AdMSC spheroids encapsulating antioxidant hybrid protein carrier for irradiation-damaged salivary gland repair
Authors:
- Byulhana KimBKByulhana Kim
- Hyerin YooHYHyerin Yoo
- Young Ju SonYSYoung Ju Son
- Seyun AhnSASeyun Ahn
- Jeonghoon LeeJLJeonghoon Lee
- Young KimYKYoung Kim
- Tae Hee KimTKTae Hee Kim
- Min Rye EomMEMin Rye Eom
- Young Bin ChoyYCYoung Bin Choy
- Justin J. ChungJCJustin J. Chung
- Seong Keun KwonSKSeong Keun Kwon
Open Access
- 1 September 2026
- journal article
- Published by KEAI Publishing in Bioactive Materials
- Vol. 63, 166-187
Abstract
Radiation therapy for head and neck cancer often causes xerostomia, a chronic salivary gland (SG) dysfunction driven by excessive reactive oxygen species (ROS), severely impacting the quality of life of patients. Existing treatments, such as artificial saliva or SG stimulants, offer only temporary relief. We developed a novel therapeutic system combining glutathione (GSH)-conjugated gelatin (Gel) hybrid protein-based cell carrier (GC) with adipose-derived mesenchymal stem cell (AdMSC) spheroids. This hybrid protein carrier (GC) extended the antioxidant activity of GSH by overcoming its short half-life and enabled efficient encapsulation and delivery of AdMSC spheroids to irradiation (IR)-damaged SGs. The 3D spheroids enhanced vascular endothelial growth factor (VEGF) expression through hypoxic core formation, promoting angiogenesis. In an IR-damaged mouse model, spheroid-encapsulated GC increased SOD2 expression and decreased 8-OHdG and NOX4 levels, effectively mitigating oxidative stress, fibrosis, and apoptosis, while accelerating angiogenesis. SG structural regeneration and functional recovery were confirmed using histological and immunohistochemical analyses following spheroid-encapsulating GC treatment. These results demonstrate the synergistic effects of ROS-scavenging activity from GC and paracrine signaling from AdMSC spheroids. This groundbreaking spheroid-encapsulating GC improves SG regeneration and functional recovery by integrating antioxidant activity with angiogenic effects, offering a paradigm-shifting solution for other oxidative stress-mediated tissue disorders.Keywords
Funding Information
- Ministry of Health and Welfare (RS-2024-00403047)
- Ministry of Health and Welfare (22A0103L1-11)
- Ministry of Trade, Industry and Energy
- Ministry of Science and ICT, South Korea (RS-2025-00561239)
- Ministry of Science and ICT, South Korea (HX23C1718)
- Ministry of Science and ICT, South Korea (25A0107L1)
- Ministry of Food and Drug Safety
- Korea Health Industry Development Institute
- Ministry of Health and Family Welfare
- National Research Foundation of Korea
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