MFG-E8 Ameliorates Nerve Injury-Induced Neuropathic Pain by Regulating Microglial Polarization and Neuroinflammation via Integrin β3/SOCS3/STAT3 Pathway in Mice

J Neuroimmune Pharmacol. 2024 Sep 21;19(1):49. doi: 10.1007/s11481-024-10150-w.

Abstract

Spinal microglial polarization plays a crucial role in the pathological processes of neuropathic pain following peripheral nerve injury. Accumulating evidence suggests that milk fat globule epidermal growth factor-8 (MFG-E8) exhibits anti-inflammatory effect and regulates microglial polarization through the integrin β3 receptor. However, the impact of MFG-E8 on microglial polarization in the context of neuropathic pain has not yet been investigated. In this study, we evaluated the effect of MFG-E8 on pain hypersensitivity and spinal microglial polarization following spared nerve injury (SNI) of the sciatic nerve in mice. We determined the molecular mechanisms underlying the effects of MFG-E8 on pain hypersensitivity and spinal microglial polarization using pain behavior assessment, western blot (WB) analysis, immunofluorescence (IF) staining, quantitative polymerase chain reaction (qPCR), enzyme-linked immunosorbent assay (ELISA), and small interfering RNA (siRNA) transfection. Our findings indicate that SNI significantly increased the levels of MFG-E8 and integrin β3 expressed in microglia within the spinal cord of mice. Additionally, we observed that intrathecal injection of recombinant human MFG-E8 (rhMFG-E8) alleviated SNI induced-mechanical allodynia and thermal hyperalgesia. Furthermore, the results suggested that rhMFG-E8 facilitated M2 microglial polarization and ameliorated neuroinflammation via integrin β3/SOCS3/STAT3 pathway in the spinal cord of mice with SNI. Importantly, these effects were negated by integrin β3 siRNA, or SOCS3 siRNA. These results demonstrate that MFG-E8 ameliorates peripheral nerve injury induced-mechanical allodynia and thermal hyperalgesia by driving M2 microglial polarization and mitigating neuroinflammation mediated by integrin β3/SOCS3/STAT3 pathway in the spinal cord of mice. MFG-E8 may serve as a promising target for the treatment of neuropathic pain.

Keywords: MFG-E8; Microglial polarization; Neuroinflammation; Neuropathic pain; SOCS3; STAT3.

MeSH terms

  • Animals
  • Antigens, Surface* / metabolism
  • Cell Polarity / drug effects
  • Cell Polarity / physiology
  • Integrin beta3* / biosynthesis
  • Integrin beta3* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microglia* / metabolism
  • Milk Proteins* / biosynthesis
  • Neuralgia* / metabolism
  • Neuroinflammatory Diseases / metabolism
  • Peripheral Nerve Injuries / complications
  • Peripheral Nerve Injuries / metabolism
  • STAT3 Transcription Factor* / metabolism
  • Signal Transduction* / physiology
  • Suppressor of Cytokine Signaling 3 Protein* / metabolism

Substances

  • Mfge8 protein, mouse
  • Suppressor of Cytokine Signaling 3 Protein
  • Antigens, Surface
  • Integrin beta3
  • STAT3 Transcription Factor
  • Milk Proteins
  • Socs3 protein, mouse
  • Stat3 protein, mouse