and IL-6 were enhanced by PA treatment. Moreover, PA activated TLR4 signalling pathway-related proteins and stimulated a strong association between TLR4 and MD2. Blocking TLR4 or MD2 reversed the PA-induced inflammatory response and TLR4 downstream signalling pathway. Thus, we speculated that SFAs act as endogenous ligands that activate TLR4/MD2, thus triggering Schwann cell inflammation during sciatic nerve injury.
坐骨神经损伤会影响生活质量。许多免疫细胞和炎症细胞因子已被报道参与坐骨神经损伤,但对于触发炎症反应的配体和受体知之甚少。通过使用改良的坐骨神经夹伤方法,我们发现坐骨神经损伤后雪旺细胞的募集和炎症反应增强。Toll 样受体 4(TLR4)是 TLR 家族的主要成员之一,在雪旺细胞中高度表达。在某些条件下,髓样分化蛋白 2(MD2)与细胞膜上的 TLR4 结合,并在炎症反应中发挥重要作用。TLR4 或 MD2 阻断后雪旺细胞募集和炎症反应的减少表明 TLR4 和 MD2 参与了坐骨神经损伤。激活炎症反应的内源性信号是什么?坐骨神经损伤后,雪旺细胞、脂肪细胞和血液中会释放大量的游离饱和脂肪酸(SFAs)。Liang 等人报道,雪旺细胞可以被棕榈酸(PA)刺激。在这里,我们发现 PA 处理增强了 TNF-α 和 IL-6 的表达和分泌。此外,PA 激活了 TLR4 信号通路相关蛋白,并刺激了 TLR4 和 MD2 之间的强烈结合。阻断 TLR4 或 MD2 逆转了 PA 诱导的炎症反应和 TLR4 下游信号通路。因此,我们推测 SFAs 作为内源性配体激活 TLR4/MD2,从而在坐骨神经损伤过程中引发雪旺细胞炎症。