Calcium microdomains and gene expression in neurons and skeletal muscle cells

被引:49
作者
Carrasco, M. Angelica
Hidalgo, Cecilia
机构
[1] Univ Chile, Fac Med, ICBM, Programa Fisiol & Biofis, Santiago 7, Chile
[2] Univ Santiago, Fac Med, Ctr FONDAP Estudios Mol Celula, Santiago, Chile
[3] Univ Chile, Fac Med, ICBM, Programa Biol Celular & Mol, Santiago 7, Chile
关键词
calcium channels; transcription factors; synaptic plasticity; muscle contraction; calcium release; nuclear calcium signals; calcium-dependent kinases; calcineurin;
D O I
10.1016/j.ceca.2006.08.021
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neurons generate particular calcium microdomains in response to different stimuli. Calcium microdomains have a central role in a variety of neuronal functions. In particular, calcium microdomains participate in long-lasting synaptic plasticity-a neuronal response presumably correlated with cognitive brain functions that requires expression of new gene products. Stimulation of skeletal muscle generates - with few milliseconds delay - calcium microdomains that have a central role in the ensuing muscle contraction. In addition, recent evidence indicates that sustained stimulation of skeletal muscle cells in culture generates calcium microdomains, which stimulate gene expression but not muscle contraction. The mechanisms whereby calcium microdomains activate signaling cascades that lead to the transcription of genes known to participate in specific cellular responses are the central topic of this review. Thus, we will discuss here the signaling pathways and molecular mechanisms, which via activation of particular calcium-dependent transcription factors regulate the expression of specific genes or set of genes in neurons or skeletal muscle cells. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:575 / 583
页数:9
相关论文
共 102 条
[1]   Molecular psychology: Roles for the ERK MAP kinase cascade in memory [J].
Adams, JP ;
Sweatt, JD .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2002, 42 :135-163
[2]   Calcium microdomains in mitochondria and nucleus [J].
Alonso, Maria Teresa ;
Villalobos, Carlos ;
Chamero, Pablo ;
Alvarez, Javier ;
Garcia-Sancho, Javier .
CELL CALCIUM, 2006, 40 (5-6) :513-525
[3]   Dihydropyridine receptors as voltage sensors for a depolarization-evoked, IP3R-mediated, slow calcium signal in skeletal muscle cells [J].
Araya, R ;
Liberona, JL ;
Cárdenas, JC ;
Riveros, N ;
Estrada, M ;
Powell, JA ;
Carrasco, MA ;
Jaimovich, E .
JOURNAL OF GENERAL PHYSIOLOGY, 2003, 121 (01) :3-16
[4]  
Baba A, 2003, J NEUROSCI, V23, P7737
[5]   The role of the endoplasmic reticulum Ca2+ store in the plasticity of central neurons [J].
Bardo, S ;
Cavazzini, MG ;
Emptage, N .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2006, 27 (02) :78-84
[6]   Excitation-transcription coupling in smooth muscle [J].
Barlow, CA ;
Rose, P ;
Pulver-Kaste, RA ;
Lounsbury, KM .
JOURNAL OF PHYSIOLOGY-LONDON, 2006, 570 (01) :59-64
[7]   Activation of nuclear factor-κB by depolarization and Ca2+ influx in MIN6 insulinoma cells [J].
Bernal-Mizrachi, E ;
Wen, W ;
Shornick, M ;
Permutt, MA .
DIABETES, 2002, 51 :S484-S488
[8]   Calcium signalling: Dynamics, homeostasis and remodelling [J].
Berridge, MJ ;
Bootman, MD ;
Roderick, HL .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (07) :517-529
[9]   Neuronal calcium signaling [J].
Berridge, MJ .
NEURON, 1998, 21 (01) :13-26
[10]   Calcium signaling in cardiac ventricular myocytes [J].
Bers, DM ;
Guo, T .
COMMUNICATIVE CARDIAC CELL, 2005, 1047 :86-98