Abstract
The neural crest (NC) arises near the neural tube during embryo development. NC cells migrate throughout the embryo and have potential to differentiate into multiple cell types, such as peripheral nerves, glial, cardiac smooth muscle, endocrine, and pigment cells, and craniofacial bone. In the present study, we induced osteoblast-like cells using whisker follicles obtained from the NC of mice. Hair follicle cells derived from the NC labeled with enhanced green fluorescent protein (EGFP) were collected from protein zero-Cre/floxed-EGFP double transgenic mice and cultured, then treated and cultured in stem cell growth medium. After growth for 14 days, results of flow cytometry analysis showed that 95% of the EGFP-positive (EGFP+) hair follicle cells derived from the NC had proliferated and 76.2% of those expressed mesenchymal stem cells markers, such as platelet-derived growth factor α and stem cell antigen-1, and also showed constitutive expression of Runx2 mRNA. Cells stimulated with bone morphogenetic protein-2 expressed osteocalcin, osterix, and alkaline phosphatase mRNA, resulting in production of mineralized matrices, which were detected by von Kossa and alizarin red staining. Moreover, EGFP+ hair follicle cells consistently expressed macrophage colony-stimulating factor and osteoprotegerin (OPG). Addition of 1α,25-dihydroxyvitamin D3 [1,25(OH)2D3] (10−8 M) to the cultures suppressed OPG expression and induced RANKL production in the cells. Furthermore, multinucleated osteoclasts appeared within 6 days after starting co-cultures of bone marrow cells with EGFP+ cells in the presence of 1,25(OH)2D3 and PGE2. These results suggest that NC-derived hair follicle cells possess a capacity for osteoblastic differentiation and may be useful for developing new bone regenerative medicine therapies.
Highlights
Neural crest cells (NCCs), a specific population of vertebrate cells originating in the dorsal neural tube [1, 2], form a variety of tissues, including the dorsal root ganglia, peripheral nerves, pigment and adipose cells, and craniofacial bone and muscle tissues [3,4,5,6]
The distribution of enhanced green fluorescent protein (EGFP)-tagged neural crest-derived cells (NCDCs) in whisker follicle samples obtained from P0-Cre/Floxed-EGFP double transgenic (P0-Cre); CAG-CAT-EGFP Tg mice was determined using fluorescence microscopy
These results showed the existence of NCDCs in the bulge and dermal papilla (DP)
Summary
Neural crest cells (NCCs), a specific population of vertebrate cells originating in the dorsal neural tube [1, 2], form a variety of tissues, including the dorsal root ganglia, peripheral nerves, pigment and adipose cells, and craniofacial bone and muscle tissues [3,4,5,6]. Kanakubo et al [16] crossed P0-Cre Tg with CAG-CAT-EGFP Tg mice [18] to establish a transgenic line in which NCCs were genetically marked with enhanced green fluorescent protein (EGFP), and these P0-Cre/Floxed-EGFP double transgenic (P0-Cre; CAG-CATEGFP Tg) mice have been widely used to study NCDCs [19,20,21,22,23]. In one of those previous studies, NCDCs were identified and isolated from bone marrow, dorsal root ganglia, and whisker follicles obtained from adult P0-Cre; CAG-CAT-EGFP Tg mice [20]. Multipotent NCDCs from the iris stroma of those mice showed great potential as a cell source for regenerative treatment of damaged corneal tissues [19]
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