Adenovirus-mediated silencing of synaptotagmin 9 inhibits Ca2+-dependent insulin secretion in islets |
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Authors: | Iezzi Mariella Eliasson Lena Fukuda Mitsunori Wollheim Claes B |
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Affiliation: | Department of Cell Physiology and Metabolism, University Medical Center, 1211 Geneva 4, Switzerland. |
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Abstract: | Synaptotagmins (Syts) are involved in Ca(2+)-dependent insulin release. However, which Syt isoform is functional in primary beta-cells remains unknown. We demonstrate by electron microscopy of pancreatic islets, the association of Syt 9 with insulin granules. Silencing of Syt 9 by RNA interference adenovirus in islet cells had no effect on the expression of Syt 5, Syt 7 and Syt 3 isoforms. The latter was localized at the plasma membrane of pancreatic polypeptide cells. Insulin release in response to glucose or tolbutamide was strongly inhibited in Syt 9 deficient islets, whereas exocytosis potentiated by raising cAMP levels, was unaltered. Thus, Syt 9 may act as Ca(2+) sensor for beta-cell secretion. |
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Keywords: | RNAi, RNA interference siRNA, small interfering RNA Syt, Synaptotagmin |
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