TY - JOUR
T1 - Spreading of human fibroblasts in serum‐free medium
T2 - Inhibition by dithiothreitol and the effect of cold insoluble globulin (plasma fibronectin)
AU - Grinnell, F.
AU - Feld, M. K.
PY - 1980/9
Y1 - 1980/9
N2 - We have tested the effect of dithiothreitol (DTT) treatment on the initial spreading of human fibroblasts in serum‐free medium in tissue culture dishes. Cell spreading was inhibited following treatment of these cells with 10 mM DTT. Inhibition occurred when the cells were treated at 37°C but not at 4° and was reversible metabolically but not by the addition of sulfhydryl oxidizing reagents. The inhibition was overcome when DTT‐treated human fibroblasts were plated on cold insoluble globulin (plasma fibronectin)—coated dishes. Under these conditions spreading appeared to be completely normal, including the formation of focal adhesions. Analysis of the fibronectin concentrations in the human fibroblasts following DTT treatment indicated that there was little decrease in the absolute level of activity as determined in a biological assay for BHK cell spreading on culture dishes. Analysis of the fibronectin distribution on the DTT‐treated human fibroblasts by indirect immunofluorescence using a specific anti‐CIG antiserum revealed that fibronectin was no longer deposited onto the culture dish surfaces. Even when the DTT‐treated human fibroblasts spread in the presence of fetal calf serum, the cell fibronectin remained for the most part in a perinuclear location. These results indicate that DTT treatment of human fibroblasts prevents the normal translocation of fibronectin from a perinuclear location to the surface of the culture dish. This study further supports our hypothesis that the initial spreading in serum‐free medium of fibroblasts from cell strains depends upon secretion of fibronectin onto the culture dish surface.
AB - We have tested the effect of dithiothreitol (DTT) treatment on the initial spreading of human fibroblasts in serum‐free medium in tissue culture dishes. Cell spreading was inhibited following treatment of these cells with 10 mM DTT. Inhibition occurred when the cells were treated at 37°C but not at 4° and was reversible metabolically but not by the addition of sulfhydryl oxidizing reagents. The inhibition was overcome when DTT‐treated human fibroblasts were plated on cold insoluble globulin (plasma fibronectin)—coated dishes. Under these conditions spreading appeared to be completely normal, including the formation of focal adhesions. Analysis of the fibronectin concentrations in the human fibroblasts following DTT treatment indicated that there was little decrease in the absolute level of activity as determined in a biological assay for BHK cell spreading on culture dishes. Analysis of the fibronectin distribution on the DTT‐treated human fibroblasts by indirect immunofluorescence using a specific anti‐CIG antiserum revealed that fibronectin was no longer deposited onto the culture dish surfaces. Even when the DTT‐treated human fibroblasts spread in the presence of fetal calf serum, the cell fibronectin remained for the most part in a perinuclear location. These results indicate that DTT treatment of human fibroblasts prevents the normal translocation of fibronectin from a perinuclear location to the surface of the culture dish. This study further supports our hypothesis that the initial spreading in serum‐free medium of fibroblasts from cell strains depends upon secretion of fibronectin onto the culture dish surface.
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U2 - 10.1002/jcp.1041040306
DO - 10.1002/jcp.1041040306
M3 - Article
C2 - 7419608
AN - SCOPUS:0019273321
SN - 0021-9541
VL - 104
SP - 321
EP - 334
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 3
ER -