1. Academic Validation
  2. Saturated fatty acids activate the inflammatory signalling pathway in Schwann cells: Implication in sciatic nerve injury

Saturated fatty acids activate the inflammatory signalling pathway in Schwann cells: Implication in sciatic nerve injury

  • Scand J Immunol. 2020 Aug;92(2):e12896. doi: 10.1111/sji.12896.
Dan Xu 1 Jie Liang 1 Mengli Cui 1 Li Zhang 1 Shurong Ren 1 Wenxiang Zheng 2 Xiaolei Dong 3 Bei Zhang 1
Affiliations

Affiliations

  • 1 Department of Immunology, Medical College of Qingdao University, Qingdao, China.
  • 2 Department of Biochemistry and Molecular Biology, Medical College of Qingdao University, Qingdao, China.
  • 3 Department of Genetics, Medical College of Qingdao University, Qingdao, China.
Abstract

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.

Keywords

Schwann cell; inflammatory response; myeloid differentiation protein 2; saturated fatty acid; sciatic nerve injury; toll-like receptor 4.

Figures
Products