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J. Biol. Chem., Vol. 266, Issue 24, 15587-15590, Aug, 1991
JE Chin, JM Tavare, L Ellis and RA Roth
Chinese hamster ovary cells and NIH 3T3 cells overexpressing mutant human
insulin receptors were examined for the presence of hybrid receptors
composed of human and rodent insulin receptors. In the present studies,
most of the endogenous rodent receptors were found to be immunoprecipitated
from the transfected cells but not the parental cells with a monoclonal
antibody specific for human receptor. These data indicate that in these
transfected cells, most of the endogenous rodent receptors are in a hybrid
complex with the overexpressed human receptor. These results together with
the in vitro studies of Treadway et al. (Treadway, J.L., Morrison, B.D.,
Soos, M.A., Siddle, K., Olefsky, J., Ullrich, A., McClain, D.A., and
Pessin, J.E. (1991) Proc. Natl. Acad. Sci. U.S.A. 88, 214-218) showing that
hybrid receptors exhibit transdominant inhibition explain the prior finding
indicating that overexpression of defective insulin receptors interferes
with the normal signaling of endogenous receptors.
Evidence for hybrid rodent and human insulin receptors in transfected cells
Department of Pharmacology, Stanford University School of Medicine, California 94305-5332.
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