Depolarization-independent net uptake of calcium into clonal insulin-releasing cells exposed to glucose.

Gylfe E, Andersson T, Rorsman P, Abrahamsson H, Arkhammar P, Hellman P, Hellman B, Oie HK, Gazdar AF

Insulin release, net fluxes of Ca2+, and glucose metabolism were studied in a clonal cell line (RINm5F) established from a transplantable rat islet tumor. The insulin content amounted to only 0.03% of that of the total protein and decreased even further with subsequent passages. The insulin secretion was as high as 10 to 20% of the total hormone content per hour. Insulin release was stimulated by K+ depolarization but not by exposure to glucose. In contrast to this secretory pattern, glucose but not K+ stimulated the net uptake of Ca2+ at micromolar concentrations of the ion. The glucose effect was not mimicked by 20 mM 3-O-methylglucose. It was as pronounced at 1 mM as at 20 mM of the sugar and corresponded to an uptake of 119 fmol cm-2 s-1. Glucose metabolism was typical for tumor cells with a high glycolytic flux and an oxidation-to-utilization ratio as low as 0.05-0.15. Maximal oxidative degradation was attained already at 1 mM. This concentration was also equivalent to the Km for glucose utilization, indicating a substantial left-hand shift of the normal dose-response curve. It is suggested that glucose induces a depolarization-independent net uptake of Ca2+ by favouring intracellular buffering of the cation.

Keywords:

Adenoma, Islet Cell

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Animals

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Biological Transport, Active

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Calcium

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Clone Cells

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Glucose

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Insulin

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Insulin Secretion

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Pancreatic Neoplasms

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Potassium

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Rats