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
[71]   The Golgi apparatus is an inositol 1,4,5-trisphosphate-sensitive Ca2+ store, with functional properties distinct from those of the endoplasmic reticulum [J].
Pinton, P ;
Pozzan, T ;
Rizzuto, R .
EMBO JOURNAL, 1998, 17 (18) :5298-5308
[72]  
Pouli AE, 1998, BIOCHEM J, V330, P1399
[73]   Investigating signal transduction with genetically encoded fluorescent probes - Delivered on 22 October 2002 at the 28th FEBS Meeting in Istanbul [J].
Pozzan, T ;
Mongillo, M ;
Rudolf, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (11) :2343-2352
[74]   PRIMARY STRUCTURE OF THE AEQUOREA-VICTORIA GREEN-FLUORESCENT PROTEIN [J].
PRASHER, DC ;
ECKENRODE, VK ;
WARD, WW ;
PRENDERGAST, FG ;
CORMIER, MJ .
GENE, 1992, 111 (02) :229-233
[75]   CHIMERIC GREEN FLUORESCENT PROTEIN AS A TOOL FOR VISUALIZING SUBCELLULAR ORGANELLES IN LIVING CELLS [J].
RIZZUTO, R ;
BRINI, M ;
PIZZO, P ;
MURGIA, M ;
POZZAN, T .
CURRENT BIOLOGY, 1995, 5 (06) :635-642
[76]   Double labelling of subcellular structures with organelle-targeted GFP mutants in vivo [J].
Rizzuto, R ;
Brini, M ;
DeGiorgi, F ;
Rossi, R ;
Heim, R ;
Tsien, RY ;
Pozzan, T .
CURRENT BIOLOGY, 1996, 6 (02) :183-188
[77]   RAPID CHANGES OF MITOCHONDRIAL CA2+ REVEALED BY SPECIFICALLY TARGETED RECOMBINANT AEQUORIN [J].
RIZZUTO, R ;
SIMPSON, AWM ;
BRINI, M ;
POZZAN, T .
NATURE, 1992, 358 (6384) :325-327
[78]   Direct monitoring of the calcium concentration in the sarcoplasmic and endoplasmic reticulum of skeletal muscle myotubes [J].
Robert, V ;
De Giorgi, F ;
Massimino, ML ;
Cantini, M ;
Pozzan, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30372-30378
[79]   Beat-to-beat oscillations of mitochondrial [Ca2+] in cardiac cells [J].
Robert, V ;
Gurlini, P ;
Tosello, V ;
Nagai, T ;
Miyawaki, A ;
Di Lisa, F ;
Pozzan, T .
EMBO JOURNAL, 2001, 20 (17) :4998-5007
[80]   Modulation of mitochondrial ATP-dependent K+ channels by protein kinase C [J].
Sato, T ;
O'Rourke, B ;
Marbán, E .
CIRCULATION RESEARCH, 1998, 83 (01) :110-114