Inositol hexakisphosphate mobilizes an endomembrane store of calcium in guard cells

被引:186
作者
Lemtiri-Chlieh, F
MacRobbie, EAC
Webb, AAR
Manison, NF
Brownlee, C
Skepper, JN
Chen, J
Prestwich, GD
Brearley, CA [1 ]
机构
[1] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[2] Univ Cambridge, Dept Plant Sci, Cambridge CB2 3EA, England
[3] Marine Biol Assoc UK, Plymouth PL1 2PB, Devon, England
[4] Univ Cambridge, Dept Anat, Multi Imaging Ctr, Cambridge CB2 3DY, England
[5] Univ Utah, Dept Med Chem, Salt Lake City, UT 84108 USA
关键词
D O I
10.1073/pnas.1133289100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
myo-Inositol hexakisphosphate (InsP(6)) is the most abundant inositol phosphate in cells, yet it remains the most enigmatic of this class of signaling molecule. InsP(6) plays a role in the processes by which the drought stress hormone abscisic acid (ABA) induces stomatal closure, conserving water and ensuring plant survival. Previous work has shown that InsP(6) levels in guard cells are elevated in response to ABA, and InsP(6) inactivates the plasma membrane inward K+ conductance (I-K,I-in) in a cytosolic calcium-dependent manner. The use of laser-scanning confocal microscopy in dye-loaded patch-clamped guard cell protoplasts shows that release of InsP(6) from a caged precursor mobilizes calcium. Measurement of calcium (barium) currents I-Ca in patch-clamped protoplasts in whole cell mode shows that InsP(6) has no effect on the calcium-permeable channels in the plasma membrane activated by ABA. The lnsP(6)-mediated inhibition Of I-K,in can also be observed in the absence of external calcium. Thus the InsP(6)-induced increase in cytoplasmic calcium does not result from calcium influx but must arise from InsP(6)-triggered release of calcium from endomembrane stores. Measurements of vacuolar currents in patch-clamped isolated vacuoles in whole-vacuole mode showed that InsP(6) activates both the fast and slow conductances of the guard cell vacuole. These data define InsP(6) as an endomembrane-acting calcium-release signal in guard cells; the vacuole may contribute to InsP(6)-triggered Ca2+ release, but other endomembranes may also be involved.
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页码:10091 / 10095
页数:5
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