The plasma membrane calcium pump displays memory of past calcium spikes - Differences between isoforms 2b and 4b

被引:76
作者
Caride, AJ
Penheiter, AR
Filoteo, AG
Bajzer, Z
Enyedi, A
Penniston, JT
机构
[1] Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Natl Inst Haematol & Immunol, H-1113 Budapest, Hungary
关键词
D O I
10.1074/jbc.M104380200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To understand how the plasma membrane Ca2+ pump (PMCA) behaves under changing Ca2+ concentrations, it is necessary to obtain information about the Ca2+ dependence of the rate constants for calmodulin activation (k(act)) and for inactivation by calmodulin removal (kin.,at). Here we studied these constants for isoforms 2b and 4b. We measured the ATPase activity of these isoforms expressed in Sf9 cells. For both PMCA4b and 2b, k(act) increased with Ca2+ along a sigmoidal curve. At all Ca2+ concentrations, 2b showed a faster reaction with calmodulin than 4b but a slower off rate. On the basis of the measured rate constants, we simulated mathematically the behavior of these pumps upon repetitive changes in Ca2+ concentration and also tested these simulations experimentally; PMCA was activated by 500 nm Ca2+ and then exposed to 50 nm Ca2+ for 10 to 150 s, and then Ca2+ was increased again to 500 nm. During the second exposure to 500 nm Ca2+, the activity reached steady state faster than during the first exposure at 500 nm Ca2+. This memory effect is longer for PMCA2b than for 4b. In a separate experiment, a calmodulin-binding peptide from myosin light chain kinase, which has no direct interaction with the pump, was added during the second exposure to 500 nm Ca2+. The peptide inhibited the activity of PMCA2b when the exposure to 50 nm Ca2+ was 150 s but had little or no effect when this exposure was only 15 s. This suggests that the memory effect is due to calmodulin remaining bound to the enzyme during the period at low Ca2+. The memory effect observed in PMCA2b and 4b will allow cells expressing either of them to remove Ca2+ more quickly in subsequent spikes after an initial activating spike.
引用
收藏
页码:39797 / 39804
页数:8
相关论文
共 33 条
[1]   Chimaeras reveal the role of the catalytic core in the activation of the plasma membrane Ca2+ pump [J].
Ba-Thein, W ;
Caride, AJ ;
Enyedi, A ;
Pászty, K ;
Croy, CL ;
Filoteo, AG ;
Penniston, JT .
BIOCHEMICAL JOURNAL, 2001, 356 :241-245
[2]  
Bautista DM, 2000, BIOPHYS J, V78, p192A
[3]   Effects of PMCA and SERCA pump overexpression on the kinetics of cell Ca2+ signalling [J].
Brini, M ;
Bano, D ;
Manni, S ;
Rizzuto, R ;
Carafoli, E .
EMBO JOURNAL, 2000, 19 (18) :4926-4935
[4]   The rate of activation by calmodulin of isoform 4 of the plasma membrane Ca2+ pump is slow and is changed by alternative splicing [J].
Caride, AJ ;
Elwess, NL ;
Verma, AK ;
Filoteo, AG ;
Enyedi, A ;
Bajzer, Z ;
Penniston, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) :35227-35232
[5]   Detection of isoform 4 of the plasma membrane calcium pump in human tissues by using isoform-specific monoclonal antibodies [J].
Caride, AJ ;
Filoteo, AG ;
Enyedi, A ;
Verma, AK ;
Penniston, JT .
BIOCHEMICAL JOURNAL, 1996, 316 :353-359
[6]   Delayed activation of the plasma membrane calcium pump by a sudden increase in Ca2+:: fast pumps reside in fast cells [J].
Caride, AJ ;
Filoteo, AG ;
Penheiter, AR ;
Pászty, K ;
Enyedi, A ;
Penniston, JT .
CELL CALCIUM, 2001, 30 (01) :49-57
[7]   THE ROLE OF CALCIUM-IONS, CALMODULIN AND TROPONIN IN THE REGULATION OF PHOSPHORYLASE-KINASE FROM RABBIT SKELETAL-MUSCLE [J].
COHEN, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1980, 111 (02) :563-574
[8]   Sensitivity of CaM kinase II to the frequency of Ca2+ oscillations [J].
De Koninck, P ;
Schulman, H .
SCIENCE, 1998, 279 (5348) :227-230
[9]   Plasma membrane Ca2+ pump isoforms 2a and 2b are unusually responsive to calmodulin and Ca2+ [J].
Elwess, NL ;
Filoteo, AG ;
Enyedi, A ;
Penniston, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (29) :17981-17986
[10]  
ENYEDI A, 1993, J BIOL CHEM, V268, P17120