Imaging the live plant cell

被引:34
作者
Shaw, SL [1 ]
机构
[1] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
关键词
live cell imaging; microscopy; digital imaging; confocal microscopy;
D O I
10.1111/j.1365-313X.2006.02653.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Observing a biological event as it unfolds in the living cell provides unique insight into the nature of the phenomenon under study. Capturing live cell data differs from imaging fixed preparations because living plants respond to the intense light used in the imaging process. In addition, live plant cells are inherently thick specimens containing colored and fluorescent molecules often removed when the plant is fixed and sectioned. For fixed cells, the straightforward goal is to maximize contrast and resolution. For live cell imaging, maximizing contrast and resolution will probably damage the specimen or rapidly bleach the probe. Therefore, the goals are different. Live cell imaging seeks a balance between image quality and the information content that comes with increasing contrast and resolution. That 'lousy' live cell image may contain all the information needed to answer the question being posed -provided the investigator properly framed the question and imaged the cells appropriately. Successful data collection from live cells requires developing a specimen-mounting protocol, careful selection and alignment of microscope components, and a clear understanding of how the microscope system generates contrast and resolution. This paper discusses general aspects of modern live cell imaging and the special considerations for imaging live plant specimens.
引用
收藏
页码:573 / 598
页数:26
相关论文
共 54 条
  • [1] AIKENS RS, 1989, METHOD CELL BIOL, V29, P291
  • [2] VIDEO-ENHANCED CONTRAST, DIFFERENTIAL INTERFERENCE CONTRAST (AVEC-DIC) MICROSCOPY - A NEW METHOD CAPABLE OF ANALYZING MICROTUBULE-RELATED MOTILITY IN THE RETICULOPODIAL NETWORK OF ALLOGROMIA LATICOLLARIS
    ALLEN, RD
    ALLEN, NS
    TRAVIS, JL
    [J]. CELL MOTILITY AND THE CYTOSKELETON, 1981, 1 (03): : 291 - 302
  • [3] VIDEOMICROSCOPY IN THE STUDY OF PROTOPLASMIC STREAMING AND CELL-MOVEMENT
    ALLEN, RD
    ALLEN, NS
    [J]. PROTOPLASMA, 1981, 109 (1-2) : 209 - 216
  • [4] AXELROD D, 1989, METHOD CELL BIOL, V30, P333
  • [5] TOTAL INTERNAL-REFLECTION FLUORESCENT MICROSCOPY
    AXELROD, D
    THOMPSON, NL
    BURGHARDT, TP
    [J]. JOURNAL OF MICROSCOPY-OXFORD, 1983, 129 (JAN): : 19 - 28
  • [6] BENSASSON KV, 1993, EXCITED STATES FREE
  • [7] Evaluation of spectral imaging for plant cell analysis
    Berg, RH
    [J]. JOURNAL OF MICROSCOPY-OXFORD, 2004, 214 : 174 - 181
  • [8] Electronic cameras for low-light microscopy
    Berland, K
    Jacobson, K
    French, T
    [J]. METHODS IN CELL BIOLOGY, VOLUME 56, 1998, 56 : 19 - 44
  • [9] FRET or no FRET: A quantitative comparison
    Berney, C
    Danuser, G
    [J]. BIOPHYSICAL JOURNAL, 2003, 84 (06) : 3992 - 4010
  • [10] Recruitment and interaction dynamics of plant penetration resistance components in a plasma membrane microdomain
    Bhat, RA
    Miklis, M
    Schmelzer, E
    Schulze-Lefert, P
    Panstruga, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (08) : 3135 - 3140