bioRxiv · 10.64898/2026.10.12.758439
GPNMB enables lysosomal adaptation required for myelin clearance and nerve regeneration after peripheral nerve injury
Abstract
Recovery from peripheral nerve injury involves coordinated axonal and immune repair programs that promote tissue regeneration. However, the mechanisms regulating immune-mediated repair remain incompletely understood. Here, we demonstrate that glycoprotein non-metastatic melanoma protein B (GPNMB) is a key regulator of repair processes following peripheral nerve injury. In a mouse sciatic nerve crush model, loss of Gpnmb impaired functional recovery after injury. MRI and histological analyses revealed persistent myelin debris accumulation, defective debris clearance, and impaired macrophage lysosomal function within injured nerves. Mechanistic studies showed that GPNMB-deficient human iPSC-derived macrophages exhibited impaired lysosomal adaptation, reduced lysosomal fitness, and defective processing of myelin-associated cargo, resulting in inefficient degradation of injury-associated material. These defects were accompanied by impaired acquisition of repair-associated cellular programs. Together, our findings identify GPNMB as a critical regulator of lysosome-dependent repair programs during nerve regeneration and demonstrate that efficient GPNMB-dependent myelin processing is required for functional recovery following peripheral nerve injury.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Ouali Alami, N., Panesar, M., Obrecht, M., Doll, T., Osinnii, I., Sansig, G., Thiel, Z., Claerr, I., Greenwood, D., Patino, C., Klein, L., Condeescu-Ivan, D., Giorgetti, E., Lambert, C., Kalamakis, G., Van Steenbergen, V., Hils, L., Manneville, C., Mueller, M., Nash, M., Labouesse, M., Shimshek, D., Beckmann, N., Dergai, O., Bidinosti, M.. 2026-10-19. GPNMB enables lysosomal adaptation required for myelin clearance and nerve regeneration after peripheral nerve injury. https://doi.org/10.64898/2026.10.12.758439
Cite the original work for its findings. Save a collection to share your selection of sources.