Page 48 - Handbook of Adhesion Promoters
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2.13 Cellular adhesion                                                41










            Figure 2.46. (a) Magnetic resonance image of octopus arm with one sucker, the scale bar equals 1 cm; (b) ultra-
            sound image of a sucker, the scale bar equals 0.5 cm; (c) histological image of octopus arm with one sucker, the
            scale bar equals 0.5 cm; (d) detail of denticle located in the infundibular portion, the scale bar equals 2 μm; (e)
            3D reconstruction from full set of 70 magnetic resonance images with 1 millimeter thickness. [Adapted, by per-
            mission, from Tramacere, F; Beccai, L; Sinibaldi, E; Laschi, C; Mazzolai, B, Procedia Computer Sci., 7, 192-3,
            2011.]
            2.13 CELLULAR ADHESION

            The cell surface recognition is the interaction of the cell with the surfaces of other cells
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            and with extracellular matrices in surroundings.  The cell-extracellular matrix interac-
            tions provide cells with anchorage, traction for cell migration, and signals for growth and
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            differentiation.   Most  cell-surroundings  interactions  depend  on  the  recognition  of  the
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            simple tripeptide Arg-Gly-Asp, RDG, by cell surface receptors, integrins.  Multiple inte-
            grins endow a cell with a great capacity to differentiate between the own extracellular
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            matrix and the matrices secreted by other cells.
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                Epithelium forms a barrier between the outside and the inside of an organism.  The
            apical  plasma  membrane  contacts  opposing  cells  and  an  extracellular  matrix.  Cell-cell
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            adhesion complexes hold epithelial cells together.
                Cells  can  form  tissues  by  directly  adhering  to  one  another,  using  transmembrane
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            receptors.  Another means of adhesion is to attach the cell to the extracellular matrix,
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            ECM, (dynamic, highly crosslinked mesh of insoluble proteins).  This is primarily medi-
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            ated by the transmembrane integrin receptors.  They anchor the cell and provide an indi-
            rect means of cell-cell adhesion when different cells connect to a common ECM between
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            them.  These features play critical roles in the construction and maintenance of tissues
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            during development and adult life.
                Keratin is a protein of human hair but it is also a protein which regulates the func-
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            tions of the liver.  Hepatocytes are the cells of the liver tissue.  Hepatocytes make up 70-
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            85% of the liver's mass.  The keratin biomaterials researchers, aiming at regulating phys-
            iological events through surface-mediated control of cellular behavior, are interested in
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            adhesion between human hair keratins and hypatocytes.  The hepatocyte adhesion to ker-
            atin substrates was not mediated by integrins of the β - or β -subtype but by hepatic glyco-
                                                      1
                                                           2
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            protein  receptor.   Glycopolymer  surfaces  preserve  the  differentiated  state  of  mature
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            hepatocytes and help maintain their ability to perform liver-specific functions.
                Scanning near-field optical microscopy, SNOM, has been employed to simultane-
            ously  acquire  high-resolution  fluorescence  images  along  with  shear-force  atomic  force
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            microscopy  from  cell  membranes  (Figure  2.47).   The  application  of  the  technique  to
            investigate cell-cell adhesion has revealed the interactions of filopodia (or microspikes are
            cytoplasmic projections that extend beyond the leading edge of cells) and their functional
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            relationship  in  establishing  adherens  junctions.   The  filopodia  from  each  cell  extend
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            across the intercellular region (Figure 2.47a).  The filopodia have diameters ranging from
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            110 to 270 nm.  These nanostructures extend approximately 4-5 μm from their originat-
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            ing lamellipodium, while some protrude over 10 mm into the intercellular space.  Filopo-
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