Fibroblast function recovery through rejuvenation effect of nanovesicles extracted from human adipose-derived stem cells irradiated with red light

Authors
Hyun, JiyuEom, JiinIm, JisooKim, Yu-JinSeo, InwooKim, Sung -WonIm, Gwang-BumKim, Yeong HwanLee, Dong-HyunPark, Hyun SuYun, Dae WonKim, Dong-IkYoon, Jeong-KeeUm, Soong HoYang, Dae HyeokBhang, Suk Ho
Issue Date
2024-04
Publisher
Elsevier BV
Citation
Journal of Controlled Release, v.368, pp.453 - 465
Abstract
Fibroblasts (hDFs) are widely employed for skin regeneration and the treatment of various skin disorders, yet research were rarely investigated about restoration of diminished therapeutic efficacy due to cell senescence. The application of stem cell and stem cell-derived materials, exosomes, were drawn attention for the restoration functionality of fibroblasts, but still have limitation for unintended side effect or low yield. To advance, stem cellderived nanovesicle (NV) have developed for effective therapeutic reagents with high yield and low risk. In this study, we have developed a method using red light irradiated human adipose-derived stem cells (hADSCs) derived NV (R-NVs) for enhancing the therapeutic efficacy and rejuvenating hDFs. Through red light irradiation, we were able to significantly increase the content of stemness factors and angiogenic biomolecules in R-NVs. Treatment with these R-NVs was found to enhance the migration ability and leading to rejuvenation of old hDFs to levels similar to those of young hDFs. In subsequent in vivo experiments, the treatment of old hDFs with R-NVs demonstrated a superior skin wound healing effect, surpassing that of young hDFs. In summary, this study successfully induced rejuvenation and leading to increased therapeutic efficacy to R-NVs treated old hDFs previously considered as biowaste.
Keywords
TRANSCRIPTIONAL REGULATION; CELLULAR SENESCENCE; GROWTH-FACTOR; PROLIFERATION; PHOTOBIOMODULATION; EXPRESSION; INVASION; TISSUE; PLURIPOTENCY; RECRUITMENT; Aging; Fibroblast; Fibroblast rejuvenation; Human adipose -derived mesenchymal stem cell; Photobiomodulation; Stem cell therapy; Stem cell nanovesicle; Wound closing
ISSN
0168-3659
URI
https://pubs.kist.re.kr/handle/201004/149887
DOI
10.1016/j.jconrel.2024.02.047
Appears in Collections:
KIST Article > 2024
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