4.5 Article

Identity of myelinated cutaneous sensory neurons projecting to nocireceptive laminae following nerve injury in adult mice

Journal

JOURNAL OF COMPARATIVE NEUROLOGY
Volume 508, Issue 3, Pages 500-509

Publisher

WILEY-LISS
DOI: 10.1002/cne.21693

Keywords

nociceptor; regeneration; spinal cord; pain; dorsal root ganglion; reinnervation

Funding

  1. NINDS NIH HHS [R01 NS052848-02, R56 NS023725, R01 NS023725-21, R01 NS052848, R01 NS044094, NS44094, R01 NS052848-03, R01 NS023725-20, R01 NS044094-05, NS23725, R01 NS023725] Funding Source: Medline

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It is widely thought that, after peripheral injury, some low-threshold mechanoreceptive (LTMR) afferents sprout into pain-specific laminae (I-II) of the dorsal horn and are responsible for chronic pain states such as mechanical allodynia. Although recent studies have questioned this hypothesis, they fail to account for a series of compelling results from single-fiber analyses showing extensive projections from large-diameter myelinated afferents into nocireceptive layers after nerve injury. Here we show that, in the thoracic spinal cord of naive adult mouse, all myelinated nociceptors gave rise to terminal projections throughout the superficial dorsal horn laminae (I-II). Most (70%) of these fibers had large-diameter axons with recurving flame-shaped central arbors that projected throughout the dorsal horn laminae I-V. This morphology was reminiscent of that attributed to sprouted LTMRs described in previous studies. After peripheral nerve axotomy, we found that LTMR afferents with narrow, uninflected somal action potentials did not sprout into superficial laminae of the dorsal horn. Only myelinated noiceptive afferents with broad, inflected somal action potentials were found to give rise to recurving collaterals and project into superficial pain-specific laminae after axotomy. We conclude that the previously undocumented central morphology of large, myelinated cutaneous nociceptors may very well account for the morphological findings previously thought to require sprouting of LTMRs.

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