A simple, rapid method to isolate salt glands for three-dimensional visualization, fluorescence imaging and cytological studies
© Tan et al; licensee BioMed Central Ltd. 2010
Received: 8 September 2010
Accepted: 19 October 2010
Published: 19 October 2010
Some plants inhabiting saline environment remove salts via the salt glands embedded in the epidermal tissues. Cytological studies of salt glands will provide valuable information to our understanding of the secretory process. Previous studies on salt gland histology relied mainly on two-dimensional microscopic observations of microtome sections. Optical sectioning properties of confocal laser scanning microscope offer alternative approach for obtaining three-dimensional structural information of salt glands. Difficulty in light penetration through intact leaves and interference from neighbouring leaf cells, however, impede the acquiring of good optical salt gland sections and limit its applications in salt gland imaging. Freeing the glands from adjacent leaf tissues will allow better manipulations for three-dimensional imaging through confocal laser scanning microscopy.
Here, we present a simple and fast method for the isolation of individual salt glands released from the interference of neighbouring cells. About 100-200 salt glands could be isolated from just one cm2 of Avicennia officinalis leaf within hours and microscopic visualization of isolated salt glands was made possible within a day. Using these isolated glands, confocal laser scanning microscopic techniques could be applied and better resolution salt gland images could be achieved. By making use of their intrinsic fluorescent properties, optical sections of the gland cells could be acquired without the use of fluorescent probes and the corresponding three-dimensional images constructed. Useful cytological information of the salt gland cells could also be obtained through the applications of fluorescent dyes (e.g., LysoTracker® Red, FM®4-64, Texas Red®).
The study of salt glands directly at the glandular level are made possible with the successful isolation of these specialized structures. Preparation of materials for subsequent microscopic observations of salt glands could be achieved within a day. Potential applications of confocal fluorescence microscopic techniques could also be performed using these isolated glands. Experiments designed and targeted directly at the salt glands were explored and cytological information obtained herein could be further incorporated towards the understanding of the mechanism underlying secretion in plant salt glands.
Salt glands are specialized adaptive structures found predominantly on the leaves and stems of halophytic species [1, 2]. They are considered to be efficient desalination devices capable of removing salts from the plant tissues via an energy-dependent secretion process . Earlier research on the histological and ultrastructural studies of salt glands had relied mainly on microtome sections of leaf tissues [1, 3–9]. Preparation of materials for conventional microtome sectioning, however, is laborious and time consuming as it involves fixation of plant tissues in appropriate fixatives followed by dehydration in alcohol series and infiltration with wax prior to embedding the samples in paraffin wax [10, 11]. Microtome sectioning of paraffin-embedded leaf samples to obtain the desired plane of sections containing the salt glands is also challenging, especially if the salt glands are sparsely distributed. In addition, observations of microtome sections are usually confined to two-dimensional imaging involving brightfield microscopy or electron microscopy as far as ultrathin microtome sections are concerned. Technical difficulty in obtaining a complete series of microtome sections  limits the use of microtomy techniques in gathering three-dimensional structural information of the salt glands. We therefore look into alternative ways for the observations of the structural organization of salt glands in greater detail and at higher resolution.
Optical sectioning microscopy, such as confocal laser scanning microscopy, is a powerful tool for biological investigation, and is currently one of the most adequate and straightforward three-dimensional imaging methods for obtaining high resolution images up to single-cell level in plant biology [12, 13]. In contrast to conventional wide-field fluorescent and light microscopy, images taken using confocal laser scanning microscopes showed much improved clarity with the successful elimination of out-of-focus background noise via the pinhole [11, 12, 14]. A series of optical sections of intact specimens can thus be collected through the use of confocal laser scanning microscopy and the corresponding three-dimensional views reconstructed using computer-aided softwares [11, 12].
Optical sectioning of intact specimens, however, has its limitation as it is difficult to obtain deep sections (>50-100 μm) from intact tissues, especially for uncleared botanical specimens such as the leaves that tend to be more opaque in nature [11, 14]. Even though the salt glands of Avicennia officinalis in the current study are distributed on the epidermal layers of the leaves, they are either sunken in deep pits or depressions for those found on the adaxial epidermal surfaces, or are intermingled with trichomes on the abaxial surfaces [4, 15]. Penetration of light through intact leaves to obtain the whole z series of the salt glands might thus be difficult and the presence of neighbouring epidermal cells or trichomes on the leaf surfaces further interfere with acquiring good optical salt gland sections. In addition, the presence of chloroplast-rich mesophyll and palisade cells in the leaves limits the use of secondary fluorochromes since red autofluorescence of the chlorophyll in these cells will obscure the signals obtained from the salt glands on the epidermal layers. Alternative approach to acquiring the entire z-stacks of the salt glands directly from intact leaves will need to be explored. Obtaining specimens that can free the salt glands from the interference of neighbouring cells will be ideal for further manipulations and imaging through confocal laser scanning microscopy.
In this paper, a method to isolate large numbers of individual salt glands as complete entities devoid of neighbouring leaf tissues is presented. Observations of isolated salt glands through brightfield, fluorescent as well as confocal laser scanning microscopy are possible, with each revealing the structural organizations of the salt glands to different degree of clarity. In contrast to visualization of salt glands directly from intact leaves, optical sectioning of the isolated salt glands showing both the top and side views is possible without the need to prepare paradermal and transverse leaf sections separately using classical microtomy techniques. The intrinsic autofluorescent nature of the salt glands also allows optical sections to be taken and subsequent three-dimensional images of the salt glands to be constructed without fluorescent dye applications.
Results and Discussion
A simple method for salt gland isolation
Microscopic views of individual salt glands revealed a general salt gland structure (Figure 3), with confocal microscopic images (Figure 3C, F) showing unambiguously the cell number within each salt gland. Both the top and side views of the salt glands could be observed from each session of salt gland isolation, in contrast to conventional microtome sectioning where paraffin-embedded samples of different orientations need to be prepared separately to obtain paradermal and transverse leaf sections. A total of 8 radially arranged secretory cells was observed from the top view of the isolated salt gland (Figure 3C). From the side view (Figure 3F), 3 secretory cells were observed and a single stalk cell was positioned at almost perpendicular to the group of secretory cells above it. The secretory cells and stalk cell were enclosed by a cuticle layer, which formed the general outline of the salt gland. A subcuticular collecting cavity above the outermost secretory cells and below the top cuticle layer was also detected (Figure 3F).
The salt glands of A. officinalis thus belong to the Type III salt gland as categorized by Thomson et al. , which are multicellular comprising a characteristic disc-shaped stalk or basal cell subtended by one or more sub-basal (collecting) cells below and several secretory cells above. The basic descriptions of the salt glands reported herein were similar to the ultrastructures of the salt glands of other Avicennia and Acanthus species studied [4, 5, 7, 8, 15–17].
Autofluorescence of salt glands
Autofluorescence of the salt gland cells revealed a total of 8 secretory cells, which was obvious from the three-dimensional top view image of isolated salt gland (Figure 6). A total of 2-4 secretory cells and 1 stalk cell enclosed in a cuticular envelope were noted from the side view of the isolated salt glands (Figures 4A-C, 5 and 7B). The base of the stalk cell was found to be about 25 μm wide and the other side in contact with the base of the secretory cells was only about 10 μm (Figure 7B). A subcuticular cavity (with no autofluorescence) between the cuticle envelope and the secretory cells was also observed (Figure 5 and figure 7B). Collecting cells located beneath the stalk cell of each salt gland as detected from the microtome section of paraffin-embedded leaf specimen (Figure 7A) were probably lost during isolation since such cells were not observed in the isolated salt gland (Figure 7B).
The total number of 6-8 secretory cells observed from isolated A. officinalis salt glands in this study was slightly lesser than that described previously on this genus [1, 4, 5, 16, 17]. A range of 8-12 secretory cells was reported for Avicennia marina salt glands [2, 5], while the salt glands of Avicennia germinans were found to contain 8 secretory cells .
Confocal fluorescent microscopic studies of isolated salt glands were made possible with the intrinsic green autofluorescent properties present in the salt glands. More plant tissues were found to show background autofluorescence compared to animal tissues due to the presence of large quantities of naturally occurring fluorochromes . One such fluorochrome is lignin, which is commonly synthesized and deposited in the cell walls. This compound shows an intense green fluorescence when excited with UV or blue light. Such autofluorescence usually poses a problem in fluorescent microscopy because of the overlapping spectra with other secondary fluorochromes used for research. On the other hand, autofluorescence can also be an advantage as it can serve as an internal structural marker [18–20].
Cytological studies of isolated salt glands with the use of various fluorochromes
The secretory cells of the salt glands were mono-nucleated (Figures 9 and 10A). Each nucleus was found to be approximately 4-6 μm in diameter (Figures 9 and 10A). Relatively large nuclei of the secretory cells were also observed in other Avicennia species and in the salt glands of other genera [1, 2, 5, 7, 16, 17]. Information on the correlation between the activity of salt gland nuclei and the activity of the salt glands, however, is lacking, even though larger nucleoli were reported in the secreting salt glands of Limonium platyphyllum in comparison to those without salt challenge .
With the availability of isolated salt glands, optical sections at different focal planes could be taken to study the distribution of organelles within the gland cells in a three-dimensional context. The location of the nuclei, for example, as revealed by optical sections of isolated salt glands stained with the nuclear stain PI, was mostly found in the middle of the secretory cells (Figure 9). Large nucleus was also reported to be located predominantly in the central region of each secretory cell in Avicennia marina. The positions of the nuclei observed herein were also similar to the green, spherical, autofluorescent structures noted in the middle of the secretory cells of these salt glands (Figures 4 and 5). In Nicotiana tobacum suspension cells, the nuclei were reported to be the main organelles that showed green autofluorescence .
Well-distributed fluorescent images of the secretory cells were observed when the isolated salt glands were stained with LysoTracker® Red DND-99 (Figure 10B, C), an acidotropic fluorescent probe that is effective in labelling typically spherical, acidic organelles by selectively accumulating itself in compartments where the pH is low . Several brightly stained structures, each about 1 μm in diameter, were detected in the secretory cells of salt glands that were exposed to the dye for 60-90 min (Figure 10B, C). More intensely stained regions of the secretory cells were also observed in these glands, with their shapes and positions coinciding with the green autofluorescence structures (Figures 4 and 5) described earlier. Negatively stained regions that appeared spherical or elliptical in shape (~1.5-3.0 μm) were consistently found towards the periphery of the secretory cells (Figure 10B).
Vacuoles of plant cells are generally acidic compartments that are similar to the vacuoles of algae and fungi and do share some properties that are also present in the mammalian lysosomes. They are usually present with their internal pH being lower when compared to the cytoplasm of the cells [24, 25]. Observations reported in this study suggest the presence of acidic spherical organelles in the secretory cells of salt glands. Micro-vacuoles or vesicles were also previously reported to be evenly distributed throughout the secretory cells of Avicennia[1, 2, 5, 7, 17].
Positive staining of the secretory cells was detected when the isolated salt glands were exposed to FM® 4-64 (Figure 10D, E), one of the lipophilic or amphiphilic styryl dyes that is weakly fluorescent or virtually non-fluorescent in aqueous medium but can fluoresce brightly when it is associated with or incorporated into the outer leaflet of the plasma membranes [20, 21, 26, 27]. Developed with animal cell systems, FM® 4-64 was found to be nontoxic to cells and may be internalized following extended staining times [21, 27–31]. The dye can thus be used as a vital stain and was reported to act as an endosomal marker in the study of endocytosis, membrane trafficking and cell division in living cells [21, 26–29, 32, 33].
In this study, the secretory cells of FM® 4-64-treated salt glands were shown to fluoresce brightly, with evident cell outlines detected (Figure 10E) without the reference from the overlapping brightfield images (inset of Figure 10E). The stain was not confined to the plasma membrane, as small, dot-like structures (estimated to be 0.5-3 μm in diameter) that fluoresce brightly were detected to be consistently distributed in the secretory cells (Figure 10D, E), a sign of internalization of dyes with prolonged staining. The stalk cell of the treated salt gland was also observed to be positively stained with FM® 4-64, with an intensely stained spherical structure in the middle of the cell being most prominent (Figure 10E).
Taken into consideration that the secretion of salts via the salt glands had always been implied to be an active process [1, 2, 34], the establishment of a mitochondrial profile within the salt gland cells will provide useful information on the metabolic status of the salt glands. Attempts were made to look into the distribution of mitochondria in the gland cells using MitoTracker® Red CM-H2XRos, a cell-permeant fluorescent dye that selectively stains mitochondria. Positive staining of the secretory cells was evident, even though MitoTracker® Red CM-H2XRos could also non-specifically stain the cuticle layer of the isolated salt gland (Figure 10F). Fricker et al.  commented that this dye did not appear to stain plant mitochondria well. Nevertheless, the patches of red fluorescent signals as observed herein seemed to indicate a high mitochondrial density in the secretory cells of salt glands, which is a common observation reported by many researchers [1, 2, 5, 7, 8, 17, 34, 35].
Establishment of the distribution of cytoskeletons in the salt glands, and their possible participation during the secretion of salts had not been reported previously in salt gland studies and will be useful in providing information towards our understanding of the secretory process. In this study, Texas Red®-X phalloidin was used to stain the isolated salt glands (Figure 10G-I). This dye is a fluorescent phalloidin derivative that can be used as a fluorescent probe in cytoskeletal studies due to their ability to bind to, and to a certain extent, stabilize F-actin [20, 21, 36]. Abundant actin-like filaments were observed in the secretory cells of isolated salt glands stained with Texas Red®-X phalloidin (Figure 10G-I). Such structures were found to be especially prominent on the periphery of the secretory cells towards the periclinal walls nearer to the cuticle layer (Figure 10H, I), or along the circumference of the secretory cells (Figure 10G). Some of these thread-like structures were also observed to extend towards the centre of the secretory cells, which were only visible from the highly magnified images (Figure 10G).
The use of commercially-available secondary fluorochromes to study the cellular structures of the isolated salt glands is thus possible as presented herein. Useful cytological information was obtained through this approach, with the presence of relatively large nuclei and abundant mini-vacuoles and/or vesicle-like structures and possibly abundant mitochondria in the secretory cells implying a high metabolic state of these specialized glands.
In this paper, we describe a simple method to isolate large numbers of salt glands from the leaves of the mangrove species A. officinalis within a day for microscopic studies. The isolated glands exist as individual entities are useful for subsequent imaging without the interference of neighbouring leaf tissues, which tend to obscure the signal from any in-focus structural information of the salt glands. Potential applications of confocal fluorescence microscopic techniques, which have made a strong impact in plant-cell imaging  could also be achieved using these isolated salt glands. Optical sectioning and subsequent three-dimensional imaging of the salt glands are now technically feasible. Structural organizations of these glands can be determined from a three-dimensional perspective even without the use of secondary fluorochromes due to their intrinsic autofluorescent nature. Successful confocal microscopic imaging of isolated salt glands stained with commercially available fluorescent dyes as presented herein further provide a new approach in obtaining useful cytological information for salt gland research.
Isolation and purification of salt glands
Abaxial epidermal layers of excised leaves of A. officinalis were removed with razor blade and the leaves were cut into segments (2 cm by 1 cm) prior to enzyme treatment. The leaf strips floated on enzyme mixture (pH 5.7; filter-sterilized) containing 0.1% (w/v) Pectolyase Y-23 (Seishin Pharmaceutical, Japan), 1.0% (w/v) Driselase (Sigma-Aldrich, USA) and 1.0% (w/v) Cellulase Y-C (Kikkoman Corporation, Japan) were vacuum infiltrated for 10 min and incubated in the dark at 30 °C, 30 rpm for 1 h. The adaxial epidermal peels obtained were rinsed, the mesophyll-palisade layers gently scraped off using a scalpel before the peels devoid of chlorophyll-containing cells were transferred to a mortar containing 3-5 ml of 1× PBS buffer (pH 7.4). These peels were then ground to release the salt glands from the epidermal peels. The grinding process was repeated several times with fresh 1× PBS buffer (pH 7.4) to release more salt glands.
The salt gland suspensions collected in centrifuge tubes were filtered through a series of Falcon® cell strainers (BD Biosciences, USA) of different pore sizes (100 μm, 70 μm followed by 40 μm) to remove the bigger cell clusters and peel debris. The isolated salt glands collected on a 20 μm cup Filcon (BD Biosciences, USA) were finally rinsed down with 2 ml of fresh 1× PBS buffer (pH 7.4) and kept on ice for subsequent observations.
Determination of salt gland density in suspension
The density of salt glands collected in suspension was determined as the number of salt glands per cm2 of leaf used. The number of salt glands was estimated with a hemocytometer. Total area of leaves used for salt gland isolation was determined with LI-3100C Area Meter (LI-COR® Biosciences, USA).
Preparation of isolated salt glands for confocal microscopic studies
Isolated salt glands in suspensions were fixed for 10 min at room temperature with freshly prepared 3.7% (w/v) paraformaldehyde dissolved in 1× PBS buffer (pH 7.4). When required, the salt glands were permeabilized with 0.1%, (v/v) Triton® × 100 prepared in 1× PBS buffer (pH 7.4) for 10 min at room temperature prior to staining. The salt glands were then stained according to the manufacturer's (see Staining procedures) protocols. All dyes were removed after staining by rinsing the isolated salt glands twice with 1× PBS buffer (pH 7.4). SlowFade® Light Antifade Kit (Molecular Probes, USA) was used after staining. The isolated salt glands was first pre-equilibrated in 10 drops of SlowFade® Light Equilibration Buffer for 5-10 min followed by the addition of SlowFade® Light antifade reagent (1-2 drops) to the sample. The salt glands were finally mounted on glass slides and sealed with nail varnish for subsequent confocal microscopic examinations.
Potential applications of various fluorescent dyes were tested on the isolated salt glands. For propidium iodide (PI) staining, isolated salt glands were permeabilized and stained for 1 h with Coulter® DNA-Prep Stain (Beckman Coulter Inc, USA) diluted to a final concentration of 8 μg ml-1 PI. For LysoTracker® Red DND-99 staining, the glands were incubated in 40 nM LysoTracker® Red DND-99 (Molecular Probes, USA) for a period of 60-90 min. FM® 4-64 [N-(3-triethylammoniumpropyl)-4-(6-(4-(diethylamino)phenyl) hexatrienyl)pyridinium dibromide); Molecular Probes, USA] was used according to Fischer-Parton et al.  and Parton et al.  with a final working solution of 8.25 nM. The isolated salt glands were stained for 30-90 min. For MitoTracker® Red CM-H2XRos staining, the isolated salt glands were permeabilized before they were stained with 100 nM MitoTracker® Red CM-H2XRos (Molecular Probes, USA) for 30 min. For Texas Red®-X phalloidin staining, the isolated salt glands were permeabilized prior to staining with 165 nM Texas Red®-X phalloidin (Molecular Probes, USA) for 20 min.
Confocal Laser Scanning Microscopy
Observations of isolated salt glands were performed with a Zeiss LSM 510 laser scanning confocal microscope. To detect autofluorescence of samples, the unstained salt glands mounted on coverslips were excited at 488 and 543 nm. The degree of autofluorescence of the salt glands at each excited wavelength was then determined and images observed in the fluorescent and transmission modes were captured simultaneously. Where possible, optical sections of each isolated salt gland were captured and the images stacked before the three-dimensional image of the corresponding salt gland was created using Imaris™ (beta) 3.0. For isolated salt glands stained with various fluorescent dyes, the excitation wavelength for all was 543 nm and emission filter was high pass 560 nm for PI, LysoTracker® Red DND-99, MitoTracker® Red CM-H2XRos and Texas Red®-X phalloidin while high pass 650 nm filter was used for FM® 4-64.
Tissues prepared for light microscopy were according to Ruzin (1999) with modifications. Briefly, the leaf tissues were fixed in FAA (formalin-acetic acid-alcohol), vacuum infiltrated and incubated in fixatives overnight at room temperature. They were then dehydrated in an alcohol series (50, 70, 85, 95 and 100%; at least 2 h in each solution), transferred to 100% TBA (Tert-butyl alcohol; 2 changes; at least 2 h for each incubation), incubated in a series of TBA: paraffin wax mixture (75:25, 50:50, 25:75, 0:100 two times) at 58 °C, with each incubation lasting for at least 4 h before the tissues were finally embedded in paraffin wax. Microtome sections of 10-μm thick were cut (Reichert-Jung 2030 Biocut, Germany) and sections with salt glands were selected and mounted on glass slides. The sections were stained with safranin O, covered with cover slips before they were observed under light microscope (Olympus).
We thank Dr. S.M. Leong of the National University of Singapore (NUS) for helpful comments on the manuscript. C.S. Loh thanks the NUS (R154-000-090-112) and NUS Environmental Research Institute (R-706-000-007-646) for research grants to carry out this project.
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