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      Micro and Nanofabrication methods to control cell-substrate interactions and cell behavior: A review from the tissue engineering perspective

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          Abstract

          Cell-substrate interactions play a crucial role in the design of better biomaterials and integration of implants with the tissues. Adhesion is the binding process of the cells to the substrate through interactions between the surface molecules of the cell membrane and the substrate. There are several factors that affect cell adhesion including substrate surface chemistry, topography, and stiffness. These factors physically and chemically guide and influence the adhesion strength, spreading, shape and fate of the cell. Recently, technological advances enabled us to precisely engineer the geometry and chemistry of substrate surfaces enabling the control of the interaction cells with the substrate. Some of the most commonly used surface engineering methods for eliciting the desired cellular responses on biomaterials are photolithography, electron beam lithography, microcontact printing, and microfluidics. These methods allow production of nano- and micron level substrate features that can control cell adhesion, migration, differentiation, shape of the cells and the nuclei as well as measurement of the forces involved in such activities. This review aims to summarize the current techniques and associate these techniques with cellular responses in order to emphasize the effect of chemistry, dimensions, density and design of surface patterns on cell-substrate interactions. We conclude with future projections in the field of cell-substrate interactions in the hope of providing an outlook for the future studies.

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          Highlights

          • This article aims to provide insight into cell-material interactions and importance of topography on cellular processes.

          • Reviewed current progress of nano and micropatterning techniques.

          • Review mainly focused on fabrication of nano-micropatterns and interaction with cells.

          • Discussed the relation between surface topography and cell adhesion, morphology, proliferation and fate.

          • Reviewed the literature on biomaterial substrate modification.

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          Most cited references125

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          The control of human mesenchymal cell differentiation using nanoscale symmetry and disorder.

          A key tenet of bone tissue engineering is the development of scaffold materials that can stimulate stem cell differentiation in the absence of chemical treatment to become osteoblasts without compromising material properties. At present, conventional implant materials fail owing to encapsulation by soft tissue, rather than direct bone bonding. Here, we demonstrate the use of nanoscale disorder to stimulate human mesenchymal stem cells (MSCs) to produce bone mineral in vitro, in the absence of osteogenic supplements. This approach has similar efficiency to that of cells cultured with osteogenic media. In addition, the current studies show that topographically treated MSCs have a distinct differentiation profile compared with those treated with osteogenic media, which has implications for cell therapies.
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            Transmembrane crosstalk between the extracellular matrix--cytoskeleton crosstalk.

            Integrin-mediated cell adhesions provide dynamic, bidirectional links between the extracellular matrix and the cytoskeleton. Besides having central roles in cell migration and morphogenesis, focal adhesions and related structures convey information across the cell membrane, to regulate extracellular-matrix assembly, cell proliferation, differentiation, and death. This review describes integrin functions, mechanosensors, molecular switches and signal-transduction pathways activated and integrated by adhesion, with a unifying theme being the importance of local physical forces.
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              Polymer surface modification for the attachment of bioactive compounds

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                Author and article information

                Contributors
                Journal
                Bioact Mater
                Bioact Mater
                Bioactive Materials
                KeAi Publishing
                2452-199X
                18 May 2018
                September 2018
                18 May 2018
                : 3
                : 3
                : 355-369
                Affiliations
                [a ]BIOMATEN, Middle East Technical University (METU) Center of Excellence in Biomaterials and Tissue Engineering, Ankara, Turkey
                [b ]METU, Department of Biomedical Engineering, Ankara, Turkey
                [c ]METU, Department of Biotechnology, Ankara, Turkey
                [d ]METU, Department of Biological Sciences, Ankara, Turkey
                Author notes
                []Corresponding author. BIOMATEN, Middle East Technical University (METU) Center of Excellence in Biomaterials and Tissue Engineering, Ankara, Turkey. vhasirci@ 123456metu.edu.tr
                [1]

                These authors contributed equally to this work.

                Article
                S2452-199X(17)30155-X
                10.1016/j.bioactmat.2018.05.005
                6026330
                29988483
                4210e3a5-99e3-4948-a3dc-71c4d4e1af63
                © 2018 The Authors. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 30 December 2017
                : 9 May 2018
                : 10 May 2018
                Categories
                Article

                microfabrication,micropattern,cell-material interaction,differentiation,cell adhesion

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