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Mitophagy induction improves salivary gland stem/progenitor cell function by reducing senescence after irradiation

Davide Cinat, Anna Lena De Souza, Abel Soto-Gamez, Anne L. Jellema-de Bruin, Robert P. Coppes, Lara Barazzuol

Radiotherapy and Oncology · 2023 · ▲ 25 citations

Abstract

BACKGROUND AND PURPOSE: Patients undergoing radiotherapy for head and neck cancer often experience a decline in their quality of life due to the co-irradiation of salivary glands. Radiation-induced cellular senescence(definition) is a key factor contributing to salivary gland dysfunction. Interestingly, mitochondrial dysfunction(definition) and cellular senescence have been reported to be strongly interconnected and thus implicated in several aging-related diseases. This study aims to investigate the role of mitochondrial dysfunction in senescence induction in salivary gland stem/progenitor cells after irradiation. MATERIALS AND METHODS: A dose of 7 Gy photons was used to irradiate mouse salivary gland organoids. Senescent markers and mitochondrial function were assessed using rt-qPCR, western blot analysis, SA-β-Gal staining and flow cytometry analysis. Mitochondrial dynamics-related proteins were detected by western blot analysis while Mdivi-1 and MFI8 were used to modulate the mitochondrial fission process. To induce mitophagy, organoids were treated with Urolithin A and PMI and subsequently stem/progenitor cell self-renewal capacity was assessed as organoid forming efficiency. RESULTS: Irradiation led to increased senescence and accumulation of dysfunctional mitochondria. This was accompanied by a strong downregulation of mitochondrial fission-related proteins and mitophagy-related genes. After irradiation, treatment with the mitophagy inducer Urolithin A attenuated the senescent phenotype and improved organoid growth and stem/progenitor cell self-renewal capacity. CONCLUSION: This study shows the important interplay between senescence and mitochondrial dysfunction after irradiation. Importantly, activation of mitophagy improved salivary gland stem/progenitor cell function thereby providing a novel therapeutic strategy to restore the regenerative capacity of salivary glands following irradiation.

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OpenAlex
DOI
10.1016/j.radonc.2023.110028
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2026-06-26 MST

Cite this

APA
Cinat, D., Souza, A.L.D., Soto-Gamez, A., Bruin, A.L.J., Coppes, R.P., &amp; Barazzuol, L. (2023). Mitophagy induction improves salivary gland stem/progenitor cell function by reducing senescence after irradiation. <em>Radiotherapy and Oncology</em>. https://doi.org/10.1016/j.radonc.2023.110028
Vancouver
Cinat D, Souza ALD, Soto-Gamez A, Bruin ALJ, Coppes RP, Barazzuol L. Mitophagy induction improves salivary gland stem/progenitor cell function by reducing senescence after irradiation. Radiotherapy and Oncology. 2023. doi:10.1016/j.radonc.2023.110028.
BibTeX
@article{davide2023Mitoph, title = {Mitophagy induction improves salivary gland stem/progenitor cell function by reducing senescence after irradiation}, author = {Davide Cinat and Anna Lena De Souza and Abel Soto-Gamez and Anne L. Jellema-de Bruin and Robert P. Coppes and Lara Barazzuol}, journal = {Radiotherapy and Oncology}, year = {2023}, doi = {10.1016/j.radonc.2023.110028}, }

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