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Updated: May 28, 2026

Identifying Microglia and Peripheral Infiltrating Macrophages in the Injured Spinal Cords Using Flow Cytometry
Published on: June 24, 2025
Site-specific subtypes of macrophages recruited after peripheral nerve injury
Tadasuke Komori1, Yoshihiro Morikawa, Takeshi Inada
1Department of Anatomy and Neurobiology, Wakayama Medical University, Wakayama, Japan.
Abstract:
After partial ligation of mouse sciatic nerve, the subtypes of macrophages were examined in the injured nerve and dorsal root ganglia (DRGs). Many M1 macrophages, which were inducible nitric oxide synthase (iNOS)-positive and arginase-1 (Arg-1)-negative, and neutrophils infiltrated the injured nerve. In contrast, almost all macrophages infiltrating the ipsilateral side of DRGs after the nerve injury were iNOS⁻/Arg-1⁺, M2 type. The infiltration of M1 and M2 macrophages was first observed in the injured nerve and ipsilateral DRGs on days 1 and 2, respectively. In addition, the macrophage infiltration preceded the activation of microglia in the ipsilateral dorsal horn of spinal cord. Thus, infiltrating macrophages after peripheral nerve injury may play unique roles dependent on the location in the development of neuropathic pain.
Insights
Peripheral nerve injury causes distinct macrophage subtypes to infiltrate different tissues. M1 macrophages target the nerve, while M2 macrophages target the dorsal root ganglia, influencing neuropathic pain development.
Area of Science:
- Neuroscience
- Immunology
- Cell Biology
Background:
- Peripheral nerve injury triggers complex cellular responses.
- Macrophages are key immune cells involved in tissue repair and inflammation.
- Understanding macrophage subtypes and their roles is crucial for developing neuropathic pain treatments.
Purpose of the Study:
- To investigate the subtypes and locations of macrophages infiltrating the sciatic nerve and dorsal root ganglia (DRGs) after injury.
- To determine the temporal dynamics of macrophage infiltration and microglial activation.
- To explore the potential roles of distinct macrophage populations in neuropathic pain development.
Main Methods:
- Partial ligation of the mouse sciatic nerve model.
- Immunohistochemical analysis to identify macrophage subtypes (M1 and M2) and neutrophils.
- Examination of injured nerve, ipsilateral DRGs, and spinal cord dorsal horn.
Main Results:
- M1 macrophages (iNOS-positive, Arg-1-negative) and neutrophils infiltrated the injured sciatic nerve.
- M2 macrophages (iNOS-negative, Arg-1-positive) predominantly infiltrated the ipsilateral DRGs.
- Macrophage infiltration preceded microglial activation in the spinal cord dorsal horn.
Conclusions:
- Distinct macrophage subtypes (M1 and M2) exhibit site-specific infiltration following peripheral nerve injury.
- Infiltrating macrophages may play unique, location-dependent roles in the pathogenesis of neuropathic pain.
- These findings highlight macrophages as potential therapeutic targets for managing nerve injury-induced pain.
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