Monitoring of free calcium in the neuronal endoplasmic reticulum: an overview of modern approaches

被引:77
作者
Solovyova, N [1 ]
Verkhratsky, A [1 ]
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
endoplasmic reticulum; intraluminal Ca2+; Ca2+ release; fluorescent dyes; aequorin; GFP;
D O I
10.1016/S0165-0270(02)00300-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The concentration of free calcium within the lumen of the endoplasmic reticulum ([Ca2+](L)) fluctuates between 100 and 1000 muM. High [Ca2+](L) provides an electro-driving force for Ca2+ release and supports high Ca2+ diffusion rate within the endoplasmic reticulum lumen. Fluctuations in [Ca2+](L) also regulate numerous chaperones, responsible for postranslational protein processing. Thus, [Ca2+](L), integrates various signalling events and establishes a link between fast signalling, associated with the endoplasmic reticulum Ca2+ release/uptake, and long-lasting adaptive responses relying primarily on the regulation of protein synthesis. This paper overviews modem approaches for the direct monitoring of [Ca2+](L) which rely on three classes of low-affinity Ca2+ probes: ER-targeted aequorin, synthetic fluorescent Ca2+ dyes and GFP-based ER-targeted Ca2+ probes. These techniques, especially as applied to neurones, may substantially widen our appreciation of the endoplasmic reticulum as a universal signalling organelle. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 95 条
[31]   WAVELENGTH MUTATIONS AND POSTTRANSLATIONAL AUTOXIDATION OF GREEN FLUORESCENT PROTEIN [J].
HEIM, R ;
PRASHER, DC ;
TSIEN, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12501-12504
[32]   IMPROVED GREEN FLUORESCENCE [J].
HEIM, R ;
CUBITT, AB ;
TSIEN, RY .
NATURE, 1995, 373 (6516) :663-664
[33]  
HEIM R, 1996, CURR BIOL, V6, P176
[34]   Free [Ca2+] dynamics measured in agonist-sensitive stores of single living intact cells:: a new look at the refilling process [J].
Hofer, AM ;
Landolfi, B ;
Debellis, L ;
Pozzan, T ;
Curci, S .
EMBO JOURNAL, 1998, 17 (07) :1986-1995
[35]   DIRECT MEASUREMENT OF FREE CA IN ORGANELLES OF GASTRIC EPITHELIAL-CELLS [J].
HOFER, AM ;
MACHEN, TE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (03) :G442-G451
[36]   TECHNIQUE FOR INSITU MEASUREMENT OF CALCIUM IN INTRACELLULAR INOSITOL 1,4,5-TRISPHOSPHATE-SENSITIVE STORES USING THE FLUORESCENT INDICATOR MAG-FURA-2 [J].
HOFER, AM ;
MACHEN, TE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2598-2602
[37]   Ionic selectivity of low-affinity ratiometric calcium indicators: mag-Fura-2, Fura-2FF and BTC [J].
Hyrc, KB ;
Bownik, JM ;
Goldberg, MP .
CELL CALCIUM, 2000, 27 (02) :75-86
[38]   SOLUTION STRUCTURE OF A CALMODULIN-TARGET PEPTIDE COMPLEX BY MULTIDIMENSIONAL NMR [J].
IKURA, M ;
CLORE, GM ;
GRONENBORN, AM ;
ZHU, G ;
KLEE, CB ;
BAX, A .
SCIENCE, 1992, 256 (5057) :632-638
[39]   CLONING AND SEQUENCE-ANALYSIS OF CDNA FOR THE LUMINESCENT PROTEIN AEQUORIN [J].
INOUYE, S ;
NOGUCHI, M ;
SAKAKI, Y ;
TAKAGI, Y ;
MIYATA, T ;
IWANAGA, S ;
MIYATA, T ;
TSUJI, FI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (10) :3154-3158
[40]  
KANO M, 1995, J PHYSIOL-LONDON, V487, P1