METHOD FOR OBSERVING BIOLOGICAL TISSUE SAMPLE

Abstract

A method for observing a biological tissue sample includes: forming a sample block; cutting up the sample block into a plurality of sample pieces and fixing each of the sample pieces to a sample piece placement member to form a plurality of observation samples; specifying an observation target area for performing precise observation; specifying and registering a coordinate of the observation target area on the sample piece for each of the observation samples; milling including irradiating the observation target area of the sample piece with an ion beam using gas as an ion source or a neutral particle beam with reference to the coordinate and exposing an observation surface inside the sample piece; and obtaining a SEM image of the observation surface with a scanning electron microscope.

Claims

1. An observation method of a biological tissue sample for observing a three-dimensional structure of the biological tissue sample, the method comprising: cutting out a sample from the biological tissue, staining the sample, and embedding the sample in a resin to form a sample block; cutting up the sample block into a plurality of sample pieces and fixing each of the sample pieces to a sample piece placement member to form a plurality of observation samples; observing each of the observation samples with an optical microscope and specifying an observation target area for performing precise observation; observing the observation target area with a scanning electron microscope and specifying and registering a coordinate of the observation target area on the sample piece for each of the observation samples; milling the sample piece comprising irradiating the observation target area of the sample piece with an ion beam using gas as an ion source or a neutral particle beam with reference to the coordinate and exposing an observation surface inside the sample piece; and obtaining a scanning electron microscope (SEM) image of the observation surface with the scanning electron microscope.

2. The method for observing a biological tissue sample according to claim 1, wherein the milling of the sample piece and the obtaining of the SEM image are alternately performed a plurality of times to obtain the SEM image in a thickness direction of the observation target area of the sample piece.

3. The method for observing a biological tissue sample according to claim 2, wherein the sample piece is left on the sample piece placement member after the milling of the sample piece and the obtaining of the SEM image are alternately performed the plurality of times.

4. The method for observing a biological tissue sample according to claim 1, wherein the sample piece has a thickness in a range of 100 nm or more and 300 nm or less.

5. The method for observing a biological tissue sample according to claim 1, wherein the cutting up of the sample block comprises cutting out the plurality of sample pieces continuous in a depth direction from the sample block embedded in the resin so that each of the sample pieces to have a thickness in a range of 100 nm or more and 300 nm or less by using a cutter.

6. The method for observing a biological tissue sample according to claim 1, wherein the gas used in the milling of the sample piece is argon or xenon.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0023] FIG. 1 is a flowchart showing a method for observing a biological tissue sample of the present disclosure in stages;

[0024] FIG. 2 is an external view showing a plurality of observation samples to which sample pieces are fixed; and

[0025] FIG. 3 is a schematic configuration diagram showing a scanning electron microscope.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0026] Hereinafter, the present illustrative embodiment is described in detail while referring to the drawings as appropriate. In the drawings used in the following description, for the sake of convenience, characteristic parts may be shown in an enlarged manner in order to make characteristics of the present disclosure easy to understand, and a dimensional ratio or the like of each constituent element may be different from actual one. Materials, dimensions, or the like exemplified in the following description are merely examples, the present disclosure is not limited thereto, and they can be appropriately changed and carried out within a range in which the effects of the present disclosure are taken.

[0027] FIG. 1 is a flowchart showing a method for observing a biological tissue sample of the present disclosure in stages.

[0028] Examples of the biological tissue applied to the present illustrative embodiment include tissue pieces and cell aggregations of various organs, mini organs produced from iPS cells, or the like. First, such a biological tissue is shaped (trimmed) into a cylindrical shape having a diameter of about several mm or a rectangular parallelepiped having a square of several mm by using a knife, for example, a single edged razor (trimming step S1). In a case where an original size is about 1 mm as that of a mini organ or the like, the trimming step Si can be omitted.

[0029] Next, the trimmed biological tissue is fixed with a formalin solution or the like, and then a staining treatment is performed (staining step S2). Various stains can be used for staining the biological tissue, for example, a toluidine blue solution can be used. Toluidine blue is a basic tar-based pigment and shows abnormal staining (metachromasia) on acidic mucus polysaccharides in a biological tissue, such as connective tissues (hyaluronic acid, chondroitin sulfate B), cartilage matrixes (mucoitin sulfate, chondroitin sulfate A and C), mast cells (heparin), and intraepithelial mucus.

[0030] Next, a dehydration treatment of the biological tissue after staining is performed (dehydration step S3). Dehydration of the biological tissue is performed by, for example, ethanol dehydration. At this time, whether or not embedding in a resin is successful is determined by whether or not the dehydration by ethanol having a concentration of 100 wt % is strictly performed, and thus the ethanol having a concentration of 100 wt % may be prepared and used by using anhydrous copper sulfate in advance.

[0031] Next, the biological tissue after dehydration is embedded in a resin to obtain a sample block (embedding step S4). In the embedding step S4, it is necessary to promote penetration of the embedding resin into the biological tissue in advance. For example, a hydrophobic resin such as an epoxy resin is not easily dissolved even in ethanol having a concentration of 100 wt %. In order to diffuse the resin for embedding to every corner of the biological tissue at an electron microscope level, it is necessary to substitute both ethanol and the resin with a solvent (substituting agent) having a high affinity.

[0032] In a case where an epoxy resin is used in the resin for embedding, propylene oxide is preferably used as such a substituting agent. For example, an epoxy resin is dissolved in propylene oxide to conform to the biological tissue. Then, propylene oxide is evaporated and then embedded in the epoxy resin. Thereafter, by drying at about 60° C. to 80° C., the sample block in which the biological tissue is embedded in a resin is obtained.

[0033] Next, the sample block is cut into a plurality of sample pieces, and each sample piece is fixed to a glass plate which is a sample piece placement member to form a plurality of observation samples (fixing step S5). A plastic slide or the like may be used instead of the glass plate. First, in order to cut the sample block embedded in a resin into a plurality of sample pieces, for example, the sample block embedded in a resin is attached to a microtome. In order to cut out the sample piece from the sample block, for example, a plurality of sample pieces continuous in a depth direction are cut out from the sample block so as to have a thickness in a range of, for example, 100 nm or more and 300 nm or less by using, for example, a glass knife.

[0034] The cut-out sample piece is placed on water droplets dropped on the glass plate (slide glass) to evaporate water. Accordingly, as shown in FIG. 2, a plurality of observation samples 13a to 13f in which continuous sample pieces 12a to 12f are fixed to a glass plate 11 are obtained.

[0035] Next, each of the observation samples 13a to 13f obtained in this manner is observed with an optical microscope, and an observation target area to be subjected to precise observation is specified (observation target area specifying step S6). In the observation target area specifying step S6, the observation samples 13a to 13f are sequentially set on a sample stage of the optical microscope, each of the sample pieces 12a to 12f is observed, and the observation target area in which stereoscopic observation in the depth direction is performed is determined.

[0036] Next, the observation target area for performing stereoscopic observation specified in the observation target area specifying step S6 is observed using a scanning electron microscope (SEM), and a coordinate of the observation target area on the sample pieces 12a to 12f is specified and registered for each of the observation samples 13a to 13f (coordinate specifying step S7).

[0037] In the coordinate specifying step S7, a SEM image of a surface of each of the observation samples 13a to 13f is obtained by the SEM, and based on the SEM image, the coordinate value (X axis, Y axis) of the observation target area on the sample pieces 12a to 12f, which is specified in the observation target area specifying step S6, is stored in a controller of the SEM.

[0038] Next, as shown in FIG. 3, the observation samples 13a to 13f (see FIG. 2) are sequentially set on the scanning electron microscope (SEM) 20 to obtain SEM images of observation surfaces on the sample pieces 12a to 12f (imaging step S8).

[0039] In observation of the biological tissue using the SEM 20, charging of the biological tissue can be reduced by using a low-vacuum scanning electron microscope (low-vacuum SEM). In the SEM 20, the sample pieces 12a to 12f are irradiated with an electron beam EB from an electron beam column 21, and reflected electrons (e.g., backscattered electrons) BE and secondary electrons SE generated from the sample pieces 12a to 12f are detected by a detection tube 22.

[0040] Accordingly, an image signal based on the reflected electrons and an image signal based on the secondary electrons are obtained. The SEM image may be a reflected electron SEM image using only an image signal based on the reflected electrons, or may be a secondary electron SEM image based on the secondary electrons. In addition, the SEM image may be based on an image signal obtained by adding the image signal based on the reflected electrons and the image signal based on the secondary electrons. The controller 23 of the SEM 20 stores image data of the obtained SEM images (first time) of the sample pieces 12a to 12f.

[0041] In addition, in the imaging step S8, an irradiation position of the electron beam EB irradiated from the electron beam column 21 on the sample pieces 12a to 12f is performed by reading the coordinate value (X axis, Y axis) of the observation target area on the sample pieces 12a to 12f, which is obtained in the coordinate specifying step S7. This makes it possible to accurately irradiate the observation target area for stereoscopic observation specified in the observation target area specifying step S6 with the electron beam EB to obtain a target SEM image.

[0042] Next, the observation target area of the sample pieces 12a to 12f is irradiated with a gas ion beam GB using gas as, for example, argon or xenon as an ion source from a gas ion column 24 to expose a new observation surface inside the sample pieces 12a to 12f (milling step S9).

[0043] In the milling step S9, in addition to using the gas ion beam GB, a rare gas element such as argon or a neutral particle beam such as oxygen can be used. By using the neutral particle beam, it is possible to reduce an influence of charge-up.

[0044] The gas ion beam column 24 can be irradiated at a low acceleration voltage of about 1 kV by ionizing gas such as argon gas. Since such a gas ion beam GB has a lower converging property than a converging ion beam (FIB) or the like used for sample processing, an etching rate on the sample pieces 12a to 12f is low. Therefore, precise shaving can be performed without significantly damaging the soft sample pieces 12a to 12f of the biological tissue or the like.

[0045] In addition, in the milling step S9, an irradiation position of the gas ion beam GB irradiated from the gas ion beam column 24 on the sample pieces 12a to 12f is obtained by reading the coordinate value (X axis, Y axis) of the observation target area on the sample pieces 12a to 12f, which is obtained in the coordinate specifying step S7. Accordingly, the observation target area for performing the stereoscopic observation specified in the observation target area specifying step S6 can be accurately irradiated with the gas ion beam GB to be shaved so as to reduce a thickness of the observation target area.

[0046] After the milling step S9, it is preferable to confirm a thickness of the sample pieces 12a to 12f as appropriate (thickness confirmation step S10). In the thickness confirmation step S10, the thickness can be measured by energy dispersive X-ray spectroscopy (EDS) or a change in intensity of the reflected electrons.

[0047] Next, a SEM image of a new observation surface obtained by shaving the sample pieces 12a to 12f exposed by the milling step S9 in the depth direction is obtained (imaging step S8). Image data of the SEM image (second time) of the new observation surface is stored.

[0048] As described above, the milling step S9 and the imaging step S8 are repeated until a predetermined depth of the sample pieces 12a to 12f set in advance or a predetermined number of imaging times set in advance. Accordingly, a predetermined number of times of SEM images (n times) continuous in the depth direction in the observation target area of the sample pieces 12a to 12f are obtained.

[0049] Thereafter, in the controller 23, image processing is performed on n times of SEM images of each of the sample pieces 12a to 12f as three-dimensional SEM images, and image processing is performed in which the three-dimensional SEM images are aligned in the depth direction separately toward the sample pieces 12a to 12f, whereby a three-dimensional SEM image in the depth direction in the observation target area of the entire sample block can be obtained.

[0050] It is also preferable to set the sample pieces 12a to 12f to remain in a predetermined thickness separately after the SEM images of all the imaging times are obtained. Hereby, the observation samples 13a to 13f having the remaining sample pieces 12a to 12f can be used or preserved as different observation materials, and re-verification or the like can be performed later.

[0051] As described above, according to the method for observing the biological tissue sample of the present illustrative embodiment, the sample block obtained by embedding the biological tissue in a resin is cut into a plurality of sample pieces, and a SEM image is obtained while shaving each of the sample pieces in the depth direction by milling, so that when the plurality of sample pieces were cut from the sample block, a thickness of each of the sample pieces can be cut out thicker (about 100 nm to 200 nm) than that in the related art. Accordingly, it is possible to easily cut out a sample piece which requires an advanced technology in the related art.

[0052] In addition, in order to shave the observation target area of each of the sample pieces in the depth direction, milling is performed by the gas ion beam, and thus it is possible to expose the observation surface set inside the depth direction without damaging cells or the like of a resin embedding object of the biological tissue which is a relatively soft sample. Then, by synthesizing the SEM images of all the observation surfaces as three-dimensional images, it is possible to easily obtain the three-dimensional SEM image of the observation target area present in the biological tissue of the sample.

[0053] In addition, by first observing the sample piece with an optical microscope to determine the observation target area and recording the observation target area coordinate with the SEM, it is possible to accurately shave the observation target area in the depth direction to obtain a SEM image in the milling step S9 and the imaging step S8.

[0054] Further, if the sample piece is set to remain in a predetermined thickness after the SEM images of all the number of times of imaging are obtained, it is possible to preserve the remaining sample pieces and to perform re-verification or the like later.

[0055] Although the illustrative embodiment of the present disclosure has been described above, the illustrative embodiment is presented as an example, and are not intended to limit the scope of the invention. The illustrative embodiment can be carried out in various other modes, and various omissions, substitutions, and changes can be performed without departing from the spirit of the invention. The illustrative embodiment and a modification thereof are included in the scope of the invention, and are similarly included in the invention described in the claims and a scope equivalent thereto.

[0056] As discussed above, the disclosure may provide at least the following illustrative, non-limiting aspects.

[0057] That is, the present disclosure may provide a method of observing a biological tissue sample of the present disclosure is an observation method of a biological tissue sample for observing a three-dimensional form of the biological tissue sample, including: a resin embedding step of forming a sample block; a fixing step of cutting up the sample block into a plurality of sample pieces and fixing each of the sample pieces to a sample piece placement member to form a plurality of observation samples; an observation target area specifying step of observing each of the observation samples with an optical microscope and specifying an observation target area for performing precise observation; a coordinate specifying step of observing the observation target area with a scanning electron microscope and specifying and registering a coordinate of the observation target area on the sample piece for each of the observation samples; a milling step of irradiating the observation target area of the sample piece with an ion beam using gas as an ion source or a neutral particle beam with reference to the coordinate and exposing an observation surface inside the sample piece; and an imaging step of obtaining a SEM image of the observation surface with the scanning electron microscope.