Molecular Diversity of Plasma Membrane Ca2+ Transporting ATPases: Their Function Under Normal and Pathological Conditions

被引:13
作者
Hegedus, Luca [1 ]
Zambo, Boglarka [2 ]
Paszty, Katalin [3 ]
Padanyi, Rita [4 ]
Varga, Karolina [4 ]
Penniston, John T. [5 ]
Enyedi, Agnes [4 ]
机构
[1] Univ Clin Essen, Ruhrlandklin, Dept Thorac Surg, Essen, Germany
[2] Hungarian Acad Sci, Inst Enzymol, Res Ctr Nat Sci, Budapest, Hungary
[3] Semmelweis Univ, Dept Biophys, Budapest, Hungary
[4] Semmelweis Univ, Dept Pathol 2, Budapest, Hungary
[5] Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
来源
CALCIUM SIGNALING, 2ND EDITION | 2020年 / 1131卷
关键词
Plasma membrane Ca2+ ATPase (PMCA); ATP2B1-4; Alternative splice; Calmodulin; Phosphatidylinositol-4; 5-bisphosphate; Actin cytoskeleton; Ca2+ signal; Genetic variation; Altered expression; Pathological condition; NITRIC-OXIDE SYNTHASE; CALMODULIN-BINDING DOMAIN; SARCOLEMMAL CALCIUM-PUMP; SINGLE-NUCLEOTIDE POLYMORPHISM; BLOOD-CELL POLYMORPHISMS; GENOME-WIDE ASSOCIATION; ISOFORM; 4B; UP-REGULATION; VITAMIN-D; 1,25-DIHYDROXYVITAMIN D-3;
D O I
10.1007/978-3-030-12457-1_5
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
Plasma membrane Ca2+ transport ATPases (PMCA1-4, ATP2B1-4) are responsible for removing excess Ca2+ from the cell in order to keep the cytosolic Ca2+ ion concentration at the low level essential for normal cell function. While these pumps take care of cellular Ca2+ homeostasis they also change the duration and amplitude of the Ca2+ signal and can create Ca2+ gradients across the cell. This is accomplished by generating more than twenty PMCA variants each having the character - fast or slow response, long or short memory, distinct interaction partners and localization signals - that meets the specific needs of the particular cell-type in which they are expressed. It has become apparent that these pumps are essential to normal tissue development and their malfunctioning can be linked to different pathological conditions such as certain types of neurodegenerative and heart diseases, hearing loss and cancer. In this chapter we summarize the complexity of PMCA regulation and function under normal and pathological conditions with particular attention to recent developments of the field.
引用
收藏
页码:92 / 129
页数:38
相关论文
共 248 条
  • [1] c-Myb-binding sites mediate G1/S-associated repression of the plasma membrane Ca2+-ATPase-1 promoter
    Afroze, T
    Husain, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) : 9062 - 9069
  • [2] Changes in islet plasma membrane calcium-ATPase activity and isoform expression induced by insulin resistance
    Alzugaray, Maria E.
    Garcia, Maria E.
    Del Zotto, Hector H.
    Raschia, Maria A.
    Palomeque, Julieta
    Rossi, Juan P. F. C.
    Gagliardino, Juan J.
    Flores, Luis E.
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 490 (01) : 17 - 23
  • [3] A C-terminal di-leucine motif controls plasma membrane expression of PMCA4b
    Antalffy, Geza
    Paszty, Katalin
    Varga, Karolina
    Hegedus, Luca
    Enyedi, Agnes
    Padanyi, Rita
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2013, 1833 (12): : 2561 - 2572
  • [4] CASK interacts with PMCA4b and JAM-A on the mouse sperm flagellum to regulate Ca2+ homeostasis and motility
    Aravindan, Rolands G.
    Fomin, Victor P.
    Naik, Ulhas P.
    Modelski, Mark J.
    Naik, Meghna U.
    Galileo, Deni S.
    Duncan, Randall L.
    Martin-Deleon, Patricia A.
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2012, 227 (08) : 3138 - 3150
  • [5] A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
    Arking, Dan E.
    Pfeufer, Arne
    Post, Wendy
    Kao, W. H. Linda
    Newton-Cheh, Christopher
    Ikeda, Morna
    West, Kristen
    Kashuk, Carl
    Akyol, Mahmut
    Perz, Siegfried
    Jalilzadeh, Shapour
    Illig, Thomas
    Gieger, Christian
    Guo, Chao-Yu
    Larson, Martin G.
    Wichmann, H. Erich
    Marban, Eduardo
    O'Donnell, Christopher J.
    Hirschhorn, Joel N.
    Kaeaeb, Stefan
    Spooner, Peter M.
    Meitinger, Thomas
    Chakravarti, Aravinda
    [J]. NATURE GENETICS, 2006, 38 (06) : 644 - 651
  • [6] Differences in intestinal calcium and phosphate transport between low and high bone density mice
    Armbrecht, HJ
    Boltz, MA
    Hodam, TL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 282 (01): : G130 - G136
  • [7] Novel functional interaction between the plasma membrane Ca2+ pump 4b and the proapoptotic tumor suppressor Ras-associated factor 1 (RASSF1)
    Armesilla, AL
    Williams, JC
    Buch, MH
    Pickard, A
    Emerson, M
    Cartwright, EJ
    Oceandy, D
    Vos, MD
    Gillies, S
    Clark, GJ
    Neyses, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (30) : 31318 - 31328
  • [8] Plasma membrane Ca2+-ATPase expression during colon cancer cell line differentiation
    Aung, Cho S.
    Kruger, Wade A.
    Poronnik, Philip
    Roberts-Thomson, Sarah J.
    Monteith, Gregory R.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 355 (04) : 932 - 936
  • [9] Evolution of substrate specificities in the P-type ATPase superfamily
    Axelsen, KB
    Palmgren, MG
    [J]. JOURNAL OF MOLECULAR EVOLUTION, 1998, 46 (01) : 84 - 101
  • [10] Chimaeras reveal the role of the catalytic core in the activation of the plasma membrane Ca2+ pump
    Ba-Thein, W
    Caride, AJ
    Enyedi, A
    Pászty, K
    Croy, CL
    Filoteo, AG
    Penniston, JT
    [J]. BIOCHEMICAL JOURNAL, 2001, 356 : 241 - 245