Dual Roles of Graphene Oxide in Chondrogenic Differentiation of Adult Stem Cells: Cell-Adhesion Substrate and Growth Factor-Delivery Carrier

Here, it is shown that graphene oxide (GO) can be utilized as both a cell‐adhesion substrate and a growth factor protein‐delivery carrier for the chondrogenic differentiation of adult stem cells. Conventionally, chondrogenic differentiation of stem cells is achieved by culturing cells in pellets and...

Full description

Saved in:
Bibliographic Details
Published inAdvanced functional materials Vol. 24; no. 41; pp. 6455 - 6464
Main Authors Yoon, Hee Hun, Bhang, Suk Ho, Kim, Taeho, Yu, Taekyung, Hyeon, Taeghwan, Kim, Byung-Soo
Format Journal Article
LanguageEnglish
Published Blackwell Publishing Ltd 05.11.2014
Subjects
Online AccessGet full text
ISSN1616-301X
1616-3028
DOI10.1002/adfm.201400793

Cover

More Information
Summary:Here, it is shown that graphene oxide (GO) can be utilized as both a cell‐adhesion substrate and a growth factor protein‐delivery carrier for the chondrogenic differentiation of adult stem cells. Conventionally, chondrogenic differentiation of stem cells is achieved by culturing cells in pellets and adding the protein transforming growth factor‐β3 (TGF‐β3), a chondrogenic factor, to the culture medium. However, pellets mainly provide cell‐cell interaction and diffusional limitation of TGF‐β3 may occur inside the pellet both of these factors may limit the chondrogenic differentiation of stem cells. In this study, GO sheets (size = 0.5–1 μm) were utilized to adsorb fibronectin (FN, a cell‐adhesion protein) and TGF‐β3 and were then incorporated in pellets of human adipose‐derived stem cells (hASCs). The hybrid pellets of hASC‐GO enhanced the chondrogenic differentiation of hASCs by adding the cell‐FN interaction and supplying TGF‐β3 effectively. This method may provide a new platform for stem cell culture for regenerative medicine. Graphene oxide can be used as both a cell‐adhesion substrate and a growth factor delivery carrier for the chondrogenic differentiation of adult stem cells.
Bibliography:National Research Foundation of Korea - No. 2013036054; No. 2013035745
ArticleID:ADFM201400793
ark:/67375/WNG-96GB7SBW-0
Korea Health 21 R&D Project, Ministry of Health and Welfare - No. H12C0199
istex:91002B2A7ED72089DF0EAC86FEDB0E3DE7679599
These authors contributed equally.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.201400793