TY - JOUR
T1 - Differentiation of induced pluripotent stem cells into dental mesenchymal cells
AU - Otsu, Keishi
AU - Kishigami, Ryota
AU - Oikawa-Sasaki, Ai
AU - Fukumoto, Satoshi
AU - Yamada, Aya
AU - Fujiwara, Naoki
AU - Ishizeki, Kiyoto
AU - Harada, Hidemitsu
N1 - Copyright:
Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2012/5/1
Y1 - 2012/5/1
N2 - Similar to embryonic stem cells, induced pluripotent stem (iPS) cells can differentiate into various cell types upon appropriate induction, and thus, may be valuable cell sources for regenerative medicine. However, iPS cells have not been reported to differentiate into odontogenic cells for tooth regeneration. Here we demonstrated that neural crest-like cells (NCLC) derived from mouse iPS cells have the potential to differentiate into odontogenic mesenchymal cells. We developed an efficient culture protocol to induce the differentiation of mouse iPS cells into NCLC. We confirmed that the cells exhibited neural crest (NC) cell markers as evidenced by immunocytochemistry, flow cytometry, and real-time reverse transcription-polymerase chain reaction. Further, in recombination cultures of NCLC and mouse dental epithelium, NCLC exhibited a gene expression pattern involving dental mesenchymal cells. Some NCLC also expressed dentin sialoprotein. Conditioned medium of mouse dental epithelium cultures further enhanced the differentiation of NCLC into odontoblasts. These results suggest that iPS cells are useful cell sources for tooth regeneration and tooth development studies.
AB - Similar to embryonic stem cells, induced pluripotent stem (iPS) cells can differentiate into various cell types upon appropriate induction, and thus, may be valuable cell sources for regenerative medicine. However, iPS cells have not been reported to differentiate into odontogenic cells for tooth regeneration. Here we demonstrated that neural crest-like cells (NCLC) derived from mouse iPS cells have the potential to differentiate into odontogenic mesenchymal cells. We developed an efficient culture protocol to induce the differentiation of mouse iPS cells into NCLC. We confirmed that the cells exhibited neural crest (NC) cell markers as evidenced by immunocytochemistry, flow cytometry, and real-time reverse transcription-polymerase chain reaction. Further, in recombination cultures of NCLC and mouse dental epithelium, NCLC exhibited a gene expression pattern involving dental mesenchymal cells. Some NCLC also expressed dentin sialoprotein. Conditioned medium of mouse dental epithelium cultures further enhanced the differentiation of NCLC into odontoblasts. These results suggest that iPS cells are useful cell sources for tooth regeneration and tooth development studies.
UR - http://www.scopus.com/inward/record.url?scp=84860198185&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84860198185&partnerID=8YFLogxK
U2 - 10.1089/scd.2011.0210
DO - 10.1089/scd.2011.0210
M3 - Article
C2 - 22085204
AN - SCOPUS:84860198185
SN - 1547-3287
VL - 21
SP - 1156
EP - 1164
JO - Stem cells and development
JF - Stem cells and development
IS - 7
ER -