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|Title:||Differential effects of lysophospholipids on exocytosis in rat PC12 cells||Authors:||Ma, M.-T.
|Issue Date:||Mar-2010||Citation:||Ma, M.-T., Yeo, J.-F., Farooqui, A.A., Zhang, J., Chen, P., Ong, W.-Y. (2010-03). Differential effects of lysophospholipids on exocytosis in rat PC12 cells. Journal of Neural Transmission 117 (3) : 301-308. ScholarBank@NUS Repository. https://doi.org/10.1007/s00702-009-0355-1||Abstract:||Secretory phospholipase A2 (SPLA2) activity is present in the CNS and the SPLA2-IIA isoform has been shown to induce exocytosis in cultured hippocampal neurons. However, little is known about possible contributions of various lysophospholipid species to exocytosis in neuroendocrine cells. This study was therefore carried out to examine the effects of several lysophospholipid species on exocytosis on rat pheochromocytoma-12 (PC 12) cells. An increase in vesicle fusion, indicating exocytosis, was observed in PC 12 cells after external infusion of Iysophosphatidylinositol (LPI), but not lysophosphatidylcholine or lysophosphatidylserine by total internal reflection microscopy. Similarly, external infusion of LPI induced significant increases in capacitance, or number of spikes detected at amperometry, indicating exocytosis. Depletion of cholesterol by pre-incubation of cells with methyl beta cyclodextrin and depletion of Ca2+ by thapsigargin and incubation in zero external Ca2+ resulted in attenuation of LPI induced exocytosis, indicating that exocytosis was dependent on the integrity of lipid rafts and intracellular Ca2+. Moreover, LPI induced a rise in intracellular Ca2+ suggesting that this could be the trigger for exocytosis. It is postulated that LPI may be an active participant in sPLA2mediated exocytosis in the CNS. © Springer-Verlag 2010.||Source Title:||Journal of Neural Transmission||URI:||http://scholarbank.nus.edu.sg/handle/10635/79885||ISSN:||03009564||DOI:||10.1007/s00702-009-0355-1|
|Appears in Collections:||Staff Publications|
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