Cell differentiation assay method, cell isolation method, method for producing induced pluripotent stem cells, and method for producing differentiated cells
Provided are a method for accurately evaluating the differentiation status of stem cells by selectively staining only stem cells in an undifferentiated state, and a method for positively isolating only stem cells in an undifferentiated state. Specifically provided is a method for determining differentiation of a cell comprising a step of contacting a test cell with a probe comprising protein (A) or (B) below and a step of detecting the presence of binding of the probe to the test cell. The method for determining differentiation of a cell is capable of detecting the presence or absence of an undifferentiated stem cell in test cells by using a probe that specifically reacts with undifferentiated stem cells and detecting the presence of bonding to the test cell. (A) A protein comprising an amino acid sequence shown in SEQ ID NO: 1 and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc;” and (B) a protein comprising an amino acid sequence showing 80% or more similarity to the amino acid sequence shown in SEQ ID NO: 1 and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc.”
1. A method for determining differentiation of a cell comprising:
a step of contacting a test cell with a probe comprising a protein (A) or (B) below and
a step of detecting the presence of binding of the probe to the test cell:
(A) a protein comprising an amino acid sequence shown in SEQ ID NO: 1 and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GlcNAc;” and
(B) a protein comprising an amino acid sequence in which one or two amino acids in the amino acid sequence shown in SEQ ID NO: 1 are deleted, substituted, inserted, or added, and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc;”
wherein binding of the probe to the test cell indicates an undifferentiated state.
2. The method for determining differentiation of a cell according to claim 1 , wherein the test cell is an undifferentiated stem cell or a stem cell subjected to a differentiation induction treatment.
3. The method for determining differentiation of a cell according to claim 2 , wherein the undifferentiated stem cell is a stem cell treated for the maintenance of an undifferentiated state or a somatic cell subjected to pluripotency induction treatment.
4. The method for determining differentiation of a cell according to claim 3 , wherein the probe comprises a detectable labeling substance.
5. A cell separation method comprising:
a step of contacting a test cell with a probe comprising a protein (A) or (B) below and
a step of separating a cell binding to the probe and a cell not binding thereto:
(A) a protein comprising an amino acid sequence shown in SEQ ID NO: 1 and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GlcNAc;” and
(B) a protein comprising an amino acid sequence in which one or two amino acids in the amino acid sequence shown in SEQ ID NO: 1 are deleted, substituted, inserted, or added, and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc;”
wherein the cell binding to the probe indicates an undifferentiated state and
wherein the cell not binding thereto indicates a differentiated state.
6. The cell separation method according to claim 5 ,
wherein the probe comprises an optically detectable label, and
wherein the separation of the cell binding to the probe and the cell not binding thereto is performed using a flow cytometer equipped with a cell sorter.
7. The cell separation method according to claim 5 ,
wherein the probe comprises a magnetically detectable label, and
wherein the separation of the cell binding to the probe and the cell not binding thereto is performed using a magnetic cell separation apparatus.
8. A method for producing an induced pluripotent stem cell, comprising:
a step of subjecting a somatic cell to a pluripotency induction treatment,
a step of contacting the pluripotency-induced cell with a probe comprising a protein (A) or (B) below, and
a step of isolating a cell binding to the probe:
(A) a protein comprising an amino acid sequence shown in SEQ ID NO: 1 and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GlcNAc;” and
(B) a protein comprising an amino acid sequence in which one or two amino acids in the amino acid sequence shown in SEQ ID NO: 1 are deleted, substituted, inserted, or added, and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc;”
wherein the cell binding to the probe indicates an undifferentiated state.
9. A method for producing a differentiated cell, comprising:
a step of subjecting a stem cell to a differentiation induction treatment,
a step of contacting the differentiation-induced cell with a probe comprising a protein (A) or (B) below, and
a step of isolating a cell not binding to the probe:
(A) a protein comprising an amino acid sequence shown in SEQ ID NO: 1 and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GlcNAc;” and
(B) a protein comprising an amino acid sequence in which one or two amino acids in the amino acid sequence shown in SEQ ID NO: 1 are deleted, substituted, inserted, or added, and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc;”
wherein the cell not binding to the probe indicates a differentiated state.
10. The method for determining differentiation of a cell according to claim 2 , wherein the probe comprises a detectable labeling substance.
11. The method for determining differentiation of a cell according to claim 1 , wherein the probe comprises a detectable labeling substance.
12. The method for determining differentiation of a cell according to claim 1 , wherein the probe comprises the protein (A).
13. The method for determining differentiation of a cell according to claim 1 , wherein the probe comprises the protein (B) comprising an amino acid sequence in which one amino acid in the amino acid sequence shown in SEQ ID NO: 1 is deleted, substituted, inserted, or added, and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GalNAc.
14. The method for determining differentiation of a cell according to claim 1 , wherein the probe comprises the protein (B) comprising an amino acid sequence in which two amino acids in the amino acid sequence shown in SEQ ID NO: 1 are deleted, substituted, inserted, or added, and recognizing a sugar chain structure of “Fucα1-2Galβ1-3GlcNAc” and/or “Fucα1-2Galβ1-3GlcNAc.
15. The method for determining differentiation of a cell according to claim 12 , wherein the test cell is an undifferentiated stem cell or a stem cell subjected to a differentiation induction treatment.
16. The method for determining differentiation of a cell according to claim 13 , wherein the test cell is an undifferentiated stem cell or a stem cell subjected to a differentiation induction treatment.
17. The method for determining differentiation of a cell according to claim 14 , wherein the test cell is an undifferentiated stem cell or a stem cell subjected to a differentiation induction treatment.
18. The method for determining differentiation of a cell according to claim 12 , wherein the probe comprises a detectable labeling substance.
19. The method for determining differentiation of a cell according to claim 13 , wherein the probe comprises a detectable labeling substance.
20. The method for determining differentiation of a cell according to claim 14 , wherein the probe comprises a detectable labeling substance.