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Updated: Aug 16, 2026

Intravital Imaging of Axonal Interactions with Microglia and Macrophages in a Mouse Dorsal Column Crush Injury
Published on: November 23, 2014
Adoptive cell transfer of macrophages following peripheral nerve injury in mice
Atul Rawat1, Mithilesh Kumar Jha1, Brett Michael Morrison1
1Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Abstract:
Macrophages are key innate immune cells involved in multiple biological processes, including peripheral nerve regeneration. Here, we describe a protocol for the adoptive cell transfer of bone-marrow-derived macrophages (BMDMs) following sciatic nerve crush injury (SNCI). This procedure involves isolating BMDMs from a donor mouse, potentially manipulating them ex vivo, and reintroducing them into an animal following SNCI. Preclinical studies show that BMDMs can infiltrate injured nerves and impact functional recovery, potentially providing a novel therapy for nerve injuries. For complete details on the use and execution of this protocol, please refer to Jha et al.1.
Insights
This study details a method for transferring bone-marrow-derived macrophages (BMDMs) to aid peripheral nerve regeneration after injury. These cells can improve functional recovery, offering a potential new therapy for nerve damage.
Area of Science:
- Immunology
- Neuroscience
- Regenerative Medicine
Background:
- Macrophages are crucial innate immune cells.
- They play a significant role in biological processes, including peripheral nerve regeneration.
- Understanding macrophage function is key to developing new therapeutic strategies for nerve injuries.
Purpose of the Study:
- To describe a protocol for the adoptive cell transfer of bone-marrow-derived macrophages (BMDMs) after sciatic nerve crush injury (SNCI).
- To highlight the potential of BMDMs as a therapeutic agent for enhancing nerve regeneration and functional recovery.
Main Methods:
- Isolation of BMDMs from donor mice.
- Optional ex vivo manipulation of BMDMs.
- Adoptive transfer of BMDMs into recipient animals following SNCI.
Main Results:
- BMDMs can infiltrate injured peripheral nerves.
- Adoptive transfer of BMDMs can positively impact functional recovery after SNCI.
- This protocol provides a reproducible method for studying macrophage-mediated nerve repair.
Conclusions:
- Adoptive cell transfer of BMDMs is a viable strategy for promoting peripheral nerve regeneration.
- BMDMs hold promise as a novel cell-based therapy for nerve injuries.
- Further research utilizing this protocol can elucidate the mechanisms of macrophage-driven nerve repair.

