Calcium Pumps: Why So Many?

被引:28
|
作者
Brini, Marisa [1 ]
Cali, Tito [1 ]
Ottolini, Denis [2 ]
Carafoli, Ernesto [3 ]
机构
[1] Univ Padua, Dept Comparat Biomed & Food Sci, Legnaro Padova, Italy
[2] Univ Padua, Dept Biomed Sci, Padua, Italy
[3] Venetian Inst Mol Med VIMM, Padua, Italy
关键词
PLASMA-MEMBRANE CA2+; SARCOPLASMIC-RETICULUM CA2+-ATPASE; SECRETORY PATHWAY CA2+/MN2+-ATPASE; TRANSIENT KINETIC ANALYSES; CALMODULIN-BINDING DOMAIN; P-TYPE ATPASE; CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE; TWITCH SKELETAL-MUSCLE; NMR SOLUTION STRUCTURE; HAILEY-HAILEY-DISEASE;
D O I
10.1002/cphy.c110034
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Ca2+- ATPases ( pumps) are key to the regulation of Ca2+ in eukaryotic cells: nine are known today, belonging to three multigene families. The three endo(sarco) plasmic reticulum (SERCA) and the four plasma membrane ( PMCA) pumps have been known for decades, the two Secretory Pathway Ca2+ ATPase (SPCA) pumps have only become known recently. The number of pump isoforms is further increased by alternative splicing processes. The three pump types share the basic features of the catalytic mechanism, but differ in a number of properties related to tissue distribution, regulation, and role in the cellular homeostasis of Ca2+. The molecular understanding of the function of all pumps has received great impetus from the solution of the three-dimensional ( 3D) structure of one of them, the SERCA pump. This landmark structural advance has been accompanied by the emergence and rapid expansion of the area of pump malfunction. Most of the pump defects described so far are genetic and produce subtler, often tissue and isoform specific, disturbances that affect individual components of the Ca2+- controlling and/ or processing machinery, compellingly indicating a specialized role for each Ca2+ pump type and/ or isoform. (C) 2012 American Physiological Society. Compr Physiol 2:1045-1060, 2012.
引用
收藏
页码:1045 / 1060
页数:16
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