Cell-permeant cytoplasmic blue fluorophores optimized for in vivo two-photon microscopy with low-power excitation

被引:15
作者
Hayek, Ali
Grichine, Alexei
Huault, Thomas
Ricard, Clement
Bolze, Frederic
Van Der Sanden, Boudewijn
Vial, Jean-Claude
Mely, Yves
Duperray, Alain
Baldeck, Patrice Lilian
Nicoud, Jean-Francois
机构
[1] Univ Louis Pasteur Strasbourg 1, CNRS, UMR 7504, Inst Phys & Chem Mat,Organ Mat Grp, F-67034 Strasbourg, France
[2] Univ Grenoble 1, Inst Albert Bonniot IFR 73, F-38042 Grenoble, France
[3] Univ Grenoble 1, CNRS, UMR 5588, Spectrometrie Phys Lab, F-38402 St Martin Dheres, France
[4] Acad Hosp, INSERM, U594, F-38043 Grenoble, France
[5] European Synchrotron Radiat Facil, INSERM, U647, F-38043 Grenoble, France
[6] CNRS, UMR 7175, Inst Gilbert Laustriat, Fac Pharm, F-67401 Illkirch Graffenstaden, France
[7] INSERM, F-38706 Grenoble, France
[8] Univ Grenoble 1, Grp Rech Canc Poumon, Inst Albert Bonniot, F-38706 Grenoble, France
关键词
two-photon dyes; cell microscopy; FLIM; FRAP; photostability; mouse brain imaging; BBB;
D O I
10.1002/jemt.20493
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Because of the spreading of nonlinear microscopies in biology, there is a strong demand for specifically engineered probes in these applications. Herein, we report on the imaging properties in living cells and nude mice brains of recently developed water soluble blue fluorophores that show efficient diffusion through cell membranes and blood-brain barriers. They are characterized by two-photon absorption cross-sections of 100-150 Goeppert-Mayer range in the near IR and fluorescence efficiencies of up to 72% in water. They were found to stain homogeneously the cytoplasm of cultured living cells within minutes. Moreover, their diffusion times and fluorescence characteristics in the cytoplasm suggest a hydrophebic association with intracellular membranes. Their intracellular fluorescent decays were found to be almost mono-exponential, a very favorable feature for fluorescence lifetime imaging. Two photon images of living cells were obtained with a good signal to noise ratio using laser powers in the sub-milliwatt range. This allows continuous imaging without significant photobleaching for tens of minutes. In addition, these fluorophores allowed in vivo three-dimensional two-photon imaging of mice cortex vasculatures and extra vasculature structures, with no sign of toxicity.
引用
收藏
页码:880 / 885
页数:6
相关论文
共 22 条
[1]   Dimethyl-pepep: a DNA probe in two-photon excitation cellular imaging [J].
Abbotto, A ;
Baldini, G ;
Beverina, L ;
Chirico, G ;
Collini, M ;
D'Alfonso, L ;
Diaspro, A ;
Magrassi, R ;
Nardo, L ;
Pagani, GA .
BIOPHYSICAL CHEMISTRY, 2005, 114 (01) :35-41
[2]   Novel heterocycle-based two-photon absorbing dyes [J].
Abbotto, A ;
Beverina, L ;
Bozio, R ;
Facchetti, A ;
Ferrante, C ;
Pagani, GA ;
Pedron, D ;
Signorini, R .
ORGANIC LETTERS, 2002, 4 (09) :1495-1498
[3]   Large two-photon absorption properties of polyphenyls and polyfluorenes [J].
Anémian, R ;
Baldeck, PL ;
Andraud, C .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 2002, 374 (01) :335-342
[4]   Dynamic behavior of T cells and thymocytes in lymphoid organs as revealed by two-photon microscopy [J].
Bousso, P ;
Robey, EA .
IMMUNITY, 2004, 21 (03) :349-355
[5]   Imaging cellular network dynamics in three dimensions using fast 3D laser scanning [J].
Goebel, Werner ;
Kampa, Bjoern M. ;
Helmchen, Fritjof .
NATURE METHODS, 2007, 4 (01) :73-79
[6]  
Grichine A, 2001, PHOTOCHEM PHOTOBIOL, V73, P267, DOI 10.1562/0031-8655(2001)073<0267:IOTSOV>2.0.CO
[7]  
2
[8]   Synthesis and characterization of water-soluble two-photon excited blue fluorescent chromophores for bioimaging [J].
Hayek, A ;
Bolze, F ;
Nicoud, JF ;
Baldeck, PL ;
Mély, Y .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2006, 5 (01) :102-106
[9]   Deep tissue two-photon microscopy [J].
Helmchen, F ;
Denk, W .
NATURE METHODS, 2005, 2 (12) :932-940
[10]   Noninvasive two-photon imaging reveals retinyl ester storage structures in the eye [J].
Imanishi, Y ;
Batten, ML ;
Piston, DW ;
Baehr, W ;
Palczewski, K .
JOURNAL OF CELL BIOLOGY, 2004, 164 (03) :373-383