Proliferation and stemness preservation of human adipose-derived stem cells by surface-modified in situ TiO₂ nanofibrous surfaces
Two important criteria of an ideal biomaterial in the field of stem cells research are to regulate the cell proliferation without the loss of its pluripotency and to direct the differentiation into a specific cell lineage when desired. The present study describes the influence of TiO2 nanofibrous su...
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Published in: | International journal of nanomedicine Vol. 9; pp. 5389 - 5401 |
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21-11-2014
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Abstract | Two important criteria of an ideal biomaterial in the field of stem cells research are to regulate the cell proliferation without the loss of its pluripotency and to direct the differentiation into a specific cell lineage when desired. The present study describes the influence of TiO2 nanofibrous surface structures on the regulation of proliferation and stemness preservation of adipose-derived stem cells (ADSCs). TiO2 nanofiber arrays were produced in situ onto Ti-6Al-4V substrate via a thermal oxidation process and the successful fabrication of these nanostructures was confirmed by field emission scanning electron microscopy (FESEM), energy dispersive spectrometer (EDS), X-ray diffractometer (XRD), and contact angle measurement. ADSCs were seeded on two types of Ti-6Al-4V surfaces (TiO2 nanofibers and flat control), and their morphology, proliferation, and stemness expression were analyzed using FESEM, AlamarBlue assay, flow cytometry, and quantitative real-time polymerase chain reaction (qRT-PCR) after 2 weeks of incubation, respectively. The results show that ADSCs exhibit better adhesion and significantly enhanced proliferation on the TiO2 nanofibrous surfaces compared to the flat control surfaces. The greater proliferation ability of TiO2 nanofibrous surfaces was further confirmed by the results of cell cycle assay. More importantly, TiO2 nanofibrous surfaces significantly upregulate the expressions of stemness markers Sox-2, Nanog3, Rex-1, and Nestin. These results demonstrate that TiO2 nanofibrous surfaces can be used to enhance cell adhesion and proliferation while simultaneously maintaining the stemness of ADSCs, thereby representing a promising approach for their potential application in the field of bone tissue engineering as well as regenerative therapies. |
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AbstractList | Two important criteria of an ideal biomaterial in the field of stem cells research are to regulate the cell proliferation without the loss of its pluripotency and to direct the differentiation into a specific cell lineage when desired. The present study describes the influence of TiO2 nanofibrous surface structures on the regulation of proliferation and stemness preservation of adipose-derived stem cells (ADSCs). TiO2 nanofiber arrays were produced in situ onto Ti-6Al-4V substrate via a thermal oxidation process and the successful fabrication of these nanostructures was confirmed by field emission scanning electron microscopy (FESEM), energy dispersive spectrometer (EDS), X-ray diffractometer (XRD), and contact angle measurement. ADSCs were seeded on two types of Ti-6Al-4V surfaces (TiO2 nanofibers and flat control), and their morphology, proliferation, and stemness expression were analyzed using FESEM, AlamarBlue assay, flow cytometry, and quantitative real-time polymerase chain reaction (qRT-PCR) after 2 weeks of incubation, respectively. The results show that ADSCs exhibit better adhesion and significantly enhanced proliferation on the TiO2 nanofibrous surfaces compared to the flat control surfaces. The greater proliferation ability of TiO2 nanofibrous surfaces was further confirmed by the results of cell cycle assay. More importantly, TiO2 nanofibrous surfaces significantly upregulate the expressions of stemness markers Sox-2, Nanog3, Rex-1, and Nestin. These results demonstrate that TiO2 nanofibrous surfaces can be used to enhance cell adhesion and proliferation while simultaneously maintaining the stemness of ADSCs, thereby representing a promising approach for their potential application in the field of bone tissue engineering as well as regenerative therapies. Two important criteria of an ideal biomaterial in the field of stem cells research are to regulate the cell proliferation without the loss of its pluripotency and to direct the differentiation into a specific cell lineage when desired. The present study describes the influence of TiO 2 nanofibrous surface structures on the regulation of proliferation and stemness preservation of adipose-derived stem cells (ADSCs). TiO 2 nanofiber arrays were produced in situ onto Ti-6Al-4V substrate via a thermal oxidation process and the successful fabrication of these nanostructures was confirmed by field emission scanning electron microscopy (FESEM), energy dispersive spectrometer (EDS), X-ray diffractometer (XRD), and contact angle measurement. ADSCs were seeded on two types of Ti-6Al-4V surfaces (TiO 2 nanofibers and flat control), and their morphology, proliferation, and stemness expression were analyzed using FESEM, AlamarBlue assay, flow cytometry, and quantitative real-time polymerase chain reaction (qRT-PCR) after 2 weeks of incubation, respectively. The results show that ADSCs exhibit better adhesion and significantly enhanced proliferation on the TiO 2 nanofibrous surfaces compared to the flat control surfaces. The greater proliferation ability of TiO 2 nanofibrous surfaces was further confirmed by the results of cell cycle assay. More importantly, TiO 2 nanofibrous surfaces significantly upregulate the expressions of stemness markers Sox-2, Nanog3, Rex-1, and Nestin. These results demonstrate that TiO 2 nanofibrous surfaces can be used to enhance cell adhesion and proliferation while simultaneously maintaining the stemness of ADSCs, thereby representing a promising approach for their potential application in the field of bone tissue engineering as well as regenerative therapies. |
Author | Chua, Kien Hui Tay, Lelia Akbar, Sheikh Ali Ahmad, Roslina Pingguan-Murphy, Belinda Tan, Ai Wen |
AuthorAffiliation | 1 Department of Biomedical Engineering, University of Malaya, Kuala Lumpur, Malaysia 3 Department of Mechanical Engineering, University of Malaya, Kuala Lumpur, Malaysia 2 Department of Physiology, Faculty of Medicine, National University of Malaysia, Kuala Lumpur, Malaysia 4 Department of Materials Science and Engineering, The Ohio State University, Columbus, OH, USA |
AuthorAffiliation_xml | – name: 4 Department of Materials Science and Engineering, The Ohio State University, Columbus, OH, USA – name: 1 Department of Biomedical Engineering, University of Malaya, Kuala Lumpur, Malaysia – name: 2 Department of Physiology, Faculty of Medicine, National University of Malaysia, Kuala Lumpur, Malaysia – name: 3 Department of Mechanical Engineering, University of Malaya, Kuala Lumpur, Malaysia |
Author_xml | – sequence: 1 givenname: Ai Wen surname: Tan fullname: Tan, Ai Wen organization: Department of Biomedical Engineering, University of Malaya, Kuala Lumpur, Malaysia – sequence: 2 givenname: Lelia surname: Tay fullname: Tay, Lelia organization: Department of Physiology, Faculty of Medicine, National University of Malaysia, Kuala Lumpur, Malaysia – sequence: 3 givenname: Kien Hui surname: Chua fullname: Chua, Kien Hui organization: Department of Physiology, Faculty of Medicine, National University of Malaysia, Kuala Lumpur, Malaysia – sequence: 4 givenname: Roslina surname: Ahmad fullname: Ahmad, Roslina organization: Department of Mechanical Engineering, University of Malaya, Kuala Lumpur, Malaysia – sequence: 5 givenname: Sheikh Ali surname: Akbar fullname: Akbar, Sheikh Ali organization: Department of Materials Science and Engineering, The Ohio State University, Columbus, OH, USA – sequence: 6 givenname: Belinda surname: Pingguan-Murphy fullname: Pingguan-Murphy, Belinda organization: Department of Biomedical Engineering, University of Malaya, Kuala Lumpur, Malaysia |
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CitedBy_id | crossref_primary_10_1002_biot_201500519 crossref_primary_10_1016_j_ijpharm_2020_119656 crossref_primary_10_1016_j_nano_2019_01_008 crossref_primary_10_1016_j_jiec_2017_08_047 crossref_primary_10_1002_smll_201904099 crossref_primary_10_2174_1874325001610010920 crossref_primary_10_3390_ijms24043551 crossref_primary_10_1016_j_ijpharm_2021_120733 crossref_primary_10_1016_j_bioactmat_2018_12_004 crossref_primary_10_1016_j_colsurfb_2021_112019 crossref_primary_10_1007_s40883_019_00091_9 crossref_primary_10_1038_srep21828 |
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Copyright | 2014 Tan et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License 2014 |
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Keywords | stem cells thermal oxidation pluripotency titania nanofibers |
Language | English |
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SubjectTerms | Adipocytes - drug effects Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Cell Physiological Phenomena - drug effects Cells, Cultured Humans Nanofibers - chemistry Original Research Pluripotent Stem Cells - drug effects Surface Properties Titanium - chemistry |
Title | Proliferation and stemness preservation of human adipose-derived stem cells by surface-modified in situ TiO₂ nanofibrous surfaces |
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