Journal articles: 'Cell surfaces'

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Pasternak, C. A. "Cell Surfaces." Interdisciplinary Science Reviews 10, no. 1 (March 1985): 42–55. http://dx.doi.org/10.1179/isr.1985.10.1.42.

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Sentandreu, Rafael, and Teun Boekhout. "Yeast cell surfaces." FEMS Yeast Research 6, no. 7 (November 2006): 947–48. http://dx.doi.org/10.1111/j.1567-1364.2006.00168.x.

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Lamponi, Stefania, Clara Dl Canio, and Rolando Barbucci. "Heterotypic Cell-Cell Interaction on Micropatterned Surfaces." International Journal of Artificial Organs 32, no. 8 (August 2009): 507–16. http://dx.doi.org/10.1177/039139880903200805.

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Purpose The aim of this paper was to study the influence of chemical and topographical signals on cell behavior and to obtain a heterotypic cell-cell interaction on microstructured domains. Methods The polysaccharide hyaluronic acid (Hyal) was photoimmobilized on glass surfaces in order to obtain a pattern with squares and rectangles of different dimensions and chemistry. The microstructured surfaces were characterized by Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM). The behavior of Human Coronary Artery Endothelial Cells (HCAEC) and human tumoral dermal fibroblasts (C54) was investigated on these micropatterned surfaces by adhesion studies. Moreover, heterotypic interaction among C54 and HCAEC adherent on patterned surfaces was evaluated by time-lapse video microscopy. Results Surface analysis revealed the presence of a pattern consisting of alternating glass and Hyal microstructures whose dimensions decreased from the center to the edge of the sample. Neither HCAEC nor C54 adhered to the immobilized Hyal but both adapted their shape to the different sizes of the glass squares and rectangles. The number of adherent cells depended on the dimensions of both the glass domains and the nuclei of the cells. Co-cultured C54 on HCAEC patterned surfaces showed a heterotypic cell-cell interaction in the same chemical and topographic domain. Conclusions A heterotypic cell-cell interaction occurred in the same chemical and topographic micro-domains but in narrow areas only. Moreover, the number of cells adhering to the glass domains and cell morphology depended on the dimensions of both adhesive areas and cell nuclei.

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Qi, Jing, Weishuo Li, Xiaoling Xu, Feiyang Jin, Di Liu, Yan Du, Jun Wang, et al. "Cyto-friendly polymerization at cell surfaces modulates cell fate by clustering cell-surface receptors." Chemical Science 11, no. 16 (2020): 4221–25. http://dx.doi.org/10.1039/c9sc06385d.

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Abbina, Srinivas, Erika M. J. Siren, Haisle Moon, and Jayachandran N. Kizhakkedathu. "Surface Engineering for Cell-Based Therapies: Techniques for Manipulating Mammalian Cell Surfaces." ACS Biomaterials Science & Engineering 4, no. 11 (September 11, 2017): 3658–77. http://dx.doi.org/10.1021/acsbiomaterials.7b00514.

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Sedláčková, P., M. Čeřovský, I. Horsáková, and M. Voldřich. "Cell surface characteristic of Asaia bogorensis – spoilage microorganism of bottled water." Czech Journal of Food Sciences 29, No. 4 (August 10, 2011): 457–61. http://dx.doi.org/10.17221/96/2011-cjfs.

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The ability of bacteria to attach to a surface and develop a biofilm has been of considerable interest for many groups in the food industry. Biofilms may serve as a chronic source of microbial contamination and the research into biofilms and cells interactions might help to improve general understanding of the biofilm resistance mechanisms. Multitude of factors, including surface conditioning, surface charge and roughness and hydrophobicity, are thought to be involved in the initial attachment. Hydrophobic interactions have been widely suggested as responsible for much of the adherence of cells to surfaces. Cell-surface hydrophobicity is an important factor in the adherence and subsequent proliferation of microorganisms on solid surfaces and at interfaces. In the present study, we have estimated the cell-surface characteristics of Asaia bogorensis – isolated contamination of flavoured bottled water and compared its ability to colonise surfaces which are typical in the beverage production – stainless steel, glass and plastic materials.

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Dalby, Matthew J. "Nanostructured surfaces: cell engineering and cell biology." Nanomedicine 4, no. 3 (April 2009): 247–48. http://dx.doi.org/10.2217/nnm.09.1.

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Akiyama, Y. "Design of Temperature-Responsive Cell Culture Surfaces for Cell Sheet Engineering." Cyborg and Bionic Systems 2021 (February 3, 2021): 1–15. http://dx.doi.org/10.34133/2021/5738457.

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Temperature-responsive cell culture surfaces, which modulate cell attachment/detachment characteristics with temperature, have been used to fabricate cell sheets. Extensive study on fabrication of cell sheet with the temperature-responsive cell culture surface, manipulation, and transplantation of the cell sheet has established the interdisciplinary field of cell sheet engineering, in which engineering, biological, and medical fields closely collaborate. Such collaboration has pioneered cell sheet engineering, making it a promising and attractive technology in tissue engineering and regenerative medicine. This review introduces concepts of cell sheet engineering, followed by designs for the fabrication of various types of temperature-responsive cell culture surfaces and technologies for cell sheet manipulation. The development of various methods for the fabrication of temperature-responsive cell culture surfaces was also summarized. The availability of cell sheet engineering for the treatment and regeneration of damaged human tissue has also been described, providing examples of the clinical application of cell sheet transplantation in humans.

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Toss, Henrik, Susanna Lönnqvist, David Nilsson, Anurak Sawatdee, Josefin Nissa, Simone Fabiano, Magnus Berggren, Gunnar Kratz, and Daniel T. Simon. "Ferroelectric surfaces for cell release." Synthetic Metals 228 (June 2017): 99–104. http://dx.doi.org/10.1016/j.synthmet.2017.04.013.

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Félez, J. "Plasminogen binding to cell surfaces." Fibrinolysis and Proteolysis 12, no. 4 (July 1998): 183–89. http://dx.doi.org/10.1016/s0268-9499(98)80012-x.

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MIZUSHIMA, Shoji. "Studies on bacterial cell surfaces." Journal of the agricultural chemical society of Japan 63, no. 1 (1989): 1–8. http://dx.doi.org/10.1271/nogeikagaku1924.63.1.

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Keough, K. M. W., P. Hyam, D. A. Pink, and B. Quinn. "Cell surfaces and fractal dimensions." Journal of Microscopy 163, no. 1 (July 1991): 95–99. http://dx.doi.org/10.1111/j.1365-2818.1991.tb03163.x.

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Clark, Peter. "Cell behaviour on micropatterned surfaces." Biosensors and Bioelectronics 9, no. 9-10 (1994): 657–61. http://dx.doi.org/10.1016/0956-5663(94)80062-6.

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Kou, Peng Meng, Zvi Schwartz, Barbara D. Boyan, and Julia E. Babensee. "Dendritic cell responses to surface properties of clinical titanium surfaces." Acta Biomaterialia 7, no. 3 (March 2011): 1354–63. http://dx.doi.org/10.1016/j.actbio.2010.10.020.

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Falconnet, Didier, Gabor Csucs, H. Michelle Grandin, and Marcus Textor. "Surface engineering approaches to micropattern surfaces for cell-based assays." Biomaterials 27, no. 16 (June 2006): 3044–63. http://dx.doi.org/10.1016/j.biomaterials.2005.12.024.

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Llopis-Grimalt, Maria Antonia, Andreu Miquel Amengual-Tugores, Marta Monjo, and Joana Maria Ramis. "Oriented Cell Alignment Induced by a Nanostructured Titanium Surface Enhances Expression of Cell Differentiation Markers." Nanomaterials 9, no. 12 (November 22, 2019): 1661. http://dx.doi.org/10.3390/nano9121661.

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A key factor for dental implant success is a good sealing between the implant surface and both soft (gum) and hard (bone) tissues. Surface nanotopography can modulate cell response through mechanotransduction. The main objective of this research was the development of nanostructured titanium (Ti) surfaces that promote both soft and hard tissue integration with potential application in dental implants. Nanostructured Ti surfaces were developed by electrochemical anodization—nanopores (NPs) and nanonets (NNs)—and characterized by atomic force microscopy, scanning electronic microscopy, and contact angle analysis. In addition, nanoparticle release and apoptosis activation were analyzed on cell culture. NP surfaces showed nanoparticle release, which increased in vitro cell apoptosis. Primary human gingival fibroblasts (hGFs) and human bone marrow mesenchymal stem cells (hBM-MSCs) were used to test cell adhesion, cytotoxicity, metabolic activity, and differentiation markers. Finally, cell orientation on the different surfaces was analyzed using a phalloidin staining. NN surfaces induced an oriented alignment of both cell types, leading in turn to an improved expression of differentiation markers. Our results suggest that NN structuration of Ti surfaces has great potential to be used for dental implant abutments to improve both soft and hard tissue integration.

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Wang, Chenlu, Sagar Chowdhury, Meghan Driscoll, Carole A. Parent, S. K. Gupta, and Wolfgang Losert. "The interplay of cell–cell and cell–substrate adhesion in collective cell migration." Journal of The Royal Society Interface 11, no. 100 (November 6, 2014): 20140684. http://dx.doi.org/10.1098/rsif.2014.0684.

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Collective cell migration often involves notable cell–cell and cell–substrate adhesions and highly coordinated motion of touching cells. We focus on the interplay between cell–substrate adhesion and cell–cell adhesion. We show that the loss of cell-surface contact does not significantly alter the dynamic pattern of protrusions and retractions of fast migrating amoeboid cells ( Dictyostelium discoideum ), but significantly changes their ability to adhere to other cells. Analysis of the dynamics of cell shapes reveals that cells that are adherent to a surface may coordinate their motion with neighbouring cells through protrusion waves that travel across cell–cell contacts. However, while shape waves exist if cells are detached from surfaces, they do not couple cell to cell. In addition, our investigation of actin polymerization indicates that loss of cell-surface adhesion changes actin polymerization at cell–cell contacts. To further investigate cell–cell/cell–substrate interactions, we used optical micromanipulation to form cell–substrate contact at controlled locations. We find that both cell-shape dynamics and cytoskeletal activity respond rapidly to the formation of cell–substrate contact.

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Hembree, D. M., J. C. Oswald, and N. R. Smyrl. "Surface-Enhanced Raman Microspectroscopy at Electrode Surfaces." Applied Spectroscopy 41, no. 2 (February 1987): 267–72. http://dx.doi.org/10.1366/000370287774986787.

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Surface-enhanced Raman microspectroscopy has been developed as a technique for characterizing processes occurring at the electrode/electrolyte interface. A spectroelectrochemical cell was designed to obtain Raman spectra of electrochemical species with the use of microscope optics, which allowed unambiguous placement of the laser focus at the electrode surface with spatial resolution on the order of 1 µm. It was also possible to visually inspect the surface morphology of the electrode with the use of the Raman microscope in the reflected-light mode. The capabilities of the spectroelectrochemical cell were demonstrated by observation of surface-enhanced Raman scattering (SERS) for a variety of model systems (pyridine, pyridinium ion, potassium cyanide) with the use of silver, copper, and nickel electrodes. The electrochemical behavior of a commercially important gold electroplating process is also reported.

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KOBAYASHI, Akira, and Toshihiro AKAIKE. "Biological Surfaces. Surface Modification and Control of Cell Functions by Design of Cell Specific Materials." Journal of the Surface Finishing Society of Japan 45, no. 2 (1994): 152–59. http://dx.doi.org/10.4139/sfj.45.152.

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Martínez-Campos, Enrique, Tamara Elzein, Alice Bejjani, Maria Jesús García-Granda, Ana Santos-Coquillat, Viviana Ramos, Alexandra Muñoz-Bonilla, and Juan Rodríguez-Hernández. "Toward Cell Selective Surfaces: Cell Adhesion and Proliferation on Breath Figures with Antifouling Surface Chemistry." ACS Applied Materials & Interfaces 8, no. 10 (March 7, 2016): 6344–53. http://dx.doi.org/10.1021/acsami.5b12832.

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Banerjee, P., D. J. Irvine, A. M. Mayes, and L. G. Griffith. "Polymer latexes for cell-resistant and cell-interactive surfaces." Journal of Biomedical Materials Research 50, no. 3 (June 5, 2000): 331–39. http://dx.doi.org/10.1002/(sici)1097-4636(20000605)50:3<331::aid-jbm6>3.0.co;2-t.

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Moussa, Hassan, Megan Logan, Kingsley Wong, Zheng Rao, Marc Aucoin, and Ting Tsui. "Nanoscale-Textured Tantalum Surfaces for Mammalian Cell Alignment." Micromachines 9, no. 9 (September 13, 2018): 464. http://dx.doi.org/10.3390/mi9090464.

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Tantalum is one of the most important biomaterials used for surgical implant devices. However, little knowledge exists about how nanoscale-textured tantalum surfaces affect cell morphology. Mammalian (Vero) cell morphology on tantalum-coated comb structures was studied using high-resolution scanning electron microscopy and fluorescence microscopy. These structures contained parallel lines and trenches with equal widths in the range of 0.18 to 100 μm. Results showed that as much as 77% of adherent cell nuclei oriented within 10° of the line axes when deposited on comb structures with widths smaller than 10 μm. However, less than 20% of cells exhibited the same alignment performance on blanket tantalum films or structures with line widths larger than 50 μm. Two types of line-width-dependent cell morphology were observed. When line widths were smaller than 0.5 μm, nanometer-scale pseudopodia bridged across trench gaps without contacting the bottom surfaces. In contrast, pseudopodia structures covered the entire trench sidewalls and the trench bottom surfaces of comb structures with line-widths larger than 0.5 μm. Furthermore, results showed that when a single cell simultaneously adhered to multiple surface structures, the portion of the cell contacting each surface reflected the type of morphology observed for cells individually contacting the surfaces.

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Dubin-Thalor, Benjamin, and Michael P. Sheetz. "LS3A2 TIRF Analyses of Cell Spreading On Matrixcoated Surfaces Reveals STEPs : stochastic, timed extension periods." Seibutsu Butsuri 42, supplement2 (2002): S224. http://dx.doi.org/10.2142/biophys.42.s224_1.

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Hanein, D., H. Sabanay, L. Addadi, and B. Geiger. "Selective interactions of cells with crystal surfaces. Implications for the mechanism of cell adhesion." Journal of Cell Science 104, no. 2 (February 1, 1993): 275–88. http://dx.doi.org/10.1242/jcs.104.2.275.

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In this study we have characterized the mode of cell adhesion to calcite and calcium (R,R)-tartrate tetrahydrate crystals. The use of crystals as adhesion substrata was motivated by their well-established chemical nature and structurally defined surfaces. We show that calcite binds A6 Xenopus laevis epithelial cells rapidly and efficiently, most likely via surface-adsorbed proteins. Surface topology had only a limited effect on the adhesive interactions. Calcium (R,R)-tartrate tetrahydrate crystals exhibits two chemically equivalent, yet structurally distinct faces that differ mainly in the surface distribution of their lattice water molecules and charges. However, despite the gross similarity between the two faces striking differences were noted in their adhesive behavior. One of the faces was highly adhesive for cells, leading to protein-independent attachment and spreading followed by cell death. In contrast, cell adhesion to the other surface of tartrate was slow (> 24 h) and apparently mediated by RGD-containing protein(s). It was further shown that the latter face of tartrate crystals could be “conditioned” by long (24 h) incubation with serum-containing medium, after which it becomes highly adhesive. The results presented here indicate that crystal surfaces may serve as excellent, structurally defined, substrata for cell adhesion, that cell binding may occur directly or via RGD-containing proteins and that cell adhesion may be dramatically modulated by variations in surface structure. The implications of the results to the mechanism of cell-substratum adhesion are discussed.

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Rezania, Alireza, Robert Johnson, Anthony R. Lefkow, and Kevin E. Healy. "Bioactivation of Metal Oxide Surfaces. 1. Surface Characterization and Cell Response." Langmuir 15, no. 20 (September 1999): 6931–39. http://dx.doi.org/10.1021/la990024n.

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Mwenifumbo, Steven, Mingwei Li, Jianbo Chen, Aboubaker Beye, and Wolé Soboyejo. "Cell/surface interactions on laser micro-textured titanium-coated silicon surfaces." Journal of Materials Science: Materials in Medicine 18, no. 1 (January 2007): 9–23. http://dx.doi.org/10.1007/s10856-006-0658-9.

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Fu, G., and W. O. Soboyejo. "Cell/surface interactions of human osteo-sarcoma (HOS) cells and micro-patterned polydimelthylsiloxane (PDMS) surfaces." Materials Science and Engineering: C 29, no. 6 (August 2009): 2011–18. http://dx.doi.org/10.1016/j.msec.2009.03.017.

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Shi, Peng, Enguo Ju, Jiasi Wang, Zhengqing Yan, Jinsong Ren, and Xiaogang Qu. "Host–guest recognition on photo-responsive cell surfaces directs cell–cell contacts." Materials Today 20, no. 1 (January 2017): 16–21. http://dx.doi.org/10.1016/j.mattod.2016.12.006.

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Okano, Teruo. "Thermo-Intelligent Surfaces for Cell Culture." Advances in Science and Technology 53 (October 2006): 70–73. http://dx.doi.org/10.4028/www.scientific.net/ast.53.70.

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In order to avoid several complications resulted from biodegradable scaffolds or single cell injection, we have developed “cell sheet engineering”. Our concept is novel tissue reconstruction not from single cells but from cell sheets. In order to prepare cell sheets, temperature-responsive culture dishes are utilized. Since temperature-responsive polymers are covalently grafted on the dishes, various types of cells adhere and proliferate on them at 37°C, but are spontaneously detached only by reducing temperature below 32°C without any need for proteolytic enzyme. All the confluent cells are noninvasively harvested as a single contiguous cell sheets with intact cell-cell junctions and deposited extracellular matrix. We have utilized these harvested cell sheets for various tissue reconstructions including ocular surfaces, periodontal ligament, cardiac patches as well as bladder.

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Yang, Joseph, Masayuki Yamato, and Teruo Okano. "Cell-Sheet Engineering Using Intelligent Surfaces." MRS Bulletin 30, no. 3 (March 2005): 189–93. http://dx.doi.org/10.1557/mrs2005.51.

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AbstractThe possibility of recreating various tissues and organs for the purpose of regenerative medicine has received much interest. However, the field of tissue engineering has been restricted by the limitations of conventional approaches. A method to circumvent the need for traditional scaffold-based technologies is cell-sheet engineering, which uses temperature-responsive culture dishes. These surfaces, which are created by grafting the temperature-responsive polymer poly(N-isopropylacrylamide) onto ordinary culture dishes, enable the non-invasive harvesting of cells as intact sheets by simple temperature reduction. This article reviews current research on the applications of cell-sheet engineering for the reconstruction of various tissues, as well as the intelligent surfaces used by this novel technology.

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Araujo, W. W. R., F. S. Teixeira, G. N. da Silva, D. M. F. Salvadori, M. C. Salvadori, and I. G. Brown. "Cell growth on 3D microstructured surfaces." Materials Science and Engineering: C 63 (June 2016): 686–89. http://dx.doi.org/10.1016/j.msec.2016.03.026.

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Dutta, Debjit, Abigail Pulsipher, Wei Luo, Hugo Mak, and Muhammad N. Yousaf. "Engineering Cell Surfaces via Liposome Fusion." Bioconjugate Chemistry 22, no. 12 (December 21, 2011): 2423–33. http://dx.doi.org/10.1021/bc200236m.

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Magnani, Agnese, Alfredo Priamo, Daniela Pasqui, and Rolando Barbucci. "Cell behaviour on chemically microstructured surfaces." Materials Science and Engineering: C 23, no. 3 (March 2003): 315–28. http://dx.doi.org/10.1016/s0928-4931(02)00284-9.

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Pfeiffer, Friederike, Bertram Herzog, Dieter Kern, Lutz Scheideler, Jürgen Geis-Gerstorfer, and Hartwig Wolburg. "Cell reactions to microstructured implant surfaces." Microelectronic Engineering 67-68 (June 2003): 913–22. http://dx.doi.org/10.1016/s0167-9317(03)00154-0.

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Diamond, R. D. "Fungal Cell Surfaces: Summary of Session." Clinical Infectious Diseases 10, Supplement 2 (August 1, 1988): S413—S414. http://dx.doi.org/10.1093/cid/10.supplement_2.s413.

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Roby, Dominique, Alain Toppan, and Marie-Thérèse Esquerré-Tugayé. "Cell Surfaces in Plant-Microorganism Interactions." Plant Physiology 81, no. 1 (May 1, 1986): 228–33. http://dx.doi.org/10.1104/pp.81.1.228.

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Woodland, David L. "Inflammatory Responses at Epithelial Cell Surfaces." Viral Immunology 24, no. 3 (June 2011): 177–78. http://dx.doi.org/10.1089/vim.2011.ed.24.3.

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Roby, Dominique, Alain Toppan, and Marie-Thérèse Esquerré-Tugayé. "Cell Surfaces in Plant-Microorganism Interactions." Plant Physiology 77, no. 3 (March 1, 1985): 700–704. http://dx.doi.org/10.1104/pp.77.3.700.

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Goulet-Hanssens, Alexis, Karen Lai Wing Sun, Timothy E. Kennedy, and Christopher J. Barrett. "Photoreversible Surfaces to Regulate Cell Adhesion." Biomacromolecules 13, no. 9 (August 30, 2012): 2958–63. http://dx.doi.org/10.1021/bm301037k.

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Ebara, Mitsuhiro. "Shape-memory surfaces for cell mechanobiology." Science and Technology of Advanced Materials 16, no. 1 (February 25, 2015): 014804. http://dx.doi.org/10.1088/1468-6996/16/1/014804.

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Kellam, Barrie, Paul A. De Bank, and Kevin M. Shakesheff. "Chemical modification of mammalian cell surfaces." Chemical Society Reviews 32, no. 6 (2003): 327. http://dx.doi.org/10.1039/b211643j.

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Hoch, John, Bruce E. Jarrell, Timothy Schneider, and Stuart K. Williams. "Endothelial Cell Interactions with Native Surfaces." Annals of Vascular Surgery 3, no. 2 (April 1989): 153–59. http://dx.doi.org/10.1016/s0890-5096(06)62009-8.

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Day, Daniel, and Min Gu. "Femtosecond fabricated surfaces for cell biology." Journal of Optics 12, no. 8 (July 15, 2010): 084005. http://dx.doi.org/10.1088/2040-8978/12/8/084005.

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Duncan, Gregg A., D. Howard Fairbrother, and Michael A. Bevan. "Diffusing colloidal probes of cell surfaces." Soft Matter 12, no. 21 (2016): 4731–38. http://dx.doi.org/10.1039/c5sm02637g.

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Consigny, Paul Macke. "Endothelial Cell Seeding on Prosthetic Surfaces." Journal of Long-Term Effects of Medical Implants 10, no. 1-2 (2000): 17. http://dx.doi.org/10.1615/.v10.i12.80.

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Peng, Yingjie, Dae Hee Kim, Teresa M. Jones, Diana I. Ruiz, and Richard A. Lerner. "Engineering Cell Surfaces for Orthogonal Selectability." Angewandte Chemie 125, no. 1 (December 13, 2012): 354–58. http://dx.doi.org/10.1002/ange.201201844.

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Horna, David, Juan Carlos Ramírez, Anna Cifuentes, Antonio Bernad, Salvador Borrós, and Manuel A. González. "Efficient Cell Reprogramming Using Bioengineered Surfaces." Advanced Healthcare Materials 1, no. 2 (February 16, 2012): 177–82. http://dx.doi.org/10.1002/adhm.201200017.

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Peng, Yingjie, Dae Hee Kim, Teresa M. Jones, Diana I. Ruiz, and Richard A. Lerner. "Engineering Cell Surfaces for Orthogonal Selectability." Angewandte Chemie International Edition 52, no. 1 (December 12, 2012): 336–40. http://dx.doi.org/10.1002/anie.201201844.

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Bosetti, M., M. Santin, A. W. Lloyd, S. P. Denyer, M. Sabbatini, and M. Cannas. "Cell behaviour on phospholipids-coated surfaces." Journal of Materials Science: Materials in Medicine 18, no. 4 (April 2007): 611–17. http://dx.doi.org/10.1007/s10856-007-2309-1.

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Sato, Hiroko, Hiroshi Tsuji, Shinichi Ikemura, Shigeo Ikeda, Junzo Ishikawa, and Sei-Ichi Nishimoto. "Enhanced Surfaces for Endothelial Cell Seeding." Journal of Biomaterials Applications 14, no. 2 (October 1999): 169–83. http://dx.doi.org/10.1177/088532829901400203.

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Journal articles on the topic 'Cell surfaces'

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