Method Article

Long-term, High-resolution Confocal Time Lapse Imaging of Arabidopsis Cotyledon Epidermis during Germination

DOI:

10.3791/4426

December 31st, 2012

In This Article

Summary

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We describe a protocol using chamber slides and media to immobilize plant cotyledons for confocal imaging of the epidermis over several days of development, documenting stomatal differentiation. Fluorophore-tagged proteins can be tracked dynamically by expression and subcellular localization, increasing understanding of their possible roles during cell division and cell-type differentiation.

Abstract

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Imaging in vivo dynamics of cellular behavior throughout a developmental sequence can be a powerful technique for understanding the mechanics of tissue patterning. During animal development, key cell proliferation and patterning events occur very quickly. For instance, in Caenorhabditis elegans all cell divisions required for the larval body plan are completed within six hours after fertilization, with seven mitotic cycles1; the sixteen or more mitoses of Drosophila embryogenesis occur in less than 24 hr2. In contrast, cell divisions during plant development are slow, typically on the order of a day 3,4,5 . This imposes a unique challenge and a need for long-term live imaging for documenting dynamic behaviors of cell division and differentiation events during plant organogenesis. Arabidopsis epidermis is an excellent model system for investigating signaling, cell fate, and development in plants. In the cotyledon, this tissue consists of air- and water-resistant pavement cells interspersed with evenly distributed stomata, valves that open and close to control gas exchange and water loss. Proper spacing of these stomata is critical to their function, and their development follows a sequence of asymmetric division and cell differentiation steps to produce the organized epidermis (Fig. 1).

This protocol allows observation of cells and proteins in the epidermis over several days of development. This time frame enables precise documentation of stem-cell divisions and differentiation of epidermal cells, including stomata and epidermal pavement cells. Fluorescent proteins can be fused to proteins of interest to assess their dynamics during cell division and differentiation processes. This technique allows us to understand the localization of a novel protein, POLAR6, during the proliferation stage of stomatal-lineage cells in the Arabidopsis cotyledon epidermis, where it is expressed in cells preceding asymmetric division events and moves to a characteristic area of the cell cortex shortly before division occurs. Images can be registered and streamlined video easily produced using public domain software to visualize dynamic protein localization and cell types as they change over time.

Protocol

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1. Seed Sterilization

  1. Prepare seed sterilization solution: 33% household bleach, 0.1% Triton X-100.
  2. Place seeds carrying desired fluorescent reporter construct(s) and genotype(s) in 1.7 ml tube and apply 1 ml of sterilization solution. Incubate on nutator for 15 min.
  3. In a sterile hood, use a pipettor to remove sterilization solution from tube, leaving seeds behind. Rinse with 1 ml sterile water. Repeat four times.
  4. Incubate at 4 °C for two days or more.

2. Preparation of Chamber Slide Media

  1. Mix 20 ml of 0.5% solution of Bacto Agar (not pure agarose) in water in a 200 ml flask, ....

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Results

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A set of informative time points collected with this method is shown in Figure 3. Cell membranes are labeled with RFP (pm-rb) and GFP is fused to POLAR protein under its native promoter (POLAR::POLAR-GFP)6 At the 30-min time scale, we see cell divisions along with the changes in protein localization preceding them. Asymmetric cell divisions in the stomatal lineage form stem-cell-like stomatal precursors called meristemoids, which retain the ability to undergo further asymmetric divisi.......

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Discussion

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This time-lapse confocal technique allows longitudinal studies of fluorescently tagged protein expression and localization in individual cells of the Arabidopsis cotyledon epidermis, which in the case of POLAR and other dynamically changing proteins is critical to a proper understanding of their function. Previously, sustained time lapse imaging has been used to examine Arabidopsis root fungal infection11 and meristem growth5,12, but adding the cotyledon epidermis expands the vers.......

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Disclosures

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No conflicts of interest declared.

Acknowledgements

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We thank Amanda Rychel for assistance in developing the time lapse protocol and Lynn Pillitteri for constructing POLAR::POLAR-eGFP. We are also grateful to ABRC for providing the pm-rb construct. This protocol was developed through a support from the PRESTO award from Japan Science Technology and Agency. Research on POLAR was also supported by the University of Washington Royalty Research Fund (RRF-4098) and the National Science Foundation (MCB-0855659). KMP is an NSF Graduate Research Fellow (DGE-0718124), and KUT is an HHMI-GBMF investigator.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Bacto AgarBD214010
One-chamber slideNunc (Thermo Scientific)155360Or two-chamber (155379)
Laser scanning confocal microscopeZeissLSM700Zen 2009 software
20x objective lensZeiss420650-9901NA 0.8, Plan-APOCHROMAT
Dissecting microscopeBenz (National)431TBLIlluminates from below
#5 forceps, biology tipRoboz Surgical InstrumentRS-4978Very fine tips are critical

References

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  1. Sulston, J. E., Schierenberg, E., White, J. G., Thomson, J. N. The Embryonic Cell Lineage of the Nematode Caenorhabditis elegans. Developmental Biology. 100, 64(1983).
  2. Foe, V., Odell, G., Edgar, B. A. Chapter 3 Mitosis and Morphogenesis: Point and Counterpoint. Development of Drosophila melanogaster. Bate, ....

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Tags

Arabidopsis CotyledonConfocal Time LapseEpidermal DevelopmentGermination ImagingProtein LocalizationCell Division DynamicsStomatal LineageFluorescent Protein FusionZ Series AcquisitionMulti Position Scan

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