TY - JOUR
T1 - Inhibition of the mobility of mouse lymphocyte surface immunoglobulins by locally bound concanavalin A
AU - Henis, Y. I.
AU - Elson, E. L.
PY - 1981
Y1 - 1981
N2 - Fluorescence photobleaching recovery was used to study directly and quantitatively the inhibition of the lateral mobility of surface immunoglobulins (sIg) on mouse lymphocytes by localized binding of concanavalin A (Con A) coupled to platelets. Up to a threshold occupancy of about 10% of the upper cell surface by Con A-platelets, the diffusion coefficient and mobile fraction of sIg remained as in untreated cells (5.3 x 10-10cm2/sec and 0.65, respectively). At higher surface occupancy, these values decreased to 8 x 10-11 cm2/sec and 0.11. The magnitude of the effect was independent of the percentage occupancy above the threshold and of the distance from the bound Con A-platelets, indicating a cooperative and propagated phenomenon. Treatment with colchicine or cytochalasin B separately induced only partial reversal of the Con A-induced modulation. Treatment with both drugs together was synergistic and fully reversed the mobility inhibition. The modulation was unaffected by NaN3 and 2-deoxyglucose, suggesting no dependence on metabolic energy. Con A-platelets did not affect the mobility of a lipid probe. Models for the Con A-induced modulation and the relationship between the effects of ConA on sIg mobility and patch formation are discussed.
AB - Fluorescence photobleaching recovery was used to study directly and quantitatively the inhibition of the lateral mobility of surface immunoglobulins (sIg) on mouse lymphocytes by localized binding of concanavalin A (Con A) coupled to platelets. Up to a threshold occupancy of about 10% of the upper cell surface by Con A-platelets, the diffusion coefficient and mobile fraction of sIg remained as in untreated cells (5.3 x 10-10cm2/sec and 0.65, respectively). At higher surface occupancy, these values decreased to 8 x 10-11 cm2/sec and 0.11. The magnitude of the effect was independent of the percentage occupancy above the threshold and of the distance from the bound Con A-platelets, indicating a cooperative and propagated phenomenon. Treatment with colchicine or cytochalasin B separately induced only partial reversal of the Con A-induced modulation. Treatment with both drugs together was synergistic and fully reversed the mobility inhibition. The modulation was unaffected by NaN3 and 2-deoxyglucose, suggesting no dependence on metabolic energy. Con A-platelets did not affect the mobility of a lipid probe. Models for the Con A-induced modulation and the relationship between the effects of ConA on sIg mobility and patch formation are discussed.
UR - http://www.scopus.com/inward/record.url?scp=0019863719&partnerID=8YFLogxK
U2 - 10.1073/pnas.78.2.1072
DO - 10.1073/pnas.78.2.1072
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AN - SCOPUS:0019863719
SN - 0027-8424
VL - 78
SP - 1072
EP - 1076
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 2 II
ER -