EVIDENCE FOR SEPARATE RECEPTORS FOR INSULIN AND INSULIN-LIKE GROWTH FACTOR-I IN CHOROID-PLEXUS OF RAT-BRAIN BY QUANTITATIVE AUTORADIOGRAPHY

Binding of insulin and insulin-like growth factor-I (IGF-I) to the choroid plexus was quantitatively characterized using autoradiography and computer densitometry. Slide-mounted brain slices were incubated in 0.1 nM [125I]-insulin or [125I]-[Thr59]IGF-I. To determine specificity of the binding sites, the labeled peptides were mixed with unlabeled analogues. Autoradiography was done with LKB Ultrofilm and analyzed with a computer image analysis system and program for densitometry. Results showed that binding was time and temperature dependent and reversible. Binding of the iodinated insulin and IGF-I was inhibited by unlabeled peptides in a dose-dependent manner. The rank order of potency of these peptides in competing for the choroid plexus iodoinsulin binding sites was: chicken insulin > porcine insulin > desoctapeptide insulin > IGF-I. IGF-I was more potent than porcine insulin in competing for the choroid plexus iodolGF-I binding sites. somatostatin was ineffective. Non-linear regression analysis revealed the presence of high- (K(d) 1.3 ± 0.2 nM) and low-affinity (K(d) 36 ± 1.4 nM) binding sites for insulin and a single high-affinity binding site (K(d) 3.1 ± 0.3 nM) for IGF-I in the choroid plexus. There were approximately 50 times more binding sites (B(max)) for IGF-I than for insulin high-affinity sites, whereas the number of low-affinity sites for insulin was about equal to the number of IGF-I high-affinity sites. The results of these binding studies with iodinated insulin and [Thr59]IGF-I support the conclusion that the rat choroid plexus has separate high-affinity receptors for insulin and IGF-I, and that the IGF-I receptors outnumber the insulin receptors.