An Acoustically Driven Microliter Flow Chamber on a Chip (μFCC) for Cell–Cell and Cell–Surface Interaction Studies

ChemPhysChem ◽  
2008 ◽  
Vol 9 (4) ◽  
pp. 641-645 ◽  
Author(s):  
Matthias F. Schneider ◽  
Zeno Guttenberg ◽  
Stefan W. Schneider ◽  
Kumudesh Sritharan ◽  
Vanessa M. Myles ◽  
...  
Keyword(s):  
Cell Surface ◽  
Flow Chamber ◽  
Surface Interaction ◽  
Interaction Studies ◽  
Cell Cell

Tailored interfaces for biosensors and cell-surface interaction studies via activation and derivatization of polystyrene-block-poly(tert-butyl acrylate) thin films

2007 ◽  
Vol 43 (6) ◽  
pp. 2177-2190 ◽  
Author(s):  
Chuan Liang Feng ◽  
Anika Embrechts ◽  
Ilona Bredebusch ◽  
Anita Bouma ◽  
Jürgen Schnekenburger ◽  
...  
Keyword(s):  
Thin Films ◽  
Cell Surface ◽  
Butyl Acrylate ◽  
Surface Interaction ◽  
Tert Butyl ◽  
Interaction Studies

scholarly journals Keratin 19 maintains E-cadherin localization at the cell surface and stabilizes cell-cell adhesion of MCF7 cells

2021 ◽  
Vol 15 (1) ◽  
pp. 1-17
Author(s):  
Sarah Alsharif ◽  
Pooja Sharma ◽  
Karina Bursch ◽  
Rachel Milliken ◽  
Van Lam ◽  
...  
Keyword(s):  
Cell Adhesion ◽  
Cell Surface ◽  
Mcf7 Cells ◽  
Keratin 19 ◽  
E Cadherin ◽  
Cell Cell

scholarly journals The upgraded TOMAS device: A toroidal plasma facility for wall conditioning, plasma production, and plasma–surface interaction studies

2021 ◽  
Vol 92 (2) ◽  
pp. 023506
Author(s):  
A. Goriaev ◽  
T. Wauters ◽  
S. Möller ◽  
R. Brakel ◽  
S. Brezinsek ◽  
...  
Keyword(s):  
Surface Interaction ◽  
Plasma Production ◽  
Plasma Surface ◽  
Toroidal Plasma ◽  
Interaction Studies

Lymphoid Cell Surface Interaction Structures Detected Using Cytolysis-Inhibiting Monoclonal Antibodies

1982 ◽  
Vol 68 (1) ◽  
pp. 5-42 ◽  
Author(s):  
Pierre Golstein ◽  
Christo Goridis ◽  
Anne-Marie Schmitt-Verhulst ◽  
Brigitte Hayot ◽  
Anne Pierres ◽  
...  
Keyword(s):  
Monoclonal Antibodies ◽  
Cell Surface ◽  
Lymphoid Cell ◽  
Surface Interaction

scholarly journals Remodeling the cell surface distribution of membrane proteins during the development of epithelial cell polarity.

1992 ◽  
Vol 116 (4) ◽  
pp. 889-899 ◽  
Author(s):  
D A Wollner ◽  
K A Krzeminski ◽  
W J Nelson
Keyword(s):  
Epithelial Cell ◽  
Membrane Proteins ◽  
Cell Surface ◽  
Mdck Cells ◽  
Apical Cell ◽  
Cell Contact ◽  
Surface Polarity ◽  
Lateral Membrane ◽  
E Cadherin ◽  
Cell Cell

The development of polarized epithelial cells from unpolarized precursor cells follows induction of cell-cell contacts and requires resorting of proteins into different membrane domains. We show that in MDCK cells the distributions of two membrane proteins, Dg-1 and E-cadherin, become restricted to the basal-lateral membrane domain within 8 h of cell-cell contact. During this time, however, 60-80% of newly synthesized Dg-1 and E-cadherin is delivered directly to the forming apical membrane and then rapidly removed, while the remainder is delivered to the basal-lateral membrane and has a longer residence time. Direct delivery of greater than 95% of these proteins from the Golgi complex to the basal-lateral membrane occurs greater than 48 h later. In contrast, we show that two apical proteins are efficiently delivered and restricted to the apical cell surface within 2 h after cell-cell contact. These results provide insight into mechanisms involved in the development of epithelial cell surface polarity, and the establishment of protein sorting pathways in polarized cells.

Studies of membrane fusion. I. Paramyxovirus-induced cell fusion, a scanning electron-microscope study

1977 ◽  
Vol 28 (1) ◽  
pp. 179-188
Author(s):  
S. Knutton ◽  
D. Jackson ◽  
M. Ford
Keyword(s):  
Cell Surface ◽  
Cell Fusion ◽  
Hela Cells ◽  
Cell Swelling ◽  
Cell Contact ◽  
Cell Agglutination ◽  
Scanning Electron Microscope Study ◽  
Virus Particles ◽  
Scanning Electron ◽  
Cell Cell

Fusion of erythrocytes and HeLa cells with Sendai and Newcastle disease viruses has been studied by scanning electron microscopy. Most virus particles are spherical but vary in diameter from approximately 200 to approximately 600 nm. At 4 degrees C virus particles bind randomly to the cell surface and at high cell densities cross-linking of adjacent cells by virus particles results in cell agglutination. Cell-cell fusion takes place when the agglutinated cell suspension is warmed to 37 degrees C. Fusion is initiated at sites of cell-cell contact and is accompanied in all cases by cell swelling. In the case of suspension HeLa cells, virally mediated cell swelling involves an ‘unfolding’ of cell surface microvilli and results in the formation of smooth-surfaced single or fused cells. With erythrocytes, swelling results in haemolysis. There is a dramatic reduction in the numbers of virus particles bound to cells following fusion.

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