Method for generating dopaminergic cells derived from neural precursors

• US 6,284,539 B1
• Filed: 10/09/1998
• Issued: 09/04/2001
• Est. Priority Date: 10/09/1998
• Status: Expired due to Term

• Current Assignee: Neuralstem Incorporated (City of Tianjin (China))
• Original Assignee: NeuralStem Biopharmaceuticals, Ltd.
• Inventors: Johe, Karl K., Bowen, David C.
• Primary Examiner(s): Priebe, Scott D.
• Assistant Examiner(s): Paras, Jr., Peter
• Application Number:
  US09/169,309
• Time in Patent Office: 1,061 Days
• Field of Search: 435/467, 435/368, 435/320.1, 435/325, 435/455, 514/44, 424/93.21, 536/23.1, 536/23.5
• US Class Current: 435/455
• 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: C12N 2501/01 Modulators of cAMP or cGMP, e.g. non-hydrolysable analogs, phosphodiesterase inhibitors, cholera toxin
• CPC Class Codes: C12N 2501/60 Transcription factors
• CPC Class Codes: C12N 2510/00 Genetically modified cells
• CPC Class Codes: C12N 5/0619 Neurons

Abstract

The present invention describes a novel method to direct a particular set of fate choice decisions by multipotential precursor cells from the central nervous system. Specifically we show that introducing the gene coding for the nuclear receptor, Nurr1, into central nervous system (CNS) stem cells causes cells to adopt a dopaminergic cell fate. One use of this technology would be to prepare in vitro neural populations enriched in dopaminergic cells for transplantation in Parkinson'"'"'s Disease or other neurological disorders. Furthermore, the finding that Nurr1 expression induces a dopaminergic phenotype suggests that introducing this gene into the brains of patients in which dopaminergic cells are degenerating or have been injured may promote the functional recovery of these neurons and thus the clinical recovery of the patient. Finally, the technology described in this application could be incorporated into a program of drug screening or gene discovery.

Claims

1. A method for generating tyrosine hydroxylase expressing cells in a culture of mammalian CNS stem cells, comprising the steps of:

a) culturing mammalian CNS stem cells in vitro;

b) introducing a polynucleotide that encodes a transcriptional regulator into the mammalian CNS stem cells in the culture,

wherein the polynucleotide encodes a transcriptional regulator selected from the group consisting of Nurr1, RNR-1, HZF-3, TINUR, and NOT, and wherein the polynucleotide is expressed;

c) incubating the mammalian CNS stem cells; and

d) identifying tyrosine hydroxylase expressing cells in the culture.

2. The method of claim 1, wherein the polynucleotide encodes Nurr1.

3. The method of claim 1, further comprising incubating the mammalian CNS stem cells with an agonist of protein kinase A activity.

4. The method of claim 3, wherein the agonist of protein kinase A activity is selected from the group consisting of forskolin;

1,9-dideoxy-forskolin;

6-[[(2-carbethoxyethyl)amino]carbonyl]-forskolin;

6-acetyl-7-deacetyl-forskolin;

6-O-[3′

-(piperidino)propionyl]-forskolin hydrochloride;

7-deacetyl-forskolin;

7-deacetyl-6-(N-acetylglycyl)-forskolin;

7-deacetyl-7-[O-(N-methylpiperazino)-g-butyryl]-forskolin, dihydrochloride;

7-deacetyl-7-O-hemisuccinyl-forskolin;

3′

,5′

cyclic monophosphate (cAMP);

8-chloro-cAMP;

8-bromo cAMP;

8-(4-chloropheylthio)-cAMP;

dibutyryl-cAMP;

dioctanoyl-cAMP;

N6-monobutyryl-cAMP;

adenosine 3′

,5′

cyclic monophosphorthioate, Sp-isomer; and

8-bromo-adenosine 3′

, 5′

cyclic monophosphorthioate, Sp-isomer.

5. The method of claim 3, wherein the agonist of protein kinase A activity is forskolin.

6. The method of claim 1, wherein the mammalian CNS stem cells are selected from the group consisting of ventral midbrain, dorsal midbrain, lateral ganglionic eminence, hippocampus, cerebral cortex, striatum, septum, diencephalon, mesencephalon, hindbrain and spinal cord.

7. The method of claim 1, wherein the mammalian CNS stem cells are human CNS stem cells.