Examining intracellular organelle function using fluorescent probes - From animalcules to quantum dots

被引:56
作者
Zorov, DB
Kobrinsky, E
Juhaszova, M
Sollott, SJ
机构
[1] NIA, Cardiovasc Sci Lab, Gerontol Res Ctr, Intramural Res Program,NIH, Baltimore, MD 21224 USA
[2] NIA, Clin Invest Lab, Gerontol Res Ctr, Intramural Res Program,NIH, Baltimore, MD 21224 USA
[3] AN Belozersky Inst Physicochem Biol, Moscow, Russia
关键词
microscopy; calcium; redox; mitochondria; fluorescent proteins;
D O I
10.1161/01.RES.0000137875.42385.8e
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fluorescence microscopy imaging has become one of the most useful techniques to assess the activity of individual cells, subcellular trafficking of signals to and between organelles, and to appreciate how organelle function is regulated. The past 2 decades have seen a tremendous advance in the rational design and development in the nature and selectivity of probes to serve as reporters of the intracellular environment in live cells. These probes range from small organic fluorescent molecules to fluorescent biomolecules and photoproteins ingeniously engineered to follow signaling traffic, sense ionic and nonionic second messengers, and report various kinase activities. These probes, together with recent advances in imaging technology, have enabled significantly enhanced spatial and temporal resolution. This review summarizes some of these developments and their applications to assess intracellular organelle function.
引用
收藏
页码:239 / 252
页数:14
相关论文
共 108 条
[11]  
Boveris A, 2000, ANN NY ACAD SCI, V899, P121
[12]   Role of mitochondria in calcium regulation of spontaneously contracting cardiac muscle cells [J].
Bowser, DN ;
Minamikawa, T ;
Nagley, P ;
Williams, DA .
BIOPHYSICAL JOURNAL, 1998, 75 (04) :2004-2014
[13]   NUCLEAR CA2+ CONCENTRATION MEASURED WITH SPECIFICALLY TARGETED RECOMBINANT AEQUORIN [J].
BRINI, M ;
MURGIA, M ;
PASTI, L ;
PICARD, D ;
POZZAN, T ;
RIZZUTO, R .
EMBO JOURNAL, 1993, 12 (12) :4813-4819
[14]  
Chalfie M, 1998, GREEN FLUORESCENT PROTEIN: PROPERTIES, APPLICATIONS, AND PROTOCOLS, pVII
[15]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[16]   Mitochondrially localized active caspase-9 and caspase-3 result mostly from translocation from the cytosol and partly from caspase-mediated activation in the organelle - Lack of evidence for Apaf-1-mediated procaspase-9 activation in the mitochondria [J].
Chandra, D ;
Tang, DG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (19) :17408-17420
[17]   Kindling fluorescent proteins for precise in vivo photolabeling [J].
Chudakov, DM ;
Belousov, VV ;
Zaraisky, AG ;
Novoselov, VV ;
Staroverov, DB ;
Zorov, DB ;
Lukyanov, S ;
Lukyanov, KA .
NATURE BIOTECHNOLOGY, 2003, 21 (02) :191-194
[18]   ER-tracker dye and BODIPY-brefeldin A differentiate the endoplasmic reticulum and Golgi bodies from the tubular-vacuole system in living hyphae of Pisolithus tinctorius [J].
Davies, D. ;
Hyde, G.J. ;
Ashford, A.E. ;
Cole, Louise .
Journal of Microscopy, 2000, 197 (03) :239-249
[19]   Direct imaging of dehydrogenase activity within living cells using enzyme-dependent fluorescence recovery after photobleaching (ED-FRAP) [J].
Combs, CA ;
Balaban, RS .
BIOPHYSICAL JOURNAL, 2001, 80 (04) :2018-2028
[20]   Requirement of ryanodine receptor subtypes 1 and 2 for Ca2+induced Ca2+ release in vascular myocytes [J].
Coussin, F ;
Macrez, N ;
Morel, JL ;
Mironneau, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (13) :9596-9603