IP Library Granted Patent US 7,060,429
Granted Patent B2
US 7,060,429 · App. 10/645,546 · Granted Jun 13, 2006

Treatment of neurodegenerative diseases by altering levels of TrkB isoforms and/or TrkC isoforms

Assignee: University of Maryland, Baltimore
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Quick Facts
Patent No.
US 7,060,429
App. No.
10/645,546
Granted
Jun 13, 2006
Kind
B2
Abstract

This invention relates to a method of treating or preventing neuro-degenerative disorders and neuro-developmental disorders by altering the ratio of the amount of full-length TrkB polypeptide to the amount of truncated TrkB polypeptides in a neuron or by altering the ratio of the amount of full-length TrkC polypeptide to the amount of truncated TrkC polypeptides in a neuron.

Claims (8)

1. A method of increasing TrkB in a neuropathic hippocampal neuron comprising the step of: contacting a neuropathic hippocampal neuron in vitro with an amount of an isolated nucleic acid encoding full-length TrkB in an amount sufficient to increase the amount of full-length TrkB in said neuron, whereby said isolated nucleic acid is expressed in said neurons compared to a neuropathic hippocampal neuron not contacted with said isolated nucleic acid.

2. The method of claim 1 , wherein said nucleic acid encodes the amino acid sequence of SEQ ID NO: 2.

3. The method of claim 1 , wherein said nucleic acid comprises the nucleotide sequence of SEQ ID NO: 1.

4. A method of increasing the ratio of the amount of full-length TrkB polypeptide to truncated TrkB polypeptide in a neuropathic hippocampal neuron wherein the neuropathic hippocampal neuron has a higher amount of truncated TrkB compared to full-length TrkB polypeptide, said method comprising contacting a neuropathic hippocampal neuron in vitro with an amount of an isolated nucleic acid encoding full-length TrkB in an amount sufficient to increase the amount of full-length TrkB in said neuron.

5. The method of claim 4 , wherein said vector comprises a nucleic acid encoding full-length TrkB.

6. The method of claim 4 , wherein said vector is selected from the group consisting of a viral vector and a plasmid.

7. The method of claim 6 , wherein said viral vector is selected from the group consisting of a herpes virus, adenovirus, adeno associated virus, retrovirus, vacccinia virus, and canary pox virus.

8. The method of claim 5 , wherein said nucleic acid comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 2.

Assignments (3)
CONFIRMATORY LICENSE Recorded Oct 20, 2016
From: UNIVERSITY OF MARYLAND, BALTIMORE
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 040070/0931 →
CONFIRMATORY LICENSE Recorded Oct 20, 2016
From: UNIVERSITY OF MARYLAND, BALTIMORE
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 040071/0171 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2006
From: KRUEGER, BRUCE K.; KINGSBURY, TAMI J.; BRAMBRICK, LINDA L.; DORSEY, SUSAN G.
To: UNIVERSITY OF MARYLAND, BALTIMORE
Reel/Frame 017287/0924 →
Continuity (4)
Continuation PCTUS021680700 · May 28, 2002
Continuation PCTUS020515100 · Feb 22, 2002
Provisional Application 6027055300 · Feb 22, 2001
Related Publication 20040110711A1 · Jun 10, 2004