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SIRT1 directly regulates SOX2 to maintain self-renewal and multipotency in bone marrow-derived mesenchymal stem cells.

Authors
 Dong Suk Yoon  ;  Yoorim Choi  ;  Yeonsue Jang  ;  Moses Lee  ;  Woo Jin Choi  ;  Sung Hwan Kim  ;  Jin Woo Lee 
Citation
 Stem Cells, Vol.32(12) : 3219-3231, 2014 
Journal Title
 Stem Cells 
ISSN
 1066-5099 
Issue Date
2014
Abstract
SOX2 is crucial for the maintenance of the self-renewal capacity and multipotency of mesenchymal stem cells (MSCs); however, the mechanism by which SOX2 is regulated remains unclear. Here, we report that RNA interference of sirtuin 1 (SIRT1) in human bone marrow (BM)-derived MSCs leads to a decrease of SOX2 protein, resulting in the deterioration of the self-renewal and differentiation capacities of BM-MSCs. Using immunoprecipitation, we demonstrated direct binding between SIRT1 and SOX2 in HeLa cells overexpressing SOX2. We further discovered that the RNA interference of SIRT1 induces the acetylation, nuclear export, and ubiquitination of SOX2, leading to proteasomal degradation in BM-MSCs. SOX2 suppression by trichostatin A (TSA), a known histone deacetylase inhibitor, was reverted by treatment with resveratrol (0.1 and 1 µM), a known activator of SIRT1 in BM-MSCs. Furthermore, 0.1 and 1 µM resveratrol reduced TSA-mediated acetylation and ubiquitination of SOX2 in BM-MSCs. SIRT1 activation by resveratrol enhanced the colony-forming ability and differentiation potential to osteogenic and adipogenic lineages in a dose-dependent manner. However, the enhancement of self-renewal and multipotency by resveratrol was significantly decreased to basal levels by RNA interference of SOX2. These results strongly suggest that the SIRT1-SOX2 axis plays an important role in maintaining the self-renewal capability and multipotency of BM-MSCs. In conclusion, our findings provide evidence for positive SOX2 regulation by post-translational modification in BM-MSCs through the inhibition of nuclear export and subsequent ubiquitination, and demonstrate that SIRT1-mediated deacetylation contributes to maintaining SOX2 protein in the nucleus.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/stem.1811/abstract
DOI
10.1002/stem.1811
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Orthopedic Surgery (정형외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
Yonsei Authors
김성환(Kim, Sung Hwan) ORCID logo https://orcid.org/0000-0001-5743-6241
윤동석(Yoon, Dong Suk)
이모세(Lee, Mo Ses)
이진우(Lee, Jin Woo) ORCID logo https://orcid.org/0000-0002-0293-9017
장연수(Jang, Yeon Sue) ORCID logo https://orcid.org/0000-0001-5683-0001
최우진(Choi, Woo Jin)
최유림(Choi, Yoo Rim)
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URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/138356
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