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Diabetes Research Center, Brussels Free University (VUB), B-1090 Brussels, Belgium
Address all correspondence and requests for reprints to: Daniël Pipeleers, Diabetes Research Center, Laarbeeklaan 103, B-1090 Brussels, Belgium. E-mail: daniel.pipeleers{at}vub.ac.be.
Insulin synthesis and release activities of ß-cells can be acutely regulated by glucose through its glycolytic and mitochondrial breakdown involving a glucokinase-dependent rate-limiting step. Isolated ß-cell populations are composed of cells with intercellular differences in acute glucose responsiveness that have been attributed to differences in glucokinase (GK) expression and activity. This study first shows that glyceraldehyde can be used as GK-bypassing oxidative substrate and then examines whether the triose can metabolically activate ß-cells with low glucose responsiveness. Glyceraldehyde 1 mM induced a similar cellular 14CO2 output and metabolic redox state as glucose 4 mM. Using flow cytometric analysis, glyceraldehyde (0.252 mM) was shown to concentration-dependently increase the percent metabolically activated cells at all tested glucose concentrations (2.520 mM). Its ability to activate ß-cells that are unresponsive to the prevailing glucose level was further illustrated in glucose low-responsive cells that were isolated by flow sorting. Metabolic activation by glyceraldehyde was associated with an activation of nutrient-driven translational control proteins and an increased protein synthetic response to glucose, however not beyond the maximal rates that are inducible by glucose alone. It is concluded that glucose low-responsive ß-cells can be metabolically activated by the GK-bypassing glyceraldehyde, increasing their acute biosynthetic response to glucose but not their maximal glucose-inducible biosynthetic capacity, which is considered subject to chronic regulation.
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