Pluripotent cell lines and methods of use thereof

Patent metadata

Field	Value
Publication number	US-9464273-B2
Application number	US-201314098890-A
Country	US
Kind code	B2
Filing date	Dec 6, 2013
Priority date	Jun 24, 2008
Publication date	Oct 11, 2016
Grant date	Oct 11, 2016

Abstract

Methods of generating cell lines with a sequence variation or copy number variation of a gene of interest, methods of use thereof, and cell lines with a sequence variation or copy number variation of a gene of interest are provided.

First claim

What is claimed is:

1. A method of producing a differentiated dopaminergic cell line, the method comprising:
a) producing induced pluripotent stem cells (iPSCs) from somatic cells harvested from a subject diagnosed with a neurodegenerative disease, wherein the somatic cells carry a genetic variation that is associated with the disease; and
b) differentiating the iPSCs towards a dopaminergic cell type, wherein the dopaminergic cell type is associated with the neurodegenerative disease and displays a phenotype of cellular protein aggregation, thereby resulting in the differentiated dopaminergic cell line.

2. The method of claim 1 , wherein the somatic cells are fibroblasts.

3. The method of claim 1 , wherein the genetic variation is a copy number variation.

4. The method of claim 3 , wherein the genetic variation is a triplication.

5. The method of claim 1 , wherein the genetic variation is a deletion, an insertion, a complex multi-state variant, a substitution, a transition, a transversion, or a duplication, of one or more nucleotides in a gene that is associated with the disease.

6. The method of claim 1 , wherein the neurodegenerative disease is Parkinson's disease, Alzheimer's disease, diffuse Lewy body disease or any other Lewy body disorder or synucleinopathy, corticobasal degeneration, multiple system atrophy, progressive supranuclear palsy, frontotemporal dementia with Parkinsonism chromosome 17, Huntington's disease, spinocerebellar ataxias, amytropic lateral sclerosis, or Creutzfeld Jakob disease.

7. The method of claim 1 , wherein the neurodegenerative disease is Parkinson's disease or Parkinson's-like disease.

8. The method of claim 7 , wherein the genetic variation is in a gene selected from PARK1 (SNCA or α-synuclein), PARK2 (Parkin), PARK5 (UCHL1), PARK6 (PINK1), PARK7 (DJ-1), PARK8 (LRRK2), and PARK 11 (GIGFY2).

9. The method of claim 8 , wherein the gene is PARK1 (SNCA or α-synuclein).

10. The method of claim 8 , wherein the gene is PARK8 (LRRK2).

11. The method of claim 9 wherein the variation is triplication of the SNCA gene.

12. The method of claim 10 , wherein the genetic variation comprises a G2019S mutation.

13. The method of claim 1 , wherein the iPSCs are differentiated towards a midbrain dopaminergic cell type.

14. The method of claim 1 , wherein the iPSCs are differentiated to adopt the cell type within 20 days.

15. The method of claim 1 , wherein the iPSCs are produced without the use of a retrovirus or a lentivirus.

16. The method of claim 1 , wherein the iPSCs are produced with a method comprising the use of three factors.

17. The method of claim 16 , wherein the three factors are OCT4, SOX2, and KLF4.

18. The method of claim 1 , wherein the differentiated dopaminergic cell line further displays a phenotype of cell viability, inclusion bodies, dystrophic neurites, apoptosis, necrosis, oxidative stress, mitochondrial dysfunction, or α-synuclein aggregation.

19. The method of claim 1 , wherein the phenotype changes when the differentiated dopaminergic cell line is in contact with a putative therapeutic agent.

20. The method of claim 1 , wherein the dopaminergic cell type is a cell type that is affected in the natural progression of the neurodegenerative disease.

21. A method of screening a putative therapeutic agent for usefulness in the treatment of a neurodegenerative disease, the method comprising:
a) producing a differentiated dopaminergic cell line by the method of claim 1 ;
b) contacting the dopaminergic cell line with an agent;
c) detecting a response to the agent in the dopaminergic cell line; and
d) determining whether the agent is useful in the treatment based on the detected response.

Assignees

• Parkinson'S Inst
• Univ Leland Stanford Junior

Inventors

• Reijo Pera Renee Ann
• Langston J William
• Schule Birgitt
• Palmer Theodore D
• Byers Blake
• Nguyen Ha Nam
• Byrne James Anthony
• Cord Branden John

Classifications

• C12N2740/15032

  Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent · CPC title

• C12N2501/71

  Oxidoreductases (EC 1.) · CPC title

• C12N2501/70

  Enzymes · CPC title

• C12N2501/50

  Cell markers; Cell surface determinants · CPC title

• C12N7/00

  Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof (preparing medicinal viral antigen or antibody compositions, e.g. virus vaccines, A61K39/00) · CPC title