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Reinforcing Stromal Cell Spheroid Through Red-Light Preconditioning for Advanced Vascularization
  • Kim, Yu Jin ;
  • Kim, Hyeok ;
  • Lee, Dong Hyun ;
  • Kim, Yeong Hwan ;
  • Park, Jae Hyun ;
  • Sim, Woo Sup ;
  • Kim, Jin Ju ;
  • Ban, Kiwon ;
  • Um, Soong Ho ;
  • Park, Hyun Ji ;
  • Davis, Michael E. ;
  • Park, Hun Jun ;
  • Bhang, Suk Ho
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Publication Year
2025-01-01
Journal
Advanced Science
Publisher
John Wiley and Sons Inc
Citation
Advanced Science
Keyword
angiogenesisarteriogenesismyocardial infarctionOPBM-preconditioningstromal cell spheroid
Mesh Keyword
AngiogenesisArteriogenesisCell spheroidsCell therapyHuman adiposeMyocardial InfarctionOLED-based photobiomodulation-preconditioningPhotobiomodulationStromal cell spheroidStromal cells
All Science Classification Codes (ASJC)
Medicine (miscellaneous)Chemical Engineering (all)Materials Science (all)Biochemistry, Genetics and Molecular Biology (miscellaneous)Engineering (all)Physics and Astronomy (all)
Abstract
Despite the promising potential of stromal cell therapy in treating myocardial infarction (MI), its effectiveness is limited by poor cell retention and engraftment in ischemic environments. This study introduces a novel strategy that combines the preconditioning of human adipose-derived stromal cells (hADSCs) using OLED-based photobiomodulation (OPBM) and culturing these cells into 3D spheroids. The preconditioned 3D spheroids (APCS group) exhibit significantly enhanced angiogenic, arterialized, and tissue remodeling capabilities compared with those of traditional 2D cultures and non-preconditioned spheroids. In vivo transplantation of these spheroids into the border zone of infarcted area significantly improve cardiac function and reduce adverse remodeling by enhancing anti-fibrosis and angiogenesis including arterialization. The combined strategy with OPBM preconditioning and 3D spheroid culture system can enhance therapeutic potential of hADSCs with multiple paracrine effects for cardiac repair. This novel approach provides next generation of cell therapeutics to overcome the limitation of adult stromal cell therapy in patients with post-MI heart failure.
ISSN
2198-3844
Language
eng
URI
https://aurora.ajou.ac.kr/handle/2018.oak/38287
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105003808920&origin=inward
DOI
https://doi.org/10.1002/advs.202500788
Journal URL
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2198-3844
Type
Article
Funding
Y.\u2010J.K. and H.K. contributed equally to this work. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (the Ministry of Science and ICT) (Nos. RS\u20102024\u201000440285, RS\u20102024\u201300405818, Republic of Korea), the Korean Fund for Regenerative Medicine (KFRM) grant funded by the Korea government (the Ministry of Science and ICT, the Ministry of Health & Welfare) (No. 21A0102L1\u201012, Republic of Korea), and from the Korea Evaluation Institute of Industrial Technology (KEIT 00434908, NTIS 2410002810), the Ministry of Trade, Industry & Energy, Republic of Korea.
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College of Bio-convergence Engineering
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