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Olfactory receptor Olfr544 responding to azelaic acid regulates glucagon secretion in alpha-cells of mouse pancreatic islets
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Title
Olfactory receptor Olfr544 responding to azelaic acid regulates glucagon secretion in alpha-cells of mouse pancreatic islets
Issued Date
2015-05
Citation
Kang, Nana. (2015-05). Olfactory receptor Olfr544 responding to azelaic acid regulates glucagon secretion in alpha-cells of mouse pancreatic islets. Biochemical and Biophysical Research Communications, 460(3), 616–621. doi: 10.1016/j.bbrc.2015.03.078
Type
Article
Author Keywords
Olfactory receptorOlfr544Pancreatic α-cellsAzelaic acidGlucagon
Keywords
BETA-CELLEXPRESSIONGenesGlucagonGUTMiceMOLECULAR-BASISODORANT RECEPTORSOlfactory ReceptorOlfr544Pancreatic Alpha-CellsPancreatic Alpha-cellsSYSTemACTIVATIONAzelaic ACID
ISSN
0006-291X
Abstract
Olfactory receptors (ORs) are extensively expressed in olfactory as well as non-olfactory tissues. Although many OR transcripts are expressed in non-olfactory tissues, only a few studies demonstrate the functional role of ORs. Here, we verified that mouse pancreatic α-cells express potential OR-mediated downstream effectors. Moreover, high levels of mRNA for the olfactory receptors Olfr543, Olfr544, Olfr545, and Olfr1349 were expressed in α-cells as assessed using RNA-sequencing, microarray, and quantitative real-time RT-PCR analyses. Treatment with dicarboxylic acids (azelaic acid and sebacic acid) increased intracellular Ca2+ mobilization in pancreatic α-cells. The azelaic acid-induced Ca2+ response as well as glucagon secretion was concentration- and time-dependent manner. Olfr544 was expressed in α-cells, and the EC50 value of azelaic acid to Olfr544 was 19.97 μM, whereas Olfr545 did not respond to azelaic acid. Our findings demonstrate that Olfr544 responds to azelaic acid to regulate glucagon secretion through Ca2+ mobilization in α-cells of the mouse pancreatic islets, suggesting that Olfr544 may be an important therapeutic target for metabolic diseases. © 2015 Elsevier Inc.All rights reserved.
URI
http://hdl.handle.net/20.500.11750/2899
DOI
10.1016/j.bbrc.2015.03.078
Publisher
Academic Press Inc.
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구재형
Koo, JaeHyung구재형

Department of New Biology

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