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KMID : 0811720160200020177
Korean Journal of Physiology & Pharmacology
2016 Volume.20 No. 2 p.177 ~ p.183
Identification of Lys49-PLA2 from crude venom of Crotalus atrox as a human neutrophil-calcium modulating protein
Md. Tipu Sultan

Li Hong Mei
Lee Yong-Zu
Lim Soon-Sung
Song Dong-Keun
Abstract
We fortuitously observed a human neutrophil intracellular free-calcium concentration ([Ca2+]i) increasing activity in the commercially available phosphodiesterase I (PDE I), which is actually dried crude venom of Crotalus atrox. As this activity was not observed with another commercially available pure PDE I, we tried to find out the causative molecule(s) present in ¡®crude¡¯ PDE, and identified Lys49- phospholipase A2 (Lys49-PLA2 or K49-PLA2), a catalytically inactive protein which belongs to the phospholipase A2 family, by activity-driven three HPLC (reverse phase, size exclusion, reverse phase) steps followed by SDS-PAGE and LC-MS/MS. K49-PLA2 induced Ca2+ influx in human neutrophils without any cytotoxic effect. Two calcium channel inhibitors, 2-aminoetoxydiphenyl borate (2-APB) (30 ¥ìM) and SKF- 96365 (20 ¥ìM) significantly inhibited K49-PLA2-induced [Ca2+]i increase. These results suggest that K49-PLA2 modulates [Ca2+]i in human neutrophils via 2-APB- and SKF- 96365-sensitive calcium channels without causing membrane disruption.
KEYWORD
Crotalus atrox, Human neutrophils, Intracellular free-calcium concentration, Lys49-PLA2, Phosphodiesterase I
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