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      Effect of Fibronectin-Coated Micro-Grooved Titanium Surface on Alignment, Adhesion, and Proliferation of Human Gingival Fibroblasts

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          Abstract

          Background

          Surface characters of culture plates affect cellular behaviors such as cellular alignment and elongation. Microgrooves guide the cell growth along the grooves and spread. The aim of this study was to observe the effect of fibronectin (FN)-coated micro-grooved titanium plates on the alignment, spread, adhesion, and proliferation of human gingival fibroblasts (HGFs).

          Material/Methods

          Micro-grooved titanium plates were fabricated, and FN was immobilized onto the micro-grooved surfaces using silanization. HGFs were cultured on the smoothed or micro-grooved (with 35 μm width, 15 μm bridge, 10 μm depth) titanium plates, with or without the FN coating. We assessed the water contact angle and blood compatibility of the surfaces, and the earlier adhesion, adhesion strength, proliferation and morphology of the cells growing on the different titanium surfaces.

          Results

          The results revealed that the blood hemolysis rates of different titanium surfaces were within the safety limits. HGFs aligned along the grooves, spread out more evidently, and showed significantly more adhesion in the FN-coated micro-grooved surface compared with other surfaces ( p<0.05).

          Conclusions

          The micro-grooved surface coated with FN guides the HGFs to align along the grooves, and promotes cell spread, adhesion and proliferation, which might be used to improve the efficacy of dental implants.

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          Most cited references18

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          Qualitative and quantitative study of human osteoblast adhesion on materials with various surface roughnesses.

          We quantitatively evaluated the adhesion of human osteoblasts on orthopedic metallic substrates (Ti6Al4V alloy) with various surface roughnesses at several times after inoculation and studied its correlation with qualitative changes in the expression of adhesion proteins and with parameters extensively describing the surface topographies. Cells were orientated in a parallel order on polished surfaces. This orientation was not affected by residual grooves after polishing. On sandblasted surfaces the cells never attained confluence and had a stellate shape, and the cell layer had no particular organization. Extracellular matrix (fibronectin, type I collagen, osteopontin) and cytoskeletal protein (actin, vinculin) orientation reflected the cell layer organization. In our experiment human osteoblasts expressed alpha3beta1 integrin but not alpha2beta1 integrin. In addition to currently analyzed roughness magnitude parameters, we calculated roughness organization parameters (fractal dimension parameters) of the substrates. We observed lower adhesion and proliferation on less organized surfaces (i.e., sandblasted ones). The significant statistical correlation observed between fractal dimension parameters (describing surface roughness organization) and cell parameters adds a new concept to the studies of substratum roughness influence on cell behavior. An attempt at modelization of the cell-surface interaction was made that includes the influence of fractal dimensions parameters. Copyright 2000 John Wiley & Sons, Inc.
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            Topographical control of cell behaviour. I. Simple step cues.

            The photolithographic techniques of the microelectronics industry have allowed us to fabricate patterned plastic substrata to investigate contact guidance of animal tissue cells. The reactions of cells to single steps on a substratum were examined using time-lapse videorecording and scanning electron microscopy. BHK cells and chick embryonic neural cell processes exhibited gradual inhibition of crossing steps with a concomitant increase in alignment at steps dependent on increasing step height. Comparison of these cells' reactions, with those of chick heart fibroblasts and rabbit neutrophils, at a 5 micron step revealed that the influence of topography is also dependent on cell type, the neutrophils being relatively unaffected. The presence of an adhesive difference at a series of steps altered BHK cells' reactions such that the frequency of crossing was dependent on the direction of approach to a step. Although our data are consistent with Dunn & Heath's proposal (1976) that the inflexibility of the cytoskeleton of a moving cell's protrusion is the cellular property determining such reactions to topography, we have found that, on encountering a topographical feature, the response of a cell may be predictable on a probabilistic basis, i.e. the topographical feature reduces the probability of a cell making a successful protrusion and contact in a given direction, that even the largest features tested did not act as absolute barriers to cell locomotion since a small proportion of a population of cells were able to overcome them, and that other guidance cues could significantly alter a cell's response. Even in situations where it is not the primary cue in directing cell locomotion, topographical control may be an important factor during morphogenesis since it must, at the very least, influence the efficiency of other cues.
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              The effect of topographic characteristics on cell migration velocity.

              The migration of cells on structured surfaces is known to be affected by its surface topography. Although the effects of topography have been extensively investigated the crucial parameters determining the cell-surface reaction are largely unknown. The present study was performed to describe and to define the role of groove/elevation (ridge) dimensions at the micrometre scale on fibroblast cell migration by correlating cell shape, migration angle alpha, cell orientation beta and velocity with these dimensions. For this a quantitative method was developed. We could show that the surface structures significantly influenced migration direction alpha, cell orientation beta and mean velocity, as well as migration speed in the directions parallel and perpendicular to the grooves/elevations in a surface structure dependant way. Cell migration velocity parallel, respectively, perpendicular to the structures was significantly affected by the geometries and dimensions of the substratum. Surface structures were not able to significantly affect distribution patterns of cell shapes. Overall, it could be shown that differently structured surfaces influenced the cells but no crucial feature could be clearly identified, suggesting that the reaction of the surface structure might be far more complex than generally is assumed.
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                Author and article information

                Journal
                Med Sci Monit
                Med. Sci. Monit
                Medical Science Monitor
                Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
                International Scientific Literature, Inc.
                1234-1010
                1643-3750
                2017
                04 October 2017
                : 23
                : 4749-4759
                Affiliations
                [1 ]School of Stomatology, Fujian Medical University, Fuzhou, Fujian, P.R. China
                [2 ]Department of Oral Implantology, Fujian Stomatological Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, P.R. China
                Author notes
                Corresponding Author: Jiang Chen, e-mail: dentistjiang@ 123456126.com
                [A]

                Study Design

                [B]

                Data Collection

                [C]

                Statistical Analysis

                [D]

                Data Interpretation

                [E]

                Manuscript Preparation

                [F]

                Literature Search

                [G]

                Funds Collection

                Article
                903883
                10.12659/MSM.903883
                5637573
                28974670
                d038727b-2327-40ec-9f2b-b4b26493aacb
                © Med Sci Monit, 2017

                This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International ( CC BY-NC-ND 4.0)

                History
                : 19 February 2017
                : 27 March 2017
                Categories
                Lab/In Vitro Research

                fibroblasts,fibronectins,titanium
                fibroblasts, fibronectins, titanium

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