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Immortalized Cell Lines Derived from Dental/odontogenic Tissue

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Journal Cell Tissue Res
Date 2023 Apr 11
PMID 37039940
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Abstract

Stem cells derived from dental/odontogenic tissue have the property of multiple differentiation and are prospective in tooth regenerative medicine and cellular and molecular studies. However, in the face of cellular senescence soon in vitro, the proliferation ability of the cells is limited, so studies are hindered to some extent. Fortunately, immortalization strategies are expected to solve the above issues. Cellular immortalization is that cells are immortalized by introducing oncogenes, human telomerase reverse transcriptase genes (hTERT), or miscellaneous immortalization genes to get unlimited proliferation. At present, a variety of immortalized stem cells from dental/odontogenic tissue has been successfully generated, such as dental pulp stem cells (DPSCs), periodontal ligament cells (PDLs), stem cells from human exfoliated deciduous teeth (SHEDs), dental papilla cells (DPCs), and tooth germ mesenchymal cells (TGMCs). This review summarized establishment and applications of immortalized stem cells from dental/odontogenic tissues and then discussed the advantages and challenges of immortalization.

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References
1.
Alcorta D, Xiong Y, Phelps D, Hannon G, Beach D, Barrett J . Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts. Proc Natl Acad Sci U S A. 1996; 93(24):13742-7. PMC: 19411. DOI: 10.1073/pnas.93.24.13742. View

2.
Maciel Palacio Alvarez M, de Carvalho R, Barbosa S, Polassi M, Nascimento F, DAlpino P . Oxidative stress induced by self-adhesive resin cements affects gene expression, cellular proliferation and mineralization potential of the MDPC-23 odontoblast-like cells. Dent Mater. 2019; 35(4):606-616. DOI: 10.1016/j.dental.2019.02.008. View

3.
Anitua E, Troya M, Zalduendo M . Progress in the use of dental pulp stem cells in regenerative medicine. Cytotherapy. 2018; 20(4):479-498. DOI: 10.1016/j.jcyt.2017.12.011. View

4.
Aranha A, Giro E, Souza P, Hebling J, de Souza Costa C . Effect of curing regime on the cytotoxicity of resin-modified glass-ionomer lining cements applied to an odontoblast-cell line. Dent Mater. 2006; 22(9):864-9. DOI: 10.1016/j.dental.2005.11.015. View

5.
Arany S, Kawagoe M, Sugiyama T . Application of spontaneously immortalized odontoblast cells in tooth regeneration. Biochem Biophys Res Commun. 2009; 381(1):84-9. DOI: 10.1016/j.bbrc.2009.02.025. View