Rice Root Hair Phenotypes Imaged by Cryo-SEM

Materials and Reagents

1. 3M^TM Micropore^TM Surgical Tape (3M, catalog number: 1533)

2. Nitrocellulose membranes with 0.8 μm pore size, 25 mm filter diameter (AAWG02500, Millipore, Gemany)

3. Rice root hair mutant Osbhlh115 seeds (Ding et al., 2009); Oryza sativa L. Xian group (also known as Hsien or Indica) wild-type Kathalath seeds

4. Sodium hypochlorite (BBI Life Sciences Corporation, China)

5. 70% ethyl alcohol (BBI Life Sciences Corporation, China)

6. Murashige and Skoog Basal Medium (Duchefa Biochemie, catalog number: M0221)

7. Phytagel (Sigma-Aldrich, catalog number: P8169-250G)

8. Carbon-rich conductive glue (Rave Scientific, catalog number: RS-MN-15-001130)

9. Gold wafer (70-AU2408, 24 × 0.2 mm, purity 99.99%. Au, Labtech, UK)

10. Argon gas (99.99% purification, Hangzhou Jingong, China)

11. Nitrogen gas (99.99% purification, Hangzhou Jingong, China)

12. Liquid nitrogen (Hangzhou Jingong, China)

Equipment

1. Horizontal shaker (Beyotime, model: TS-2000A)

2. Growth chamber (Ningbo-Jiangnan, model: GXM-1008)

3. Scanning electron microscope (HITACHI, model: S-3000N)

4. GATAN ALTO 2100 (GATAN, model: ALTO 2100)

5. HITACHI SEM equipped with a GATAN cryo-SEM preparation system

Software

1. ImageJ (Version 1.53e, National Institutes of Health, United States, https://imagej.nih.gov/ij)

2. Office 365 (Microsoft, United States, https://www.office.com/)

Procedure

1. Rice Root Hair Growth

   1. Sterilize the glume removed-rice seeds with 70% EtOH for 2 min, and remove the disinfectant alcohol. Then, sterilize the seeds with 10% sodium hypochlorite for 30 min on a horizontal shaker. Rinse the seeds thoroughly 5 times with sterile distilled water.

   2. Place the seeds on sterile absorbent paper for drying.

   3. Sow the seeds onto 0.8% phytagel half-strength MS medium (pH = 5.8).

      Note: To avoid too much moisture attached to the root hairs, it is highly recommended to seal the medium plates with 3M Micropore surgical tape.

   4. Place the medium plate vertically in the growth chamber under a temperature regime of 30°C/22°C (day/night) with 50% or lower humidity and a 12 h photoperiod (15,000 lux).

      Note: Lowering the humidity is an effective way to reduce the moisture in the plate.

   5. Use three-day-old rice roots after germination for subsequent sample treatment.

      
      

2. Preparation for Cryo-SEM

   1. Install the SEM stage cold module (Figures 1; see Video 1).

      
      

      
      Figure 1. SEM stage cold module installation. Dovetail and fit the module with a thermometer. Push the copper shaft and copper shaft sleeve together to make an interference fit connection. Ensure that the real-time module temperatures are displayed on the keypad.

      
      

      
      Video 1. SEM stage cold module installation

      
      

   2. Check the Alto 2100 keypad (or control panel) (Figure 2).

      
      

      
      Figure 2. The keypad at the very beginning of the start-up. The keypad allows control of the pump and the system’s valves, sputter coater, lighting, and heater. All temperature and pressure readings are instantly available and easy to observe on the keypad.

      
      

   3. Prep chamber precooling (Figure 3, see Video 2)

      
      

      
      Figure 3. The prep-chamber before adding liquid nitrogen. The red circles indicate the inlet and outlet for liquid nitrogen. The red ellipse indicates the pressure indicator LED display.

      
      
      
      Video 2. Pour the liquid nitrogen into the prep chamber inlet
      
      

   4. Precool the SEM cold stage module

      Pour liquid nitrogen into the open topped dewar where the pipeline is immersed (see Video 3). The pipeline is filled with high-purity nitrogen gas. The cooled gas in the pipeline cools down the SEM stage cold module below -180°C.

      
      
      
      Video 3. Pour liquid nitrogen into the open topped dewar

      Note: Ventilate the cryo-pipeline for at least 5 min before running the cryo-SEM system. A uniform flow rate of nitrogen in the pipeline is necessary for image quality.

      
      

3. Produce slush nitrogen

   1. Pour the liquid nitrogen into the slush chamber and close the lid (see Video 4).

      Note: Wear waterproof cryogloves!

      
      
      
      Video 4. Preparation of slush nitrogen
      
      

   2. Press the SLUSH/VENT button on the Alto control panel to activate slush chamber pumping (see Video 4).

   3. Allow the liquid nitrogen to boil until it solidifies. This step takes approximately two minutes.

   4. Press the SLUSH/VENT button again to stop pumping and vent the air into the chamber.

   5. Remove the lid before use.

      
      

4. Root Sample Acquisition

   1. Cut a 1-2 cm length of wild type or mutant straight growing seminal roots for use.

   2. Add a drop of carbon-rich conductive glue to the aluminum stub of the specimen holder (see Video 5).

      
      
      
      Video 5. The conductive glue was applied to the aluminum stub
      
      

   3. Place a piece of moist nitrocellulose paper, immersed in distilled water in advance, on the glue (see Video 6).

      
      
      
      Video 6. Putting the nitrocellulose paper onto the sample stage and applying gel
      
      

   4. Gently clamp the cut-off root end with tweezers and transfer the root onto nitrocellulose paper. Place the root as horizontally as possible (Figure 4).

      
      

      
      Figure 4. Clamping the rice root onto the nitrocellulose paper. First, apply conductive glue to the aluminum stub. Then, place the nitrocellulose paper on the gel. After that, spread the conductive glue to the near end of the rod. Last, stick the root cut end on the glue and lay the root flat on the nitrocellulose paper.

      
      

   5. Immerse the trimmed root end in the glue (Figure 4).

      
      

5. Root Sample Repreparation

   1. Stick together the specimen holder with a root sample on its stub and the sample holder integrated with the vacuum transfer device (VTD) (see Video 7).

   2. Buckle the sample holder (with the VTD) to the slush chamber until the VTD sits on the O-ring in the recess located on the top of the slushing chamber (see Video 7).

   3. Slide the rod in the VTD down (see Video 7).

   4. Grip the sample holder in the air above the nitrogen pool for 10 s to quickly freeze the root hair (see Video 7).

   5. Plunge the sample holder into the slushy nitrogen to rapidly cool the sample (see Video 7).

      Note: Ensure that only the sample holder is immersed in the nitrogen when slushing, otherwise the cold rod freezes the VTD’s O-ring. This has a negative influence on the subsequent push-pull operation and/or the gas tightness.

      
      

      
      Video 7. The sample immersed into the nitrogen slush
      
      

   6. Press the SLUSH/VENT button to activate slush chamber pumping.

   7. Pull the VTD rod upward and fully retract the sample holder into VTD before the nitrogen slush completely solidifies (see Video 8).

      
      
      
      Video 8. The sample waiting to leave the slushing station
      
      

   8. Push the trapdoor valve (see Video 9) (The sample is now held in the VTD under a vacuum and ready for transfer into the prep chamber).

      
      
      
      Video 9. The sample leaving the slushing station

      
      

   9. Press the SLUSH/VENT button once again to vent the slush chamber.

   10. Transfer and place the VTD in the GATE VALVE airlock (see Video 10).

       
       
       
       Video 10. Pump the Gate Value airlock vacuum
       
       

   11. Press the LOAD PUMP button on the Alto control panel to vacuum the prep chamber (Figure 2).

   12. Wait until six bars of indicator light illuminate, which is indicated by the red ellipse in Figure 3.

   13. Fully open the valve, push the rod, and insert the specimen holder into the dovetail stage in the prep chamber (Figures 5-6; see Video 11).

       
       

       
       Figure 5. The dovetail stage in the prep-chamber. The dovetail stage is convenient for the angled sides of the sample holders and is fitted with a thermometer and a heater. There is a stopper to allow the sample holder to be transferred to exactly the same position. A spring clip secures the holder and prevents vibration.

       
       

       
       Figure 6. The rice root sample before sublimating and sputtering. The white circle indicates that the sample is waiting to be sublimated and sputtered on the stage.

       
       
       
       Video 11. Transfer the sample to the prep chamber (The VTD and prep chamber valves are opened simultaneously)
       
       

   14. Set the sublimation temperature of the prep-chamber stage to -95°C (Figure 7).

       
       

       
       Figure 7. The sublimation temperature settings. By pressing the SET TEMPERATURE buttons, set the sublimation temperature to -95°C.

       
       

   15. Press the HEAT button to start warm-up (see Video 12) (For rice root hairs, maintaining at -95°C for 300 s is optimal. The sublimation time mainly depends on the humidity of the root culture environment).

       
       
       
       Video 12. The sublimation temperature keeps rising
       
       

   16. Press the HEAT button again to stop heating and recover the temperature to ≤ -140°C.

   17. Set the gold sputter time and press the SPUTTER button on the control panel (120 s is sufficient for root hairs) (Figure 8).

       Note: If the prep chamber is not equipped with a microscope device, samples can be transferred to the SEM chamber for rough viewing before sputtering. This step is extremely important for obtaining favorable samples and high-quality images.

       
       

       
       Figure 8. The sputter parameter display. The default setting of the sputter electric current is 10 mA. Before argon sputtering, the stage temperature should be cooled to ≤-140°C.

       
       

   18. The argon inlet solenoid closes automatically when the time is up (Figure 9; see Video 13).

       
       

       
       Figure 9. The rice root being sputtered. The rice root sample should be placed under the coating head during sputtering.

       
       
       
       Video 13. The sample is being sputtered
       
       

6. SEM Microscopy

   1. Open the ball valve between the preparation chamber and the SEM chamber when the indicator LED light turns green (Figures 10-11).

      
      

      
      Figure 10. The ball valve LED is red. In this situation, the mechanical interlock cannot be opened.

      
      

      
      Figure 11. The ball valve LED is green. When the vacuum in the prep chamber and the SEM equilibrates, the LED turns green, and the mechanical interlock can be opened.

      
      

   2. Transfer the specimen holder to the SEM cold stage module (see Video 14).

      
      
      
      Video 14. Transfer the sample from the prep chamber to the SEM
      
      

   3. Rotate the rod and separate the specimen holder from the rod.

   4. Retract the rod back into the prep chamber and close the ball valve. SEM imaging has now started.

   5. Open the software and click the HV button to start the preview and shooting mode.

   6. Set the SEM acceleration voltage (6 kV or 15 kV).

   7. Adjust the SEM sample stage position by rotating different control knobs for the SEM standard stage (Figure 12).

   8. Rotate the rotary functional knobs on the HITACHI control unit by adjusting MAGNIFICATION, CONTRAST, BRIGHTNESS, and FOCUS (Figure 13).

      
      

      
      Figure 12. The standard stage of the SEM. The T control knob tilts the specimen (-20 to 90°); the R control knob rotates the specimen (±360°); the X control knob moves the specimen in the longitudinal direction; the Y control knob moves the specimen in the lateral direction; the Z control knob moves the specimen in the vertical direction.

      
      

      
      Figure 13. Appearance of the SEM display unit. The rotary knob unit is shown in the yellow rectangle. The control button layout on the unit is embedded in the image.

      
      

   9. Click the mouse to open or close dialog windows and run the settings. Input characters and comments with the keyboard.

   10. Switch to different sample parts by moving the mouse wheel.

   11. Click the H.R. Capture button to scan the sample. The scanning speed is optional.

       Note: The slower the scanning speed, the higher the resolution of the image. However, a slow scanning speed occasionally causes image deformation.

   12. Click the SAVE button to save and name the acquired image in the target folder.

   13. Click the H.V. button again to turn off the SEM filament when imaging is finished.

   14. Open the BALL VALVE, and remove the specimen holder from the Cold Stage Module located by the rod.

   15. Haul the rod backwards and insert the holder into the dovetail stage in the prep chamber.

   16. Close the BALL VALVE.

   17. Haul the rod backwards to the end and shut the airlock valve.

   18. Push the LOAD PUMP button on the Alto control panel twice and vent the airlock to remove the VTD.

   19. Place the VTD on the slushing chamber and engage the trapdoor valve onto the control lever.

Data analysis

Root hair parameters were obtained from the cryo-SEM images (Figure 14). The root hairs from the region of 2-3 mm from the root apex were used for the statistics and analysis of the root hair parameters. According to the results, the root hair length in the Osbhlh115 mutant was much shorter than that in the wild type (Table 1). The difference in root hair diameter between the wild type and mutant was insignificant. Although the angles between root hairs and seminal roots of the wild type and mutant were not different, cryo-SEM provided an important tool for the study of the root hair angle parameter (Table 1).

Figure 14. Root hair phenotype analyzed by cryo-SEM. A-B. Kathalath (wild type) root hair phenotype. A is 40× magnification and B is 400× magnification; C-D. Osbhlh115 mutant root hair phenotype. C is 40× magnification and D is 400× magnification.

Table 1. Quantitative parameters of the root hairs*

*All data were obtained according to the reference instructions (Tajima and Kato, 2013)

In addition to imaging root hairs, cryo-SEM can be used to image root cell internal structures (Figure 15). After the water in the epidermal and cortical cells is removed by sublimation, the reticulate structure and layered structure, respectively, at 2,000× magnification are shown (Figure 15B). Similar cytoplasmic lamellar and reticulate structures were found in the drupelet mesocarp cells of red raspberry (Rubus indaeus L.) (Williamson and Duncan, 1989). Conventional paraffin and resin sections could not show the true structures of the cytoplasm. When resin or paraffin replaced the water in the tissue, it likely took away some of the proteins or other components in the cytoplasm. Cryo-SEM can eliminate water through sublimation, retaining the cytoplasmic contents to the greatest extent. It was reported many years ago that electron microscope freeze-fixation was better than chemical fixation (Walther and Müller, 1999).

Figure 15. Cytoplasmic contents analyzed by cryo-SEM. A. Kathalath root transverse fracture cytoplasmic structure at 180× magnification. B. Enlarged view of the red rectangular zone in B at 2,000× magnification. The red circle in B indicates a reticulate structure; the red square in B indicates a lamellar structure.

Nitrogen sludge may transform into nitrogen solids during the root hair freezing process. The root hair tubular protuberant parts were broken occasionally when the specimen holder was retracted from the slush chamber. In Figure 16, a variety of broken root hair holes are visible (Figure 16A). Root hairs exhibit a large vacuole in the protruding part (Preuss et al., 2004). After the sublimation finished, the entire vacuole was evaporated to dryness and an empty cavity was left (Figure 16B). Some of the residual particles in the cavity most likely represent cytoskeletal proteins (Walther and Müller, 1999). In conclusion, there are reasons to believe that the reticulate and layered structures displayed in Figure 15B have different functions in the formation of cell morphology, organelle positioning, signal transduction, and material transportation. Note that only a small portion of the information displayed by cryo-SEM was utilized and further exploration is needed.

Figure 16. Broken root hairs left holes. A-B. Kathalath (wild type) root hair phenotype. A is 400× magnification and B is 7,500× magnification.

Acknowledgments

This project was supported by Zhejiang Provincial Natural Science Foundation (LY19C020002), the National Science Foundation of China NSFC (31200913), the Entrepreneurship and Innovation Project for the Overseas Returnees (or Teams) in Hangzhou (4105C5062000611), China Scholarship Council (201709645003) and National Undergraduate Innovation and Entrepreneurship Training Program (1085C5212030510). This protocol was adapted from Yu et al. (2013). We give great thanks to Mr. Hanmin Chen at Zhejiang University for his technical support. Our personal heartfelt appreciation goes to Dr. Zhiming Yu’s late advisor Professor Dr. Ping Wu at Zhejiang University. The protocol presented here was developed from a previous publication (Yu et al., 2011).

Competing interests

The authors declare no competing financial interests.

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