Linoleic acid stimulates [Ca2+]i increase in rat pancreatic beta-cells through both membrane receptor- and intracellular metabolite-mediated pathways.

Yufeng Zhao, Li Wang, Jianhua Qiu, Dingjun Zha, Qiang Sun, Chen Chen

Index: PLoS ONE 8 , e60255, (2013)

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Abstract

The role of the free fatty acid (FFA) receptor and the intracellular metabolites of linoleic acid (LA) in LA-stimulated increase in cytosolic free calcium concentration ([Ca(2+)]i) was investigated. [Ca(2+)]i was measured using Fura-2 as indicator in rat pancreatic β-cells in primary culture. LA (20 µM for 2 min) stimulated a transient peak increase followed by a minor plateau increase in [Ca(2+)]i. Elongation of LA stimulation up to 10 min induced a strong and long-lasting elevation in [Ca(2+)]i. Activation of FFA receptors by the non-metabolic agonist GW9508 (40 µM for 10 min) resulted in an increase in [Ca(2+)]i similar to that of 2-min LA treatment. Inhibition of acyl-CoA synthetases by Triacsin C suppressed the strong and long-lasting increase in [Ca(2+)]i. The increase in [Ca(2+)]i induced by 2 min LA or GW9508 were fully eliminated by exhaustion of endoplasmic reticulum (ER) Ca(2+) stores or by inhibition of phospholipase C (PLC). Removal of extracellular Ca(2+) did not influence the transient peak increase in [Ca(2+)]i stimulated by 2 min LA or GW9508. The strong and long-lasting increase in [Ca(2+)]i induced by 10 min LA was only partially suppressed by extracellular Ca(2+) removal or thapsigargin pretreatment, whereas remaining elevation in [Ca(2+)]i was eliminated after exhaustion of mitochondrial Ca(2+) using triphenyltin. In conclusion, LA stimulates Ca(2+) release from ER through activation of the FFA receptor coupled to PLC and mobilizes mitochondrial Ca(2+) by intracellular metabolites in β-cells.