TY - JOUR
T1 - Isolation of dental pulp stem cells with high osteogenic potential
AU - Yasui, Takazumi
AU - Mabuchi, Yo
AU - Morikawa, Satoru
AU - Onizawa, Katsuhiro
AU - Akazawa, Chihiro
AU - Nakagawa, Taneaki
AU - Okano, Hideyuki
AU - Matsuzaki, Yumi
N1 - Funding Information:
This work was supported by Japanese Society for the Promotion of Science (JSPS) KAKENHI grants (Grant Nos. 23792293, 25861895, and 16 K11656) to T.Y.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/4/10
Y1 - 2017/4/10
N2 - Dental pulp stem cells/progenitor cells (DPSCs) can be easily obtained and can have excellent proliferative and mineralization potentials. Therefore, many studies have investigated the isolation and bone formation of DPSCs. In most previous reports, human DPSCs were traditionally isolated by exploiting their ability to adhere to plastic tissue culture dishes. DPSCs isolated by plastic adherence are frequently contaminated by other cells, which limits the ability to investigate their basic biology and regenerative properties. Additionally, the proliferative and osteogenic potentials vary depending on the isolated cells. It is very difficult to obtain cells of a sufficient quality to elicit the required effect upon transplantation. Considering clinical applications, stem cells used for regenerative medicine need to be purified in order to increase the efficiency of bone regeneration, and a stable supply of these cells must be generated. Here, we review the purification of DPSCs and studies of cranio-maxillofacial bone regeneration using these cells. Additionally, we introduce the prospective isolation of DPSCs using specific cell surface markers: low-affinity nerve growth factor and thymocyte antigen 1.
AB - Dental pulp stem cells/progenitor cells (DPSCs) can be easily obtained and can have excellent proliferative and mineralization potentials. Therefore, many studies have investigated the isolation and bone formation of DPSCs. In most previous reports, human DPSCs were traditionally isolated by exploiting their ability to adhere to plastic tissue culture dishes. DPSCs isolated by plastic adherence are frequently contaminated by other cells, which limits the ability to investigate their basic biology and regenerative properties. Additionally, the proliferative and osteogenic potentials vary depending on the isolated cells. It is very difficult to obtain cells of a sufficient quality to elicit the required effect upon transplantation. Considering clinical applications, stem cells used for regenerative medicine need to be purified in order to increase the efficiency of bone regeneration, and a stable supply of these cells must be generated. Here, we review the purification of DPSCs and studies of cranio-maxillofacial bone regeneration using these cells. Additionally, we introduce the prospective isolation of DPSCs using specific cell surface markers: low-affinity nerve growth factor and thymocyte antigen 1.
KW - Bone regeneration
KW - Cranio-maxillofacial
KW - Dental pulp stem/progenitor cell
KW - Flow cytometry
KW - Isolation
KW - Low-affinity nerve growth factor receptor
KW - Osteogenic potential
KW - THY-1
KW - Transplantation
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U2 - 10.1186/s41232-017-0039-4
DO - 10.1186/s41232-017-0039-4
M3 - Review article
AN - SCOPUS:85059967376
SN - 1880-9693
VL - 37
SP - 1
EP - 10
JO - Inflammation and Regeneration
JF - Inflammation and Regeneration
IS - 1
ER -