Materials and Reagents

0.1-10 μl pipette tips (Thermo Fisher Scientific, QSP, catalog number: 104-Q )
1-200 μl pipette tips (Thermo Fisher Scientific, QSP, catalog number: 110-B-Q )
1-1,000 μl pipette tips (Corning, Axygen^®, catalog number: T-1000-B )
1.5 ml microcentrifuge tubes
Toothpick (Yin Sha, catalog number: 918 )
Grid (Emcn, catalog number: AZH75HH )
40 holes flat embedding mold (Emcn, catalog number: DZ10590-40 )
4 weeks-old Nicotiana benthamiana plants
Agrobacterium strain GV3010
E-64d (Sigma-Aldrich, catalog number: E8640-1MG )
Paraformaldehyde (Electron Microscopy Sciences, catalog number: 157-8 )
Glutaraldehyde (Structure Probe, SPI-CHEM, catalog number: 02607-BA )
Sodium dihydrogen phosphate dehydrate (NaH₂PO₄•2H₂O) (Sigma-Aldrich, catalog number: 1.06342.1000 )
Disodium hydrogen phosphate dodecahydrate (Na₂HPO₄•12H₂O) (Sigma-Aldrich, catalog number: 04273 )
Potassium hexacyanoferrate (K₃[Fe(CN)₆]) (Sigma-Aldrich, catalog number: 702587 )
OsO₄ (Ted Pella, catalog number: 18451 )
ddH₂O
Uranyl acetate (DEUTSCHL AND LUXEMBURGPRODUZIER TSPE ZIA LCHEMIKALIEN PROD UKTION)
Lead acetate (Structure Probe, SPI-CHEM, 1161108)
Ethanol (Sinopharm Chemical Reagent, catalog number: 10009218 )
Epoxypropane (Sinopharm Chemical Reagent, catalog number: 80059118 )
1% (w/v) uranyl acetate in ddH₂O and 2% (w/v) uranyl acetate in ddH₂O
DDSA (Structure Probe, SPI-CHEM, catalog number: 02827-AF )
SPI-PON^TM812 (Structure Probe, SPI-CHEM, catalog number: 02659-AB )
NMA (Structure Probe, SPI-CHEM, catalog number: 02828-AF )
DMP-30 (Structure Probe, SPI-CHEM, catalog number: 02823-DA )
HCl (Sinopharm Chemical Reagent, catalog number: 10011008 )
NaOH (Sinopharm Chemical Reagent, catalog number: 10019762 )
Trizol reagent (Tiangen)
RNase-free DNase I (Sigma-Aldrich)
Oligo(dT)
TRANScript moloney murine leukemia virus reverse transcriptase (Tiangen)
Power SYBRGreen PCR master mix (Applied Biosystems)
Paraformaldehyde-glutaraldehyde Fixative Solution (2%/2.5%), pH 7.2 (see Recipes)
0.1 M phosphate buffer (PB), pH 7.2 (see Recipes)
OsO₄-hexacyanoferrate fixative solution (see Recipes)
1% (w/v) uranyl acetate (see Recipes)
2% (w/v) uranyl acetate (see Recipes)
0.2% lead acetate (see Recipes)
Epon 812 (see Recipes)
20 μM E-64d (see Recipes)

Equipment

Water Purification System (Merck, Milli-Q^®, model: Advantage A10 )
Art knife (FLYING EAGLE, catalog number: 74-S )
Pincette (Beijing XXBR Technology, catalog number: T5889 )
Diamond knife (DiATOME, catalog number: DU4535 )
Eppendorf Research^® plus Pipette 0.5-10 μl
Eppendorf Research^® plus Pipette 10-200 μl
Eppendorf Research^® plus Pipette 100-1,000 μl
Diaphragm vacuum pump (Tianjin Jinteng Experiment Equipment, catalog number: GM-0.50II )
Shaking incubator (Miulab, catalog number: ES-60 )
Electronic balance (Sartorius AG)
Electro-heating standing-temperature cultivator (Tianjin Taisite Instrument, model: DH4000BII )
Electrothermal constant-temperature dry box (Tianjin Taisite Instrument, model: 202-0AB )
Ultramicrotome (Leica Microsystems, model: EM UC6 )
Eyelash pen
Dyeing machine (Leica Microsystems, model: EM AC20 )
Electron microscope (Hitachi High-Technologies, model: H-7650 )
Bio-Rad CFX96 real-time PCR detection system

Procedure

Nicotiana bentiamiana plants are grown for 4 weeks in growth rooms at 25 °C under a 16-h light/8-h dark cycle.
Agrobacterium strain GV3010 containing pTRV1 and pTRV2 or its derivative GAPCs or GAPCs/ATG3 co-silencing construct are mixed at the proportion of 1:1 and infiltrated into the top two leaves of the plants to silence GAPCs and GAPCs/ATG3 in plants, respectively.
When target genes are silenced successfully at 16-18 days post infiltration (dpi), infiltrate 20 μΜ E-64d into the top two new leaves where the genes are silenced successfully.
After treatment with E-64d for 8-12 h, cut the treated leaves into small pieces (1 mm x 1 mm). Fix the small pieces of leaves in 300 μl paraformaldehyde-glutaraldehyde fixative solution (2%/2.5%, pH 7.2) in a 1.5 ml tube. Vacuumize them using the diaphragm vacuum pump at 0.1 MPa for 10-30 min until the pieces sink to the bottom of the tube. Poke the pieces with toothpicks to help them sink to the bottom of the tube. Fix these pieces with paraformaldehyde-glutaraldehyde fixative solution (2 %/2.5%, pH 7.2) on ice for 1 h.
Wash the pieces with 0.1 M PBS buffer in a shaker for 3 times, 15 min each time (Steps 5 to 10 should be achieved in a shaker).
Fix the samples with OsO₄-hexacyanoferrate fixative solution (1%/1.5%) on ice for 1 h.
Wash the pieces with 0.1 M PBS buffer at room temperature (RT) for 3 times, 15 min each time.
Wash the pieces with ddH₂O at RT for 3 times, 10 min each time.
Stain the samples with 1% uranyl acetatein the dark at RT for 1 h.
Wash the pieces with ddH₂O at RT for 3 times, 15 min each time.
Dehydrate the samples in a graded series of ethanol of 30%, 50%, 70%, 80%, 90% and 95% (v/v), 10 min each time.
Dehydrate in 100% ethanol for 3 times, 10 min each time.
Dehydrate the samples with 100% epoxypropane for 2 times, 10 min each time.
Incubate the samples with epoxypropane: epon 812 at the volume proportion of 2:1 in a shaker for 30 min at RT.
Incubate the samples with epoxypropane: epon 812 at the volume proportion of 2:1 in a shaker for 30 min at RT.
Incubate the samples with epon 812 in a shaker overnight.
Refresh the epon 812 for 3 times, 3 h each time.
Embed the samples in 40 holes flat embedding mold with epon 812.
Permeate the samples with epon 812 at 37 °C for 4 h.
Aggregate resin at 60 °C, 24-48 h.
Cut the embedding block with art knife until the sample could be saw. Continue to cut the sample with glass knife until the surface is smooth.
Cut the sample surface in trapezoidal with an art knife.
Cut the embedding block into 70-nm ultrathin sections on ultramicrotome with a diamond knife.
Collect them with eyelash pen on Formvar-coated grids.
Stain the sections with 2% uranyl acetate for 30 min and 0.2% lead acetate for 5 min using a Dyeing machine.
Examine the sections under an electron microscope.
Observe the autophagic structures in mesophyll cells, record the number of autophagic structures and the number of cells.

Data analysis

As shown in Figure 1, a lot of ultrastructure of single-membrane autophagic bodies (arrows) are observed in the vacuole of mesophyll cells of GAPCs-RNAi leaves, whereas few number of autophagic bodies are observed in control or GAPCs/ATG3-RNAi leaves. Virus-induced gene silencing (VIGS) is used here for silencing of GAPCs and ATG3. In Figure 1B, the canonical double-membrane autophagosomes (arrowhead) are observed in the cytoplasm of GAPCs-silenced plants. The black arrowheads show the autophagic bodies inside the vacuole. Figure 1C showed the relative autophagic activity of three samples. Autophagic activity is calculated through dividing the number of totalautophagic structures (both autophagic bodies and autophagosomes) by the number of mesophyll cells. The autophagic activity of TRV control is normalized and set to 1.0. Approximately 20 cells from 2-3 different embedding blocks are used to quantify autophagic structures in each treatment. The statistical analysis indicates the autophagic activity is significantly increased in GAPCs-silenced plants compared to that of control and GAPCs/ATG3-silenced leaves, indicating that silencing of GAPCs activates autophagy, and the activated autophagy is dependent on ATG3.

Figure1.Detection of autophagic like structures by TEM in control and VIGS plants. A. Representative TEM images of mesophyll cells from GAPCs-silenced, GAPCs/ATG3-silenced and control leaves. The ultrastructures of autophagic bodies (arrows) are observed in the vacuole of mesophyll cells of GAPCs-silenced plants. Cp, chloroplast; V, vacuole. Scale bar = 1 μm. B. Representative ultrastructure of autophagosomes (arrows) and autophagic bodies (arrowhead) observed in the cytoplasm of mesophyll cells. Scale bar = 500 nm. C. Relative autophagic activity in GAPCs-silenced and GAPCs/ATG3-silenced plants. Autophagic activity in TRV control plants is set to 1.0. Values represent means ± SE from 3 independent experiments. Different letters indicate significant differences (ANOVA, P < 0.05).

Notes

As plant autophagy is a rapid process, it is helpful to inhibit the autophagy process to allow the observation of transient intermediates (Yoshimoto, 2012). E-64d is a cysteine protease inhibitor which can prevent the autophagic vacuolar degradation thus increase the number of autophagic structures (Liu et al., 2005; Xu et al., 2017). Infiltration of E-64d is optional. It depends on the purpose of the experiment.
During the preparation of TEM samples, the air humidity should be controlled at a low level (< 40%).
Samples should be put into the paraformaldehyde-glutaraldehyde fixative solution quickly.
After application of the paraformaldehyde-glutaraldehyde fixative solution, OsO₄-hexacyanoferrate fixative solution and uranyl acetate solution, the samples should be washed thoroughly.
Alcohol dehydration and resin permeation of samples should be thorough.
It's crucial to identify autophagic structures properly apart from other double-membrane organelles and vesicles in cytoplasm. Pay attention to the membrane construction, size and the containing substances of the structures. In Nicotiana benthamiana, autophagosomes and autophagic bodies are 0.5-1.5 μm structures. Autophagosomes are double-membrane structures, while autophagosomes fuse with vacuole thus become single-membrane structures termed autophagic bodies. One distinct feature is that, both autophagosomes and autophagic bodies contain substrates for autophagic degradation, such as proteins, organelles, targets lipids, carbohydrates, nucleic acids and invading pathogens (Rabinowitz and White, 2010).
VIGS is used to silence gene in Nicotiana benthamiana (Liu et al., 2002), and suppress gene expression by infecting Nicotiana benthamiana with a recombinant virus vector carrying host-derived sequence.
Real-time RT PCR was used to confirm VIGS efficiency of the target genes.
1. Extract total RNAs using Trizol reagent (Tiangen) from the leaf samples. Treat the samples with RNase-free DNase I (Sigma-Aldrich) to remove potential DNA contamination. Reverse transcribe RNA using oligo(dT) primer and TRANScript moloney murine leukemia virus reverse transcriptase following the manufacturer’s manual (Tiangen).
2. Gene expression analysis. Perform real-time PCR on a Bio-Rad CFX96 real-time PCR detection system using Power SYBR Green PCR master mix (Applied Biosystems). Set real-time PCR cycles to 39. Use actin gene as the internal control (data not shown).

Recipes

Note: All the solutions are prepared with ddH₂O unless otherwise stated.

Paraformaldehyde-glutaraldehyde Fixative Solution
Components
Concentration
Paraformaldehyde
2%
Glutaraldehyde
2.5%
0.1 M phosphate buffer
Adjust pH to 7.2 (with HCl)
0.1 M phosphate buffer (PB), pH 7.2
Components
Concentration
NaH₂PO₄•2H₂O
0.028 M
Na₂HPO₄•12H₂O
0.072 M
Adjust pH to 7.2 with NaOH
OsO₄-hexacyanoferrate fixative solution
Components
Concentration
OsO₄
1% (w/v)
Potassium hexacyanoferrate
1.5% (w/v)
1% (w/v) uranyl acetate
Components
Concentration
Uranyl acetate
1%
2% (w/v) uranyl acetate
Components
Concentration
Uranyl acetate
2%
0.2% lead acetate
Components
Concentration
Lead acetate
0.2%
NaOH
4%
Epon 812 (100 ml)
Components
Content
DDSA
16 ml
SPI-PON^TM 812
50 ml
NMA
35.6 ml
DMP-30
2 ml
20 μM E-64d
1. E-64d was diluted in ethanol to a 10 mM stock solution and stored at -20 °C
2. Dilute10 mM E-64d in ddH₂O to the final concentration of 20 μM

Acknowledgments

This protocol was adapted from SJ Han et al.’s work (Han et al., 2015). This work was supported by the National Transgenic Program of China (2016ZX08009-003-001).

Competing interests

The authors declare that there are no conflicts of interest.

References

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