Long-Term Culture Reveals Passage-Dependent Decline in the Secretome of Human Adipose-Derived Mesenchymal Stem Cells After Diagnostic-Level Radiation Exposure
Authors:
- Alexander KorneevAKAlexander Korneev
- Taisia TrubchenkovaTTTaisia Trubchenkova
- Anna ChigasovaACAnna Chigasova
- Andrey OsipovAOAndrey Osipov
- Maxim IgnatovMIMaxim Ignatov
- Yuriy FedotovYFYuriy Fedotov
- Petr EreminPEPetr Eremin
- Ilia BuianovIBIlia Buianov
- Natalia VorobyevaNVNatalia Vorobyeva
- Nikolay ZyuzikovNZNikolay Zyuzikov
- Andreyan N OsipovAOAndreyan N Osipov
Preprint
- 28 November 2025
- preprint
- Published by MDPI AG in Preprints.org
Abstract
The growing use of computed tomography (CT) in medicine requires a better understanding of how low-dose radiation affects human stem cells. This study investigated the long-term consequences of CT-level radiation on the secretory profile of human adipose-derived mesenchymal stem cells (AD-MSCs). AD-MSCs were exposed to radiation regimens simulating a single or multiple head CT scans, or to a single 2 Gy therapeutic dose, and their secretion of 41 cytokines, chemokines, and growth factors was monitored during long-term culture. At the early passage, AD-MSCs receiving a single 2 Gy dose showed a coordinated increase in several lymphocyte-regulating cytokines compared to cells exposed to multiple CT scans. However, these initial differences were not sustained. Long-term culturing led to a progressive and widespread decrease in the secretion of 26 cytokines, chemokines, and growth factors across all groups. By the latest passage, all irradiated cells showed a generalized reduction in secretory function compared to non-irradiated controls. These findings demonstrate that while different radiation regimens trigger distinct immediate responses, long-term culture results in a broad decline of the AD-MSCs secretome, which is accentuated by prior radiation exposure. This underscores the importance of assessing long-term consequences to fully evaluate the functional impact of diagnostic radiation on stem cells.Keywords
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