Compartmentalization of the redox environment in PC-12 neuronal cells

被引:9
作者
Maulucci, G. [1 ]
Pani, G. [2 ]
Fusco, S. [2 ]
Papi, M. [1 ]
Arcovito, G. [1 ]
Galeotti, T. [2 ]
Fraziano, M. [3 ]
De Spirito, M. [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Ist Fis, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Ist Patol Gen, I-00168 Rome, Italy
[3] Univ Roma Tor Vergata, Dipartmento Biol, I-00133 Rome, Italy
来源
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS | 2010年 / 39卷 / 06期
关键词
ROS; Neuron; Redox environment; rxYFP; Compartmentalization; DISULFIDE BOND FORMATION; PC12; CELLS; OXYGEN; DIFFERENTIATION; GENERATION; PHENOTYPE; RADICALS;
D O I
10.1007/s00249-009-0470-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Neuronal redox phenomena are involved in numerous biochemical pathways and play a key role in many pathological events and clinical situations. The oxidation/reduction (redox) state present in biological compartments is a major target for possible pharmaceutical intervention and, consequently, the processes associated with its change have attracted increased attention in recent years. Here, we analyze the redox environment and its spatial compartmentalization in differentiated neuronal phenotype of PC-12 cells using a redox-sensitive protein (i.e., a mutant of the Yellow Fluorescent protein), employed ratiometrically. Redox maps of cells were generated with an elevate spatial resolution, and the spatial distributions of highly oxidized and highly reduced regions have been determined. A quantitative analysis of redox maps allows the disclosure of a peculiar spatial organization of the redox environment.
引用
收藏
页码:993 / 999
页数:7
相关论文
共 30 条
[1]  
[Anonymous], 1991, STAT SPATIAL DATA
[2]  
Babior BM, 2002, ISRAEL MED ASSOC J, V4, P1023
[3]  
Bindokas VP, 1996, J NEUROSCI, V16, P1324
[4]   Development of a novel GFP-based ratiometric excitation and emission pH indicator for intracellular studies [J].
Bizzarri, R ;
Arcangeli, C ;
Arosio, D ;
Ricci, F ;
Faraci, P ;
Cardarelli, F ;
Beltram, F .
BIOPHYSICAL JOURNAL, 2006, 90 (09) :3300-3314
[5]   FLUORESCENCE RATIO IMAGING MICROSCOPY - TEMPORAL AND SPATIAL MEASUREMENTS OF CYTOPLASMIC PH [J].
BRIGHT, GR ;
FISHER, GW ;
ROGOWSKA, J ;
TAYLOR, DL .
JOURNAL OF CELL BIOLOGY, 1987, 104 (04) :1019-1033
[6]   Imaging dynamic redox changes in mammalian cells with green fluorescent protein indicators [J].
Dooley, CT ;
Dore, TM ;
Hanson, GT ;
Jackson, WC ;
Remington, SJ ;
Tsien, RY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (21) :22284-22293
[7]   Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95
[8]   Oxidant signals and oxidative stress [J].
Finkel, T .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (02) :247-254
[9]   Oxygen radicals and signaling [J].
Finkel, T .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (02) :248-253
[10]   DUAL-WAVELENGTH RATIOMETRIC FLUORESCENCE MEASUREMENT OF THE MEMBRANE DIPOLE POTENTIAL [J].
GROSS, E ;
BEDLACK, RS ;
LOEW, LM .
BIOPHYSICAL JOURNAL, 1994, 67 (01) :208-216