| Literature DB >> 26225748 |
Miki Ono1, Tetsuo Suzawa2, Masamichi Takami3, Gou Yamamoto4, Tomohiko Hosono5, Atsushi Yamada6, Dai Suzuki6, Kentaro Yoshimura6, Junichi Watahiki7, Ryuhei Hayashi8, Satoru Arata5, Kenji Mishima4, Kohji Nishida8, Noriko Osumi9, Koutaro Maki7, Ryutaro Kamijo6.
Abstract
In embryos, neural crest cells emerge from the dorsal region of the fusing neural tube and migrate throughout tissues to differentiate into various types of cells including osteoblasts. In adults, subsets of neural crest-derived cells (NCDCs) reside as stem cells and are considered to be useful cell sources for regenerative medicine strategies. Numerous studies have suggested that stem cells with a neural crest origin persist into adulthood, especially those within the mammalian craniofacial compartment. However, their distribution as well as capacity to differentiate into osteoblasts in adults is not fully understood. To analyze the precise distribution and characteristics of NCDCs in adult oral tissues, we utilized an established line of double transgenic (P0-Cre/CAG-CAT-EGFP) mice in which NCDCs express green fluorescent protein (GFP) throughout their life. GFP-positive cells were scattered like islands throughout tissues of the palate, gingiva, tongue, and buccal mucosa in adult mice, with those isolated from the latter shown to form spheres, typical cell clusters composed of stem cells, under low-adherent conditions. Furthermore, GFP-positive cells had markedly increased alkaline phosphatase (a marker enzyme of osteoblast differentiation) activity and mineralization as shown by alizarin red staining, in the presence of bone morphogenetic protein (BMP)-2. These results suggest that NCDCs reside in various adult oral tissues and possess potential to differentiate into osteoblastic cells. NCDCs in adults may be a useful cell source for bone regeneration strategies.Entities:
Keywords: Adult; Cellular differentiation; Neural crest-derived cells; Oral tissues; Osteoblasts
Mesh:
Year: 2015 PMID: 26225748 DOI: 10.1016/j.bbrc.2015.07.106
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575