TY - JOUR
T1 - Applications of Mesenchymal Stem Cells and Neural Crest Cells in Craniofacial Skeletal Research
AU - Morikawa, Satoru
AU - Ouchi, Takehito
AU - Shibata, Shinsuke
AU - Fujimura, Takumi
AU - Kawana, Hiromasa
AU - Okano, Hideyuki
AU - Nakagawa, Taneaki
N1 - Funding Information:
The authors thank the members of their laboratory for helpful discussions. This work was supported by Japan Society for the Promotion of Science KAKENHI grants numbered 15K11221 (Taneaki Nakagawa) and 25463226 (Satoru Morikawa) and by the Program for Intractable Disease Research Utilizing Disease-specific iPS Cells from the Japan Science and Technology Agency (JST), Japan Agency for Medical Research and Development (A-MED), and the Ministry of Education, Science, Sports and Culture (MEXT) to Hideyuki Okano.
Publisher Copyright:
© 2016 Satoru Morikawa et al.
PY - 2016
Y1 - 2016
N2 - Craniofacial skeletal tissues are composed of tooth and bone, together with nerves and blood vessels. This composite material is mainly derived from neural crest cells (NCCs). The neural crest is transient embryonic tissue present during neural tube formation whose cells have high potential for migration and differentiation. Thus, NCCs are promising candidates for craniofacial tissue regeneration; however, the clinical application of NCCs is hindered by their limited accessibility. In contrast, mesenchymal stem cells (MSCs) are easily accessible in adults, have similar potential for self-renewal, and can differentiate into skeletal tissues, including bones and cartilage. Therefore, MSCs may represent good sources of stem cells for clinical use. MSCs are classically identified under adherent culture conditions, leading to contamination with other cell lineages. Previous studies have identified mouse- and human-specific MSC subsets using cell surface markers. Additionally, some studies have shown that a subset of MSCs is closely related to neural crest derivatives and endothelial cells. These MSCs may be promising candidates for regeneration of craniofacial tissues from the perspective of developmental fate. Here, we review the fundamental biology of MSCs in craniofacial research.
AB - Craniofacial skeletal tissues are composed of tooth and bone, together with nerves and blood vessels. This composite material is mainly derived from neural crest cells (NCCs). The neural crest is transient embryonic tissue present during neural tube formation whose cells have high potential for migration and differentiation. Thus, NCCs are promising candidates for craniofacial tissue regeneration; however, the clinical application of NCCs is hindered by their limited accessibility. In contrast, mesenchymal stem cells (MSCs) are easily accessible in adults, have similar potential for self-renewal, and can differentiate into skeletal tissues, including bones and cartilage. Therefore, MSCs may represent good sources of stem cells for clinical use. MSCs are classically identified under adherent culture conditions, leading to contamination with other cell lineages. Previous studies have identified mouse- and human-specific MSC subsets using cell surface markers. Additionally, some studies have shown that a subset of MSCs is closely related to neural crest derivatives and endothelial cells. These MSCs may be promising candidates for regeneration of craniofacial tissues from the perspective of developmental fate. Here, we review the fundamental biology of MSCs in craniofacial research.
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U2 - 10.1155/2016/2849879
DO - 10.1155/2016/2849879
M3 - Article
AN - SCOPUS:84960969653
SN - 1687-966X
VL - 2016
JO - Stem Cells International
JF - Stem Cells International
M1 - 2849879
ER -