Apoptosis Regulation in Dental Pulp Cells and PD-1/PD-L1 Expression Dynamics Under Ozone Exposure – A Pilot Approach

This study aimed to determine the effect of ozone on the expression of and genes in dental pulp cells. Additionally, the programmed cell death protein 1, programmed death-ligand 1, and CD200 antigens were determined in lymphocytes to assess their surface expression. Dental pulp cells were cultured f...

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Veröffentlicht in:Archivum Immunologiae et Therapiae Experimentalis 2024-01, Vol.72 (1)
Hauptverfasser: Ptasiewicz, Maja, Orłowski, Mirosław, Magryś, Agnieszka, Kocki, Janusz, Gosik, Krzysztof, Stachurski, Piotr, Chałas, Renata
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Sprache:eng
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Zusammenfassung:This study aimed to determine the effect of ozone on the expression of and genes in dental pulp cells. Additionally, the programmed cell death protein 1, programmed death-ligand 1, and CD200 antigens were determined in lymphocytes to assess their surface expression. Dental pulp cells were cultured from extracted healthy third molars and characterized as dental pulp stromal cells. Gene expression of and was analyzed at 0 s, 6 s, and 12 s of ozone exposure using real-time PCR. Lymphocytes from dental pulp were subjected to ozone exposure for 12 s and PD-1, PD-L1, and CD200/CD200R expression was analyzed by flow cytometry. Upon exposure to ozone for 6 s, the expression decreased significantly to −0.09, and at 12 s, it increased significantly to 0.3. gene expression level increased significantly to 0.188 after 6 s exposure, and at 12 s, to 0.16. Lymphocytes exposed to ozone for 12 s showed minimal changes in PD-1, PD-L1, and CD200/CD200R expression levels, indicating that oxidative stress does not impact the signaling pathways regulating these molecules. The significant upregulation of at 12 s highlights the cells’ effort to protect themselves from prolonged oxidative stress, possibly tipping the balance toward cell survival and tissue repair. However, the absence of changes in PD-1 and PD-L1 expression on lymphocytes under oxidative stress suggests that these molecules are not sensitive to oxidative stress in this context.
ISSN:1661-4917
1661-4917
DOI:10.2478/aite-2024-0019