Erythrocyte insulin-like growth factor-I binding in younger and older males

David Y. Moromisato, Charles Roberts, Jo Anne Brasel, Subburaman Mohan, Elizabeth Cowles, Stephen M. King, Dan M. Cooper

    Research output: Contribution to journalArticle

    7 Citations (Scopus)

    Abstract

    OBJECTIVE. Insulin-like growth factor-I (IGF-I) levels are lower in older compared with younger subjects. We tested the hypothesis that the reduction in circulating IGF-I would be accompanied by upregulation in tissue IGF-l binding in at least some tissues. We tested erythrocyte IGF-l binding since blood is an accessible tissue in humans, and there is growing evidence to suggest that erythrocyte IGF- binding is influenced by circulating IFG-I. DESIGN AND PATIENTS. We compared 9 healthy older males (61-68 years old) with 9 healthy younger males (15-19 years old). MEASUREMENTS. Standard techniques were used to assay circulating IGF-I and IGF binding proteins 1-5 (IGFBPs 1- 5). Erythrocyte IGF-I binding was first measured by studies in which native [125I]-IGF-I was displaced with unlabelled native IGF-l. In order to determine a possible role for IGF binding proteins (IGFBP), native [125]- IGF-I was displaced with des-(1-3)IGF-l, which binds with IGF receptors but not IGFBPs. RESULTS. As expected, circulating IGF-I was significantly lower in the older compared with the younger subjects. In addition, IGFBP-3 and 5 were significantly lower, and IGFBP-4 higher, in older compared with younger subjects. When native [125I]-IGF-l was displaced with unlabeled native IGF-I, the number of IGF-I binding sites per erythrocyte was higher in the older subjects (43 ± 5 vs. 18 ± 2, older vs. younger, respectively; P125I]-IGF-I was displaced with des- (1-3), IGF-I binding capacity was not different between the two age groups. CONCLUSIONS. Erythrocyte IGF binding was increased in older compared with younger subjects. Surprisingly, the mechanism of the increase may not be a simple up regulation of IGF-I receptors in response to reduced circulating IGF-I, but possibly by an increase in the levels of as yet unidentified erythrocyte membrane-associated IGF binding proteins.

    Original languageEnglish (US)
    Pages (from-to)339-345
    Number of pages7
    JournalClinical Endocrinology
    Volume48
    Issue number3
    DOIs
    StatePublished - 1998

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    Insulin-Like Growth Factor I
    Erythrocytes
    Insulin-Like Growth Factor Binding Proteins
    Insulin-Like Growth Factor Binding Protein 5
    Insulin-Like Growth Factor Binding Protein 1
    Up-Regulation
    Insulin-Like Growth Factor Binding Protein 4
    IGF Type 1 Receptor
    Insulin-Like Growth Factor Binding Protein 3
    Erythrocyte Membrane
    Membrane Proteins
    Age Groups
    Binding Sites

    ASJC Scopus subject areas

    • Endocrinology

    Cite this

    Moromisato, D. Y., Roberts, C., Brasel, J. A., Mohan, S., Cowles, E., King, S. M., & Cooper, D. M. (1998). Erythrocyte insulin-like growth factor-I binding in younger and older males. Clinical Endocrinology, 48(3), 339-345. https://doi.org/10.1046/j.1365-2265.1998.00395.x

    Erythrocyte insulin-like growth factor-I binding in younger and older males. / Moromisato, David Y.; Roberts, Charles; Brasel, Jo Anne; Mohan, Subburaman; Cowles, Elizabeth; King, Stephen M.; Cooper, Dan M.

    In: Clinical Endocrinology, Vol. 48, No. 3, 1998, p. 339-345.

    Research output: Contribution to journalArticle

    Moromisato, DY, Roberts, C, Brasel, JA, Mohan, S, Cowles, E, King, SM & Cooper, DM 1998, 'Erythrocyte insulin-like growth factor-I binding in younger and older males', Clinical Endocrinology, vol. 48, no. 3, pp. 339-345. https://doi.org/10.1046/j.1365-2265.1998.00395.x
    Moromisato, David Y. ; Roberts, Charles ; Brasel, Jo Anne ; Mohan, Subburaman ; Cowles, Elizabeth ; King, Stephen M. ; Cooper, Dan M. / Erythrocyte insulin-like growth factor-I binding in younger and older males. In: Clinical Endocrinology. 1998 ; Vol. 48, No. 3. pp. 339-345.
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    abstract = "OBJECTIVE. Insulin-like growth factor-I (IGF-I) levels are lower in older compared with younger subjects. We tested the hypothesis that the reduction in circulating IGF-I would be accompanied by upregulation in tissue IGF-l binding in at least some tissues. We tested erythrocyte IGF-l binding since blood is an accessible tissue in humans, and there is growing evidence to suggest that erythrocyte IGF- binding is influenced by circulating IFG-I. DESIGN AND PATIENTS. We compared 9 healthy older males (61-68 years old) with 9 healthy younger males (15-19 years old). MEASUREMENTS. Standard techniques were used to assay circulating IGF-I and IGF binding proteins 1-5 (IGFBPs 1- 5). Erythrocyte IGF-I binding was first measured by studies in which native [125I]-IGF-I was displaced with unlabelled native IGF-l. In order to determine a possible role for IGF binding proteins (IGFBP), native [125]- IGF-I was displaced with des-(1-3)IGF-l, which binds with IGF receptors but not IGFBPs. RESULTS. As expected, circulating IGF-I was significantly lower in the older compared with the younger subjects. In addition, IGFBP-3 and 5 were significantly lower, and IGFBP-4 higher, in older compared with younger subjects. When native [125I]-IGF-l was displaced with unlabeled native IGF-I, the number of IGF-I binding sites per erythrocyte was higher in the older subjects (43 ± 5 vs. 18 ± 2, older vs. younger, respectively; P125I]-IGF-I was displaced with des- (1-3), IGF-I binding capacity was not different between the two age groups. CONCLUSIONS. Erythrocyte IGF binding was increased in older compared with younger subjects. Surprisingly, the mechanism of the increase may not be a simple up regulation of IGF-I receptors in response to reduced circulating IGF-I, but possibly by an increase in the levels of as yet unidentified erythrocyte membrane-associated IGF binding proteins.",
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    AU - Brasel, Jo Anne

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    AU - Cowles, Elizabeth

    AU - King, Stephen M.

    AU - Cooper, Dan M.

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    N2 - OBJECTIVE. Insulin-like growth factor-I (IGF-I) levels are lower in older compared with younger subjects. We tested the hypothesis that the reduction in circulating IGF-I would be accompanied by upregulation in tissue IGF-l binding in at least some tissues. We tested erythrocyte IGF-l binding since blood is an accessible tissue in humans, and there is growing evidence to suggest that erythrocyte IGF- binding is influenced by circulating IFG-I. DESIGN AND PATIENTS. We compared 9 healthy older males (61-68 years old) with 9 healthy younger males (15-19 years old). MEASUREMENTS. Standard techniques were used to assay circulating IGF-I and IGF binding proteins 1-5 (IGFBPs 1- 5). Erythrocyte IGF-I binding was first measured by studies in which native [125I]-IGF-I was displaced with unlabelled native IGF-l. In order to determine a possible role for IGF binding proteins (IGFBP), native [125]- IGF-I was displaced with des-(1-3)IGF-l, which binds with IGF receptors but not IGFBPs. RESULTS. As expected, circulating IGF-I was significantly lower in the older compared with the younger subjects. In addition, IGFBP-3 and 5 were significantly lower, and IGFBP-4 higher, in older compared with younger subjects. When native [125I]-IGF-l was displaced with unlabeled native IGF-I, the number of IGF-I binding sites per erythrocyte was higher in the older subjects (43 ± 5 vs. 18 ± 2, older vs. younger, respectively; P125I]-IGF-I was displaced with des- (1-3), IGF-I binding capacity was not different between the two age groups. CONCLUSIONS. Erythrocyte IGF binding was increased in older compared with younger subjects. Surprisingly, the mechanism of the increase may not be a simple up regulation of IGF-I receptors in response to reduced circulating IGF-I, but possibly by an increase in the levels of as yet unidentified erythrocyte membrane-associated IGF binding proteins.

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