We have previously found that cyclin A expression is markedly reduced in pancreatic ??-cells by cell-specific overexpression of repressor inducible cyclic AMP early repressor (ICER I??) in transgenic mice. Here we further examined regulatory effects of ICER I?? on cyclin A gene expression using Min6 cells, an insulin-producing cell line. The cyclin A promoter luciferase assay showed that ICER I?? directly repressed cyclin A gene transcription. In addition, upon ICER I?? overexpression, cyclin A mRNA levels markedly decreased, thereby confirming an inhibitory effect of ICER I?? on cyclin A expression. Suppression of cyclin A results in inhibition of BrdU incorporation. Under normal culture conditions endogenous cyclin A is abundant in these cells, whereas ICER is hardly detectable. However, serum starvation of Min6 cells induces ICER I?? expression with a concomitant very low expression level of cyclin A. Cyclin A protein is not expressed unless the cells are in active DNA replication. These results indicate a potentially important anti-proliferative effect of ICER I?? in pancreatic ?? cells. Since ICER I?? is greatly increased in diabetes as well as in FFA- or high glucose-treated islets, this effect may in part exacerbate diabetes by limiting ??-cell proliferation. ?? 2005 Elsevier Inc. All rights reserved.
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Iii, A. T. P., Quick, G. A., & Reference, D. (n.d.). ATP III Guidelines At-A-Glance Quick Desk Reference.
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