| Literature DB >> 27514999 |
Katsuhiro Uzawa1, Atsushi Kasamatsu2, Tomoaki Saito3, Toshikazu Takahara3, Yasuyuki Minakawa3, Kazuyuki Koike2, Masanobu Yamatoji2, Dai Nakashima2, Morihiro Higo2, Yosuke Sakamoto2, Masashi Shiiba4, Hideki Tanzawa5.
Abstract
Because of cellular senescence/apoptosis, no effective culture systems are available to maintain replication of cells from odontogenic tumors especially for odontoma, and, thus, the ability to isolate human odontoma-derived cells (hODCs) for functional studies is needed. The current study was undertaken to develop an approach to isolate hODCs and fully characterize the cells in vitro. The hODCs were cultured successfully with a Rho-associated protein kinase inhibitor (Y-27632) for an extended period with stabilized lengths of the telomeres to sustain a similar phenotype/property as the primary tumoral cells. While the hODCs showed stable long-term expansion with expression of major dental epithelial markers including dentin sialophosphoprotein (DSPP) even in the three-dimensional microenvironment, they lack the specific markers for the characteristics of stem cells. Moreover, cells from dental pulp showed significant up-regulation of DSPP when co-cultured with the hODCs, while control fibroblasts with the hODCs did not. Taken together, we propose that the hODCs can be isolated and expanded over the long term with Y-27632 to investigate not only the development of the hODCs but also other types of benign human tumors.Entities:
Keywords: Dentin sialophosphoprotein; Long-term culture; Mineralization; Odontoma; Rho kinase inhibitor; Telomere
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Year: 2016 PMID: 27514999 DOI: 10.1016/j.yexcr.2016.08.005
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905