Reagents and methods for using human embryonic stem cells to evaluate toxicity of pharmaceutical compounds and other chemicals

• US 8,703,483 B2
• Filed: 04/10/2007
• Issued: 04/22/2014
• Est. Priority Date: 04/10/2006
• Status: Active Grant

• Current Assignee: Wisconsin Alumni Research Foundation (University of Wisconsin System)
• Original Assignee: Wisconsin Alumni Research Foundation (University of Wisconsin System)
• Inventors: Cezar, Gabriela G.
• Primary Examiner(s): Shen, Bin
• Application Number:
  US11/733,677
• Publication Number:
  US 20070248947A1
• Time in Patent Office: 2,569 Days
• Field of Search: 435/325, 435/366, 435/375
• US Class Current: 435/325
• CPC Class Codes: G01N 2500/10 involving cells
• CPC Class Codes: G01N 33/5038 involving detection of metabolites per se
• CPC Class Codes: G01N 33/5073 Stem cells
• CPC Class Codes: G01N 33/5091 for testing the pathological state of an organism

Abstract

The invention provides biomarker profiles of cellular metabolites and methods for screening chemical compounds including pharmaceutical agents, lead and candidate drug compounds and other chemicals using human embryonic stem cells (hESC) or lineage-specific cells produced therefrom. The inventive methods are useful for testing toxicity, particularly developmental toxicity and detecting teratogenic effects of such chemical compounds.

Claims

1. A method for identifying one or a plurality of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that is differentially produced in human embryonic stem cells (hESCs) or human pluripotent stem cells contacted with a test compound from a population of secreted cellular metabolites, the method comprising the steps of:

a) culturing hESCs or human pluripotent stem cells in the presence or absence of a test compound;

b) separating members of the population of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are secreted from hESCs or human pluripotent stem cells;

c) detecting one or a plurality of differentially produced cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons from hESCs or human pluripotent stem cells; and

d) identifying at least one cellular metabolite having a molecular weight of from about 10 to about 1500 Daltons that is differentially produced in cells cultured in the presence of the test compound.

2. A method according to claim 1, wherein at least one of the cellular metabolites is produced in greater amounts in the presence of the test compound than in the absence of the test compound.

3. A method according to claim 1, wherein at least one of the cellular metabolites is produced in greater amounts in the absence of the test compound than in the presence of the test compound.

4. A method according to claim 1, wherein the cellular metabolite has a molecular weight of from about 100 to about 1000 Daltons.

5. A method according to claim 1, wherein the test compound is a toxic or teratogenic compound.

6. A method according to claim 1, wherein one or a plurality of cellular metabolites is separated using a physical separation method.

7. A method according to claim 6, wherein the physical separation method is liquid chromatography/electrospray ionization time of flight mass spectrometry.

8. A method according to claim 1, wherein the cellular metabolites are tetrahydrofolate, dihydrofolate or other metabolites in the folate metabolic pathway, glutathione, or oxidized glutathione.

9. A method according to claim 1, wherein the cellular metabolites are kynurenine, 8-methoxykynurenate, N′

-formylkynurenine 7,8-dihydro-7,8-dihydroxykynurenate, 5-Hydroxytryptophan, N-acetyl-D-tryptophan, glutamate, pyroglutamic acid or other metabolites in the tryptophan or glutamate metabolic pathways, histamine, dopamine, 3,4-dihydroxybutyric acid, serotonin, or gamma-aminobutyric acid (GABA).

10. A method according to claim 1, wherein a plurality of cellular metabolites are identified.

11. A method according to claim 10 wherein the plurality of identified cellular metabolites comprise a biomarker profile.

12. A method according to claim 11, wherein one of the cellular metabolites comprising a biomarker profile is kynurenine.

13. A method according to claim 10, wherein the test compound is a toxic or teratogenic compound.

14. A method according to claim 13, wherein the plurality of identified cellular metabolites comprise a biomarker profile characteristic of hESC or human pluripotent stem cell response to a toxic or teratogenic compound.

15. A method of claim 1, further comprising the step of identifying at least one cellular metabolite having a molecular weight of from about 10 to about 1500 Daltons that is differentially produced in the cells in the presence or absence of the test compound in a biomarker profile comprising one or a plurality of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are differentially produced in human embryonic stem cells (hESCs) or human pluripotent stem cells contacted with a toxic compound or compounds.

16. The method of claim 1, wherein at least two cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are differentially produced in the cells in the presence or absence of the test compound are detected.

17. A method for screening a test compound to identify an effect of the compound on human embryonic stem cells (hESCs) or human pluripotent stem cells contacted with the test compound, the method comprising the steps of:

a) culturing hESCs or human pluripotent stem cells in the presence or absence of a test compound;

b) separating members of a population of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are secreted from hESCs or human pluripotent stem cells

c) detecting one or a plurality of differentially produced cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons; and

d) identifying the effect of a compound on human embryonic stem cells (hESCs) or human pluripotent stem cells by identifying at least one cellular metabolite having a molecular weight of from about 10 to about 1500 Daltons that is differentially secreted between cells cultured in the presence versus the absence of the test compound.

18. A method according to claim 17, wherein at least one of the cellular metabolites is produced in greater amounts in the presence of the test compound than in the absence of the test compound.

19. A method according to claim 17, wherein at least one of the cellular metabolites is produced in greater amounts in the absence of the test compound than in the presence of the test compound.

20. A method according to claim 17, wherein at least one of the cellular metabolites has a molecular weight of from about 100 to about 1000 Daltons.

21. A method according to claim 17, wherein the test compound is a toxic or teratogenic compound.

22. A method according to claim 17, wherein one or a plurality of cellular metabolites is separated using a physical separation method.

23. A method according to claim 22, wherein the physical separation method is liquid chromatography/electrospray ionization time of flight mass spectrometry.

24. A method according to claim 17, wherein the cellular metabolites are tetrahydrofolate, dihydrofolate or other metabolites in the folate metabolic pathway, glutathione, or oxidized glutathione.

25. A method according to claim 17, wherein the cellular metabolites are kynurenine, 8-methoxykynurenate, N′

-formylkynurenine 7,8-dihydro-7,8-dihydroxykynurenate, 5-Hydroxytryptophan, N-acetyl-D-tryptophan, glutamate, pyroglutamic acid or other metabolites in the tryptophan or glutamate metabolic pathways, histamine, dopamine, serotonin, gamma-aminobutyric acid (GABA) or other butyric acid species.

26. A method according to claim 17 wherein a plurality of cellular metabolites are identified.

27. A method according to claim 26, wherein the plurality of identified cellular metabolites comprise a biomarker profile.

28. A method according to claim 27, wherein one of the cellular metabolites comprising a biomarker profile is kynurenine.

29. A method according to claim 27, wherein the test compound is a toxic or teratogenic compound.

30. A method according to claim 29, wherein the plurality of identified cellular metabolites comprise a biomarker profile characteristic of hESC or human pluripotent stem cells response to a toxic or teratogenic compound.

31. A method of claim 17, further comprising the step of identifying at least one cellular metabolite having a molecular weight of from about 10 to about 1500 Daltons that is differentially produced in the cells in the presence or absence of the test compound in biomarker profile comprising one or a plurality of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are differentially produced in human embryonic stem cells (hESCs) or human pluripotent stem cells contacted with a toxic compound or compounds.

32. The method of claim 17, wherein at least two cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are differentially produced in the cells in the presence or absence of the test compound are detected.

33. A method for assaying a test compound for toxicity or teratogenicity to hESC-derived lineage-specific cells or human pluripotent stem cell-derived lineage-specific cells contacted with the test compound, the method comprising the steps of:

a) culturing hESC-derived lineage-specific cells or human pluripotent stem cell-derived lineage-specific cells in the presence or absence of a test compound;

b) separating members of a population of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons secreted from or hESC-derived lineage-specific cells or human pluripotent stem cell-derived lineage-specific cells;

c) detecting one or a plurality of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons produced by hESC-derived lineage-specific cells or human pluripotent stem cell-derived lineage-specific cells contacted with a compound; and

d) identifying the toxicity or teratogenicity of the test compounds wherein hESC-derived lineage-specific cells or human pluripotent stem cell-derived lineage-specific cells contacted with a test compound differentially produce one or a plurality of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons.

34. A method according to claim 33, wherein at least one of the cellular metabolites is produced in greater amounts in the presence of the test compound than in the absence of the test compound.

35. A method according to claim 33, wherein at least one of the cellular metabolites is produced in greater amounts in the absence of the test compound than in the presence of the test compound.

36. A method according to claim 33, wherein the cellular metabolite has a molecular weight of from about 100 to about 1000 Daltons.

37. A method according to claim 33, wherein the test compound is a toxic or teratogenic compound.

38. A method according to claim 33, wherein one or a plurality of cellular metabolites is separated using a physical separation method.

39. A method according to claim 38, wherein the physical separation method is liquid chromatography/electrospray ionization time of flight mass spectrometry.

40. A method according to claim 33, wherein the cellular metabolites are tetrahydrofolate, dihydrofolate or other metabolites in the folate metabolic pathway, glutathione, or oxidized glutathione.

41. A method according to claim 33, wherein the cellular metabolites are kynurenine, 8-methoxykynurenate, N′

-formylkynurenine 7,8-dihydro-7,8-dihydroxykynurenate 5-Hydroxytryptophan, N-acetyl-D-tryptophan, glutamate, pyroglutamic acid or other metabolites in the tryptophan or glutamate metabolic pathways, histamine, dopamine, 3,4-dihydroxybutyric acid, serotonin, gamma-aminobutyric acid (GABA) or other butyric acid species.

42. A method according to claim 33, wherein a plurality of cellular metabolites are identified.

43. A method according to claim 42, wherein the plurality of identified cellular metabolites comprise a biomarker profile.

44. A method according to claim 43, wherein one of the cellular metabolites comprising a biomarker profile is kynurenine.

45. A method according to claim 44, wherein the test compound is a toxic or teratogenic compound.

46. A method according to claim 33, wherein the plurality of identified cellular metabolites comprise a biomarker profile characteristic of hESC response to a toxic or teratogenic compound.

47. A method of claim 33, further comprising the step of identifying at least one cellular metabolite having a molecular weight of from about 10 to about 1500 Daltons that is differentially produced in the cells in the presence or absence of the test compound in a biomarker profile comprising one or a plurality of cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are differentially produced in hESC-derived lineage-specific cells or human pluripotent stem cell-derived lineage-specific cells contacted with a toxic compound or compounds.

48. The method of claim 33, wherein at least two cellular metabolites having a molecular weight of from about 10 to about 1500 Daltons that are differentially produced in the cells in the presence or absence of the test compound are detected.