Abstract
Pancreatic β-cells store insulin in secretory granules that undergo exocytosis upon glucose stimulation. Sustained stimulation depletes β-cells of their granule pool, which must be quickly restored. However, the factors promoting rapid granule biogenesis are unknown. Here we show that β-cell stimulation induces the nucleocytoplasmic translocation of polypyrimidine tract-binding protein (PTB). Activated cytosolic PTB binds and stabilizes mRNAs encoding proteins of secretory granules, thus increasing their translation, whereas knockdown of PTB expression by RNA interference (RNAi) results in the depletion of secretory granules. These findings may provide insight for the understanding and treatment of diabetes, in which insulin secretion is typically impaired.
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Acknowledgements
We thank P. De Camilli, C. Walch-Solimena and E. Ullu for critical reading of the manuscript, R. Jahn, W. Huttner, K. Moremen, A. Helenius and J. Saraste for antibodies, M. Kolpe and R. Meisterfeld for help with islet isolation and insulin radioimmunoassay, F. Theissig for preparing islet sections, F. Bucholz for advice on RNAi, K. Scheckel for providing Jurkat cells, C. Echeverri and L. Buffa for siRNA oligonucleotides, K. Pfriem for excellent secretarial assistance and M. Füssel for support. We are also very grateful to the reviewers, whose criticisms greatly improved this article. This work was supported by grants from the A. von Humboldt Foundation and the Bundesministerium für Bildung und Forschung (BMBF) to M.S. and by a Telethon Post-Doctoral Fellowship to B.B.
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Knoch, KP., Bergert, H., Borgonovo, B. et al. Polypyrimidine tract-binding protein promotes insulin secretory granule biogenesis. Nat Cell Biol 6, 207–214 (2004). https://doi.org/10.1038/ncb1099
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DOI: https://doi.org/10.1038/ncb1099
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