4.7 Article

Neural crest stem cells undergo multilineage differentiation in developing peripheral nerves to generate endoneurial fibroblasts in addition to Schwann cells

Journal

DEVELOPMENT
Volume 131, Issue 22, Pages 5599-5612

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.01429

Keywords

neural crest stem cell; peripheral nerve development; fate-mapping

Funding

  1. NCI NIH HHS [CA46592, P30 CA046592] Funding Source: Medline
  2. NIAMS NIH HHS [P30 AR048310, 1 P30 AR48310, AR20557] Funding Source: Medline
  3. NIDDK NIH HHS [P60 DK020572, P60-DK20572] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS040750, R01 NS040750-01, R01 NS40750] Funding Source: Medline

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Neural crest stem cells (NCSCs) persist in peripheral nerves throughout late gestation but their function is unknown. Current models of nerve development only consider the generation of Schwarnn cells from neural crest, but the presence of NCSCs raises the possibility of multilineage differentiation. We performed Crerecombinase fate mapping to determine which nerve cells are neural crest derived. Endoneurial fibroblasts, in addition to myelinating and non-myelinating Schwarnn cells, were neural crest derived, whereas perineurial cells, pericytes and endothelial cells were not. This identified endoneurial fibroblasts as a novel neural crest derivative, and demonstrated that trunk neural crest does give rise to fibroblasts in vivo, consistent with previous studies of trunk NCSCs in culture. The multilineage differentiation of NCSCs into glial and non-glial derivatives in the developing nerve appears to be regulated by neuregulin, notch ligands, and bone morphogenic proteins, as these factors are expressed in the developing nerve, and cause nerve NCSCs to generate Schwann cells and fibroblasts, but not neurons, in culture. Nerve development is thus more complex than was previously thought, involving NCSC self-renewal, lineage commitment and multilineage differentiation.

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