Title : Tunicamycin-mediated depletion of insulin receptors in 3T3-L1 adipocytes.

Pub. Date : 1979 Apr

PMID : 457783






5 Functional Relationships(s)
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1 Tunicamycin-mediated depletion of insulin receptors in 3T3-L1 adipocytes. Tunicamycin insulin Homo sapiens
2 Tunicamycin, an antibiotic that inhibits protein glycosylation, elicited a rapid depletion of insulin binding activity at the surface of 3T3-L1 adipocytes. Tunicamycin insulin Homo sapiens
3 Disappearance of insulin receptors occurred more rapidly in the presence of tunicamycin than when protein synthesis was inhibited by cycloheximide and was accompanied by a diminution in sensitivity of the adipocytes to the acute effects of insulin and anti-insulin receptor antibody on hexose uptake and metabolism. Tunicamycin insulin Homo sapiens
4 Disappearance of insulin receptors occurred more rapidly in the presence of tunicamycin than when protein synthesis was inhibited by cycloheximide and was accompanied by a diminution in sensitivity of the adipocytes to the acute effects of insulin and anti-insulin receptor antibody on hexose uptake and metabolism. Tunicamycin insulin Homo sapiens
5 Disappearance of insulin receptors occurred more rapidly in the presence of tunicamycin than when protein synthesis was inhibited by cycloheximide and was accompanied by a diminution in sensitivity of the adipocytes to the acute effects of insulin and anti-insulin receptor antibody on hexose uptake and metabolism. Tunicamycin insulin Homo sapiens