Merkel cell-driven BDNF signaling specifies SAI neuron molecular and electrophysiological phenotypes

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Abstract

The extent to which the skin instructs peripheral somatosensory neuron maturation is unknown. We studied this question in Merkel cell–neurite complexes, where slowly adapting type I (SAI) neurons innervate skin-derived Merkel cells. Transgenic mice lacking Merkel cells had normal dorsal root ganglion (DRG) neuron numbers, but fewer DRG neurons expressed the SAI markers TrkB, TrkC, and Ret. Merkel cell ablation also decreased downstream TrkB signaling in DRGs, and altered the expression of genes associated with SAI development and function. Skin- and Merkel cell-specific deletion of Bdnf during embryogenesis, but not postnatal Bdnf deletion or Ntf3 deletion, reproduced these results. Furthermore, prototypical SAI electrophysiological signatures were absent from skin regions where Bdnf was deleted in embryonic Merkel cells. We conclude that BDNF produced by Merkel cells during a precise embryonic period guides SAI neuron development, providing the first direct evidence that the skin instructs sensory neuron molecular and functional maturation.

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APA

Reed-Geaghan, E. G., Wright, M. C., See, L. A., Adelman, P. C., Lee, K. H., Koerber, H. R., & Maricich, S. M. (2016). Merkel cell-driven BDNF signaling specifies SAI neuron molecular and electrophysiological phenotypes. Journal of Neuroscience, 36(15), 4362–4376. https://doi.org/10.1523/JNEUROSCI.3781-15.2016

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