期刊
INTERNATIONAL IMMUNOPHARMACOLOGY
卷 84, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.intimp.2020.106492
关键词
Sciatic nerve injury; Inflammasome; NLRP3; IL-1 beta
资金
- National Natural Science Foundation of China [81072398]
The activation of the inflammasome plays an important role in the central nervous system. However, only a few studies have investigated the effects of inflammasome activation in the peripheral nerve, especially in the sciatic nerve, and the mechanism of this activation remains elusive. Moreover, how interleukin-1 beta (IL-1 beta) is produced after sciatic nerve injury is also unknown. In our study, we aimed to investigate whether the nucleotidebinding oligomerization domain-like pyrin domain containing protein 3 (NLRP3) inflammasome is activated after sciatic nerve injury and to explore its role in sciatic nerve injury. The results of immunoblotting and immunofluorescence microscopy indicate that the NLRP3 inflammasome was activated after sciatic nerve injury in wild-type (WT) mice, as demonstrated by upregulated inflammasome-related components, e.g., NLRP3, procaspase-1 and ASC. Furthermore, upregulated inflammasome-related components cis-cleavage precursor IL-1 beta (proIL-1 beta) and precursor interleukin-18 (proIL-18) to IL-1 beta and IL-18, contributing to the inflammatory response. Consequently, the inflammatory response after sciatic nerve injury in NLRP3 knockout (NLRP3-KO) mice was less severe than that in WT mice. Moreover, NLRP3-KO mice exhibited an increased sciatic functional index (SFI), which was determined by footprint analysis, suggesting that NLRP3 deficiency is beneficial to sciatic nerve recovery after injury. Therefore, our results indicate that NLRP3 is involved in the recovery from sciatic nerve injury and mediates the production of inflammatory factors, such as IL-1 beta, after sciatic nerve injury.
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