Cell reprogramming using extracellular vesicles from differentiating stem cells into white/beige adipocytes
- Authors
- Jung, Youn Jae; Kim, Hark Kyun; Cho, Yoonsuk; Choi, Ji Suk; Woo, Chang Hee; Lee, Kyoung Soo; Sul, Jae Hoon; Lee, Chan Mi; Han, Jihoon; Park, Jae Hyung; Jo, Dong-Gyu; Cho, Yong Woo
- Issue Date
- Mar-2020
- Publisher
- AMER ASSOC ADVANCEMENT SCIENCE
- Citation
- SCIENCE ADVANCES, v.6, no.13, pp 1 - 14
- Pages
- 14
- Indexed
- SCIE
SCOPUS
- Journal Title
- SCIENCE ADVANCES
- Volume
- 6
- Number
- 13
- Start Page
- 1
- End Page
- 14
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/1251
- DOI
- 10.1126/sciadv.aay6721
- ISSN
- 2375-2548
2375-2548
- Abstract
- Stem cell-derived extracellular vesicles (EVs) offer alternative approaches to stem cell-based therapy for regenerative medicine. In this study, stem cell EVs derived during differentiation are developed to use as cell-free therapeutic systems by inducing tissue-specific differentiation. EVs are isolated from human adipose-derived stem cells (HASCs) during white and beige adipogenic differentiation (D-EV and BD-EV, respectively) via tangential flow filtration. D-EV and BD-EV can successfully differentiate HASCs into white and beige adipocytes, respectively. D-EV are transplanted with collagen/methylcellulose hydrogels on the backs of BALB/c mice, and they produce numerous lipid droplets in injected sites. Treatments of BD-EV attenuate diet-induced obesity through browning of adipose tissue in mice. Furthermore, high-fat diet-induced hepatic steatosis and glucose tolerance are improved by BD-EV treatment. miRNAs are responsible for the observed effects of BD-EV. These results reveal that secreted EVs during stem cell differentiation into white adipocytes or beige adipocytes can promote cell reprogramming.
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