Stem cell-derived neural cells for cell therapy in neurological disorders

Patent metadata

Field	Value
Publication number	US-9717761-B2
Application number	US-201214359623-A
Country	US
Kind code	B2
Filing date	Nov 21, 2012
Priority date	Nov 21, 2011
Publication date	Aug 1, 2017
Grant date	Aug 1, 2017

Abstract

The present invention provides methods and uses of neural cells differentiated from adult stem cells of the oral mucosa for cell therapy of neurological and psychiatric diseases and disorders. Methods for direction of differentiation of oral mucosal stem cells into neuronal or neuron supporting cells are also provided.

First claim

The invention claimed is:

1. A method for inducing selective differentiation of oral mucosa stem cells (OMSC) into neuron-supporting glial cells, comprising:
(a) obtaining oral mucosa stem cells (OMSC) from oral mucosa;
(b) incubating the OMSC of (a) in a pre-differentiating medium, comprising N-2 supplement, basic fibroblast growth factor 2 (bFGF) and epidermal growth factor (EGF); and
(c) after incubation of the OMSC in (b), replacing the pre-differentiation medium of (b) with a differentiating medium comprising dibutyryl cyclic adenosine monophosphate (dbcAMP), IBMX (3-Isobutyl-1-methylxanthine), neuregulin, and platelet-derived growth factor (PDGF) and incubating the OMSC from (b) in the differentiation medium to selectively differentiate OMSC into neuron-supporting glial cells secreting neurotrophic factors.

2. The method according to claim 1 , wherein the OMSC are incubated in a differentiating medium comprising 0.1-10 mM dbcAMP, 0.1-10 mM IBMX, 5-500 ng/ml neuregulin, and 0.1-10 ng/ml PDGF for about 48-96 hours, for about 24-120 hours.

3. The method according to claim 1 , wherein the OMSC are incubated in a differentiating medium comprising about 0.5-2 mM dbcAMP, about 0.2-1 mM IBMX, about 20-100 ng/ml neuregulin, and about 0.5-2 ng/ml PDGF for about 48-96 hours.

4. The method according to claim 1 , wherein the OMSC are incubated in a differentiating medium comprising about 1 mM dbcAMP, about 0.5 mM IBMX, about 50 ng/ml neuregulin, and about 1 ng/ml PDGF for about 48-96 hours.

5. The method according to claim 1 , in which OMSC, separate from the OMSC selectively differentiating into neuron-supporting glial cells, are induced to selectively differentiate into a separate population of dopaminergic neural cells, further comprising:
(d) incubating a separate population of OMSC obtained from oral mucosa in a pre-differentiation medium comprising N2, bFGF and EGF; and
(e) after incubation of the OMSC in (d), replacing the pre-differentiation medium of (d) with a differentiation medium comprising a plurality of agents selected from the group consisting of B27, IBMX (3-Isobutyl-1-methylxanthine), dbcAMP, ascorbic acid, BDNF, Sonic Hedgehog (SHH), Wnt-1, fibroblast growth factor-8 (FGF-8), and bFGF and incubating the OMSC from (d) in the differentiation medium for a duration of at least 2 days to selectively differentiate the separate population of OMSC into a separate population of dopaminergic neural cells, so that when mixed with the OMSC selectively differentiated into neuron-supporting glial cells the mixture forms a mixed population of selectively differentiated neuron-supporting glial cells and selectively differentiated dopaminergic neural cells .

6. The method according to claim 5 , wherein the OMSC are incubated in a differentiating medium comprising 0.1-5% B27, 0.1-5 mM IBMX, 0.1-10 mM dbcAMP, 10-500 μM ascorbic, and 10-500 ng/ml BDNF, for about 2-4 days.

7. The method according to claim 5 , wherein the OMSC are incubated in a differentiating medium comprising 0.5% B27, 85-750 ng/mL Sonic Hedgehog, 30-300 ng/mL Wnt-1, 30-300 ng/mL FGF-8, 15-150 ng/mL BDNF, 15-150 ng/mL bFGF, and 65-600 ng/mL ascorbic acid, for at least 4 days.

8. The method according to claim 5 , wherein step (d) is performed for duration of about 48-96 hours.

9. The method according to claim 5 , wherein step (e) is performed for at least 12 days in a differentiating medium comprising 0.1-5% B27, 85-750 ng/mL Sonic Hedgehog, 30-300 ng/mL Wnt-1, 30-300 ng/mL FGF-8, 15-150 ng/mL BNDF, 15-150 ng/mL bFGF, and 65-600 ng/mL ascorbic acid.

10. The method according to claim 5 , wherein the OMSC are incubated in a differentiating medium comprising 0.5% B27, 100-400 ng/mL Sonic Hedgehog, 50-150 ng/mL Wnt-1, 50-150 ng/mL FGF-8, 25-100 ng/mL BDNF, 25-100 ng/mL bFGF, and 100-400 ng/mL of ascorbic acid for 13 days.

Assignees

• Ramot At Tel-Aviv Univ Ltd

Inventors

• Pitaru Sandu
• Ganz Javier
• Offen Daniel
• Melamed Eldad

Classifications

• A61P25/28

  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 title

• A61P25/16

  Anti-Parkinson drugs · CPC title

• A61K35/30 Primary

  Nerves; Brain; Eyes; Corneal cells; Cerebrospinal fluid; Neuronal stem cells; Neuronal precursor cells; Glial cells; Oligodendrocytes; Schwann cells; Astroglia; Astrocytes; Choroid plexus; Spinal cord tissue · CPC title

• C12N2501/11

  Epidermal growth factor [EGF] · CPC title

• C12N2501/115

  Basic fibroblast growth factor (bFGF, FGF-2) · CPC title