Imaging the live plant cell
Open Access
- 26 January 2006
- journal article
- Published by Wiley in The Plant Journal
- Vol. 45 (4) , 573-598
- https://doi.org/10.1111/j.1365-313x.2006.02653.x
Abstract
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.Keywords
This publication has 52 references indexed in Scilit:
- Dynamic Multiphoton Imaging: A Live View from Cells to SystemsPhysiology, 2005
- Expanded dynamic range of fluorescent indicators for Ca 2+ by circularly permuted yellow fluorescent proteinsProceedings of the National Academy of Sciences, 2004
- Evaluation of spectral imaging for plant cell analysisJournal of Microscopy, 2004
- Imaging plant cells by two-photon excitationProtoplasma, 2004
- Imaging molecular interactions in cells by dynamic and static fluorescence anisotropy (rFLIM and emFRET)Biochemical Society Transactions, 2003
- Intercellular movement of the putative transcription factor SHR in root patterningNature, 2001
- Green Fluorescent Protein as a Marker for Gene ExpressionScience, 1994
- Total internal reflection fluorescent microscopyJournal of Microscopy, 1983
- Videomicroscopy in the study of protoplasmic streaming and cell movementProtoplasma, 1981
- A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue CulturesPhysiologia Plantarum, 1962