IP Library Granted Patent US 9,861,600
Granted Patent B2
US 9,861,600 · App. 14/858,602 · Granted Jan 9, 2018

Methods and compositions for treating and identifying compounds to treat age-related macular degeneration treatment

Inventors: Brian McKay (Marana, AZ); John A. Martens (Tucson, AZ)
Assignee: Arizona Board of Regents, A Body Corporate Of The State Of Arizona Acting For An On Behalf Of The University of Arizona
A61K31/198A61K31/00A61K31/07A61K31/195A61K31/355A61K31/375A61K33/30A61K33/34A61K45/06A61K49/0008G01N33/5023G01N33/5041G01N2333/4704G01N2333/726G01N2500/10
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Quick Facts
Patent No.
US 9,861,600
App. No.
14/858,602
Granted
Jan 9, 2018
Kind
B2
Abstract

The present invention provides methods for treating or limiting development of age-related macular degeneration, as well as methods for identifying compound suitable for such use.

Claims (23)

1. A method for identifying candidate compounds to treat and/or limit development of age-related macular degeneration (AMD), comprising contacting a first population of cells expressing OA1 with a test compound, and identifying as positive test compounds those test compounds that increase one or both of

(i) pigment epithelium-derived factor (PEDF) expression in the first cell population relative to one or both (A) PEDF expression in the first population of cells not contacted with the test compound, and (B) a second cell population not expressing OA1, and

(ii) intracellular calcium concentration in the first cell population relative to one or both (A) intracellular calcium concentration in the first population of cells not contacted with the test compound, and (B) the second cell population not expressing OA1;

wherein the positive test compounds are candidate compounds for treating and/or limiting development of AMD.

2. The method of claim 1 wherein the identifying comprises (i) detecting pigment epithelium-derived factor (PEDF) expression in the first cell population relative to one or both (a) PEDF expression in the first population of cells not contacted with the test compound, and (b) the second cell population, and (ii) identifying as positive test compounds those test compounds that increase PEDF expression in the first cell population relative to one or both (a) PEDF expression in the first population of cells not contacted with the test compound, and (b) the second cell population.

3. The method of claim 1 wherein the identifying comprises (i) detecting levels of intracellular calcium concentration in the first cell population relative to one or both (a) intracellular calcium concentration in the first population of cells not contacted with the test compound, and (b) the second cell population; and (ii) identifying as positive test compounds those test compounds that increase intracellular calcium concentration in the first cell population relative to one or both (a) intracellular calcium concentration in the first population of cells not contacted with the test compound, and (b) the second cell population.

4. The method of claim 1 , wherein the first cell population and the second cell population are selected from the group consisting of mouse, rat, hamster, and human cells.

5. The method of claim 1 , wherein the first cell population and the second cell population are retinal pigment epithelial cells.

6. The method of claim 1 , wherein the contacting occurs in the presence of between 0 uM and 10 uM tyrosine.

7. The method of claim 1 , wherein the contacting occurs in the presence of a tyrosinase inhibitor.

8. The method of claim 2 , wherein the first cell population and the second cell population are selected from the group consisting of mouse, rat, hamster, and human cells.

9. The method of claim 2 , wherein the first cell population and the second cell population are retinal pigment epithelial cells.

10. The method of claim 2 , wherein the contacting occurs in the presence of between 0 uM and 10 uM tyrosine.

11. The method of claim 2 , wherein the contacting occurs in the presence of a tyrosinase inhibitor.

12. The method of claim 3 , wherein the first cell population and the second cell population are selected from the group consisting of mouse, rat, hamster, and human cells.

13. The method of claim 3 , wherein the first cell population and the second cell population are retinal pigment epithelial cells.

14. The method of claim 3 , wherein the contacting occurs in the presence of between 0 uM and 10 uM tyrosine.

15. The method of claim 3 , wherein the contacting occurs in the presence of a tyrosinase inhibitor.

16. The method of claim 5 , wherein the contacting occurs in the presence of between 0 uM and 10 uM tyrosine.

17. The method of claim 5 , wherein the contacting occurs in the presence of a tyrosinase inhibitor.

18. The method of claim 9 , wherein the contacting occurs in the presence of between 0 uM and 10 uM tyrosine.

19. The method of claim 9 , wherein the contacting occurs in the presence of a tyrosinase inhibitor.

20. The method of claim 13 , wherein the contacting occurs in the presence of between 0 uM and 10 uM tyrosine, and/or wherein the contacting occurs in the presence of a tyrosinase inhibitor.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 2, 2015
From: UNIVERSITY OF ARIZONA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 037032/0948 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 22, 2015
From: MCKAY, BRIAN
To: ARIZONA BOARD OF REGENTS, A BODY CORPORATE OF THE STATE OF ARIZONA ACTING FOR AND ON BEHALF OF THE UNIVERSITY OF ARIZONA
Reel/Frame 036624/0577 →
Continuity (3)
Division 12937669
Provisional Application 61124624 · Apr 18, 2008
Related Publication 20160015665A1 · Jan 21, 2016