Endoplasmic reticulum Ca2+-ATPase pump is up-regulated in calcium-transporting dental enamel cells:: a non-housekeeping role for SERCA2b

被引:34
作者
Franklin, IK [1 ]
Winz, RA [1 ]
Hubbard, MJ [1 ]
机构
[1] Univ Otago, Dept Biochem, Dunedin, New Zealand
关键词
calcium store; calcium homoeostasis; calcium toxicity; cytotoxicity; ameloblast;
D O I
10.1042/0264-6021:3580217
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
Dental enamel-forming cells face a. major challenge to avoid the cytotoxic effects of excess calcium. We have characterized sarcoplasmic/endoplasmic reticulum calcium-ATPase pumps (SERCA) in rat enamel cells to address the proposal that nonmitochondrial calcium stores play a dominant role in transcellular calcium transport. A single major isoform, SERCA2b, was detected during the protein-secretory and calcium-transport stages of enamel formation using reverse-transcriptase PCR, cDNA cloning, Northern analysis and immunoblotting. Most importantly, SERCA2b exhibited a specific 3-fold up-regulation to high expression levels during calcium transport, as determined by quantitative immunoblotting and ATPase assays. Sensitivity of the calcium-dependent ATPase to thapsigargin and three other SERCA inhibitors was characterized. These findings indicate that enamel cells are well-equipped to sequester calcium in endoplasmic reticulum stores and so protect against calcium toxicity, associate SERCA with transcellular calcium transport for the first time, and establish SERCA2b as a molecular and pharmacological target for future investigations of calcium transcytosis. The observed physiological regulation in enamel cells contradicts the widespread perception that SERCA2b is restricted to general housekeeping duties.
引用
收藏
页码:217 / 224
页数:8
相关论文
共 48 条
[1]   IN-SITU MESSENGER-RNA DISTRIBUTION OF SARCO(ENDO)PLASMIC RETICULUM CA2+-ATPASE ISOFORMS DURING ONTOGENY IN THE RAT [J].
ANGER, M ;
SAMUEL, JL ;
MAROTTE, F ;
WUYTACK, F ;
RAPPAPORT, L ;
LOMPRE, AM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (04) :539-550
[2]   EFFECTS OF THAPSIGARGIN AND CYCLOPIAZONIC ACID ON TWITCH FORCE AND SARCOPLASMIC-RETICULUM CA-2+ CONTENT OF RABBIT VENTRICULAR MUSCLE [J].
BAUDET, S ;
SHAOULIAN, R ;
BERS, DM .
CIRCULATION RESEARCH, 1993, 73 (05) :813-819
[3]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[4]   THE BIOLOGY AND MEDICINE OF CALCIUM SIGNALING [J].
BERRIDGE, MJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1994, 98 (02) :119-124
[5]   Neurodegenerative and morphogenic changes in a mouse model of temporal lobe epilepsy do not depend on the expression of the calcium-binding proteins parvalbumin, calbindin, or calretinin [J].
Bouilleret, V ;
Schwaller, B ;
Schurmans, S ;
Celio, MR ;
Fritschy, JM .
NEUROSCIENCE, 2000, 97 (01) :47-58
[6]   CALCIUM-TRANSPORT ACROSS EPITHELIA [J].
BRONNER, F .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1991, 131 :169-212
[7]  
BURK SE, 1989, J BIOL CHEM, V264, P18561
[8]   The sarco/endoplasmic reticulum calcium-ATPase 2b is an endoplasmic reticulum stress-inducible protein [J].
Caspersen, C ;
Pedersen, PS ;
Treiman, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (29) :22363-22372
[9]   Thapsigargin discriminates strongly between Ca2+-ATPase phosphorylated intermediates with different subcellular distributions in bovine adrenal chromaffin cells [J].
Caspersen, C ;
Treiman, M .
FEBS LETTERS, 1995, 377 (01) :31-36
[10]   A DIRECT COLORIMETRIC ASSAY FOR CA-2+-STIMULATED ATPASE ACTIVITY [J].
CHAN, KM ;
DELFERT, D ;
JUNGER, KD .
ANALYTICAL BIOCHEMISTRY, 1986, 157 (02) :375-380