Reporter hepatocytes and other cells for drug screening and toxicity testing

• US 20060292694A1
• Filed: 09/22/2005
• Published: 12/28/2006
• Est. Priority Date: 06/22/2005
• Status: Abandoned Application

• Current Assignee: CXR Biosciences Ltd. (Concept Life Sciences (Midco) Ltd.)
• Original Assignee: CXR Biosciences Ltd. (Concept Life Sciences (Midco) Ltd.), Roslin Institute
• Inventors: Clark, A. John, Wolf, C. Roland, Clark, Helen
• Application Number:
  US11/233,712
• Publication Number:
  US 20060292694A1
• Time in Patent Office: Days
• US Class Current: 435/370
• CPC Class Codes: C12N 2500/30 Organic components
• CPC Class Codes: C12N 2500/62 DMSO
• CPC Class Codes: C12N 2501/11 Epidermal growth factor [EGF]
• CPC Class Codes: C12N 2501/12 Hepatocyte growth factor [HGF]
• CPC Class Codes: C12N 2503/02 Drug screening
• CPC Class Codes: C12N 2506/02 from embryonic cells
• CPC Class Codes: C12N 2510/00 Genetically modified cells
• CPC Class Codes: C12N 5/067 Hepatocytes
• CPC Class Codes: G01N 33/5044 involving specific cell types
• CPC Class Codes: G01N 33/5073 Stem cells

Abstract

This invention provides a system for rapid determination of pharmacologic effects on target tissue types in cell populations cultured in vitro. The cells contain a promoter-reporter construct that reflects a toxicologic or metabolic change caused by the agent being screened. The promoter is taken from a gene known to be up- or down-regulated according to the metabolic state of the cell, and linked to a reporter gene that provides an external signal for monitoring promoter activity. The promoter-reporter cells may be produced by placing these genetic alterations into a line of human embryonic stem cells, bulking up the cells to any extent desired, and then differentiating the cells into the desired tissue type. This disclosure explains some of the powerful features of the promoter-reporter cells of this invention, and shows various ways the skilled reader can use the invention for pharmaceutical development and testing, or to monitor graft survival.

Claims

1. A population of cells differentiated from human embryonic stem (hES) cells, comprising cells that have been genetically altered so that a promoter that responds to a metabolic or toxicologic change in the cell controls expression of a reporter gene.

2. The cell population of claim 1, which is a population of neural, cardiomyocyte, or hepatocyte lineage cells.

4. The cell population of claim 1, wherein the promoter responds to apoptosis, such as a promoter for a PUMA gene.

5. The cell population of claim 1, wherein the promoter responds to DNA damage, such as a promoter for a p21 OR p21/WAF1 gene.

6. The cell population of claim 1, wherein the promoter responds to hyperplasia, such as a promoter for a Ki-67 gene.

7. The cell population of claim 1, wherein the promoter responds to oxidative stress.

8. The cell population of claim 7, wherein the promoter is a promoter for a heme oxygenase 1, superoxide dismutase, γ

-glutamyl cysteinyl ligase, or metallothionine gene.

9. The cell population of claim 1, wherein the promoter is a promoter for a PXR, CAR, aryl hydrocarbon receptor (AhR), or Nrf2 gene.

10. The cell population of claim 1, wherein the promoter is a promoter for an androgen, estrogen, or pPAG responsive gene, such as prostate specific antigen (PSA).

11. The cell population of claim 1, wherein the promoter is a promoter for a cytochrome P450 enzyme.

12. The cell population of claim 11, wherein the promoter is a promoter for CYP3A4 or CYP1A1.

13. The cell population of claim 1, wherein the promoter is a promoter for a drug transporter gene, such as MDR1;

or a gene that affects the contraction rate or the QT interval of the heart, such as a calcium flux gene.

14. The cell population of claim 1, wherein the reporter gene encodes a protein that produces a fluorescent or phosphorescent signal when expressed, such as green fluorescent protein.

15. The cell population of claim 1, wherein the reporter gene encodes a protein that is excretable by the kidney, such as human chorionic gonadotropin.

16. The cell population of claim 1, which has also been genetically altered so that a second promoter that is tissue specific controls expression of a second reporter gene.

17. The cell population of claim 16, wherein the second promoter is a promoter for a hepatocyte specific marker selected from albumin, α

1-antitrypsin, α

-fetoprotein, γ

-glutamyl tranpeptidase, glucose-6-phosphatase, catalase, and monooxygenase.

18. The cell population of claim 1, which has been genetically altered to express a gene encoding a variant of an endogenous drug target or drug metabolizing enzyme.

19. The cell population of claim 1, wherein at least 20% of the cells have the following characteristics of the hepatocyte lineage:

antibody-detectable expression of α

₁-antitrypsin (AAT);

antibody-detectable expression of albumin; and

evidence of glucose-6-phosphatase activity.

20. The cell population of claim 1, along with undifferentiated cells from the same line of hES cells from which they were derived, for producing more of said differentiated cells.

3. A population of non-cancer-derived hepatocytes comprising cells that have been genetically altered so that a promoter that responds to a metabolic or toxicologic change in the cell controls expression of a reporter gene.