Premium
Neural crest‐derived cells sustain their multipotency even after entry into their target tissues
Author(s) -
Motohashi Tsutomu,
Kitagawa Daisuke,
Watanabe Natsuki,
Wakaoka Takanori,
Kunisada Takahiro
Publication year - 2014
Publication title -
developmental dynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.634
H-Index - 141
eISSN - 1097-0177
pISSN - 1058-8388
DOI - 10.1002/dvdy.24072
Subject(s) - sox10 , neural crest , biology , microbiology and biotechnology , embryonic stem cell , stem cell , cellular differentiation , immunology , embryo , genetics , gene
Background: Neural crest cells (NC cells) are highly migratory multipotent cells. Their multipotency is transient at the early stage of their generation; soon after emerging from the neural tube, these cells turn into lineage‐restricted precursors. However, recent studies have disputed this conventionally believed paradigm. In this study, we analyzed the differentiation potency of NC‐derived cells after their arrival at target tissues. Results: Using Sox10‐IRES‐Venus mice, we found that the NC‐derived cells in the skin, DRG, and inner ear could be divided into two populations: Sox10‐positive/Kit‐negative cells (Sox10+/Kit‐ cells) and Sox10‐ and Kit‐positive cells (Sox10+/Kit+ cells). Only the Sox10+/Kit‐ cells were detected in the intestines. Unexpectedly, the Sox10+/Kit+ cells differentiated into neurons, glial cells, and melanocytes, showing that they had maintained their multipotency even after having entered the target tissues. The Sox10+/Kit+ cells in the DRG maintained their multipotency for a restricted period during the earlier embryonic stages, whereas those in the skin and inner ear were multipotent yet even in later embryonic stages. Conclusions: We showed that NC‐derived Sox10+/Kit+ cells maintained their multipotency even after entry into the target tissues. This unexpected differentiation potency of these cells in tissues seems to have been strictly restricted by the tissue microenvironment. Developmental Dynamics 243:368–380, 2014 . © 2013 Wiley Periodicals, Inc.