Nonlinear microscopy: new techniques and applications

被引:118
作者
Mertz, J [1 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
关键词
D O I
10.1016/j.conb.2004.08.013
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Nonlinear microscopy, a general term that embraces any microscopy technique based on nonlinear optics, is further establishing itself as an important tool in neurobiology. Recent advances in labels, labeling techniques, and the use of native or genetically encoded contrast agents have bolstered the capacity of nonlinear microscopes to image the structure and function of not just single cells but of entire networks of cells. Along with novel strategies to image over exceptionally long durations and with increased depth penetration in living brains, these advances are opening new opportunities in neurobiology that were previously unavailable.
引用
收藏
页码:610 / 616
页数:7
相关论文
共 79 条
[1]
Time-multiplexed multifocal multiphoton microscope [J].
Andresen, V ;
Egner, A ;
Hell, SW .
OPTICS LETTERS, 2001, 26 (02) :75-77
[2]
Four-dimensional multiphoton imaging of brain entry, amyloid binding, and clearance of an amyloid-β ligand in transgenic mice [J].
Bacskai, BJ ;
Hickey, GA ;
Skoch, J ;
Kajdasz, ST ;
Wang, YM ;
Huang, GF ;
Mathis, CA ;
Klunk, WE ;
Hyman, BT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12462-12467
[3]
Fluorescence resonance energy transfer determinations using multiphoton fluorescence lifetime imaging microscopy to characterize amyloid-beta plaques [J].
Bacskai, BJ ;
Skoch, J ;
Hickey, GA ;
Allen, R ;
Hyman, BT .
JOURNAL OF BIOMEDICAL OPTICS, 2003, 8 (03) :368-375
[4]
Microfluorometric detection of catecholamines with multiphoton-excited fluorescence [J].
Balaji, J ;
Reddy, CS ;
Kaushalya, SK ;
Maiti, S .
APPLIED OPTICS, 2004, 43 (12) :2412-2417
[5]
Epifluorescence collection in two-photon microscopy [J].
Beaurepaire, E ;
Mertz, J .
APPLIED OPTICS, 2002, 41 (25) :5376-5382
[6]
Ultra-deep two-photon fluorescence excitation in turbid media [J].
Beaurepaire, E ;
Oheim, M ;
Mertz, J .
OPTICS COMMUNICATIONS, 2001, 188 (1-4) :25-29
[7]
Two-photon fluorescence absorption and emission spectra of dyes relevant for cell imaging [J].
Bestvater, F ;
Spiess, E ;
Stobrawa, G ;
Hacker, M ;
Feurer, T ;
Porwol, T ;
Berchner-Pfannschmidt, U ;
Wotzlaw, C ;
Acker, H .
JOURNAL OF MICROSCOPY, 2002, 208 (02) :108-115
[8]
New modal wave-front sensor: application to adaptive confocal fluorescence microscopy and two-photon excitation fluorescence microscopy [J].
Booth, MJ ;
Neil, MAA ;
Wilson, T .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 2002, 19 (10) :2112-2120
[9]
In vivo monitoring of neuronal network activity in zebrafish by two-photon Ca2+ imaging [J].
Brustein, E ;
Marandi, N ;
Kovalchuk, Y ;
Drapeau, P ;
Konnerth, A .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2003, 446 (06) :766-773
[10]
Stimulating neurons with light [J].
Callaway, EM ;
Yuste, R .
CURRENT OPINION IN NEUROBIOLOGY, 2002, 12 (05) :587-592