We thank Dr. R. Terada, Dr. Z. Shimatani, and Dr. H. Tsuji for providing us with the OsMADS15-mOrange seeds; Dr. D. Kurihara for providing us with the NGCN construction; and Dr. R. Shim for editing our manuscript. This work was funded by JSPS KAKENHI (grant numbers JP20H05912, 20H05778, 20H05779) and by the SATREPS program (no. JPMJSA1706) of the JST and JICA.

1. Preparation of the fixative solution
<ol>
	<li>Transfer 70 mL of sterile water into a glass bottle and add 10 g of paraformaldehyde (PFA). 
	CAUTION: PFA is toxic; hence, wearing gloves is recommended.</li>
	<li>Add 2 mL of 1 N NaOH to dissolve the PFA solution.</li>
	<li>Dissolve the PFA solution with continuous stirring (300-500 rpm) at 60 &#176;C for about 1 h until the PFA solution is transparent.</li>
	<li>Add sterilized water to increase the volume of the PFA solution to 100 mL. 
	NOTE: The PFA solution was prepared freshly before use. Moreover, a PFA solution stored at 4 &#176;C can be used for approximately 2 months.</li>
	<li>Immediately before sampling, add 25 mL of 60 mM HEPES (pH 7.4), 3 mL of 1 M sucrose, and 2 mL of sterile water into 20 mL of 10 % PFA to prepare a 50 mL fixative solution.</li>
</ol>
2. Preparation of the clearing solution (CS)
<ol>
	<li>Weigh and mix 7.5 g of sodium deoxycholate, 5 g of xylitol, and 12.5 g of urea (see Table of Materials) in 50 mL of sterile water. 
	NOTE: Sodium deoxycholate powder was weighed in a general laboratory draft chamber to prevent airborne dispersion.</li>
	<li>Dissolve the ingredients (step 2.1.) using a magnetic stirrer to prepare the CS. 
	NOTE: The present study used in-house prepared clearing solution (CS), but a commercially available clearing solution, ClearSee (see Table of Materials), can also be used.</li>
	<li>Transfer the CS into a 50 mL conical tube and store it at room temperature (15-30 &#176;C) in the dark. 
	&#8203;NOTE: The CS can be stored for more than 1 year.</li>
</ol>
3. Sampling
<ol>
	<li>Cut the roots carefully without damaging the plants. Wash the plants with water to remove the dirt. 
	NOTE: This method studied the observation of tissues from the three-leaf stage (LS) to flag LS. The present study used the rice cultivars Nipponbare (Nip) and Taichung 65 (T65) at the 8-10 LS.</li>
	<li>Peel off the old outer leaves with hands and tweezers. There were about 2-3 leaves left.</li>
	<li>Cut the tissue from the SAM/young panicle to the base with a single-edged razor using a sliding motion to avoid crushing the cells (Figure 1A-C). If the position of the SAM/young panicle is not visible, cut it longer.</li>
	<li>Since the cross-section of the rice shoot has&#160;an oval shape (Figure 1D), shave off one side of the oval thinly in the direction of its long axis with a double-edged razor (Figure 1E-F). 
	NOTE: This step made it easier for the fixative solution to penetrate the sample. A horizontal cutting surface makes the sample easier to stick to a vibrating micro-slicer (see Table of Materials) tray.</li>
	<li>Confirm the position of the SAM/young panicle by the appearance of a whitish color in the sample (Figure 1G). Trim off excess tissue. 
	NOTE: The length of the sample should be adjusted to the maximum length that can be trimmed using a vibrating micro-slicer. If the sample is too long, divide it into several pieces.</li>
</ol>
4. Fixation of the samples
<ol>
	<li>Pipette 1 mL of the fixative solution (prepared in step 1.) to a 1.5 mL microcentrifuge tube and immediately put in the samples. 
	NOTE: Ensure that the amount of sample does not exceed 20% of the volume of the fixative solution.</li>
	<li>Cut a piece of paraffin film into 2.5 cm2. Shape the paraffin film into balls and place them on top of the samples to prevent them from floating out of the fixative solution.</li>
	<li>Place the tube containing the sample in a desiccator. Then, close the lid of the desiccator and start the vacuum pump to depressurize the inside of the desiccator until &#8722;0.095 MPa slowly.</li>
	<li>After closing the desiccator at &#8722;0.095 MPa, turn off the vacuum pump and allow it to stand for 30 min at room temperature. 
	NOTE: The vacuum level was such that bubbles appeared gradually in the samples.</li>
	<li>Open the desiccator slightly and slowly return it to atmospheric pressure. Reduce the pressure of the desiccator to &#8722;0.095 MPa, turn off the vacuum pump, and allow the mixture to stand for 30 min at room temperature.</li>
	<li>Open the desiccator slightly and slowly return it to atmospheric pressure. If the sample is correctly fixed, it sinks into the fixative solution. If it did not sink, reduce the pressure again.</li>
	<li>Remove the paraffin film, close the lid, and keep the tubes overnight at 4 &#176;C. 
	&#8203;NOTE: Samples were fixed in fixative solution for at least 2 h. It can be stored for ~1 week.</li>
</ol>
5. Trimming the fixed sample
<ol>
	<li>Remove the excess fixative solution from the sample using lint-free wipes. 
	NOTE: Excess fixative solution prevents the sample from sticking properly onto the tray.</li>
	<li>Fix the sample on a vibrating micro-slicer tray with instant glue. Place it on a tray with the flat side down, which was shaved off during sampling. 
	NOTE: Due to the structure of the rice shoot, it must be trimmed from the base toward the SAM/young panicle.</li>
	<li>Set the trimming conditions according to the fixed sample. 
	NOTE: In this study, trimming was set to THICK, 130 &#181;m; WIDE, 15 mm; FREQUENCY, 15%; and CUTTING SPEED, 32 mm.</li>
	<li>Adjust the sample position with the RVS or FWD button and the UP or DOWN button. Fill the tray with deionized water until all the samples are immersed. After filling the tray, press the START button. Place the trimmed samples on a glass slide with a drop of 1x PBS. 
	NOTE: Shift the position of the sample to the other side after each trimming since the hard sample wears out the razor blade.</li>
	<li>After checking the sample containing the target site under a stereomicroscope, transfer the trimmed sample to a multiwell plate with 1 mL of 1x PBS. 
	&#8203;NOTE: Choose the number of wells according to the size of the sample. In this study, a 12-multiwell plate was used.</li>
</ol>
6. Treatment with the clearing solution
<ol>
	<li>Remove the 1x PBS from the multiwell plate and add fresh 1x PBS. Let it stand for 1 min.</li>
	<li>Remove 1x PBS and add the CS. 
	NOTE: The amount of CS must be five times the sample volume.</li>
	<li>Place the multiwell plate containing the sample in a desiccator. Then, close the lid of the desiccator and start the vacuum pump to depressurize the inside of the desiccator until &#8722;0.09&#160;MPa slowly.</li>
	<li>After closing the desiccator at &#8722;0.09 MPa, turn off the vacuum pump and let it stand for 1 h at room temperature.</li>
	<li>Open the desiccator slightly and slowly return it to atmospheric pressure.</li>
	<li>Pour deionized water into the gap between the wells to prevent the evaporation of the CS. Store the multiwell plates at room temperature in the dark for clearing. 
	NOTE: Gently shake the multiwell plate every 1-2 days to diffuse the chlorophyll and other components.</li>
	<li>When the CS turns green, replace it with fresh solution.</li>
</ol>
7. Cell wall staining with chemical dye
<ol>
	<li>Pipet the calcofluor white solution (1 mL, final concentration: 1 mg/mL in the clearing solution, see Table of Materials) into a multiwell plate. Place the samples in the dye solution and incubate for 1 h. 
	NOTE: The volume of the dye must not exceed 10% of the volume of the CS.</li>
	<li>Wash the stained samples in another multiwell plate with 1 mL of the CS for at least 1 h.</li>
</ol>
8. Observation with a confocal laser microscope
<ol>
	<li>Place a drop of CS onto a microscope slide and transfer the treated (with CS) samples onto the slide. 
	NOTE: As the treated samples are soft, they must be carefully handled with tweezers.</li>
	<li>Cover the sample with a glass coverslip to prevent the evaporation of the CS. 
	NOTE: The CS precipitates easily.</li>
	<li>Observe the treated samples under a confocal laser microscope. 
	NOTE: After observation, the treated samples can be returned to the CS for further observations later.</li>
</ol>

<ol>
	<li>Kurihara, D., Mizuta, Y., Sato, Y., Higashiyama, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=ClearSee:+A+rapid+optical+clearing+reagent+for+whole-plant+fluorescence+imaging.">ClearSee: A rapid optical clearing reagent for whole-plant fluorescence imaging.</a> Development. 142 (23), 4168-4179 (2015).</li><li>Hasegawa, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Three-dimensional+imaging+of+plant+organs+using+a+simple+and+rapid+transparency+technique.">Three-dimensional imaging of plant organs using a simple and rapid transparency technique.</a> Plant and Cell Physiology. 57 (3), 462-472 (2016).</li><li>Musielak, T. J., Slane, D., Liebig, C., Bayer, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+versatile+optical+clearing+protocol+for+deep+tissue+imaging+of+fluorescent+proteins+in+Arabidopsis+thaliana.">A versatile optical clearing protocol for deep tissue imaging of fluorescent proteins in Arabidopsis thaliana.</a> PLoS One. 11 (8), 0161107 (2016).</li><li>Pandey, K. B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Plant+roots+sense+soil+compaction+through+restricted+ethylene+diffusion.">Plant roots sense soil compaction through restricted ethylene diffusion.</a> Science. 371 (6526), 276-280 (2021).</li><li>Ejaza, M., Bencivenga, S., Tavaresa, R., Busha, M., Sablowski, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=ARABIDOPSIS+THALIANA+HOMEOBOX+GENE+1+controls+plant+architecture+by+locally+restricting+environmental+responses.">ARABIDOPSIS THALIANA HOMEOBOX GENE 1 controls plant architecture by locally restricting environmental responses.</a> Proceedings of the National Academy of Sciences of the United States of America. 118 (17), (2021).</li><li>Smetana, O., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High+levels+of+auxin+signalling+define+the+stem-cell+organizer+of+the+vascular+cambium.">High levels of auxin signalling define the stem-cell organizer of the vascular cambium.</a> Nature. 565 (7740), 485-489 (2019).</li><li>Chu, T. T. H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sub-cellular+markers+highlight+intracellular+dynamics+of+membrane+proteins+in+response+to+abiotic+treatments+in+rice.">Sub-cellular markers highlight intracellular dynamics of membrane proteins in response to abiotic treatments in rice.</a> Rice. 11 (1), 23 (2018).</li><li>Nagaki, K., Yamaji, N., Murata, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=ePro-ClearSee:+A+simple+immunohistochemical+method+that+does+not+require+sectioning+of+plant+samples.">ePro-ClearSee: A simple immunohistochemical method that does not require sectioning of plant samples.</a> Scientific Reports. 7, 42203 (2017).</li><li>Sato, M., Akashi, H., Sakamoto, Y., Matsunaga, S., Tsuji, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Whole-tissue+three-dimensional+imaging+of+rice+at+single-cell+resolution.">Whole-tissue three-dimensional imaging of rice at single-cell resolution.</a> International Journal of Molecular Sciences. 23 (1), 40 (2022).</li><li>Matsuo, T., Hoshikawa, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Science+of+the+Rice+Plant:+Morphology.">Science of the Rice Plant: Morphology.</a> Food and Agriculture Policy Research Center. , (1993).</li><li>Kobayashi, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inflorescence+meristem+identity+in+rice+is+specified+by+overlapping+functions+of+three+AP1/FUL-Like+MADS+box+genes+and+PAP2,+a+SEPALLATA+MADS+box+gene.">Inflorescence meristem identity in rice is specified by overlapping functions of three AP1/FUL-Like MADS box genes and PAP2, a SEPALLATA MADS box gene.</a> Plant Cell. 24 (5), 1848-1859 (2012).</li><li>Tamaki, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=FT-like+proteins+induce+transposon+silencing+in+the+shoot+apex+during+floral+induction+in+rice.">FT-like proteins induce transposon silencing in the shoot apex during floral induction in rice.</a> Proceedings of the National Academy of Sciences of the United States of America. 112 (8), 901-910 (2015).</li><li>Kodama, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Time+gating+of+chloroplast+autofluorescence+allows+clearer+fluorescence+imaging+In+Planta.">Time gating of chloroplast autofluorescence allows clearer fluorescence imaging In Planta.</a> PLoS One. 11 (3), 0152484 (2016).</li><li>Sakamoto, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Improved+clearing+method+contributes+to+deep+imaging+of+plant+organs.">Improved clearing method contributes to deep imaging of plant organs.</a> Communications Biology. 5 (1), 12 (2022).</li><li>Kurihara, D., Mizuta, Y., Nagahara, S., Higashiyama, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=ClearSeeAlpha:+Advanced+optical+clearing+for+whole-plant+imaging.">ClearSeeAlpha: Advanced optical clearing for whole-plant imaging.</a> Plant and Cell Physiology. 62 (8), 1302-1310 (2021).</li></ol>

The authors have no conflicts of interest to declare.

Critical steps of the protocol 
The critical steps in this protocol are fixation and trimming. Rice shoots have hard, thick, or layered tissues that limit penetration of the fixative solution. To improve the permeability of the fixative solution, one side of the tissue was thinly shaved at sampling, as shown in Figure 1E-F.&#160;In addition, the vacuum treatments were repeated twice using higher pressure. Furthermore, the samples were fixed overnight at 4 &#176;C instead of the usual 2 h fixation at 4 &#176;C.
The key point in the trimming step is to determine the thickness of the tissues to be prepared to observe the fluorescent proteins while preserving their internal structure following a short period of CS treatment. As shown in Figure 2C, the 1 mm thick samples, hand-trimmed as thin as possible, became transparent in only a limited number of tissues even after 3 months of CS treatment. Therefore, the trimming step is essential for deep fluorescence observation of adult rice shoots. In this study, the samples were trimmed to a thickness of 130 &#181;m, as shown in Figure 2D. The 130 &#181;m thickness allowed for clearing the leaves after 1 week of CS treatment and the whole sample after 2 weeks. Adult rice shoots at the 9-10 LS were used in this study. Thick but softer tissues from younger rice shoots may be cleared faster with the CS treatment. The thickness of the samples and the duration of the CS treatment should be adjusted according to the tissue type, condition, and thickness of the 3D structure to be observed.
Modifications and troubleshooting methods 
The CS precipitated easily at low temperatures. The precipitated CS cannot preserve the fluorescent proteins; hence, care must be taken when storing the samples at the proper temperature. In addition, both the CS and fixative solution&#160;have no antiseptic effect; therefore, fluorescent proteins will be degraded if contaminated. Soil-grown rice is prone to fungal growth; hence, the sampling and handling of samples must be performed with care to avoid contamination.
Excess fluorescent dyes in the buffer may give off background fluorescence and interfere with microscopic observations. For example, a calcofluor white solution containing Evans blue dye was previously used. After staining for 1 h and washing for 1 h, the fluorescent proteins of OsMADS15-mOrange were observed using a 555 nm laser. However, fluorescent proteins could not be observed because of the background fluorescence derived from Evans blue dye. This background fluorescence was almost eliminated by washing the samples for 2 h. Moreover, the fluorescent proteins were clearer if the samples were left overnight. Therefore, a pure calcofluor white solution was used in this study. Background fluorescence derived from the fluorescent dye should be checked using different laser wavelengths before observations.
Limitations of the method 
As shown in Figure 3, deep fluorescent proteins were observed in the samples that were 130 &#181;m thick after 2 weeks of CS treatment. This is consistent with the results shown in Figure 2D, where the 130 &#181;m thick sample became transparent after 2 weeks of CS treatment. However, as shown in Figure 3A, auto-fluorescence of the cytoplasm was still noticeable in the nodes after 2 weeks and was only completely removed after 4 weeks of CS treatment. Nodes have a high cell density and, therefore, require a longer time to remove auto-fluorescent materials.
As shown in Figure 3C, deep fluorescent proteins were observed in the leaves without CS treatment, but the brightness was weaker than that in the nodes and internodes at the same depth of 20 &#181;m. After 1 week of CS treatment, the fluorescent proteins were brighter. Chlorophyll is abundant in leaves and absorbs 488 nm of excitation light. They also have orange/red auto-fluorescence, which can interfere with the observation of fluorescent proteins using a 555 nm laser. After 1 week of CS treatment, chlorophyll and other auto-fluorescent materials were removed, resulting in high signal-to-noise ratio images.
The depths that could be observed in tissues after 2 weeks and 4 weeks of CS treatment were not significantly different, although the fluorescent proteins appeared weaker after 4 weeks (Figure 3). Normally, the brightness of fluorescent proteins and auto-fluorescence weakens with time, resulting in a higher signal-to-noise ratio. Therefore, fluorescent proteins can be observed more clearly by adjusting the microscopic conditions and image processing. Based on these results, it was concluded that 2 weeks of CS treatment could facilitate the observation of deep fluorescent proteins, given our sample conditions. However, 4 weeks are needed to observe clearer images that completely exclude the auto-fluorescent materials.
Structures with strong autofluorescence, such as vascular bundles and multi-arm cells, cannot be cleared in the CS. To observe these structures without autofluorescence, it is necessary to use a time-gating method12 or to obtain images by spectroscopy of the fluorescence spectrum. A two-photon microscope may be more suitable for observing deeper tissues if thicker tissues are observed.
Significance of the method with respect to existing and alternative methods 
Generally, the internal structures of rice plants have been observed using either cryostat or vibratome sectioning. A cryostat is suitable for preparing thin sections, which allow easier observation, but the preparation of the samples and the operation of the equipment are time-consuming. Reconstructing the original 3D structure from thin sections is also difficult. The vibratome is relatively easy to operate and suitable for producing thick sections. However, thick sections of target tissues only allow observations of the cut surface and not deep tissues that light cannot reach. For these reasons, neither method is suitable for deep fluorescence observations.
This study addressed challenges in deep fluorescence observation in rice shoots, such as the limited tissue penetration of the CS and the poor object resolution under a confocal microscope, by combining existing methods. As shown in Figure 4, we observed fluorescent proteins (OsMADS15-mOrange) expressed in the deep tissues of adult rice shoots from the young panicle to the base. Figure 4D focuses on the floret and shows deep fluorescent proteins at 3 &#181;m intervals. Tissues over &#8722;130 &#181;m depth were observed after 2 weeks of CS treatment, but only the tissues within &#8722;27 &#181;m depth were observed (data not shown) in the floret at the same size and growth stage without CS treatment. The current improved protocol allowed observation not only of overexpression of genes but also natural gene expression in the deep tissues of adult rice shoots.
Importance and potential applications of the method in specific research areas 
This protocol, which optimizes the deep fluorescence observation of adult rice shoots, enables the efficient clearing of hard, thick, or layered tissues by trimming off unnecessary tissues and increasing the permeability of the CS. In addition, the thickness of the samples for analysis was optimized to allow continuous and structural deep fluorescence observation using a confocal laser microscope, which normally cannot resolve thick or opaque tissues.
It is difficult to compare rice samples at different growth stages because the fluorescent proteins degrade over time in the fixative and PBS solutions. However, the fluorescent proteins in the CS can be stored for more than 5 months1. The long shelf life of the CS is a major advantage for deep fluorescence observation in rice.
Recently, many clearing technologies have been developed, making it possible to observe deep tissues in 3D while preserving their internal structures. These technologies have continued to evolve, and new clearing solutions have been developed. A good example is iTOMEI14, which enables efficient chlorophyll removal and brighter fluorescence detection. Another example is ClearSeeAlpha15, which prevents the browning of tissues during clearing treatment and makes them appear transparent. Combining these clearing solutions with the present method may allow more efficient and effective clearing.
It is expected that the current method will help gain new insights through deep imaging of not only rice but also other plants.

Recently developed clearing technology has made it possible to observe the deep tissues of plants while preserving their internal structure1,2,3. In the dicot model plant Arabidopsis, many studies on fluorescent protein imaging have been conducted using clearing technology to eliminate refractive index mismatches and remove auto-fluorescent materials4,5,6. Although the use of clearing technology7,8 and 3D imaging at cellular resolution9 have been reported in rice (Oryza sativa L.), a monocot model plant and a globally important crop, these are limited to relatively thin and soft organs, such as roots, leaves, and shoot apical meristem (SAM), which are easy to observe.
The shoot is the main organ constituting the aboveground parts of vascular plants. In rice, shoots are composed of a series of vertically stacked &#34;phytomers,&#34; comprising axillary buds, leaves, and the stem10. At the tip of the shoot, the SAM is composed of undifferentiated stem cells in the center. Phytomers are formed by the differentiation of cells derived from the SAM. After the plants shift from the vegetative to the reproductive phase, rice stems elongate and the SAM differentiates into young panicles10. This developmental change is accompanied by fluctuations in the expression of various genes in the stems and SAM/young panicles. To understand the mechanisms underlying cell differentiation into various tissues, it is important to structurally observe the cell morphology and gene expression in internal shoot tissues. However, the deep imaging of stems (nodes and internodes) in the shoot presents a challenge because of the inefficiency of clearing solutions to penetrate the tissue. Stems immediately undergo a rapid volume increase from lateral growth after differentiation from the SAM. The hardening of the rice node tissues due to the thickening of the vascular bundles and the horizontal complex link of the nodal vascular anastomosis, in addition to the high repellency of rice shoots, all contribute to limiting the penetration of the CS in stems10.
This study aimed to observe changes in gene expression in rice shoot tissues using a structural deep fluorescence technique. This work optimizes a clearing protocol for rice to continuously observe gene expression from the SAM/young panicle to the base in a 3D structure, rather than on a flat surface, using a confocal laser microscope.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1.5 mL microcentrifuge tube</td>
			<td>BIO-BIK</td>
			<td>ST-0150F</td>
			<td></td>
		</tr>
		<tr>
			<td>12-multiwell plate</td>
			<td>Corning</td>
			<td>353043</td>
			<td></td>
		</tr>
		<tr>
			<td>50 mL conical tube</td>
			<td>Corning</td>
			<td>352070</td>
			<td></td>
		</tr>
		<tr>
			<td>Calcofluor white solution</td>
			<td>Sigma-Aldrich</td>
			<td>910090</td>
			<td></td>
		</tr>
		<tr>
			<td>ClearSee</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>031-25151</td>
			<td>This can be made or purchased.</td>
		</tr>
		<tr>
			<td>Confocal laser microscope</td>
			<td>Carl Zeiss</td>
			<td>LSM700</td>
			<td></td>
		</tr>
		<tr>
			<td>Desiccator</td>
			<td>SANPLATEC</td>
			<td></td>
			<td>Custom made of acrylic. 30 cm (L), 30 cm (W), 14.5 cm (H)</td>
		</tr>
		<tr>
			<td>Glass coverslip (18 &#215; 18 No.1)</td>
			<td>MATSUNAMI</td>
			<td>C018181</td>
			<td></td>
		</tr>
		<tr>
			<td>HEPES</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>342-01375</td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope slide (76 &#215; 26)</td>
			<td>MATSUNAMI</td>
			<td>S2441</td>
			<td></td>
		</tr>
		<tr>
			<td>Paraffin film</td>
			<td>Bemis</td>
			<td>PM-996</td>
			<td></td>
		</tr>
		<tr>
			<td>Paraformaldehyde</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>162-16065</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium deoxycholate</td>
			<td>Tokyo Chemical Industry</td>
			<td>C0316</td>
			<td></td>
		</tr>
		<tr>
			<td>Sucrose</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>190-00013</td>
			<td></td>
		</tr>
		<tr>
			<td>UBQpro::NLS-sGFP-nClover3-mNeonGreen (UBQpro::NGCN)</td>
			<td>provided by Dr. Kurihara</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Urea</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>211-01213</td>
			<td></td>
		</tr>
		<tr>
			<td>Vacuum pump</td>
			<td>AS One</td>
			<td>AS-01</td>
			<td></td>
		</tr>
		<tr>
			<td>Vibrating micro-slicer</td>
			<td>DOSAKA</td>
			<td>DTK-3000</td>
			<td></td>
		</tr>
		<tr>
			<td>Xylitol</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>248-00545</td>
			<td></td>
		</tr>
	</tbody>
</table>

deep fluorescence observation in rice shoots via clearing technology

The recently developed clearing technology that eliminates refractive index mismatches and diminishes auto-fluorescent material has made it possible to observe plant tissues in three dimensions (3D) while preserving their internal structures. In rice (Oryza sativa L.), a monocot model plant and a globally important crop, clearing technology has been reported in organs that are relatively easy to observe, such as the roots and leaves. Applications of clearing technology in shoot apical meristem (SAM) and stems have also been reported, but only to a limited degree because of the poor penetration of the clearing solution (CS) in these tissues. The limited efficiency of the clearing solutions in these tissues has been attributed to auto-fluorescence, thickening, and hardening of the tissues in the stem as the vascular bundles and epidermis develop and layering of the SAM with water-repellent leaves. The present protocol reports the optimization of a clearing approach for continuous and 3D observation of gene expression from the SAM/young panicle to the base of the shoots during development. Fixed tissue samples expressing a fluorescent protein reporter were trimmed into sections using a vibrating micro-slicer. When an appropriate thickness was achieved, the CS was applied. By specifically targeting the central tissue, the penetration rate and uniformity of the CS increased, and the time required to make the tissue transparent decreased. Additionally, clearing of the trimmed sections enabled the observation of the internal structure of the whole shoot from a macro perspective. This method has potential applications in deep imaging of tissues of other plant species that are difficult to clear.

First, the extent to which the hard and thick tissues of adult rice plants could be made transparent by the clearing treatment was validated. Nip at the 9-10 LS, which is the panicle formation stage, and 12-16 mm long tissues cut out from the young panicle to the base of the shoot were used. These samples, including the young panicle, were fixed in the fixative solution and observed before and after 1-4 weeks of the clearing treatment (Figure 2). The untrimmed samples remained green and did not become transparent after 4 weeks or even after 3 months of treatment with the clearing solution (Figure 2A). In samples that were peeled off all leaves, the internodes&#160;turned white&#160;after 1 week of treatment with the CS, although the nodes remained green. This sample did not become transparent after 4 weeks (Figure 2B). After 3 months of the treatment with the CS, only the young panicle became transparent. The hand-trimmed samples changed to white, except for the outer leaves and vascular bundles, after 1 week of treatment with the CS. Some parts of the leaves, young panicle, and internodes became translucent but did not become transparent after 4 weeks (Figure 2C). After 3 months, only the young panicle and inner leaves became transparent. The samples that were trimmed to 130 &#181;m thickness with the vibrating micro-slicer became translucent after 1 week of treatment with the CS, with the leaves turning transparent. After 2 weeks, the sample was almost transparent and remained unchanged after 4 weeks (Figure 2D). After 3 months, the samples became completely transparent.
Next, the depth by which the clearing treatment allowed gene expression observations in the shoot of T65 at the 8 LS was validated. The UBQpro::NLS-sGFP-nClover3-mNeonGreen (UBQpro::NGCN, see Table of Materials) expressed shoots were used. Tissue samples were fixed in the fixative solution before trimming them to 130 &#181;m thickness using a vibrating micro-slicer. The samples were then observed under a confocal laser microscope (laser: 488 nm/13%, objective: 20x, pinhole: 0.93 AU, averaging: 16, detector gain: 800) at 10 &#181;m intervals in the z-axis direction every week from 0-4 weeks of treatment with the CS. The representative results are shown in Figure 3. All figures were adjusted with the same processing to compare the fluorescence intensity. In the node without the treatment, faint fluorescent signals were observed at a depth of &#8722;40 &#181;m (Figure 3A). The observable depth was &#8722;60 &#181;m after 1 week of the CS treatment and &#8722;90 &#181;m after 2 weeks, but auto-fluorescence of the cytoplasm was noticeable at both weeks at a depth of &#8722;20 &#181;m. The autofluorescence became somewhat weaker after 3 weeks and was no longer visible after 4 weeks. Fluorescent signals were observed at a depth of &#8722;80 &#181;m at 3 weeks and at a depth of &#8722;100 &#181;m at 4 weeks. In the internode, fluorescent signals were observed at a depth of &#8722;60 &#181;m without the CS treatment (Figure 3B). The observable depth was &#8722;90 &#181;m after 1 week to 3 weeks of the CS treatment and &#8722;100 &#181;m after 4 weeks, but auto-fluorescence in the cytoplasm was noticeable at a depth of &#8722;20 &#181;m after 1 week. Auto-fluorescence was no longer visible after 2 weeks. In the leaves, fluorescent signals were observed at a depth of &#8722;90 &#181;m without the CS treatment (Figure 3C). The fluorescent signals were observed deeper in the leaves than in the nodes and internodes. However, the fluorescent signals were weaker. The fluorescent signals became clear after 1 week of CS treatment and were observed at a depth of &#8722;120 &#181;m. After 2 weeks and 3 weeks, fluorescent signals were observed at a depth of &#8722;110 &#181;m and, after 4 weeks, at a depth of &#8722;120 &#181;m.
Finally, the expression of the transcription factor OsMADS1511 fused with mOrange12 was observed, which regulates the transition of SAM from the vegetative to the reproductive phase13. Tissue samples from Nip at the 10 LS with OsMADS15-mOrange were fixed, trimmed to 130 &#181;m thickness, and treated with the CS for 2 weeks. Figure 4 shows that the clearing solution could be used simultaneously to observe the fluorescent proteins (OsMADS15-mOrange) of natural gene expression and fluorescent dye staining (calcofluor white). The whole floret at depths from 0 to &#8722;130 &#181;m was observed, and the 3D image was reconstructed from 43 z-stack images at 3 &#181;m intervals (Figure 4E).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/64116/64116fig01.jpg" /> 
Figure 1: Sampling position and processing. (A) Nip seedling at the 8 LS under the short-day condition. (B) Enlarged view of the base. (C) A sample cut-out from the SAM/young panicle to the base. (D) An oval cross-section from C (inset). (E) Thinly shaving off one side of the shoot with a blade. (F) Thinly shaved surface. (G) Sample showing internode elongation. The whitish section indicated by the arrowheads is nodes. The upper side of the upper node has the young panicle. Scale bars: (A) 10 cm, (B-C,E-G) 1 cm, (D) 0.5 cm. <a href="https://www.jove.com/files/ftp_upload/64116/64116fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/64116/64116fig02.jpg" /> 
Figure 2: Tissue clearing depends on the sample thickness and CS treatment period. (A) Untrimmed samples with partial shoots including the young panicle. Maximum thickness: 4 mm. (B) All leaves peeled off from the samples to expose the young panicle. Maximum thickness: 2.5 mm. yp: young panicle, in: internode; arrowheads indicate node. (C) Samples that were hand-trimmed to 1 mm thickness. (D) Samples trimmed with the vibrating micro-slicer to 130 &#181;m thickness. Scale bar: 5 mm. <a href="https://www.jove.com/files/ftp_upload/64116/64116fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/64116/64116fig03.jpg" /> 
Figure 3: The depth of fluorescence observation depends on the tissue type and CS treatment period. Deep imaging of UBQpro::NGCN in the (A) node, (B) internode, and (C) leaf. &#34;Merge&#34; means the images were fused with the differential interference contrast (DIC) image and all z-stack images. Images in which no fluorescence was observed were marked as &#34;n.d.&#34; (not detected). Settings of the confocal laser microscopy are as follows: laser: 488 nm/13%, objective: 20x, pinhole: 0.93 AU, averaging: 16, detector gain: 800, interval: 10 &#181;m. Scale bars: 50 &#181;m. <a href="https://www.jove.com/files/ftp_upload/64116/64116fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/64116/64116fig04.jpg" /> 
Figure 4: Deep fluorescence observation of OsMADS15-mOrange. (A) The DIC image of Nip at the 10 LS. yp: young panicle, le: leaf, no: node, in: internode; arrowheads indicate florets. (B) Fluorescence image of OsMADS15-mOrange. Yellow dots indicate the fluorescent proteins of OsMADS15-mOrange at the nucleus. The cell wall was stained cyan with the calcofluor white solution. (C) Enlarged view of the young panicle. (D) Deep imaging of the floret. pa: palea, le: lemma, fm: floral meristem; asterisks indicate stamen primordia. The confocal laser microscope was set as follows: OsMADS15-mOrange; laser: 555 nm/13%, objective: 20x, pinhole: 0.96 AU, averaging: 16, detector gain: 800, interval: 3 &#181;m. Calcofluor white; laser: 405 nm/3%, objective: 20x, pinhole: 0.93 AU, averaging: 16, detector gain: 470, interval: 3 &#181;m. (E) The 3D image of the figure (D) constructed from the z-stack images. Scale bars: (A-B) 1 mm, (C) 500 &#181;m, (D) 40 &#181;m. <a href="https://www.jove.com/files/ftp_upload/64116/64116fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Deep Fluorescence Observation in Rice Shoots via Clearing Technology at JoVE.com

Deep Fluorescence Observation in Rice Shoots via Clearing Technology

The present protocol describes a clearing technique for rice shoots, which are difficult to prepare for internal structural observations owing to the hard, thick, or layered nature of the tissues. This method facilitates continuous and deep fluorescence observations, even in adult rice plants.

Deep Fluorescence Observation in Rice Shoots via Clearing Technology

The recently developed clearing technology that eliminates refractive index mismatches and diminishes auto-fluorescent material has made it possible to ...

deep-fluorescence-observation-in-rice-shoots-via-clearing-technology

Research

JoVE Journal

Biology

2.7K Views.  Nagoya University. The present protocol describes a clearing technique for rice shoots, which are difficult to prepare for internal structural observations owing to the hard, thick, or layered nature of the tissues. This method facilitates continuous and deep fluorescence observations, even in adult rice plants.

Video: Deep Fluorescence Observation in Rice Shoots via Clearing Technology

In vivo Imaging of Deep Cortical Layers using a Microprism

We present a protocol for in vivo imaging of cortical tissue using a deep-brain imaging probe in the shape of a microprism.  Microprisms are 1-mm in size and have a reflective coating on the hypotenuse to allow internal reflection of excitation and emission light.  The microprism probe simultaneously images multiple cortical layers with a perspective typically seen only in slice preparations.  Images are collected with a large field-of-view (~900 &mu;m).  In addition, we provide details on the non-survival surgical procedure and microscope setup.  Representative results include images of layer V pyramidal neurons from Thy-1 YFP-H mice showing their apical dendrites extending through the superficial cortical layer and extending into tufts.  Resolution was sufficient to image dendritic spines near the soma of layer V neurons.  A tail-vein injection of fluorescent dye reveals the intricate network of blood vessels in the cortex.  Line-scanning of red blood cells (RBCs) flowing through the capillaries reveals RBC velocity and flux rates can be obtained. This novel microprism probe is an elegant, yet powerful new method of visualizing deep cellular structures and cortical function in vivo.

In vivo Imaging of Deep Cortical Layers using a Microprism

Right-angle microprisms inserted into the mouse neocortex allows for deep imaging of multiple cortical layers with a viewpoint typically found in slice. One-millimeter microprisms offer a wide field-of-view (~900 &mu;m) and spatial resolutions sufficient to resolve dendritic spines. We demonstrate layer V neuronal imaging and neocortical vascular imaging using microprisms.

We present a protocol for in vivo imaging of cortical tissue using a deep-brain imaging probe in the shape of a microprism.  Microprisms are 1-mm in size ...

Measuring Diffusion Coefficients via Two-photon Fluorescence Recovery After Photobleaching

Multi-fluorescence recovery after photobleaching is a microscopy technique used to measure the diffusion coefficient (or analogous transport parameters) of macromolecules, and can be applied to both in vitro and in vivo biological systems. Multi-fluorescence recovery after photobleaching is performed by photobleaching a region of interest within a fluorescent sample using an intense laser flash, then attenuating the beam and monitoring the fluorescence as still-fluorescent molecules from outside the region of interest diffuse in to replace the photobleached molecules. We will begin our demonstration by aligning the laser beam through the Pockels Cell (laser modulator) and along the optical path through the laser scan box and objective lens to the sample. For simplicity, we will use a sample of aqueous fluorescent dye. We will then determine the proper experimental parameters for our sample including, monitor and bleaching powers, bleach duration, bin widths (for photon counting), and fluorescence recovery time. Next, we will describe the procedure for taking recovery curves, a process that can be largely automated via LabVIEW (National Instruments, Austin, TX) for enhanced throughput. Finally, the diffusion coefficient is determined by fitting the recovery data to the appropriate mathematical model using a least-squares fitting algorithm, readily programmable using software such as MATLAB (The Mathworks, Natick, MA).

In this article we will describe the procedure for measuring diffusion coefficients using multi-photon fluorescence recovery after photobleaching. We will begin by aligning the laser along the optical path to the sample and determining the proper experimental parameters, then continue generating and finally fitting fluorescence recovery curves.

Multi-fluorescence recovery after photobleaching is a microscopy technique used to measure the diffusion coefficient (or analogous transport parameters) ...

Time-lapse Imaging of Mitosis After siRNA Transfection

Changes in cellular organization and chromosome dynamics that occur during mitosis are tightly coordinated to ensure accurate inheritance of genomic and cellular content. Hallmark events of mitosis, such as chromosome movement, can be readily tracked on an individual cell basis using time-lapse fluorescence microscopy of mammalian cell lines expressing specific GFP-tagged proteins. In combination with RNAi-based depletion, this can be a powerful method for pinpointing the stage(s) of mitosis where defects occur after levels of a particular protein have been lowered. In this protocol, we present a basic method for assessing the effect of depleting a potential mitotic regulatory protein on the timing of mitosis. Cells are transfected with siRNA, placed in a stage-top incubation chamber, and imaged using an automated fluorescence microscope. We describe how to use software to set up a time-lapse experiment, how to process the image sequences to make either still-image montages or movies, and how to quantify and analyze the timing of mitotic stages using a cell-line expressing mCherry-tagged histone H2B. Finally, we discuss important considerations for designing a time-lapse experiment. This strategy is complementary to other approaches and offers the advantages of 1) sensitivity to changes in kinetics that might not be observed when looking at cells as a population and 2) analysis of mitosis without the need to synchronize the cell cycle using drug treatments. The visual information from such imaging experiments not only allows the sub-stages of mitosis to be assessed, but can also provide unexpected insight that would not be apparent from cell cycle analysis by FACS.

Here we describe a basic protocol to image and quantify the mitotic timing of live mammalian tissue culture cells after siRNA transfection.

Changes in cellular organization and chromosome dynamics that occur during mitosis are tightly coordinated to ensure accurate inheritance of genomic and ...

Basic Caenorhabditis elegans Methods: Synchronization and Observation

Research into the molecular and developmental biology of the nematode Caenorhabditis elegans was begun in the early seventies by Sydney Brenner and it has since been used extensively as a model organism 1. C. elegans possesses key attributes such as simplicity, transparency and short life cycle that have made it a suitable experimental system for fundamental biological studies for many years 2. Discoveries in this nematode have broad implications because many cellular and molecular processes that control animal development are evolutionary conserved 3.
C. elegans life cycle goes through an embryonic stage and four larval stages before animals reach adulthood. Development can take 2 to 4 days depending on the temperature. In each of the stages several characteristic traits can be observed. The knowledge of its complete cell lineage 4,5 together with the deep annotation of its genome turn this nematode into a great model in fields as diverse as the neurobiology 6, aging 7,8, stem cell biology 9 and germ line biology 10. 
An additional feature that makes C. elegans an attractive model to work with is the possibility of obtaining populations of worms synchronized at a specific stage through a relatively easy protocol. The ease of maintaining and propagating this nematode added to the possibility of synchronization provide a powerful tool to obtain large amounts of worms, which can be used for a wide variety of small or high-throughput experiments such as RNAi screens, microarrays, massive sequencing, immunoblot or in situ hybridization, among others. 
Because of its transparency, C. elegans structures can be distinguished under the microscope using Differential Interference Contrast microscopy, also known as Nomarski microscopy. The use of a fluorescent DNA binder, DAPI (4',6-diamidino-2-phenylindole), for instance, can lead to the specific identification and localization of individual cells, as well as subcellular structures/defects associated to them.

Basic Caenorhabditis elegans Methods: Synchronization and Observation

The easiness of maintaining and propagating the nematode C. elegans make it a nice model organism to work with. The possibility of synchronizing worms allows the work with a significant amount of subjects at the same developmental stage, what facilitates the study of one particular process in many animals.

Research into the molecular and developmental biology of the nematode Caenorhabditis elegans was begun in the early seventies by Sydney Brenner and it has ...

Internalization and Observation of Fluorescent Biomolecules in Living Microorganisms via Electroporation

The ability to study biomolecules in vivo is crucial for understanding their function in a biological context. One powerful approach involves fusing molecules of interest to fluorescent proteins such as GFP to study their expression, localization and function. However, GFP and its derivatives are significantly larger and less photostable than organic fluorophores generally used for in vitro experiments, and this can limit the scope of investigation. 
We recently introduced a straightforward, versatile and high-throughput method based on electroporation, allowing the internalization of biomolecules labeled with organic fluorophores into living microorganisms. Here we describe how to use electroporation to internalize labeled DNA fragments or proteins into Escherichia coli and Saccharomyces cerevisi&#230;, how to quantify the number of internalized molecules using fluorescence microscopy, and how to quantify the viability of electroporated cells. Data can be acquired at the single-cell or single-molecule level using fluorescence or FRET. The possibility of internalizing non-labeled molecules that trigger a physiological observable response in vivo is also presented. Finally, strategies of optimization of the protocol for specific biological systems are discussed.

Studies of biomolecules in vivo are crucial for understanding molecular function in a biological context. Here we describe a novel method allowing the internalization of fluorescent biomolecules, such as DNA or proteins, into living microorganisms. Analysis of in vivo data recorded by fluorescence microscopy is also presented and discussed.

The ability to study biomolecules in vivo is crucial for understanding their function in a biological context. One powerful approach involves fusing ...

Development of a Quantitative Recombinase Polymerase Amplification Assay with an Internal Positive Control

It was recently demonstrated that recombinase polymerase amplification (RPA), an isothermal amplification platform for pathogen detection, may be used to quantify DNA sample concentration using a standard curve. In this manuscript, a detailed protocol for developing and implementing a real-time quantitative recombinase polymerase amplification assay (qRPA assay) is provided. Using HIV-1 DNA quantification as an example, the assembly of real-time RPA reactions, the design of an internal positive control (IPC) sequence, and co-amplification of the IPC and target of interest are all described. Instructions and data processing scripts for the construction of a standard curve using data from multiple experiments are provided, which may be used to predict the concentration of unknown samples or assess the performance of the assay. Finally, an alternative method for collecting real-time fluorescence data with a microscope and a stage heater as a step towards developing a point-of-care qRPA assay is described. The protocol and scripts provided may be used for the development of a qRPA assay for any DNA target of interest.

Provided is a protocol for developing a real-time recombinase polymerase amplification assay to quantify initial concentration of DNA samples using either a thermal cycler or a microscope and stage heater. Also described is the development of an internal positive control. Scripts are provided for processing raw real-time fluorescence data.

It was recently demonstrated that recombinase polymerase amplification (RPA), an isothermal amplification platform for pathogen detection, may be used to ...

Observation and Quantification of Telomere and Repetitive Sequences Using Fluorescence In Situ Hybridization (FISH) with PNA Probes in Caenorhabditis elegans

Telomere is a ribonucleoprotein structure that protects chromosomal ends from aberrant fusion and degradation. Telomere length is maintained by telomerase or an alternative pathway, known as alternative lengthening of telomeres (ALT)1. Recently, C. elegans has emerged as a multicellular model organism for the study of telomere and ALT2. Visualization of repetitive sequences in the genome is critical in understanding the biology of telomeres. While telomere length can be measured by telomere restriction fragment assay or quantitative PCR, these methods only provide the averaged telomere length. On the contrary, fluorescence in situ hybridization (FISH) can provide the information of the individual telomeres in cells. Here, we provide protocols and representative results of the method to determine telomere length of C. elegans by fluorescent in situ hybridization. This method provides a simple, but powerful, in situ procedure that does not cause noticeable damage to morphology. By using fluorescently labeled peptide nucleic acid (PNA) and digoxigenin-dUTP-labeled probe, we were able to visualize two different repetitive sequences: telomere repeats and template of ALT (TALT) in C. elegans embryos and gonads.

Observation and Quantification of Telomere and Repetitive Sequences Using Fluorescence In Situ Hybridization FISH with PNA Probes in Caenorhabditis elegans

We report a concise procedure of fluorescence in situ hybridization (FISH) in the gonad and embryos of Caenorhabditis elegans for observing and quantifying repetitive sequences. We successfully observed and quantified two different repetitive sequences, telomere repeats and template of alternative lengthening of telomeres (TALT).

Telomere is a ribonucleoprotein structure that protects chromosomal ends from aberrant fusion and degradation. Telomere length is maintained by telomerase ...

Observation and Quantification of Mating Behavior in the Pinewood Nematode, Bursaphelenchus xylophilus

A method for observing and quantifying the mating behavior of the pinewood nematode, Bursaphelenchus xylophilus, was established under a stereomicroscope. To improve the mating efficiency of B. Xylophilus and to increase the chances of mating observation, virgin adults were cultured and used for the investigation. Eggs were obtained by keeping the nematodes in water and allowing the females to lay eggs for 10 min. The second-stage juveniles (J2) were synchronized by incubating the eggs for 24 h at 25 &#176;C in the dark, and the early J4 were obtained by culturing the J2 with grey mold, Botrytis cinerea, for another 52 h. At this time point, most J4 nematodes could be clearly distinguished as being male or female using their genital morphology. The male and female J4 were collected and cultured separately in two different Petri dishes for 24 h to get virgin adult nematodes. A virgin male and a virgin female were paired in a drop of water in the well of a concave slide. The mating behavior was filmed with a video recorder under a stereomicroscope. The whole period of the mating process was 82.8 &#177;3.91 min (mean &#177;SE) and could be divided into 4 different phases: searching, contacting, copulating, and lingering. The mean minutes of duration were 21.8 &#177; 2.0, 28.0 &#177; 1.9, 25.8 &#177; 0.7 and 7.2 &#177; 0.5, respectively. Eleven sub-behaviors were described: cruising, approaching, encountering, touching, hooping, locating, attaching, ejaculating, separating, quiescence, and roaming. Interestingly, obvious intra-sexual competition was observed when one female was grouped with 3 males or one male with 3 females. This protocol is useful and valuable, not only in investigating the mating behavior of B. xylophilus, but also in acting as a reference for ethological studies of other nematodes.

Observation and Quantification of Mating Behavior in the Pinewood Nematode, Bursaphelenchus xylophilus

A protocol for investigating the mating behavior of the pinewood nematode, Bursaphelenchus xylophilus, is presented. Behavioral features of B. xylophilus are described in the mating process.

A method for observing and quantifying the mating behavior of the pinewood nematode, Bursaphelenchus xylophilus, was established under a stereomicroscope. ...

Light Sheet Fluorescence Microscopy of Plant Roots Growing on the Surface of a Gel

One of the key questions in understanding plant development is how single cells behave in a larger context of the tissue. Therefore, it requires the observation of the whole organ with a high spatial- as well as temporal resolution over prolonged periods of time, which may cause photo-toxic effects. This protocol shows a plant sample preparation method for light-sheet microscopy, which is characterized by mounting the plant vertically on the surface of a gel. The plant is mounted in such a way that the roots are submerged in a liquid medium while the leaves remain in the air. In order to ensure photosynthetic activity of the plant, a custom-made lighting system illuminates the leaves. To keep the roots in darkness the water surface is covered with sheets of black plastic foil. This method allows long-term imaging of plant organ development in standardized conditions.

This protocol shows a plant sample preparation method for light-sheet microscopy. The setup is characterized by mounting the plant vertically on the surface of a gel and letting it grow in controlled bright conditions. This allows long-term observation of plant organ development in standardized conditions.

One of the key questions in understanding plant development is how single cells behave in a larger context of the tissue. Therefore, it requires the ...

Exploring Adipose Tissue Structure by Methylsalicylate Clearing and 3D Imaging

Obesity is a major worldwide public health issue that increases the risk to develop cardiovascular diseases, type-2 diabetes, and liver diseases. Obesity is characterized by an increase in adipose tissue (AT) mass due to adipocyte hyperplasia and/or hypertrophia, leading to profound remodeling of its three-dimensional structure. Indeed, the maximal capacity of AT to expand during obesity is pivotal to the development of obesity-associated pathologies. This AT expansion is an important homeostatic mechanism to enable adaptation to an excess of energy intake and to avoid deleterious lipid spillover to other metabolic organs, such as muscle and liver. Therefore, understanding the structural remodeling that leads to the failure of AT expansion is a fundamental question with high clinical applicability. In this article, we describe a simple and fast clearing method that is routinely used in our laboratory to explore the morphology of mouse and human white adipose tissue by fluorescent imaging. This optimized AT clearing method is easily performed in any standard laboratory equipped with a chemical hood, a temperature-controlled orbital shaker and a fluorescent microscope. Moreover, the chemical compounds used are readily available. Importantly, this method allows one to resolve the 3D AT structure by staining various markers to specifically visualize the adipocytes, the neuronal and vascular networks, and the innate and adaptive immune cells distribution.

Here, we describe a simple, inexpensive and fast clearing method to resolve the 3D structure of both mouse and human white adipose tissue using a combination of markers to visualize vasculature, nuclei, immune cells, neurons, and lipid-droplet coat proteins by fluorescent imaging.

Obesity is a major worldwide public health issue that increases the risk to develop cardiovascular diseases, type-2 diabetes, and liver diseases. Obesity ...

Deep Fluorescence Observation in Rice Shoots via Clearing Technology

Summary

Explore More Videos

Chapters in this video

In vivo Imaging of Deep Cortical Layers using a Microprism

Measuring Diffusion Coefficients via Two-photon Fluorescence Recovery After Photobleaching

Time-lapse Imaging of Mitosis After siRNA Transfection

Basic Caenorhabditis elegans Methods: Synchronization and Observation

Internalization and Observation of Fluorescent Biomolecules in Living Microorganisms via Electroporation

Development of a Quantitative Recombinase Polymerase Amplification Assay with an Internal Positive Control

Observation and Quantification of Telomere and Repetitive Sequences Using Fluorescence In Situ Hybridization (FISH) with PNA Probes in Caenorhabditis elegans

Observation and Quantification of Mating Behavior in the Pinewood Nematode, Bursaphelenchus xylophilus

Light Sheet Fluorescence Microscopy of Plant Roots Growing on the Surface of a Gel

Exploring Adipose Tissue Structure by Methylsalicylate Clearing and 3D Imaging