Calcium pumps of plasma membrane and cell interior

被引:129
作者
Strehler, EE
Treiman, M
机构
[1] Mayo Clin, Coll Med, Dept Biochem & Mol Biol, Rochester, MN USA
[2] Univ Copenhagen, Dept Med Physiol, Copenhagen, Denmark
[3] CHARC, Copenhagen, Denmark
关键词
D O I
10.2174/1566524043360735
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Calcium entering the cell from the outside or from intracellular organelles eventually must be returned to the extracellular milieu or to intracellular storage organelles. The two major systems capable of pumping Ca2+ against its large concentration gradient out of the cell or into the sarco/endoplasmatic reticulum are the plasma membrane Ca2+ ATPases (PMCAs) and the sarco/endoplasmic reticulum Ca2+ ATPases (SERCAs), respectively. In mammals, multigene families code for these Ca2+ pumps and additional isoform subtypes are generated via alternative splicing. PMCA and SERCA isoforms show developmental-, tissue- and cell type-specific patterns of expression. Different PMCA and SERCA isoforms are characterized by different regulatory and kinetic properties that likely are optimized for the distinct functional tasks fulfilled by each pump in setting resting cytosolic or intra-organellar Ca2+ levels, and in shaping intracellular Ca2+ signals with spatial and temporal resolution. The loss or malfunction of specific Ca2+ pump isoforms is associated with defects such as deafness, ataxia or heart failure. Understanding the involvement of different Ca2+ pump isoforms in the pathogenesis of disease allows their identification as therapeutic targets for the development of selective strategies to prevent or combat the progression of these disorders.
引用
收藏
页码:323 / 335
页数:13
相关论文
共 163 条
[21]   CA-ATPASE ISOZYME EXPRESSION IN SARCOPLASMIC-RETICULUM IS ALTERED BY CHRONIC STIMULATION OF SKELETAL-MUSCLE [J].
BRIGGS, FN ;
LEE, KF ;
FEHER, JJ ;
WECHSLER, AS ;
OHLENDIECK, K ;
CAMPBELL, K .
FEBS LETTERS, 1990, 259 (02) :269-272
[22]   IDENTIFICATION OF 2 DOMAINS WHICH MEDIATE THE BINDING OF ACTIVATING PHOSPHOLIPIDS TO THE PLASMA-MEMBRANE CA2+ PUMP [J].
BRODIN, P ;
FALCHETTO, R ;
VORHEER, T ;
CARAFOLI, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (02) :939-946
[23]  
BURK SE, 1992, J BIOL CHEM, V267, P19683
[24]  
BURK SE, 1989, J BIOL CHEM, V264, P18561
[25]   CALCIUM-PUMP OF THE PLASMA-MEMBRANE [J].
CARAFOLI, E .
PHYSIOLOGICAL REVIEWS, 1991, 71 (01) :129-153
[26]   BIOGENESIS - PLASMA-MEMBRANE CALCIUM-ATPASE - 15 YEARS OF WORK ON THE PURIFIED ENZYME [J].
CARAFOLI, E .
FASEB JOURNAL, 1994, 8 (13) :993-1002
[27]   mRNA encoding four isoforms of the plasma membrane calcium pump and their variants in rat kidney and nephron segments [J].
Caride, AJ ;
Chini, EN ;
Homma, S ;
Penniston, JT ;
Dousa, TP .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1998, 132 (02) :149-156
[28]   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
[29]   The plasma membrane calcium pump displays memory of past calcium spikes - Differences between isoforms 2b and 4b [J].
Caride, AJ ;
Penheiter, AR ;
Filoteo, AG ;
Bajzer, Z ;
Enyedi, A ;
Penniston, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (43) :39797-39804
[30]   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