Mast cells can contribute to axon-glial dissociation and fibrosis in peripheral nerve

Kelly R. Monk, Jianqiang Wu, Jon P. Williams, Brenda A. Finney, Maureen E. Fitzgerald, Marie Dominique Filippi, Nancy Ratner

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Expression of the human epidermal growth factor receptor (EGFR) in murine Schwann cells results in loss of axon-Schwann cell interactions and collagen deposition, modeling peripheral nerve response to injury and tumorigenesis. Mast cells infiltrate nerves in all three situations. We show that mast cells are present in normal mouse peripheral nerve beginning at 4 weeks of age, and that the number of mast-cells in EGFR+ nerves increases abruptly at 5-6 weeks of age as axons and Schwann cells dissociate. The increase in mast cell number is preceded and accompanied by elevated levels of mRNAs encoding the mast-cell chemoattractants Rantes, SCF and VEGF. Genetic ablation of mast cells and bone marrow reconstitution in W41 x EGFR+ mice indicate a role for mast cells in loss of axon-Schwann cell interactions and collagen deposition. Pharmacological stabilization of mast cells by disodium cromoglycate administration to EGFR+ mice also diminished loss of axon-Schwann cell interaction. Together these three lines of evidence support the hypothesis that mast cells can contribute to alterations in peripheral nerves.

Original languageEnglish (US)
Pages (from-to)233-244
Number of pages12
JournalNeuron Glia Biology
Volume3
Issue number3
DOIs
StatePublished - Aug 2007

Keywords

  • EGFR
  • NF1
  • Remak bundle
  • Schwann cell

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology

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