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Neutrophils Are Critical for Myelin Removal in a Peripheral Nerve Injury Model of Wallerian Degeneration.

Wallerian degeneration (WD) is considered an essential preparatory stage to the process of axonal regeneration. In the peripheral nervous system, infiltrating monocyte-derived macrophages, which use the chemokine receptor CCR2 to gain entry to injured tissues from the bloodstream, are purportedly necessary for efficient WD. However, our laboratory has previously reported that myelin clearance in the injured sciatic nerve proceeds unhindered in the Ccr2-/- mouse model. Here, we extensively characterize WD in male Ccr2-/- mice and identify a compensatory mechanism of WD that is facilitated primarily by neutrophils. In response to the loss of CCR2, injured Ccr2-/- sciatic nerves demonstrate prolonged expression of neutrophil chemokines, a concomitant extended increase in the accumulation of neutrophils in the nerve, and elevated phagocytosis by neutrophils. Neutrophil depletion substantially inhibits myelin clearance after nerve injury in both male WT and Ccr2-/- mice, highlighting a novel role for these cells in peripheral nerve degeneration that spans genotypes.SIGNIFICANCE STATEMENT The accepted view in the basic and clinical neurosciences is that the clearance of axonal and myelin debris after a nerve injury is directed primarily by inflammatory CCR2+ macrophages. However, we demonstrate that this clearance is nearly identical in WT and Ccr2-/- mice, and that neutrophils replace CCR2+ macrophages as the primary phagocytic cell. We find that neutrophils play a major role in myelin clearance not only in Ccr2-/- mice but also in WT mice, highlighting their necessity during nerve degeneration in the peripheral nervous system. These degeneration studies may propel improvements in nerve regeneration and draw critical parallels to mechanisms of nerve degeneration and regeneration in the CNS and in the context of peripheral neuropathies.

Pubmed ID: 28912156 RIS Download

Mesh terms: Animals | Disease Models, Animal | Female | Male | Mice | Mice, 129 Strain | Mice, Inbred C57BL | Mice, Knockout | Myelin Sheath | Nerve Crush | Neutrophils | Peripheral Nerve Injuries | Phagocytosis | Random Allocation | Sciatic Neuropathy | Wallerian Degeneration

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Data used in this publication

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Associated grants

  • Agency: NEI NIH HHS, Id: P30 EY011373
  • Agency: NIDDK NIH HHS, Id: R56 DK097223
  • Agency: NIH HHS, Id: S10 OD016164
  • Agency: NIDDK NIH HHS, Id: R01 DK097223
  • Agency: NINDS NIH HHS, Id: R01 NS095017
  • Agency: NINDS NIH HHS, Id: T32 NS067431
  • Agency: NINDS NIH HHS, Id: F31 NS093694

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