Methodology article
Open Access

Single-cell-based system to monitor carrier driven cellular auxin homeostasis

  • Elke Barbez1, 2,
  • Martina Laňková3,
  • Markéta Pařezová3,
  • Alexis Maizel4,
  • Eva Zažímalová3,
  • Jan Petrášek3,
  • Jiří Friml1, 5 and
  • Jürgen Kleine-Vehn1, 2Email author
BMC Plant Biology201313:20

https://doi.org/10.1186/1471-2229-13-20

©  Barbez et al.; licensee BioMed Central Ltd. 2013

Received: 2 October 2012

Accepted: 31 January 2013

Published: 4 February 2013

Abstract

Background

Abundance and distribution of the plant hormone auxin play important roles in plant development. Besides other metabolic processes, various auxin carriers control the cellular level of active auxin and, hence, are major regulators of cellular auxin homeostasis. Despite the developmental importance of auxin transporters, a simple medium-to-high throughput approach to assess carrier activities is still missing. Here we show that carrier driven depletion of cellular auxin correlates with reduced nuclear auxin signaling in tobacco Bright Yellow-2 (BY-2) cell cultures.

Results

We developed an easy to use transient single-cell-based system to detect carrier activity. We use the relative changes in signaling output of the auxin responsive promoter element DR5 to indirectly visualize auxin carrier activity. The feasibility of the transient approach was demonstrated by pharmacological and genetic interference with auxin signaling and transport. As a proof of concept, we provide visual evidence that the prominent auxin transport proteins PIN-FORMED (PIN)2 and PIN5 regulate cellular auxin homeostasis at the plasma membrane and endoplasmic reticulum (ER), respectively. Our data suggest that PIN2 and PIN5 have different sensitivities to the auxin transport inhibitor 1-naphthylphthalamic acid (NPA). Also the putative PIN-LIKES (PILS) auxin carrier activity at the ER is insensitive to NPA in our system, indicating that NPA blocks intercellular, but not intracellular auxin transport.

Conclusions

This single-cell-based system is a useful tool by which the activity of putative auxin carriers, such as PINs, PILS and WALLS ARE THIN1 (WAT1), can be indirectly visualized in a medium-to-high throughput manner. Moreover, our single cell system might be useful to investigate also other hormonal signaling pathways, such as cytokinin.

Keywords

Auxin homeostasis DR5 Auxin carrier Auxin transport

Background

The phytohormone auxin is crucial to control plant growth and development. At the cellular level, auxin regulates cell division, cell expansion, and cellular differentiation [1]. Auxin largely exerts its action through a multistep signaling pathway: Aux/IAA proteins are repressors of the AUXIN RESPONSE FACTOR (ARF) transcription factors. Auxin directly binds to the nuclear co-receptors TRANSPORT INHITOR RESPONSE/AUXIN F-BOX PROTEIN (TIR/AFB) and the Aux/IAA. Auxin binding causes the subsequent degradation of Aux/IAA transcriptional repressors [2–4]. Subsequently, auxin perception leads to the de-repression of the ARF transcription factors, initiating transcriptional reprogramming.

The spatial and temporal distribution of auxins depends on auxin metabolism (biosynthesis, conjugation, and degradation) and the activity of cellular auxin transporters [5]. To date, various auxin carriers have been identified [6], among which the most prominent are auxin influx carriers of the AUXIN RESISTANT1/LIKE AUX1 (AUX/LAX) class, ABC transporters of the MULTIDRUG RESISTANCE (B-type) subfamily, and PIN-FORMED (PIN) auxin carriers [7–9]. Pharmacological and genetic interference with auxin carriers have illustrated the importance of auxin transport mechanisms for various aspects of plant development [10]. In particular, classical auxin transport inhibitors, such as 1-naphthylphthalamic acid (NPA) [11–13], are valuable tools to assess various auxin carrier-mediated developmental processes. Typically, auxin carriers mediate the cellular auxin import or export at the plasma membrane and, thus, regulate the auxin availability for nuclear auxin signaling (carrier-driven cellular auxin homeostasis). However, recently, a subclass of PIN proteins, such as PIN5 and PIN8, has been shown to reside at the endoplasmic reticulum (ER) and to control cellular auxin homeostasis presumably via the regulation of intracellular auxin compartmentalization into the ER lumen [14–16]. Yet another evolutionary distinct PIN-LIKES (PILS) putative auxin carrier family functions at the ER, indicating broad developmental and evolutionary importance of intracellular auxin transport [17–19].

The transport capacity of a multitude of auxin carriers and their sensitivity to auxin transport inhibitors has been analyzed in plant cell systems, such as Arabidopsis protoplasts or Bright Yellow-2 (BY-2) cell cultures of tobacco (Nicotiana tabacum), and in heterologous cell systems, such as yeast and mammalian cells [9, 14, 20–23]. These elaborate auxin transport assays are important tools to study transport activities and mechanisms. However, it would be desirable to develop easier methods to asses auxin carrier activity. An alternative approach has been proposed for the indirect visualization of the carrier-driven auxin homeostasis [24, 25]. This bioassay utilizes the stimulating effect of free auxin levels on root hair elongation. The root hair-specific expression of an auxin carrier and its action on the root hair length is used to indirectly visualize carrier driven auxin homeostasis. However, auxin fluxes in neighboring tissues also contribute to the regulation of root hair growth [26], preventing the combined use of ectopic carrier expression and its sensitivity to auxin transport inhibitors. Moreover, the time-consuming generation of stable transgenic lines might limit the use of this bioassay for high-throughput applications.

Another frequently used tool to monitor auxin signaling is the synthetic, highly auxin responsive promoter DR5, created by tandem repeats of the auxin responsive element (AuxRE) from the soybean GH3 promoter [27]. Previously, the DR5 promoter activity has been suggested to indicate the relative rate of nuclear auxin signaling in various tissues [28–33]. DR5 has been used to visualize auxin signaling maxima and minima which, however, do not correlate in all cells with the actual auxin levels possibly due to cell type-dependent cues [32, 34, 35].

Here, we present a novel single cell based system, using the DR5 promoter, to address cellular mechanisms that affect cellular auxin homeostasis and ultimately auxin signaling. We show the correlation between DR5 promoter activity and fluctuations in cellular auxin levels in tobacco BY-2 cells. Our data suggest that the transient expression of DR5rev:monomeric RED FLUORESCENT PROTEIN (mRFP) reporter for nuclear auxin signaling can be used to illustrate the relative state of cellular auxin signaling in tobacco BY-2 cells. By means of this single-cell-based system, the relative auxin carrier induced changes in cellular auxin signaling were monitored, indirectly indicating auxin carrier activity. As a proof of concept, we assessed the prominent PIN auxin carrier activity and confirmed their effects on cellular auxin homeostasis/signaling [14, 21]. Moreover, a pharmacological approach revealed that the activity regulation of PIN2 at the plasma membrane and PIN5 at the ER are distinct. Furthermore, we show that this single-cell-based system could be analogously used to investigate other putative carriers, such as PILS and WAT1, or potentially even other hormonal pathways, such as cytokinin.

Results

Indirect visualization of auxin carrier activity in tobacco BY-2 cells

In previous studies, the synthetic auxin-responsive promoter element DR5 fused to the monomeric RFP or GFP reporter gene (DR5rev:mRFP/GFP) [30, 36, 37] was used to visualize the auxin response maxima within tissues and it was proposed to indirectly estimate auxin distribution [29, 30, 33]. However, auxin distribution and DR5-based auxin signaling does not always correlate in plant tissues presumably due to cell type-dependent cues [32].

To reduce cell type dependent effects, we tested whether the DR5 promoter could be used in tobacco BY-2 cell cultures to indirectly estimate auxin carrier activity. In order to address the correlation between auxin carrier activity and DR5 promoter activity in tobacco BY-2 cells, we stably transformed the DR5rev:mRFP construct into transgenic BY-2 lines carrying the construct for inducible PIN1 GFP[38] or PIN7[21] expression. PIN1 and PIN7 are plasma membrane localized auxin efflux carriers important for plant growth and development [6, 21]. Induction of PIN1 GFP and PIN7, which causes cellular auxin depletion [21], decreased DR5rev:mRFP signal intensity compared to non-induced cells, reflecting lower nuclear auxin signaling (Figure 1A–1F, Additional file 1: Figure S1A). The DR5rev:RFP signal intensity is represented by the average mean gray value (MGV) of the induced cell population (n > 150 single cells) relative to the average MGV of the uninduced control population (n > 150).
Figure 1

Correlation between altered DR5 promoter activity and cellular auxin accumulation in stably transformed tobacco BY- 2 cells. Tobacco BY-2 cells stably transformed with the auxin responsive DR5rev:mRFP and the estradiol (Est) inducible XVE-PIN1-GFP or the dexamethasone (Dex) inducible GVG-PIN7 construct. (A,B) Induction of PIN1-GFP (in green) with estradiol visibly decreases DR5rev:mRFP (in red) signal intensity compared to non-induced cells as visualized by confocal imaging. (C,D) Dexamethasone-dependent induction of PIN7 visibly decreases DR5rev:mRFP signal intensity compared to non-induced cells. (E) Graph depicts mean gray values (MGV) of the DR5rev:mRFP signal intensity in PIN1 induced and non-induced cells (n = 150). (F) MGV of the DR5rev:mRFP signal intensity in PIN7 induced and non-induced cells (n = 150). (G) [3H]NAA accumulation assays in non-induced and estradiol-induced (XVE-PIN1-GFP) cells. Error bars represent standard error. Statistical significance was evaluated with the unpaired student T-test (* P < 0.05, ** P < 0.01, *** P < 0.0001).

Within the estradiol induced PIN1-GFP expressing BY-2 cell population, we observed a negative correlation between DR5rev:mRFP and PIN1-GFP signal intensity (Additional file 1: Figure S1B and S1C), suggesting lower levels of nuclear auxin signaling in case of high PIN1-GFP activity.

To unambiguously depict auxin carrier activity of PIN1-GFP and PIN7, we performed auxin accumulation assays on the same cell lines and observed lower accumulation of the radiolabelled synthetic auxin 1-naphtylacetic acid ([3H]NAA) in estradiol induced PIN1-GFP expressing cells compared to non-induced cells (Figure 1G). Our findings indicate that DR5rev:mRFP signal intensity (Figure 1A–F) correlates with cellular auxin accumulation (Figure 1G), presumably due to carrier induced changes in cellular auxin content and subsequent alterations in auxin signaling.

We conclude that under our experimental conditions the DR5 promoter activity can be used in BY-2 cells to indirectly visualize auxin carrier-dependent regulation of cellular auxin homeostasis.

Procedure for transient auxin carrier expression in a single-cell-based system

In BY-2 cells, the visualization of auxin signaling could be used to indirectly monitor carrier driven cellular auxin homeostasis. To establish a medium-to-high throughput assay, we elaborated on procedures to transiently express auxin carriers. Particle bombardment is an easy to use procedure that enables high transformation efficiencies at low plasmid concentrations and has, in case of partial automatization, the potential for high-throughput use [39, 40]. We adjusted the previously described particle bombardment procedure [39, 40] for efficient, transient tobacco BY-2 transformation (see Materials and methods). To obtain high protein expression levels, BY-2 cell cultures in the exponential growth phase were used. DNA concentrations ranging from 0.05 μg/μl to 1 μg/μl were sufficient for transient expression and resulted in a correlation between DNA concentration and expression levels, allowing fine-tuning of the gene expression (data not shown). The co-transformation efficiency was tested by transformation of two plasmids at different concentration ratios and the co-transformation levels were calculated (Additional file 1: Table S1). Although dependent on concentration, in general the co-transformation efficiency was very high (approximately 90% at 0.05 μg/μl for both plasmids), enabling the two plasmids to be efficiently co-transformed (Additional file 1: Table S1). Thus, BY-2 particle bombardment can be used as a suitable method to efficiently co-express genes of interest.

Transient single-cell-based-system to monitor auxin signaling

To initially test whether the transient DR5 expression in BY-2 cells could be used to visualize qualitative differences in levels of auxin signaling between two samples of interest, we transiently co-transformed tobacco BY-2 cells with the auxin responsive DR5rev:mRFP construct and the stabilized auxin signaling repressor IAA17mImII fused to the activator domain of the herpes simplex virus VP16. This construct leads to constitutive auxin signaling in plant cells [41, 42]. As expected, the mean gray value (MGV) of DR5rev:mRFP (reflecting auxin signaling) was higher in cells co-transformed with DR5rev:mRFP and 35S:VP16 IAA17mImII than in control cells expressing DR5rev:mRFP and the inert endoplasmic reticulum (ER) marker 35S:HDEL GFP (Figure 2A–2C). To further elaborate on the relative changes in DR5/auxin signaling, we subdivided the transformed cell population in 4 classes according to the relative MGV. Individual cells were scored as low (-) with a relative MGV below 0.5 (2-1), medium (+) with a relative MGV above 0.5 (2-1) and below 1 (20), high (++) with a relative MGV between 1 (20) and 2 (21) and very high (+++) with a relative MGV value higher than 2 (21). (Figure 2E and Additional file 1: Figure S2). This alternative visualization allows us to trace the shifts in relative cell numbers with low, medium, high and very high RFP signal intensity between two samples and to compare even more subtle differences in DR5rev:mRFP signal intensities. 35S:VP16-IAA17mImII enhanced auxin signaling in our system and accordingly reduced the relative cell numbers with low/medium and increased the cell numbers with strong, or very strong RFP signal intensity (Figure 2E).
Figure 2

Effect of altered auxin signaling and transport capacity on cellular auxin homeostasis. (A,B) Graphs represent the relative average mean gray values (MGV) of the DR5rev:mRFP signal intensity. Error bars represent standard error (n = 60). Statistical significance was evaluated with the unpaired student T-test (* P < 0.05, ** P < 0.01, *** P < 0.0001). (A) Coexpression of DR5rev:mRFP and the stabilized version of IAA17 fused to a VP16 activator domain (35S:VP16-IAA17mImII), causing constitutive auxin signaling, significantly increased the relative average MGV compared to the 35S:HDEL-GFP-expressing control cells. (B) NPA treatment leads to an increased MGV/DR5 signaling compared to transformants maintained in standard cultivation medium. (C) 10 representative pictures are shown for the control cells (left panel) and the cells overexpressing VP16-IAA17-mImII (right panel). (D) 10 representative pictures are shown for the untreated control cells (left panel) and the cells treated with NPA (right panel). (E,F) Graphs depict the changes in relative number of transformed cells displaying a low (-), medium (+), high (++), and very high (+++) DR5rev:mRFP signal between the two samples addressing VP16-IAA17-mImII expression or NPA treatment (for detailed description of the quantification, see Additional file 1: Figure S2). Error bars represent standard error (n = 3 repetitions with at least 50 counted cells). Statistical significance was evaluated with the ANOVA test; the P-value is indicated.

These findings indicate that the transient DR5rev:mRFP expression in BY-2 cells can be used to monitor the qualitative differences in nuclear auxin signaling.

Next, we examined whether our single-cell-based system can be used to address mechanisms of auxin transport. Therefore we treated the DR5rev:mRFP-transformed cell population with the auxin transport inhibitor NPA that reduces cellular auxin efflux and, hence, increases cellular auxin levels [43]. As expected, NPA treatment significantly increased the relative rate of DR5 signaling in our transient assay (Figure 2B, 2D and 2F), revealing that NPA action on cellular auxin efflux and cellular auxin homeostasis can be monitored in our single-cell-based system.

Our findings suggest that the DR5- and single-cell-based system can be used to qualitatively monitor changes in auxin signaling. However, in order to use this system in a meaningful way, the experimental design needs to be carefully chosen, because DR5 activity has been suggested not to solely reflect auxin signaling. The phytohormone brassinolide affects the expression of several auxin responsive genes as well as the activity of the DR5 promoter in Arabidopsis thaliana[34, 35] (Additional file 1: Figure S3A and S3B). Nevertheless, in our experimental conditions, brassinolide treatment did not increase the average MGV of DR5rev:mRFP transformed tobacco BY-2 cells (Additional file 1: Figure S3C–S3E). This finding indicates that either brassinosteroids do not increase auxin signaling in BY-2 cells or that our approach is not sensitive enough to trace subtle differences, such as brassinosteroid-induced auxin signaling.

Auxin carrier trafficking and localization in the single-cell-based system

To further assess the usability of the method, we studied the effect of the PIN auxin carrier activity on the cellular auxin signaling. Initially, a time-frame of presumably high PIN protein activity was defined by investigating the PIN trafficking/localization after transient BY-2 transformation. Transmembrane proteins, such as PIN proteins, are co-translationally inserted into the ER membrane. Plasma membrane-localized PIN proteins, such as PIN1, are exported subsequently from the ER and sorted to the plasma membrane [44]. In contrast, PIN5 proteins remain at the ER membrane, where they function as regulators of (intra)cellular auxin homeostasis [14].

Ten hours after transformation, we observed colocalization of PIN1-RFP with the inert ER marker HDEL:GFP in most of the transformed cells (87%) (Figure 3A and 3D), implying high levels of newly synthesized PIN proteins, whereas 16 h after transformation, in most analyzed cells, PIN1-RFP was absent from the ER and solely visible (at the given confocal setting) at the plasma membrane (Figure 3B and 3D) where it is active [21]. Afterwards, the percentage of cells with a strong PIN1-RFP signal at the plasma membrane diminished over time (Figure 3D). This decrease in PIN1 localization at the plasma membrane correlated with an increase of the PIN1-RFP occurrence in the vacuole (Figure 3C and 3D), hinting at a PIN1 turnover by lytic degradation [45].
Figure 3

Cellular localization and trafficking of PIN1-RFP. (A) Colocalization of PIN1 proteins (in red) with the ER marker HDEL-GFP (in green) 10 h after transformation. (B) PIN1-RFP preferentially localizes to the plasma membrane (PM) after 16 h. (C) 24 h after transformation, PIN1-RFP shows vacuolar localization indicating lytic turnover. (D) Relative number of cells showing pronounced PIN1-RFP signal in the ER, PM, and in the vacuole over a time course of 24 h after transformation. Cells showing PIN1-RFP both at PM and either at the ER or vacuole were ascertained as ER or vacuole positive, respectively. Bars = 10 μm.

Altogether, PIN1 proteins displayed a pronounced localization and, presumably, high activity at the plasma membrane between 16 h-18 h after transformation. At that time point (17 h after transformation), also other PIN proteins, such as PIN2-GFP and PIN5-GFP, strongly localized at the plasma membrane and ER (Figure 4A and 4B), respectively. We conclude 16 h to 18 h as a suitable time frame for the analysis of PIN auxin carrier activity.
Figure 4

Effect of PIN protein activity on cellular auxin homeostasis. (A) Preferential PIN2-GFP localization at the plasma membrane. (B) Typical perinuclear ER localization of PIN5-GFP. (C,D) PIN2-GFP and PIN5-GFP localization is not affected in the presence of the auxin transport inhibitor NPA (application with 10 μM NPA-enriched medium). Arrowheads depict preferential PIN2 and PIN5 localizations at the PM and ER, respectively. Bars = 10 μm. (E,I,F,J) Cells co-transformed with DR5rev:mRFP and either 35S:PIN2-GFP or 35S:PIN5-GFP had a lower DR5rev:mRFP signal intensity than the control cells expressing DR5rev:mRFP and the inert ER marker 35S:HDEL-GFP. (G,H,K,L) In the presence of NPA, PIN5-GFP but not PIN2-GFP expression decreases DR5rev:mRFP signal intensity. (E-H) Graphs represent the relative average mean gray values (MGV) of the DR5rev:mRFP signal intensity. Error bars represent standard error (n = 60). Statistical significance was evaluated with the unpaired student T-test (* P < 0.05, ** P < 0.01, *** P < 0.0001). (I-L) Graphs depict the change in relative number of transformed cells displaying a low (-), medium (+), high (++), and very high (+++) DR5rev:mRFP signal intensity between the two samples (for detailed description of the quantification, see Additional file 1: Figure S2). Error bars represent standard error (n = 3 repetitions with at least 50 counted cells). Statistical significance was evaluated with the ANOVA test; the P- value is indicated.

Activity of the PIN auxin transport proteins affects auxin signaling

Next, we investigated the effect of the PIN auxin carrier activity on the cellular auxin signaling using the DR5- and single-cell-based system. Cells cotransformed with DR5rev:mRFP and 35S:PIN2-GFP had a lower DR5rev:mRFP signal intensity than the control cells expressing DR5rev:mRFP and the inert ER marker 35S:HDEL-GFP (Figure 4A, 4E and 4I). These observations are in agreement with the PIN induced decrease in cellular auxin accumulation (Figure 1A–I) and indicate a decreased auxin signaling due to the enhanced PIN2-auxin efflux carrier activity at the plasma membrane.

PIN5 is an ER localized auxin carrier described to facilitate auxin transport from the cytosol into the ER. This auxin sequestration into the ER presumably reduces the availability of auxin for nuclear auxin signaling [14]. In agreement with these assumptions, the PIN5 GFP expression caused a significant decrease in the DR5rev:mRFP signal intensity (Figure 4B, 4F and 4J).

We conclude that the DR5- and single-cell-based system can be used to indirectly monitor the activity of plasma membrane and ER localized PIN auxin transporters.

Auxin transport inhibitor NPA inhibits PIN2, but not PIN5 action in the single cell system

As described above, the expression of PIN2 GFP facilitates the auxin efflux from cells and, hence, lowers the levels of intracellular auxin signaling (Figure 4E and 4I). After treatment with the auxin transport inhibitor NPA, PIN2 expression did not decrease auxin signaling compared to NPA treated HDEL GFP expressing control cells (Figure 4G and 4K). Importantly, NPA did not visibly affect the transient PIN2 localization at the plasma membrane (Figure 4C), indicating that our single-cell-based system monitors the inhibitory effect of NPA on the auxin transport activity of PIN2 [21, 23].

In contrast to PIN2, the PIN5 GFP expression (Figure 4D) reduced the auxin signaling even in the presence of NPA (Figure 4H and 4L). This difference in NPA sensitivity indicates that the mechanisms of NPA action and/or auxin transport mechanisms of PIN2 and PIN5 are distinct. This finding is in agreement with a NPA binding activity at the plasma membrane [46]. To further assess the NPA insensitivity of putative auxin carriers at the ER, we analyzed PILS putative auxin carrier activity in our system. PILS5 localizes to the ER and was recently described to decrease nuclear auxin signaling presumably due to auxin sequestration into the ER [17]. Similar to PIN5, we observed a PILS5 dependent decrease in DR5 signaling in the presence of NPA (Additional file 1: Figure S4). Hence, we assume that NPA inhibits intercellular, but not intracellular auxin transport at the ER in BY-2 cell cultures.

We conclude that the single-cell-based system is a sensitive approach not only to monitor the carrier-driven auxin homeostasis, but also to assess the auxin carrier sensitivity to auxin transport inhibitors. These data demonstrate that our transient approach can be used to investigate the genetic or pharmacological interferences with auxin carrier function.

WAT1 protein activity affects cellular auxin homeostasis

To assess whether the approach is suitable to monitor also the activity of other putative transporters, we co-expressed DR5rev:mRFP with WALLS ARE THIN1 (WAT1) (Figure 5A). WAT1 is a tonoplast-localized transmembrane protein that belongs to the drug/metabolite transporter superfamily. WAT1 activity has an impact on auxin homeostasis by affecting tryptophan and/or auxin metabolism via an unknown mechanism [47]. We used our single-cell-based system to investigate whether WAT1 affects the cellular auxin signaling in BY-2 cells. Cells co-transformed with DR5rev:mRFP and 35S:WAT1:GFP had a lower DR5rev:mRFP signal intensity than control cells expressing DR5rev:mRFP and 35S:GFP:GFP (Figure 5B and 5C), implying a negative effect of WAT1 protein activity on nuclear auxin signaling. These data show that our single-cell-based system visualizes the effect of WAT1 on cellular auxin homeostasis and that it could be in principle used to indirectly asses the activity of a wide range of carrier proteins.
Figure 5

Effect of WAT1: GFP protein activity on cellular auxin homeostasis. (A) Preferential WAT1:GFP localization at the tonoplast (arrowheads). Bar = 10 μm. (b,c) Lower DR5rev:mRFP intensity in cells expressing 35S:WAT1:GFP than control cells co-expressing DR5rev:mRFP and 35S:GFP:GFP. (B) Graph represents the relative average mean gray values (MGV) of the DR5rev:mRFP signal intensity. Error bars represent standard error (n = 60). Statistical significance was evaluated with the unpaired student T-test (* P < 0.05, ** P < 0.01, *** P < 0.0001). (C) Graph depicts the change in relative number of transformed cells displaying a low (-), medium (+), high (++), and very high (+++) DR5rev:mRFP signal intensity between the two samples (for detailed description of the quantification, see Additional file 1: Figure S2). Error bars represent standard error (n = 3 repetitions with at least 50 counted cells). Statistical significance was evaluated with the ANOVA test; the P-value is indicated.

Indirect visualization of the cellular cytokinin homeostasis

As the single-cell-based system enables the indirect monitoring of carrier driven cellular auxin homeostasis, we tested whether the method could be used analogously for other hormonal pathways. The synthetic cytokinin-responsive promoter TWO-COMPONENT-OUTPUT-SENSOR (TCS):GFP was expressed transiently in tobacco BY-2 cells for indirect visualization of the cellular cytokinin signaling [48]. The distribution characteristics of the cells transiently transformed with TCS:GFP were similar to those previously observed for DR5rev:mRFP. Analogously, we measured the average MGV of the transformed cell population and furthermore categorized the cells in subpopulations with very strong, strong, medium, and low TCS:GFP signal intensity (Figure 6A–C). The TCS:GFP activity was higher in transformants treated with 6-benzylaminopurine (BAP), a native aromatic cytokinin [1], than in those grown in standard cultivation medium (Figure 6A and 6B), suggesting an enhanced cytokinin signaling in BY-2 cells upon cytokinin application.
Figure 6

Effect of exogenous 6- benzylaminopurine (BAP) on cellular cytokinin signaling. BAP treatment (application with 10 μM BAP-enriched medium) led to an increased TCS:GFP signaling compared to transformants maintained in the standard cultivation medium (control). (A) Graph represents the relative average mean gray values (MGV) of the TCS:GFP transformed BY-cells. Error bars represent standard error (n = 60). Statistical significance was evaluated with the unpaired student T-test (* P < 0.05, ** P < 0.01, *** P < 0.0001). (B) Representative pictures show the TCS:GFP signal intensities of 10 untreated (left) and BAP treated (right) transformed cells. (C) Graph depicts the change in relative number of transformed cells displaying a low (-), medium (+), high (++), and very high (+++) TCS:GFP signal intensity between the two samples (for detailed description of the quantification, see Additional file 1: Figure S2). Error bars represent standard error (n = 3 repetitions with at least 50 counted cells). Statistical significance was evaluated with the ANOVA test; the P-value is indicated.

These results suggest that our single-cell-based system could eventually be extended to other applications, such as the indirect visualization of cellular cytokinin signaling.

Discussion and conclusion

The phytohormone auxin plays a key role in many aspects of plant growth and development. The cellular auxin content is tightly controlled by local auxin metabolism (biosynthesis, conjugation/deconjugation, or oxidation) and auxin transport facilitators [5, 28, 49–52]. Whereas the complex interplay of these factors still needs to be unraveled, it is clear that various transporters have pronounced effects on the cellular auxin homeostasis [7, 9, 17, 21, 47, 53]. Furthermore, the steady release of new annotated genomes increases the number of putative auxin carriers and enables the study of their molecular evolution. The scientific progress in auxin carrier identification emphasizes the growing demand for suitable approaches to assess carrier-driven cellular auxin homeostasis.

Here, we present a single-cell-based system that allows us to monitor qualitative differences in nuclear auxin signaling between two samples of interest. Thanks to this easy approach, carrier-driven auxin homeostasis and its sensitivity to auxin transport inhibitors can be visualized. The transient approach enables (possibly in combination with automated imaging systems) medium-to-high throughput work flows that can be used for chemical genomic or gain- and loss-of-function screens. The DR5rev:mRFP signal intensity can be easily estimated by measuring the mean grey values. Ratiometric imaging of DR5 signaling and a constitutive (auxin independent) marker could furthermore increase the sensitivity of the approach. Also the usage of the so-called novel auxin signaling sensor (Aux/IAA-based) termed DII-VENUS [54] could be useful to improve the temporal resolution of the system, because DII is not based on gene regulation, but on auxin-dependent protein degradation. For high-throughput work flows, automation, such as qRT-PCR or luciferase-based detection, might be most beneficial.

Various transient expression approaches, such as gold particle bombardment, micro-injection, polyethylene glycol (PEG)-mediated DNA uptake, and electroporation of protoplasts [55–58] have been successfully used to transiently transform plant cells. Whereas transient transformation of protoplasts has been proven to be highly efficient in high-throughput work flows, particle bombardment of plant cells might be preferable for investigating auxin carrier activity, because it does not affect the cell wall integrity that might be required for auxin carrier trafficking and function [59–61]. Accordingly, here we utilized particle bombardment of BY-2 cells as a transient transformation system to establish a single-cell-based system to monitor cellular auxin homeostasis.

As a proof of concept, we investigated prominent PIN auxin efflux carriers and visualized their action on the cellular auxin signaling. In stably transformed BY-2 cell lines, we illustrate that PIN-dependent reduction in cellular accumulation of exogenous auxin correlates with decreased (DR5-based) nuclear auxin signaling. Using the single-cell-based system, we reveal the differential sensitivities of PIN2, PIN5 and PILS5 to the auxin transport inhibitor NPA. Under our experimental condition, NPA blocks PIN2 action at the plasma membrane, but does not diminish PIN5 and PILS5 function at the ER, indicating that auxin transport mechanisms at the plasma membrane and at the ER could be partially distinct. These findings are in agreement with the assumption that NPA action on auxin carrier activity might be restricted to the plasma membrane [46]. As such, NPA could be applied to distinguish between intercellular and intracellular auxin transport. We assume that the differential sensitivity of PIN2 and PIN5 to NPA indicate the suitability of the system for chemical genetic approaches.

Besides the analysis on PIN2, PIN5 and PILS5, we also confirmed that WAT1 negatively affects cellular auxin signaling. WAT1 localizes to the tonoplast and has been suggested to regulate cellular auxin homeostasis [47], possibly by sequestering a yet to be identified auxinic compound into the vacuole. How WAT1 affects auxin homeostasis is still unclear and the mechanism awaits in-depth characterization. Nevertheless, WAT1 activity could be visualized indirectly with our system that might be helpful to further characterize its functionality.

In summary, we established an easy and useful tool to visualize carrier activities that affect cellular auxin signaling. This complementary method bridges the gap between highly elaborated direct auxin transport assays and indirect approaches such as root hair-based visualization of carrier-driven cellular auxin homeostasis [9, 14, 20–25]. Given the transient nature of our approach, it allows, for instance, the rapid and systematic pre-screening of several mutant versions of an auxin carrier of interest. Subsequently, interesting candidates could be analyzed in depth in other, more elaborated systems.

This single-cell-based system could be also used to analyze other molecular components involved in auxin homeostasis, such as regulators of the auxin signaling or metabolism. Moreover, it could be eventually extended to investigate other hormonal pathways by means of different reporter constructs, such as the cytokinin-responsive element TCS:GFP [48]. However, compared to the DR5 auxin reporter, further in depth characterization of TCS:GFP activity in BY-2 cells is needed to use the system analogously.

Methods

Plant material and growth conditions

Nicotiana tabacum L. cv. Bright Yellow-2 cell line [62] was cultivated at 25°C in darkness on an orbital incubator at 150 rpm in liquid medium (3% sucrose, 4.3 g L-1 Murashige and Skoog salts, 100 mg L-1 inositol, 1 mg L-1 thiamin, 0.2 mg L-1 2,4-dichlorophenoxyacetic acid (2,4-D) and 200 mg L-1 KH2PO4, pH 5.8) and subcultured weekly (50x dilution). The used constructs for transient BY-2 cell transformation have been described previously: DR5rev:mRFP[37], XVE::PIN1:GFP[38], GVG PIN7[21], 35S:PIN2 GFP[63], 35S:PIN5 GFP[14], 35S:PILS5_D[17], 35S:HDEL GFP[64], 35S:PIN1 RFP[59], 35S:VP16 IAA17mImII[38], 35S:WAT1:GFP[47], 35S:GFP:GFP[47], and TCS:GFP[48]. Expression of PIN1 GFP in XVE:PIN1 GFP/DR5:mRFP1 genes was induced by the addition of β-estradiol (1 μM, 48 h) and PIN7 in GVG:PIN7/DR5:mRFP by the addition of dexamethasone (3 μM, 48 h) at the beginning of the subculture interval. The solvent DMSO (estradiol) or H2O (dexamethasone) were also added to control samples. We used Arabidopsis thaliana of ecotype Columbia 0 (Col-0). Seedlings were grown vertically on half Murashige and Skoog medium. Plants were grown under long-day (16 h light/8 h dark) conditions at 20–22°C. The Arabidopsis thaliana DR5rev:GFP line was described previously [30]. Treatment with 1 μM brassinolide for 18h was performed on 7 day old seedlings in liquid growth medium.

Stable transformation of BY-2 cells

The basic transformation protocol of An [65] was used. For the transformation, BY-2 lines carrying PIN1:GFP gene, under the estradiol-inducible transactivator XVE, (XVE-PIN1:GFP) [38] or PIN7 gene under dexamethasone-inducible promoter (line GVG-PIN7) [21] were used. Three-day-old BY-2 cells were co-incubated with Agrobacterium tumefaciens strain GV2260 carrying DRrev5:mRFP construct. Resulting double transformed lines were maintained in culture media containing 100 μg/mL kanamycin, 100 μg/mL hygromycin and 100 μg/ml cefotaxim.

Verification of transgene expression using Quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR)

Tobacco total RNA was extracted from stably transformed BY-2 cells (induction of expression GVG-PIN7 by the dexamethasone (3 μM, 24 h)) using SpectrumTM Plant Total RNA Kit (Sigma - Aldrich) and treated with DNAse from DNA-freeTM Kit (Ambion). M-MLV Reverse Transcriptase (H-) (Promega) was used to generate cDNA, according to the manufacturer's instructions. qPCR was performed using DyNAmoTM Flash SYBR® Green qPCR Kit (Finnzymes). Specific primers: AtPIN7 forward 5′-GGGAAGAAGAGTCGGAGAG-3′, reverse 5′-AAGAGCCCAAATGAGACCAA-3′; Ta = 56°C. Resulting values are expressed as a ratio of relative expression of particular gene in induced cells against relative expression of this gene in non-induced cells. Actin was used as reference gene.

Auxin accumulation measurements

Auxin accumulation in 2-day-old cells was measured using radioactively labelled auxins according to [66], as modified by [21]. Treatments were replicated at least three times and the average values (± standard errors) were expressed as pmols of the particular auxin accumulated per million cells. At the beginning of the accumulation assay 3H]NAA (20 Ci mmoL-1; American Radiolabeled Chemicals, Inc., St Louis, MO, USA) (as a good substrate of auxin efflux carriers) was added to the PIN1-GFP induced BY-2 cell line XVE-PIN1:GFP/DR5rev:mRFP (non-induced line was used as a control) to give a final concentration 2nM of 3H]NAA.

Transient transformation of BY-2 cells

Adjusted from previously described procedures [39, 40] 10 ml of three-day-old cells were harvested on filter paper by vacuum filtration and kept on plates with BY-2 medium solidified with 0,6% agar. The cells were transformed via particle bombardment with a PDS 1000/He biolistic system (Bio-Rad) according to the manufacturer's instructions (http://www.bio-rad.com/webroot/web/pdf/lsr/literature/Bulletin_9075.pdf). To coat the gold particles with DNA, 2 μl of plasmid DNA (if not indicated differently, 0.05 μg/μl of each construct to transform) was added to 6.25 μl of 1.6-μm diameter gold particles (dissolved in 50% glycerol). The suspension was supplemented with 2.5 μl spermidine (0.1 M stock solution) and 6.25 μl CaCl2 (2.5 M stock solution). For 35S:PIN2 GFP, 35S:PIN5 GFP, 35S:HDEL:GFP, and 35S:VP16 IAA17mImII, 0.1 μg/μl was used for the transformation. The particles were pelleted by centrifugation, washed twice with 70% and 100% ethanol and, subsequently, resuspended in 10 μl of 100% ethanol. Cells were bombarded under a pressure of 1100 psi. Pharmacological treatments were done by applying 0.5 ml of BY-2 growth medium, enriched with 10 μM NPA, 10 μM 6-benzylaminopurine (BAP) (Duchefa) or 1 μM brassinolide (BR) (Fuji Chemical Industries) directly after transformation. The plates were sealed with parafilm and kept in the dark for 18 h at 25°C. For microscopic analysis, cells were gently transferred (with a spatula) from the filter to a microscopy slide (in water) and subsequently covered with a cover slip. Samples were analyzed via confocal microscopy.

Microscopy

Live-cell confocal microscopy was done with a Zeiss 710 microscope. Fluorescence signals for GFP (excitation 488 nm, emission peak 509 nm) and mRFP1 (excitation 561 nm, emission peak 607 nm) were detected. Sequential scanning was used for double labeling to avoid crosstalk between channels. The DR5rev:mRFP expression was evaluated by defining the mean gray value (MGV) of each imaged cell (middle sections). For each experiment, confocal settings were defined based on the DR5rev:mRFP signal of the control cells and remained unchanged during the respective experiment. Transformants were identified based on the fluorescence of both proteins, imaged with a 40x objective, and subdivided into four clusters (very low, low, medium, and high) according to the relative MGV (See also Additional file 1: Figure S2). Every experiment was done in triplicate (independent transformations) and for each condition, a total number of at least 60 transformed cells were imaged. The means and standard errors were calculated and the statistical significance (independence between the two populations) was obtained by student t-test (for the analysis of the MGV) and ANOVA analysis (for the subdivision into clusters).

Abbreviations

BY-2: 

Bright Yellow-2

PIN: 

Pin-formed

ER: 

Endoplasmic reticulum

NPA: 

1-naphthylphthalamic acid

PILS: 

PIN-likes

WAT1: 

Walls are thin1

ARF: 

Auxin response factor

TIR/AFB: 

Transport inhibitor repsonse/auxin F-box protein

AUX/LAX: 

Auxin resistant1/like aux1

GH3: 

Gretchen Hagen 3

mRFP: 

Monomeric red fluorescent protein

NAA: 

1-Naphthylacetic acid

MGV: 

Mean gray value

GFP: 

Green flurorescent protein

TCS: 

Two-component-output-sensor

BAP: 

6-benzylaminopurine

PEG: 

Polyethylene glycol.

Declarations

Acknowledgements

We thank T.J. Guilfoyle, C. Luschnig, D. Goffner, J. Sheen and P. Pimpl for sharing published materials and M. De Cock for help in preparing the manuscript. This work was supported by the Vienna Science and Technology Fund (WWTF) (to J.K.-V.), the Agency for Innovation by Science and Technology (IWT) and Fonds voor Wetenschappelijk Onderzoek (FWO) (predoctoral fellowship and travel grant to E.B.), the Odysseus program of the Research Foundation-Flanders (to J.F) Grant Agency of the Czech Republic, projects CZ.1.07/2.3.00/20.0043, CZ.1.05/1.1.00/02.0068 (to J.F.), P305/11/2476 (to J.P.) and P305/11/0797 (to E.Z.) and the Land Baden-Württemberg, the Chica und Heinz Schaller Stiftung and the CellNetworks cluster of excellence of the Heidelberg university (to A.M.).

Authors’ Affiliations

(1)
Department of Plant Systems Biology, VIB and Department of Plant Biotechnology and Genetics, Ghent University
(2)
Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences
(3)
Institute of Experimental Botany, The Academy of Sciences of the Czech Republic
(4)
Department of Stem Cell Biology, Center for Organismal Studies, University of Heidelberg
(5)
Department of Functional Genomics and Proteomics, Faculty of Science, and CEITEC, Masaryk University

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