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Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments
Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments
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Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments
Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments

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Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments
Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments
Journal Article

Invasive Behavior of Mouse Sarcoma Cells is Inhibited by Blocking a 37,000-Dalton Plasma Membrane Glycoprotein with Fab Fragments

1984
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Overview
Abercrombie's confronted explant technique was used to study the role of tumor surface antigens in malignant invasion. Plasma membranes were isolated from mouse sarcoma cells (FS9) and a mouse cell line (L929) of the same H-2 haplotype. FS9 cells are highly invasive when confronted with chicken heart fibroblasts, whereas the L929 cells are not [Abercrombie, M. (1979) Nature (London) 281, 259-262]. The FS9 plasma membranes contained significantly higher concentrations of a 37,000-dalton glycoprotein. When antiserum directed against FS9 plasma membranes was preabsorbed with L929 cells, the antibodies remaining reacted predominantly with the 37,000-dalton antigen. Fab fragment prepared from the preabsorbed antiserum inhibited the invasion of chicken heart fibroblasts by FS9 cells. Fab prepared from a monoclonal antibody directed against the 37,000-dalton antigen also inhibited invasivity, whereas monoclonal antibodies reacting with two other FS9 cell surface antigens did not. The results imply a relationship between the increased concentration of the 37,000-dalton glycoprotein on the surface of the FS9 cells and their invasivity.