Up-Regulation of CX3CL1 via STAT3 Contributes to SMIR-Induced Chronic Postsurgical Pain

Neurochem Res. 2018 Mar;43(3):556-565. doi: 10.1007/s11064-017-2449-8. Epub 2018 Jan 8.

Abstract

Chronic postsurgical pain (CPSP) often occurs after surgery and has a strong impact on patients' daily lives. However, the underlying mechanism of CPSP remains unknown. Here, we used a skin/muscle incision and retraction (SMIR) model to investigate the role of CX3CL1 in SMIR-induced pain and its underlying mechanism. We found that up-regulation of CX3CL1 in the spinal dorsal horn contributed to SMIR-induced mechanical allodynia. The use of a CX3CL1-neutralizing antibody to block CX3CL1 attenuated mechanical allodynia induced by SMIR surgery. We also found that phospho-STAT3 co-localizes with CX3CL1 in spinal neurons after SMIR surgery and that this contributes to SMIR-induced mechanical allodynia. Intrathecal administration of the STAT3 inhibitor S3I-201 suppressed up-regulation of CX3CL1 at both the protein and mRNA levels after SMIR surgery. Chromatin immunoprecipitation further demonstrated that SMIR promotes the recruitment of STAT3 to the cx3cl1 gene promoter (- 1032/- 1022). These findings suggest that activation of STAT3 after SMIR mediates the up-regulation of CX3CL1, leading to mechanical allodynia, and that this upregulation may partly be due to the enhanced recruitment of STAT3 to the cx3cl1 gene promoter after SMIR.

Keywords: CX3CL1; Chronic postsurgical pain; P-STAT3; Skin/muscle incision and retraction.

MeSH terms

  • Animals
  • Chemokine CX3CL1 / metabolism*
  • Chronic Pain / metabolism*
  • Disease Models, Animal
  • Hyperalgesia / metabolism
  • Male
  • Muscles / surgery
  • Pain Measurement / methods
  • Pain, Postoperative / metabolism*
  • Rats, Sprague-Dawley
  • STAT3 Transcription Factor / metabolism*
  • Skin / injuries
  • Transcriptional Activation / physiology
  • Up-Regulation*

Substances

  • Chemokine CX3CL1
  • Cx3cl1 protein, rat
  • STAT3 Transcription Factor
  • Stat3 protein, rat