Cell assessment method, cell assessment device, and cell assessment program

The present invention relates to a cell assessment method, a cell assessment device, and a cell assessment program.

Human-derived stem cells such as ES cells and iPS cells have an ability to differentiate into many kinds of cells (pluripotency), and have attracted attention in that they enable large-scale pharmacometrics and medical applications using human cells which have been difficult, such as analysis of diseases, drug discovery screening, toxicity testing, and regenerative medicine. A differentiation efficiency in differentiation induction from these stem cells into desired cells is considered to be largely dependent on the state of the stem cells as starting materials. That is, the efficiency of differentiation induction is lowered, unless the stem cells maintain pluripotency and keep an undifferentiated state. Thus, quality control of the stem cells is extremely important for industrial application of the stem cells, and the stem cells need to be monitored and noninvasively assessed for their states.

In addition, since these stem cells form a confluent cell population (colony) by adhesion (contact) of approximately thousands to tens of thousands of stem cells, quality control is also usually conducted in increments of colonies.

For example, Patent Document 1 discloses a cell analytical method in a cell analyzer for analyzing a cell colony using an optical path length image of a cell colony composed of a large number of cells, which is characterized by comprising an obtention step of obtaining the optical path length image of the cell colony by an obtention means in the cell analyzer, an extraction step of extracting a circular shape corresponding to the cell nucleus of the cell in the obtained optical path length image by an extraction means in the cell analyzer, a comparison step of comparing an inner optical path length with an outer optical path length of the extracted circular shape by the comparison means of the cell analyzer, and an analysis step of analyzing the cell colony by an analysis means in the cell analyzer based on the compared results.

In addition, Non-Patent Document 1 describes that mean optical path lengths in cytoplasm regions in CHO cells, HeLa cells and osteoclast-like (OC) cells which were differentiated cells were smaller than those in their nuclear areas, on the contrary, a mean optical path length in cytoplasm region in each hiPS cell in the colony was larger than that in its nuclear area, and that a ratio (cytoplasm/nucleus) of optical path lengths can be a simple indicator for discriminating between the hiPS cells and other types of differentiated cells.

Patent Literature

Patent Document 1: Japanese Patent Application Laid-Open No. 2012-231709

Non Patent Literature

Non-Patent Document 1: Biomedical Optics Express, Vol. 3, issue 9, pp. 2175-2183 (2012).

Problems to be Solved by the Invention

According to Patent Document 1, an “optical path length” is a result of multiplying “refractive index” by “physical thickness” (optical path length =refractive index×physical thickness) and the refractive index of a cell nucleus (inside of the cell nucleus) is generally lower than the refractive index of cytoplasm (outside of the cell nucleus) (refractive index of the inside of the cell nucleus<refractive index of the outside of the cell nucleus).

Stem cells of good quality that form a colony have shapes such as shown in FIG. 12 with distances between adjacent stem cells being close and the cytoplasm being thick between cell nuclei so that the physical thicknesses at the inside and the outside of the cell nucleus are substantially equal (physical thickness of the inside of the cell nucleus≈physical thickness of the outside of the cell nucleus) and in regard to the optical path length, it is deemed that “optical path length of the inside of the cell nucleus<optical path length of the outside of the cell nucleus” holds.

On the other hand, with stem cells of poor quality that form a colony, the distances between adjacent stem cells are far and the cytoplasm between cell nuclei is thin so that physical thickness of the inside of the cell nucleus is much thicker than the physical thickness of the outside (physical thickness of the inside of the cell nucleus>>physical thickness of the outside of the cell nucleus) and in regard to the optical path length, it is deemed that “optical path length of the inside of the cell nucleus>optical path length of the outside of the cell nucleus” holds.

Thus in Patent Document 1, it is deemed that whether or not “optical path length of the inside of the cell nucleus<optical path length of the outside of the cell nucleus” holds depends on the physical thickness of the outside of the cell nucleus, and the physical thickness of the outside of the cell nucleus depends on the shape of the cell.

On the other hand, in order to maintain stem cells, it is essential to perform subculturing by dissociating a stem cell colony into small clumps and making these proliferate. Although in the process of subculturing, it is desirable to assess the quality of the dissociated small clump product obtained from the stem cell colony and then make these proliferate, the shapes of the stem cells forming the stem cell colony are not necessarily maintained in the process of dissociating the stem cell colony into small clumps because the adhesion (contact) of a stem cell with other cells is severed partially or completely. For example, FIG. 1 is an image acquired by observing, under a bright field microscope, a single ES cell that is a dissociated small clump product obtained from an ES cell colony (bright field image; a single ES cell region is provided with the symbol W), and in FIG. 1 , the cell nucleus of the single ES cell is biased in position and the thickness of the cytoplasm is also non-uniform.

It was thus considered that for a stem cell forming a small cell clump, “optical path length of the inside of the cell nucleus<optical path length of the outside of the cell nucleus” does not hold.

On the other hand, although it was known that with differentiated cells, the average optical path length of cytoplasmic regions is less than the average optical path length of nucleus regions and that with respective hiPS cells in a colony, the average optical path length of cytoplasmic regions is greater than the average optical path length of nucleus regions ( FIG. 13 ), it was predicted that when an hiPS cell colony is dissociated into small clumps, “optical path length of the inside of the cell nucleus<optical path length of the outside of the cell nucleus” will not hold.

However, the present inventors found that even for a stem cell forming a small cell clump, “optical path length of the inside of the cell nucleus<optical path length of the outside of the cell nucleus” holds regardless of shape and noticed that it is possible to assess whether or not a cell forming a small cell clump is a stem cell by comparing the optical path length of the inside of the cell nucleus region and the optical path length of the outside.

The present invention is based on this unexpected finding and an object thereof is to provide a cell assessment method, a cell assessment device, and a cell assessment program for assessing whether or not a cell forming a small cell clump is a stem cell.

Means for Solving the Problems

The present invention that achieves the above object is a cell assessment method characterized in including an acquisition step of acquiring an optical path length image of a small cell clump, an extraction step of extracting a cell nucleus region within the acquired optical path length image, a comparison step of comparing an optical path length of an inside and an optical path length of an outside of the extracted cell nucleus region, and an assessment step of assessing whether or not a cell is a stem cell based on the comparison results.

Also, the present invention is a cell assessment device characterized in including an acquisition means acquiring an optical path length image of a small cell clump, an extraction means extracting a cell nucleus region within the acquired optical path length image, a comparison means comparing an optical path length of an inside and an optical path length of an outside of the extracted cell nucleus region, and an assessment means assessing whether or not a cell is a stem cell based on the comparison results.

Further, the present invention is a program arranged to make a computer function as an acquisition means acquiring an optical path length image of a small cell clump, an extraction means extracting a cell nucleus region within the acquired optical path length image, a comparison means comparing an optical path length of an inside and an optical path length of an outside of the extracted cell nucleus region, and an assessment means assessing whether or not a cell is a stem cell based on the comparison results.

In the present invention, a “small cell clump” means a cell cluster that includes not more than 200 cells, and a “stem cell” means a cell having an ability to differentiate into cells of multiple lineages (pluripotency) and an ability to maintain the pluripotency even after undergoing cell division (replication competence).

Also, “optical path length” is synonymous with “phase difference” or “optical thickness” and is a result of multiplying “refractive index” by “physical thickness” (optical path length=refractive index×physical thickness). An “optical path length image” is an image from which an optical path length can be acquired.

For a stem cell forming a small cell clump, “optical path length of the inside of the cell nucleus region<optical path length of the outside of the cell nucleus region” holds regardless of shape and therefore, by the present invention, whether or not cells are stem cells can be assessed even with cells that form a small cell clump.

Also, if the small cell clump is a dissociated small clump product obtained from a colony of pluripotent stem cells, for example, iPS cells or ES cells, the dissociated small clump product may be selected and used, based on the assessment result, for example, as that suited for proliferation to a pluripotent stem cell colony or that suited for gene cloning.

Also, the small cell clump may be a single cell. By the cell assessment method of the present invention that further includes a second extraction step of extracting a single cell region within the acquired optical path length image, extraction of just the single cell region is made possible. The cell assessment method may be performed by the cell assessment device of the present invention that further includes a second extraction means extracting a single cell region within the acquired optical path length image.

According to the present invention, it can be assessed whether or not a cell forming a small cell clump is a stem cell.

FIG. 1 is a bright field image of a single ES cell.

FIG. 2 is a quantitative phase image of the single ES cell.

FIG. 3 is a three-dimensional plot image expressing optical path lengths of the single ES cell as brightness.

FIG. 4 is an image of a small ES cell clump that has been immunostained by an anti-nanog antibody.

FIG. 5 shows a graph of optical path lengths ( FIG. 5A ) and a graph of CN ratios ( FIG. 5B ) of ES cells that form the small ES cell clump.

FIG. 6 is an image of a small differentiated cell clump that has been immunostained by the anti-nanog antibody.

FIG. 7 shows a graph of optical path lengths ( FIG. 7A ) and a graph of CN ratios ( FIG. 7B ) of differentiated cells that form the small differentiated cell clump.

FIG. 8 is an arrangement diagram of a cytometer 1 .

FIG. 9 is a schematic diagram of the hardware arrangement of a cell assessment device D.

FIG. 10 is a schematic diagram of the functional arrangement of the cell assessment device D.

FIG. 11 is a flowchart of a cell assessment method.

FIG. 12 is a quantitative phase image of stem cells of a stem cell colony.

FIG. 13 shows bright field images (upper row of FIG. 13A ), quantitative phase images (lower row of FIG. 13A ), a graph of optical path lengths of cell nuclei and cytoplasm ( FIG. 13B ), and a graph of optical path length ratios (cytoplasm/nucleus) ( FIG. 13C ) of CHO cells, HeLa cells, OC cells, and hiPS cells.

The present invention is based on the unexpected finding that even for a stem cell forming a small cell clump “optical path length of the inside of the cell nucleus region<optical path length of the outside of the cell nucleus region” holds regardless of shape and therefore this finding shall be explained first.

FIG. 2 is an image (quantitative phase image) acquired by observing a single ES cell with a quantitative phase microscope (and is provided with the symbol W), and FIG. 3 is a three-dimensional plot image expressing optical path lengths of the single ES cell as brightness. Both horizontal axes (X and Y directions) of FIG. 3 express the number of picture elements (pixels) and the vertical axis (Z axis) expresses brightness. A greater numerical value along the vertical axis indicates a greater brightness and a smaller optical path length.

From FIG. 3 , it can be understood that “optical path length of the inside of the cell nucleus region<optical path length of the outside of the cell nucleus region” holds even for a single ES cell that does not have a shape like that of a stem cell of a stem cell colony.

Also, from FIG. 4 and FIG. 5 , it can be understood in a small ES cell clump, “optical path length of the inside of the cell nucleus region<optical path length of the outside of the cell nucleus region,” that is, “optical path length of the outside of the cell nucleus region/optical path length of the inside of the cell nucleus region” (CN ratio) is greater than 1 and from FIG. 6 and FIG. 7 , it can be understood that in a small differentiated cell clump induced from ES cells by retinoic acid (small differentiated cell clump), the CN ratio is less than 1.

FIG. 4 is an image of a small ES cell clump that has been immunostained by an anti-nanog antibody, which is an undifferentiated marker, and bright regions of the image correspond to ES cells that form the small ES cell clump. FIG. 5 shows a graph of optical path lengths ( FIG. 5A ) and a graph of CN ratios ( FIG. 5B ) of the cells that form the same small ES cell clump, and from FIG. 5 , it is calculated that with the ES cells forming the small ES cell clump, CN ratio=1.06±0.0642 (n=34; the value provided with±is the standard deviation). A comparison of FIG. 4 and FIG. 5 shows that the CN ratios of the cells forming the small ES cell clump are greater than 1.

On the other hand, FIG. 6 is an image of a small cell clump that has been induced from ES cells by retinoic acid and has been immunostained by the anti-nanog antibody, which is an undifferentiated cell marker, and from there being no bright regions in the image, it is confirmed that the small cell clump is a small differentiated cell clump. FIG. 7 shows a graph of optical path lengths ( FIG. 7A ) and a graph of CN ratios ( FIG. 7B ) of the cells that form the small differentiated cell clump, and from FIG. 7 , it is calculated that with the differentiated cells forming the small differentiated cell clump, CN ratio=0.973±0.122 (n=27; the value provided with±is the standard deviation). A comparison of FIG. 6 and FIG. 7 shows that the CN ratios of the differentiated cells forming the small differentiated cell clump are less than 1.

Preferred embodiments of a cell assessment method, cell assessment device, and cell assessment program of the present invention shall now be described in detail. In the description of the drawings, elements that are the same are provided with the same symbols and redundant description shall be omitted.

(Small Cell Clump)

A “small cell clump” means a cell cluster that includes not more than 200 cells. Although the number of cells may be 1 or may be 2 or more, it is 1 to 100, particularly 1 to 60, and above all 1 to 20. When the number of cells is 1, the small cell clump is a single cell. A small cell clump includes that which cannot proliferate under the presence of an apoptosis inhibitor (for example, the ROCK inhibitor).

The small cell clump may include a stem cell (small stem cell clump) and, in particular, may be constituted only of a stem cell. A single stem cell is a small cell clump, for which the number of stem cells is 1 and which does not include cells besides the stem cell. An example of a cell that is included in a small cell clump and is other than a stem cell is a differentiated cell.

A “stem cell” means a cell having an ability to differentiate into cells of multiple lineages (pluripotency) and an ability to maintain the pluripotency even after undergoing cell division (replication competence). As examples of a stem cell, pluripotent cells, such as an ES cell, iPS cell, mesenchymal stem cell, etc., can be cited, and the stem cell is not restricted to a human stem cell and may be a stem cell of a mouse, monkey, rabbit, dog, cat, etc.

The small cell clump may be a dissociated small clump product obtained from a stem cell colony. As a dissociated small clump product obtained from a stem cell colony, that obtained by dissociating a stem cell colony into small clumps by a physical or chemical means, for example, by pipetting or by treatment by an enzyme, such as trypsin, Accutase, etc., can be cited. With a stem cell, with which adhesion (contact) with other cells has been severed partially or completely in the process of dissociating a stem cell colony into small clumps, the shape of the cell when it formed the stem cell colony is ordinarily not maintained.

Dissociated small clump products obtained from a pluripotent stem cell colony include those capable of proliferating and forming a pluripotent stem cell colony again and those incapable of proliferating and forming a pluripotent stem cell colony again.

Although there is no restriction in regard to a method for acquiring a small cell clump, a method of making a stem cell colony into small cell clumps by dissociation into small clumps can be cited as a method for acquiring a small cell clump, and the dissociation into small clumps may be performed in the process of subculturing the stem cells. As mentioned above, means for dissociation into small clumps include physical and chemical means, for example, pipetting and enzymatic treatment using trypsin, Accutase, etc.

(Measurement Sample)

The small cell clump is then made into a measurement sample S. The measurement sample S is prepared, for example, by injecting a solution, containing the small cell clump, into a slide chamber. A small clump of pluripotent stem cells is ordinarily made to adhere to (contact) the slide chamber.

(Cytometer)

The arrangement of a cytometer 1 to be used shall now be described. FIG. 8 is an arrangement diagram of a cytometer 1 .

As shown in FIG. 8 , the cytometer 1 is mainly arranged from a quantitative phase microscope A and a cell assessment device D.

(Quantitative Phase Microscope)

The quantitative phase microscope A includes, at a light incidence side, a lens A 2 , facing an emission side end face B 1 of an optical fiber B that guides irradiation light H 0 (laser light) from an unillustrated light emitting portion, and a reflecting portion A 3 reflecting the irradiation light HO transmitted through the lens A 2 . On the other hand, an image pickup device C, such as a CCD camera, etc., that captures and obtains an image of an interference fringe (not illustrated; the same applies hereinafter) formed by an optical interference portion A 7 is provided at a light emission side of the quantitative phase microscope.

The quantitative phase microscope A includes a microscope main body A 1 provided with a sample stage A 4 that supports the measurement sample S, an objective lens A 5 , a reflecting portion A 6 , and the light interference portion A 7 .

The sample stage A 4 includes, for example, a light transmitting portion A 41 , which allows transmission of light, at a center, is substantially plate-shaped, and has a placement surface A 42 enabling placement of the measurement sample S on an upwardly facing surface. Arrangements are made so that by irradiating light from above in a state where the measurement sample S is placed on the placement surface A 42 , light (measured light H 1 ) transmitted through the measurement sample S is transmitted through the light transmitting portion A 41 and directed toward the objective lens A 5 . The light transmitting portion A 41 may, for example, be that which is formed from glass or other member capable of transmitting light or may simply be a hole. Based, for example, on an operation of an operation portion (not illustrated), the objective lens AS magnifies the incident measured light H 1 by a predetermined magnification in accordance with the operation and emits the light as parallel light. The reflecting portion A 6 is, for example, a total reflection type mirror and can totally reflect the measured light H 1 from the objective lens A 5 to introduce it to the light interference portion A 7 . The light interference portion A 7 includes a light splitting element A 71 , splitting the measured light H 1 into two lights H 1 a and H 1 b , a condenser lens A 72 , converting the measured light H 1 (H 1 a , H 1 b ) emitted from the light splitting element A 71 into convergent light H 2 (H 2 a , H 2 b ), a spatial filter A 73 disposed at a convergence position of the convergent light H 2 , and a combining lens A 75 combining an object light H 3 transmitted through the spatial filter A 73 and a reference light H 4 to form interference fringes. Here, the light splitting element A 71 is arranged using a diffraction grating. Further, the light splitting element A 71 may be a polarizing light splitting element that splits light into two lights that differ mutually in polarization direction. In this case, the light interference portion A 7 includes the light splitting element A 71 , splitting the measured light H 1 into two lights H 1 a and H 1 b that differ mutually in polarization direction, the condenser lens A 72 , performing conversion into convergent light H 2 (H 2 a , H 2 b ), the spatial filter A 73 disposed at the convergence position of the convergent light H 2 , a half-wave plate A 74 disposed at an emission side of the object light H 3 transmitted through the spatial filter A 73 , the reference light H 4 , and the spatial filter A 73 , and the combining lens A 75 combining the object light H 3 and the reference light H 4 , which have been aligned in polarization direction by the half-wave plate A 74 , to form interference fringes. Or, a polarizer may be disposed in place of the half-wave plate A 74 disposed at the emission side of the spatial filter A 73 to align the polarization directions of the object light H 3 and the reference light H 4 .

(Cell Assessment Device)

The arrangement of the cell assessment device D shall now be described. FIG. 9 is a schematic diagram of the hardware arrangement of the cell assessment device D, and FIG. 10 is a schematic diagram of the functional arrangement of the cell assessment device D.

As shown in FIG. 9 , the cell assessment device D is physically arranged as an ordinary computer that includes a CPU D 11 , main storage devices, such as a ROM D 12 and a RAM D 13 , etc., an input device D 14 , such as a keyboard and a mouse, etc., an output device D 15 , such as a display, etc., a communication module D 16 , such as a network card, etc., arranged to perform sending and receiving of data with another device, for example, the image pickup device C, etc., an auxiliary storage device D 17 , such as a hard disk, etc. The respective functions of the cell assessment device D to be described below are realized by making predetermined computer software be read into the hardware, such as the CPU D 11 , the ROM D 12 , the RAM D 13 , etc., to make the input device D 14 , the output device D 15 , and the communication module D 16 operate under the control of the CPU D 11 and perform reading and writing of data from and into the main storage devices D 12 and D 13 and the auxiliary storage device D 17 .

As shown in FIG. 10 , the cell assessment device D includes, as functional components, an acquisition means D 1 , an extraction means D 2 , a comparison means D 3 , an assessment means D 4 , and a display means D 5 .

The acquisition means D 1 acquires an image (quantitative phase image) from the image pickup device C. The extraction means D 2 extracts a cell nucleus region within the acquired quantitative phase image. If a single cell region is to be extracted from within the quantitative phase image, the cell assessment device D further includes a second extraction means (not illustrated) that extracts a single cell region within the acquired quantitative phase image. The comparison means D 3 compares an optical path length of an inside and an optical path length of an outside of the extracted cell nucleus region. The assessment means D 4 assesses whether or not a cell is a stem cell based on the comparison results. The display means D 5 displays the assessment result.

(Cell Assessment Program)

A cell assessment program makes a computer function as the above-mentioned acquisition means D 1 , the extraction means D 2 , the comparison means D 3 , the assessment means D 4 , and the display means D 5 . The computer is made to operate as the cell assessment device D by making the computer read the cell assessment program. The cell assessment program is presented, for example, by being stored in a recording medium. As examples of the recording medium, recording media, such as flexible disks, CDs, DVDs, etc., storage media, such as ROMs, etc., semiconductor memories, etc., can be cited.

(Cell Assessment Method)

A cell assessment method performed by the cell assessment device D shall now be described. FIG. 11 is a flowchart of the cell assessment method. By the cell assessment method performed by the cell assessment device D, the assessment of whether or not a cell forming a small cell clump is a stein cell can be made quantitatively and automatically with high precision. Although up until now, whether or not a cell is a stem cell was assessed subjectively by an assessor, it becomes possible to make assessments objectively regardless of the assessor. That is, ambiguous elements, such as the subjectivity and physical condition of an assessor and variation among assessors, can be eliminated and cell assessment based on fixed criteria that is not dependent on the skills of assessors can be performed.

[Acquisition Step S 1 ]

First, the acquisition means D 1 acquires the quantitative phase image of the small cell clump from the image pickup device C. Image processing, for example, magnification, reduction, brightness adjustment, or conversion of the quantitative phase image may be performed as necessary.

[Extraction Step S 2 ]

Next, the extraction means D 2 extracts a cell nucleus region within the acquired quantitative phase image. Although the extraction means is not restricted in particular, if the brightness of the quantitative phase image is proportional to optical path length, it is also possible to extract the cell nucleus region from the quantitative phase image. Also, a cell nucleus region may be extracted from an image acquired by observation of the same small cell clump by another microscope, for example, a bright field image of the same small cell clump and the corresponding cell nucleus region within the quantitative phase image may be extracted.

If the small cell clump is constituted of two or more cells and images of the two or more cells are included within the quantitative phase image, arrangements may be made to extract the cell nuclear regions of the two or more cells within the quantitative phase image.

If a single cell region is to be extracted from within the quantitative phase image, a second extraction step of extracting a single cell region within the acquired quantitative phase image is further included. The second extraction means calculates an area of an independent cell region present within the quantitative phase image and if the area is less than an area of a single cell region that has been set in advance, the cell region is assessed to be a single cell region and extracted, and oppositely if the area is greater than the area of the single cell region that has been set in advance, the cell region is assessed not to be a single cell region and prevented from being extracted.

Also, if the cytometer 1 includes an interference reflection microscope, just a region of a small cell clump adhered to (contacting) the slide chamber may be extracted.

[Comparison Step S 3 ]

Next, the comparison means D 3 compares the optical path length of the inside and the optical path length of the outside of the cell nucleus region extracted in the extraction step S 2 and extracts the result. The comparison means D 3 may extract the value of “optical path length of the outside of the cell nucleus region/optical path length of the inside of the cell nucleus region” (CN ratio) as the result.

If the small cell clump is constituted of two or more cells and the images of the two or more cells are included within the quantitative phase image, arrangements may be made to extract the comparison results for the two or more cells.

[Assessment Step S 4 ]

Next, the assessment means D 4 assesses whether or not the cell is a stem cell based on the comparison result extracted in the comparison step S 3 . The assessment means D 4 assesses the cell to be a stem cell if the comparison result of the comparison step S 3 is such that the optical path length of the outside of the cell nucleus region is greater than the optical path length of the inside, that is, if “optical path length of the inside of the cell nucleus<optical path length of the outside of the cell nucleus,” and assesses the cell not to be a stem cell if the optical path length of the outside of the cell nucleus region is less than the optical path length of the inside, that is, if “optical path length of the inside of the cell nucleus>optical path length of the outside of the cell nucleus.” If the comparison result is the CN ratio, it is assessed that the cell is a stem cell if the CN ratio is greater than 1 and assessed that the cell is not a stem cell if the CN ratio is less than 1.

Also, a degree of differentiation of the cell may be assessed based on the CN ratio. If the value is greater than 1, the degree of differentiation of the cell will also be low, and if the value is less than 1, the degree of differentiation of the cell will also be high.

If the small cell clump is constituted of two or more cells and the images of the two or more cells are included within the quantitative phase image, arrangements may be made to perform the assessment of whether or not a cell is a stem cell for the two or more cells and the proportion of stern cells within the small cell clump may be assessed.

[Display Step S 5 ]

Next, the display means D 5 displays the result of assessment in the assessment step S 4 . For example, whether or not the cell is a stem cell, the value of “optical path length of the outside of the cell nucleus region/optical path length of the inside of the cell nucleus region,” the degree of differentiation of the cell, etc., are displayed by the display means D 5 .

(After the End of Assessment)

After the end of assessment, the small cell clump may be discarded or may be used for another purpose.

Especially in a case where the small cell clump is a dissociated small clump product of a colony of pluripotent stem cells, for example, iPS cells or ES cells, the dissociated small clump product may be selected and used, based on the assessment result, for example, as that suited for proliferation to a pluripotent stem cell colony or that suited for gene cloning.

Although an embodiment in which the optical path length image is a quantitative phase image has been described in detail above, the optical path length image is not restricted to a quantitative phase image. The optical path length image suffices to be an image from which acquisition of optical path length is possible, and the optical path length image may be an image acquired using a phase difference microscope, for example, an image of a phase difference contrast microscope (a phase difference contrast image). In this case, the device is inexpensive and leads to cost savings.

The single ES cell used to acquire the images of FIG. 1 to FIG. 3 was acquired as follows.

Human ES cells (khES3) were cultured in an mTeSR1 medium (made by STEMCELL Technologies Inc.; registered trademark) using matrigel (made by Becton, Dickinson and Company; registered trademark) as a substrate to form a colony of human ES cells. Thereafter, the cells were peeled off from the substrate and treated with 0.25% trypsin to disperse single human ES cells in the medium. 10 μM of ROCK inhibitor (Y27632: trans-4-[(1R)-1-aminoethyl]-N-4-pyridinylcyclohexanecarboxamide dihydrochloride) were added to the medium. The cells were cultured in the single ES cell state for approximately 3 hours and adhered onto a bottom surface of a dish.

W . . . single ES cell, 1 . . . cytometer, A . . . quantitative phase microscope, A 1 . . . microscope main body, B . . . optical fiber, C . . . image pickup device, D . . . cell assessment device, D 1 . . . acquisition means, D 2 . . . extraction means, D 3 . . . comparison means, D 4 . . . assessment means, D 5 . . . display means.