Tae Hoon Seo
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Tae Hoon Seo has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Jung-Suk Sung
Department of Life Science, Dongguk University-Seoul, Goyang-si, Republic of Korea
1 shared publication Myung Jong Kim
Applied Quantum Composites Research Center, Korea Institute of Science and Technology, Jeonbuk 565-905, Republic of Korea
1 shared publicationSeula Lee
Applied Quantum Composites Research Center, Korea Institute of Science and Technology, Jeonbuk 565-905, Republic of Korea
1 shared publicationWonhee Jang
Department of Life Science, Dongguk University, Goyang, Gyeonggi-do, 10326, Republic of Korea
1 shared publicationYoo‐Jung Lee
Department of Life Science, Dongguk University, Goyang, Gyeonggi-do, 10326, Republic of Korea
1 shared publication
Latest Publications
- 23 September 2017
- Published by Wiley in Journal of Biomedical Materials Research Part A
- Vol. 106 (1) , 43-51
Neuronal differentiation of human mesenchymal stem cells in response to the domain size of graphene substrates
Graphene is a noncytotoxic monolayer platform with unique physical, chemical, and biological properties. It has been demonstrated that graphene substrate may provide a promising biocompatible scaffold for stem cell therapy. Because chemical vapor deposited graphene has a two dimensional polycrystalline structure, it is important to control the individual domain size to obtain desirable properties for nano‐material. However, the biological effects mediated by differences in domain size of graphene have not yet been reported. On the basis of the control of graphene domain achieved by one‐step growth (1step‐G, small domain) and two‐step growth (2step‐G, large domain) process, we found that the neuronal differentiation of bone marrow‐derived human mesenchymal stem cells (hMSCs) highly depended on the graphene domain size. The defects at the domain boundaries in 1step‐G graphene was higher (×8.5) and had a relatively low (13% lower) contact angle of water droplet than 2step‐G graphene, leading to enhanced cell‐substrate adhesion and upregulated neuronal differentiation of hMSCs. We confirmed that the strong interactions between cells and defects at the domain boundaries in 1step‐G graphene can be obtained due to their relatively high surface energy, which is stronger than interactions between cells and graphene surfaces. Our results may provide valuable information on the development of graphene‐based scaffold by understanding which properties of graphene domain influence cell adhesion efficacy and stem cell differentiation. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 43–51, 2018.
- 23 September 2017
- Published by Wiley in Journal of Biomedical Materials Research Part A
- Vol. 106 (1) , 43-51
Neuronal differentiation of human mesenchymal stem cells in response to the domain size of graphene substrates
Graphene is a noncytotoxic monolayer platform with unique physical, chemical, and biological properties. It has been demonstrated that graphene substrate may provide a promising biocompatible scaffold for stem cell therapy. Because chemical vapor deposited graphene has a two dimensional polycrystalline structure, it is important to control the individual domain size to obtain desirable properties for nano‐material. However, the biological effects mediated by differences in domain size of graphene have not yet been reported. On the basis of the control of graphene domain achieved by one‐step growth (1step‐G, small domain) and two‐step growth (2step‐G, large domain) process, we found that the neuronal differentiation of bone marrow‐derived human mesenchymal stem cells (hMSCs) highly depended on the graphene domain size. The defects at the domain boundaries in 1step‐G graphene was higher (×8.5) and had a relatively low (13% lower) contact angle of water droplet than 2step‐G graphene, leading to enhanced cell‐substrate adhesion and upregulated neuronal differentiation of hMSCs. We confirmed that the strong interactions between cells and defects at the domain boundaries in 1step‐G graphene can be obtained due to their relatively high surface energy, which is stronger than interactions between cells and graphene surfaces. Our results may provide valuable information on the development of graphene‐based scaffold by understanding which properties of graphene domain influence cell adhesion efficacy and stem cell differentiation. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 43–51, 2018.