Effects of IGF-I and glucose on protein and proteoglycan synthesis by human fetal mesangial cells in culture

A. Moran, D. M. Brown, Y. Kim, D. J. Klein

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58 Scopus citations

Abstract

Abnormalities in proteoglycan metabolism have been implicated in the pathogenesis of diabetic nephropathy. Whether hyperglycemia plays a direct role in these events is unknown. To evaluate the effects of high glucose concentrations and insulinlike growth factor I (IGF-I) on kidney proteoglycan and protein metabolism, we incubated quiescent, subconfluent human fetal mesangial cells for 24 h in serum-free media containing either physiological (5.6-mM) or elevated (25-mM) glucose concentrations with or without 1.3 x 10-9 M IGF-I. In the presence of physiological glucose concentrations, IGF-I stimulated incorporation of [3H]leucine into protein and [35S]sulfate or [3H]glucosamine into proteoglycans. High glucose concentrations significantly amplified IGF-I-mediated stimulation of protein synthesis but totally abolished IGF-I-induced proteoglycan synthesis. The hydrodynamic size and proportions of heparan-35SO4 and chondroitin/dermatan-35SO4 proteoglycans in all experimental media were the same. However, high glucose concentrations decreased the iduronic acid content of dermatan-35SO4. In separate experiments, quiescent cells were cultured for 7 days in media supplemented with 2% fetal calf serum. IGF-I had no effect on mesangial cell proliferation, but as cells reached confluence, high glucose concentrations significantly inhibited cell proliferation. This inhibition was not mimicked by isoosmolar concentrations of mannitol. After 7 days, uptake of radioactive precursors into proteoglycans and proteins over 24 h was similar under all culture conditions. However, IGF-I decreased the ratio of [35S]sulfate to [3H]glucosamine in proteoglycans and their glycosaminoglycan side chains. This difference persisted in disaccharides derived by chondroitin ABC lyase digestion of dermatan-35SO4. A higher specific activity of [3H]glucosamine without a change in [35S]sulfate uptake or proteoglycan structure indicated that IGF-I treatment of confluent mesangial cells altered the glucosamine pool size. Thus, in subconfluent human mesangial cells, high concentrations of glucose amplified IGF-I-stimulated protein synthesis but abrogated IGF-I-stimulated proteoglycan synthesis, resulting in a relatively proteoglycan-depleted state. This effect was not seen in cells that had been confluent for several days.

Original languageEnglish (US)
Pages (from-to)1346-1354
Number of pages9
JournalDiabetes
Volume40
Issue number10
DOIs
StatePublished - 1991

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