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<RECORD>
	<REFERENCE_TYPE>31</REFERENCE_TYPE>
	<AUTHORS>
		<AUTHOR>Peyot, M. L.</AUTHOR>
		<AUTHOR>Guay, C.</AUTHOR>
		<AUTHOR>Latour, M. G.</AUTHOR>
		<AUTHOR>Lamontagne, J.</AUTHOR>
		<AUTHOR>Lussier, R.</AUTHOR>
		<AUTHOR>Pineda, M.</AUTHOR>
		<AUTHOR>Ruderman, N. B.</AUTHOR>
		<AUTHOR>Haemmerle, G.</AUTHOR>
		<AUTHOR>Zechner, R.</AUTHOR>
		<AUTHOR>Joly, E.</AUTHOR>
		<AUTHOR>Madiraju, S. R.</AUTHOR>
		<AUTHOR>Poitout, V.</AUTHOR>
		<AUTHOR>Prentki, M.</AUTHOR>
	</AUTHORS>
	<YEAR>2009</YEAR>
	<TITLE>Adipose triglyceride lipase is implicated in fuel- and non-fuel-stimulated insulin secretion</TITLE>
	<SECONDARY_TITLE>J Biol Chem</SECONDARY_TITLE>
	<VOLUME>284</VOLUME>
	<NUMBER>25</NUMBER>
	<PAGES>16848-59</PAGES>
	<DATE>Jun 19</DATE>
	<ISBN>0021-9258 (Print)</ISBN>
	<ACCESSION_NUMBER>19389712</ACCESSION_NUMBER>
	<ABSTRACT>Reduced lipolysis in hormone-sensitive lipase-deficient mice is associated with impaired glucose-stimulated insulin secretion (GSIS), suggesting that endogenous beta-cell lipid stores provide signaling molecules for insulin release. Measurements of lipolysis and triglyceride (TG) lipase activity in islets from HSL(-/-) mice indicated the presence of other TG lipase(s) in the beta-cell. Using real time-quantitative PCR, adipose triglyceride lipase (ATGL) was found to be the most abundant TG lipase in rat islets and INS832/13 cells. To assess its role in insulin secretion, ATGL expression was decreased in INS832/13 cells (ATGL-knockdown (KD)) by small hairpin RNA. ATGL-KD increased the esterification of free fatty acid (FFA) into TG. ATGL-KD cells showed decreased glucose- or Gln + Leu-induced insulin release, as well as reduced response to KCl or palmitate at high, but not low, glucose. The K(ATP)-independent/amplification pathway of GSIS was considerably reduced in ATGL-KD cells. ATGL(-/-) mice were hypoinsulinemic and hypoglycemic and showed decreased plasma TG and FFAs. A hyperglycemic clamp revealed increased insulin sensitivity and decreased GSIS and arginine-induced insulin secretion in ATGL(-/-) mice. Accordingly, isolated islets from ATGL(-/-) mice showed reduced insulin secretion in response to glucose, glucose + palmitate, and KCl. Islet TG content and FFA esterification into TG were increased by 2-fold in ATGL(-/-) islets, but glucose usage and oxidation were unaltered. The results demonstrate the importance of ATGL and intracellular lipid signaling for fuel- and non-fuel-induced insulin secretion.</ABSTRACT>
	<NOTES>Journal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tUnited States</NOTES>
	<URL>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=PubMed&amp;dopt=Citation&amp;list_uids=19389712</URL>
</RECORD>
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