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Long-term passage impacts human dental pulp stem cell activities and cell response to drug addition in vitro.
Patntirapong, Somying; Khankhow, Juthaluck; Julamorn, Sikarin.
Affiliation
  • Patntirapong S; Thammasat University Research Unit in Dental and Bone Substitute Biomaterials, Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.
  • Khankhow J; Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.
  • Julamorn S; Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.
PeerJ ; 12: e17913, 2024.
Article in En | MEDLINE | ID: mdl-39193517
ABSTRACT

Background:

Dental pulp stem cells (DPSCs) possess mesenchymal stem cell characteristics and have potential for cell-based therapy. Cell expansion is essential to achieve sufficient cell numbers. However, continuous cell replication causes cell aging in vitro, which usually accompanies and potentially affect DPSC characteristics and activities. Continuous passaging could alter susceptibility to external factors such as drug treatment. Therefore, this study sought to investigate potential outcome of in vitro passaging on DPSC morphology and activities in the absence or presence of external factor.

Methods:

Human DPSCs were subcultured until reaching early passages (P5), extended passages (P10), and late passages (P15). Cells were evaluated and compared for cell and nuclear morphologies, cell adhesion, proliferative capacity, alkaline phosphatase (ALP) activity, and gene expressions in the absence or presence of external factor. Alendronate (ALN) drug treatment was used as an external factor.

Results:

Continuous passaging of DPSCs gradually lost their normal spindle shape and increased in cell and nuclear sizes. DPSCs were vulnerable to ALN. The size and shape were altered, leading to morphological abnormality and inhomogeneity. Long-term culture and ALN interfered with cell adhesion. DPSCs were able to proliferate irrespective of cell passages but the rate of cell proliferation in late passages was slower. ALN at moderate dose inhibited cell growth. ALN caused reduction of ALP activity in early passage. In contrast, extended passage responded differently to ALN by increasing ALP activity. Late passage showed higher collagen but lower osteocalcin gene expressions compared with early passage in the presence of ALN.

Conclusion:

An increase in passage number played critical role in cell morphology and activities as well as responses to the addition of an external factor. The effects of cell passage should be considered when used in basic science research and clinical applications.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Adhesion / Alendronate / Dental Pulp / Cell Proliferation Limits: Humans Language: En Journal: PeerJ Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Adhesion / Alendronate / Dental Pulp / Cell Proliferation Limits: Humans Language: En Journal: PeerJ Year: 2024 Document type: Article Affiliation country: Country of publication: