Characterization of Silk Fibroin Modified Surface : A Proteomic View of Cellular Response Proteins Induced by Biomaterials
The purpose of this study was to develop the pathway of silk fibroin (SF) biopolymer surface induced cell membrane protein activation. Fibroblasts were used as an experimental model to evaluate the responses of cellular proteins induced by biopolymer material using a mass spectrometry-based profilin...
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Published in | BioMed Research International Vol. 2014; no. 2014; pp. 1 - 13 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Puplishing Corporation
01.01.2014
Hindawi Publishing Corporation Hindawi Limited John Wiley & Sons, Inc |
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Abstract | The purpose of this study was to develop the pathway of silk fibroin (SF) biopolymer surface induced cell membrane protein activation. Fibroblasts were used as an experimental model to evaluate the responses of cellular proteins induced by biopolymer material using a mass spectrometry-based profiling system. The surface was covered by multiwalled carbon nanotubes (CNTs) and SF to increase the surface area, enhance the adhesion of biopolymer, and promote the rate of cell proliferation. The amount of adhered fibroblasts on CNTs/SF electrodes of quartz crystal microbalance (QCM) greatly exceeded those on other surfaces. Moreover, analyzing differential protein expressions of adhered fibroblasts on the biopolymer surface by proteomic approaches indicated that CD44 may be a key protein. Through this study, utilization of mass spectrometry-based proteomics in evaluation of cell adhesion on biopolymer was proposed. |
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AbstractList | The purpose of this study was to develop the pathway of silk fibroin (SF) biopolymer surface induced cell membrane protein activation. Fibroblasts were used as an experimental model to evaluate the responses of cellular proteins induced by biopolymer material using a mass spectrometry-based profiling system. The surface was covered by multiwalled carbon nanotubes (CNTs) and SF to increase the surface area, enhance the adhesion of biopolymer, and promote the rate of cell proliferation. The amount of adhered fibroblasts on CNTs/SF electrodes of quartz crystal microbalance (QCM) greatly exceeded those on other surfaces. Moreover, analyzing differential protein expressions of adhered fibroblasts on the biopolymer surface by proteomic approaches indicated that CD44 may be a key protein. Through this study, utilization of mass spectrometry-based proteomics in evaluation of cell adhesion on biopolymer was proposed. The purpose of this study was to develop the pathway of silk fibroin (SF) biopolymer surface induced cell membrane protein activation. Fibroblasts were used as an experimental model to evaluate the responses of cellular proteins induced by biopolymer material using a mass spectrometry-based profiling system. The surface was covered by multiwalled carbon nanotubes (CNTs) and SF to increase the surface area, enhance the adhesion of biopolymer, and promote the rate of cell proliferation. The amount of adhered fibroblasts on CNTs/SF electrodes of quartz crystal microbalance (QCM) greatly exceeded those on other surfaces. Moreover, analyzing differential protein expressions of adhered fibroblasts on the biopolymer surface by proteomic approaches indicated that CD44 may be a key protein. Through this study, utilization of mass spectrometry-based proteomics in evaluation of cell adhesion on biopolymer was proposed.The purpose of this study was to develop the pathway of silk fibroin (SF) biopolymer surface induced cell membrane protein activation. Fibroblasts were used as an experimental model to evaluate the responses of cellular proteins induced by biopolymer material using a mass spectrometry-based profiling system. The surface was covered by multiwalled carbon nanotubes (CNTs) and SF to increase the surface area, enhance the adhesion of biopolymer, and promote the rate of cell proliferation. The amount of adhered fibroblasts on CNTs/SF electrodes of quartz crystal microbalance (QCM) greatly exceeded those on other surfaces. Moreover, analyzing differential protein expressions of adhered fibroblasts on the biopolymer surface by proteomic approaches indicated that CD44 may be a key protein. Through this study, utilization of mass spectrometry-based proteomics in evaluation of cell adhesion on biopolymer was proposed. |
Audience | Academic |
Author | Chen, Wen-Cheng Tsai, Wan-Chi Tyan, Yu Chang Lin, Po-Chiao Lu, Chi Yu Chung, Tze Wen Jong, Shiang-Bin Yang, Ming Hui Chiang, Pei-Wen Yuan, Shyng Shiou |
AuthorAffiliation | 7 Department of Medical Imaging and Radiological Sciences, Kaohsiung Medical University, Kaohsiung 807, Taiwan 5 School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan 8 Department of Nuclear Medicine, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 807, Taiwan 15 Center of Biomedical Engineering and System Biology, Kaohsiung Medical University, Kaohsiung 807, Taiwan 14 Department of Chemistry, National Sun Yat-Sen University, Kaohsiung 804, Taiwan 10 National Sun Yat-Sen University-Kaohsiung Medical University Joint Research Center, Kaohsiung 804, Taiwan 9 Department of Biochemistry, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan 3 Translational Research Center, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 807, Taiwan 13 Department of Fiber and Composite Materials, College of Engineering, Feng Chia University, Taichung 407, Taiwan 2 Department of Medical Research, Kaohsiung Medical Universi |
AuthorAffiliation_xml | – name: 7 Department of Medical Imaging and Radiological Sciences, Kaohsiung Medical University, Kaohsiung 807, Taiwan – name: 8 Department of Nuclear Medicine, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 807, Taiwan – name: 4 Department of Obstetrics and Gynecology, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 807, Taiwan – name: 9 Department of Biochemistry, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan – name: 12 Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan – name: 13 Department of Fiber and Composite Materials, College of Engineering, Feng Chia University, Taichung 407, Taiwan – name: 11 Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan – name: 2 Department of Medical Research, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 807, Taiwan – name: 10 National Sun Yat-Sen University-Kaohsiung Medical University Joint Research Center, Kaohsiung 804, Taiwan – name: 1 Instrument Technology Research Center, National Applied Research Laboratories, Hsinchu 300, Taiwan – name: 14 Department of Chemistry, National Sun Yat-Sen University, Kaohsiung 804, Taiwan – name: 15 Center of Biomedical Engineering and System Biology, Kaohsiung Medical University, Kaohsiung 807, Taiwan – name: 3 Translational Research Center, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 807, Taiwan – name: 5 School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan – name: 6 Department of Biomedical Engineering, National Yang-Ming University, Taipei 112, Taiwan |
Author_xml | – sequence: 1 fullname: Lin, Po-Chiao – sequence: 2 fullname: Chiang, Pei-Wen – sequence: 3 fullname: Tyan, Yu Chang – sequence: 4 fullname: Yang, Ming Hui – sequence: 5 fullname: Chen, Wen-Cheng – sequence: 6 fullname: Tsai, Wan-Chi – sequence: 7 fullname: Lu, Chi Yu – sequence: 8 fullname: Yuan, Shyng Shiou – sequence: 9 fullname: Chung, Tze Wen – sequence: 10 fullname: Jong, Shiang-Bin |
BackLink | https://cir.nii.ac.jp/crid/1873399490521803904$$DView record in CiNii https://www.ncbi.nlm.nih.gov/pubmed/24818131$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s10570_021_04126_9 crossref_primary_10_1155_2016_1917394 crossref_primary_10_3389_fbioe_2022_816513 crossref_primary_10_1038_s41545_022_00170_5 crossref_primary_10_3389_fbioe_2021_793778 crossref_primary_10_3762_bjnano_10_133 crossref_primary_10_1007_s10854_019_01751_w crossref_primary_10_1021_acsami_9b09066 crossref_primary_10_1002_jbm_b_33560 |
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ContentType | Journal Article |
Contributor | Chen, Wen-Cheng Tsai, Wan-Chi Tyan, Yu Chang Lin, Po-Chiao Lu, Chi Yu Chung, Tze Wen Jong, Shiang-Bin Yang, Ming Hui Chiang, Pei-Wen Yuan, Shyng Shiou |
Contributor_xml | – sequence: 1 fullname: Lin, Po-Chiao – sequence: 2 fullname: Chiang, Pei-Wen – sequence: 3 fullname: Tyan, Yu Chang – sequence: 4 fullname: Yang, Ming Hui – sequence: 5 fullname: Chen, Wen-Cheng – sequence: 6 fullname: Tsai, Wan-Chi – sequence: 7 fullname: Lu, Chi Yu – sequence: 8 fullname: Yuan, Shyng Shiou – sequence: 9 fullname: Chung, Tze Wen – sequence: 10 fullname: Jong, Shiang-Bin |
Copyright | Copyright © 2014 Ming-Hui Yang et al. COPYRIGHT 2014 John Wiley & Sons, Inc. Copyright © 2014 Ming-Hui Yang et al. Ming-Hui Yang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright © 2014 Ming-Hui Yang et al. 2014 |
Copyright_xml | – notice: Copyright © 2014 Ming-Hui Yang et al. – notice: COPYRIGHT 2014 John Wiley & Sons, Inc. – notice: Copyright © 2014 Ming-Hui Yang et al. Ming-Hui Yang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. – notice: Copyright © 2014 Ming-Hui Yang et al. 2014 |
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Snippet | The purpose of this study was to develop the pathway of silk fibroin (SF) biopolymer surface induced cell membrane protein activation. Fibroblasts were used as... |
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SubjectTerms | Animals Biocompatible Materials Biocompatible Materials - pharmacology Biomedical materials Biomedical research Bromodeoxyuridine Bromodeoxyuridine - metabolism Cell Adhesion Cell adhesion & migration Cell Adhesion - drug effects Cell Proliferation Cell Proliferation - drug effects Cell Shape Cell Shape - drug effects Electrodes Fibroblasts Fibroblasts - cytology Fibroblasts - drug effects Fibroins Fibroins - pharmacology Gene Ontology Hospitals Hyaluronan Receptors Hyaluronan Receptors - metabolism Immunohistochemistry Mass Spectrometry Microscopy, Atomic Force Nanotubes, Carbon Nanotubes, Carbon - chemistry Proteins Proteins - metabolism Proteomics Quartz Crystal Microbalance Techniques Research Article Science Silk Spectroscopy, Fourier Transform Infrared Surface Properties |
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Title | Characterization of Silk Fibroin Modified Surface : A Proteomic View of Cellular Response Proteins Induced by Biomaterials |
URI | https://search.emarefa.net/detail/BIM-454746 https://dx.doi.org/10.1155/2014/209469 https://cir.nii.ac.jp/crid/1873399490521803904 https://www.ncbi.nlm.nih.gov/pubmed/24818131 https://www.proquest.com/docview/1517833486 https://www.proquest.com/docview/1524174670 https://www.proquest.com/docview/1524423193 https://pubmed.ncbi.nlm.nih.gov/PMC3982454 |
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