Document Type
Article
Language
eng
Publication Date
2-23-2018
Publisher
Taylor & Francis
Source Publication
Artificial Cells, Nanomedicine, and Biotechnology: An International Journal
Source ISSN
2169-141X
Abstract
Placenta-derived amniotic epithelial cells (AECs), a great cell source for tissue engineering and stem cell therapy, are immunologically inert in their native state; however, immunological changes in these cells after culture and differentiation have challenged their applications. The aim of this study was to investigate the effect of 2D and 3D scaffolds on human lymphocyte antigens (HLA) expression by AECs. The effect of different preparation parameters including pre-freezing time and temperature was evaluated on 3D chitosan–gelatine scaffolds properties. Evaluation of MHC class I, HLA-DR and HLA-G expression in AECs after 7 d culture on 2D bed and 3D scaffold of chitosan–gelatine showed that culture of AECs on the 2D substrate up-regulated MHC class I and HLA-DR protein markers on AECs surface and down-regulated HLA-G protein. In contrast, 3D scaffold did not increase protein expression of MHC class I and HLA-DR. Moreover, HLA-G protein expression remained unchanged in 3D culture. These results confirm that 3D scaffold can remain AECs in their native immunological state and modification of physical properties of the scaffold is a key regulator of immunological markers at the gene and protein expression levels; a strategy which circumvents rejection challenge of amniotic stem cells to be translated into the clinic.
Recommended Citation
Azizian, Sara; Katami, Fatemeh; Modaresifar, Khashayar; Mosaffa, Nariman; Peirovi, Habibollah; Tayebi, Lobat; Bahrami, Soheyl; Redl, Heinz; and Niknejad, Hassan, "Immunological Compatibility Status of Placenta-Derived Stem Cells is Mediated by Scaffold 3D Structure" (2018). School of Dentistry Faculty Research and Publications. 272.
https://epublications.marquette.edu/dentistry_fac/272
Comments
Accepted version. Artificial Cells, Nanomedicine, and Biotechnology: An International Journal, Vol. 46, Supplement 1 (2018):876-884. DOI. © 2018 Taylor and Francis. Used with permission.