Methods of differentiating and protecting cells by modulating the P38/MEF2 pathway

• US 7,919,317 B2
• Filed: 06/05/2001
• Issued: 04/05/2011
• Est. Priority Date: 06/05/2000
• Status: Expired due to Fees

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Sanford-Burnham Medical Research Institute (Sanford Burnham Prebys Medical Discovery Institute)
• Inventors: Lipton, Stuart A., Okamoto, Shu-ichi
• Primary Examiner(s): FALK, ANNE MARIE
• Application Number:
  US09/876,187
• Publication Number:
  US 20020090603A1
• Time in Patent Office: 3,591 Days
• Field of Search: 435/325, 435/366, 435/368, 435/377, 435/455
• US Class Current: 435/377
• CPC Class Codes: A61K 35/12 Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells vaccines or medicinal preparations containing antigens or antibodies A61K39/00
• CPC Class Codes: A61P 25/00 Drugs for disorders of the nervous system
• CPC Class Codes: A61P 25/16 Anti-Parkinson drugs
• CPC Class Codes: A61P 25/28 for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• CPC Class Codes: C12N 2501/385 of the family of the retinoic acid recptor, e.g. RAR, RXR; Peroxisome proliferator-activated receptor [PPAR]
• CPC Class Codes: C12N 2501/60 Transcription factors
• CPC Class Codes: C12N 2503/00 Use of cells in diagnostics
• CPC Class Codes: C12N 2506/02 from embryonic cells
• CPC Class Codes: C12N 2510/00 Genetically modified cells
• CPC Class Codes: C12N 5/0619 Neurons
• CPC Class Codes: G01N 33/6887 from muscle, cartilage or connective tissue

Abstract

The present invention provides a method of differentiating progenitor cells to produce a population containing protected neuronal cells. A method of the invention includes the steps of contacting the progenitor cells with a differentiating agent; and introducing into the progenitor cells a nucleic acid molecule encoding a MEF2 polypeptide or an active fragment thereof, thereby differentiating the progenitor cells to produce a population containing protected neuronal cells. In one embodiment, the MEF2 polypeptide is human MEF2C or an active fragment thereof.

Claims

1. A method of differentiating progenitor cells in vitro to produce a cell population containing neuronal cells protected from apoptotic cell death, comprising the steps of:

(a) contacting in vitro said progenitor cells with a differentiating agent; and

(b) introducing in vitro into said progenitor cells a nucleic acid molecule encoding a constitutively active MEF2 polypeptide or an active fragment thereof, wherein said constitutively active MEF2 polypeptide or active fragment thereof has transactivation activity that is independent of phosphorylation,

thereby differentiating said progenitor cells in vitro to produce a cell population containing neuronal cells protected from apoptotic cell death.

2. The method of claim 1, wherein said MEF2 polypeptide is human MEF2C, or an active fragment thereof.

3. The method of claim 1, wherein said constitutively active MEF2 polypeptide is a MEF2/VP16 fusion protein.

4. The method of claim 1, wherein said constitutively active MEF2 polypeptide contains one or more serine/threonine to aspartic acid/glutamic acid substitutions in the MEF2 transactivation domain.

5. The method of claim 1, further comprising inhibiting caspase activity in said progenitor cells.

6. The method of claim 1, wherein said progenitor cells are human stem cells.

7. The method of claim 1, wherein said progenitor cells are embryonic stem cells.

8. The method of claim 7, wherein said embryonic stem cells are human embryonic stem cells.

9. The method of claim 1, wherein said progenitor cells are hematopoietic progenitor cells.

10. The method of claim 9, wherein said hematopoietic progenitor cells are human hematopoietic progenitor cells.

11. The method of claim 1, further comprising selecting CD133-positive human progenitor cells.

12. The method of claim 1, further comprising selecting CD133-positive/CD34-positive human progenitor cells.

13. The method of claim 1, further comprising selecting CD133-positive/CD34-negative human progenitor cells.

14. The method of claim 1, further comprising selecting CD133-positive/CD34-negative/CD45-negative human progenitor cells.

15. The method of claim 1, further comprising selecting CD34-negative/CD38-negative/Lin-negative human progenitor cells.

16. The method of claim 1, further comprising selecting CD34-positive/CD38-negative/Lin-negative/Thy-1-negative human progenitor cells.

17. The method of claim 1, wherein said differentiating agent is retinoic acid.

18. The method of claim 1, wherein said differentiating agent is selected from the group consisting of neurotrophic factor 3, epidermal growth factor, insulin-like growth factor 1 and a platelet-derived growth factor.

19. The method of claim 1, wherein said population containing protected neuronal cells comprises at least 50% neuronal cells.

20. The method of claim 1, wherein said nucleic acid molecule is stably introduced into said progenitor cells.