IP Library Granted Patent US 8,044,018
Granted Patent B2
US 8,044,018 · App. 12/101,710 · Granted Oct 25, 2011

Reagents and methods for smooth muscle therapies

Assignee: Arizona Board of Regents
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Quick Facts
Patent No.
US 8,044,018
App. No.
12/101,710
Granted
Oct 25, 2011
Kind
B2
Abstract

The present invention provides novel polypeptides comprising heat shock protein 20 (HSP20)-derived polypeptides to treat or inhibit smooth muscle vasospasm, as well to treat and inhibit smooth muscle cell proliferation and migration.

Claims (52)

1. A method for inhibiting smooth muscle cell proliferation and/or migration, comprising contacting the smooth muscle cells with an amount effective to inhibit smooth muscle cell proliferation and/or migration of the following polypeptide:

X2-SEQ ID NO: 300-X6

X2 is absent or is a cell transduction domain;

X6 is absent or is a cell transduction domain; and wherein at least one of X2 and

X6 comprise a transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

2. A method for inhibiting smooth muscle cell proliferation and/or migration, comprising contacting the smooth muscle cells with an amount effective to inhibit smooth muscle cell proliferation and/or migration of the following polypeptide:

X2-SEQ ID NO: 300

X2 is a cell transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

3. A method for treating or inhibiting a disorder selected from the group consisting of intimal hyperplasia, stenosis, restenosis, and/or atherosclerosis, comprising contacting a subject in need thereof with an amount effective to treat or inhibit intimal hyperplasia, stenosis, restenosis, and/or atherosclerosis with the following polypeptide:

X2-SEQ ID NO: 300-X6

X2 is absent or is a cell transduction domain;

X6 is absent or is a cell transduction domain; and wherein at least one of X2 and

X6 comprise a transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

4. A method for treating or inhibiting a disorder selected from the group consisting of intimal hyperplasia, stenosis, restenosis, and/or atherosclerosis, comprising contacting a subject in need thereof with an amount effective to treat or inhibit intimal hyperplasia, stenosis, restenosis, and/or atherosclerosis of the following polypeptide:

X2-SEQ ID NO: 300

X2 is a cell transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

5. A method for treating or inhibiting smooth muscle spasm, comprising contacting a subject in need thereof with an amount effective to inhibit vasoconstriction of the following polypeptide:

X2-SEQ ID NO: 300-X6

X2 is absent or is a cell transduction domain;

X6 is absent or is a cell transduction domain; and wherein at least one of X2 and

X6 comprise a transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

6. A method for treating or inhibiting smooth muscle spasm, comprising contacting a subject in need thereof with an amount effective to inhibit vasoconstriction of the following polypeptide

X2-SEQ ID NO: 300

X2 is a cell transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

7. A method of reducing graft failure in a subject with a graft, comprising administering to the subject an effective amount of the following polypeptide

X2-SEQ ID NO: 300-X6

X2 is absent or is a cell transduction domain;

X6 is absent or is a cell transduction domain; and wherein at least one of X2 and

X6 comprise a transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

8. A method of reducing graft failure in a subject with a graft, comprising administering to the subject an effective amount of the following polypeptide:

X2-SEQ ID NO: 300

X2 is a cell transduction domain;

(SEQ ID NO: 300) is Trp Leu Arg Arg Ala Ser Ala Pro Leu Pro Gly Leu Lys; and

the serine in SEQ ID NO: 300 is phosphorylated.

9. The method of claim 1 wherein the method is used to treat or inhibit one or more of angina, coronary vasospasm, Prinzmetal's angina, ischemia, stroke, bradycardia, hypertension, pulmonary hypertension, asthma, toxemia of pregnancy, pre-term labor, pre-eclampsia, eclampsia, Raynaud's disease or phenomenon, hemolytic-uremia, non-occlusive mesenteric ischemia, anal fissure, achalasia, impotence, migraine, ischemic muscle injury associated with smooth muscle spasm, and vasculopathy in the subject.

10. The method of claim 2 , wherein the method is used to treat or inhibit one or more of angina, coronary vasospasm, Prinzmetal's angina, ischemia, stroke, bradycardia, hypertension, pulmonary hypertension, asthma, toxemia of pregnancy, pre-term labor, pre-eclampsia, eclampsia, Raynaud's disease or phenomenon, hemolytic-uremia, non-occlusive mesenteric ischemia, anal fissure, achalasia, impotence, migraine, ischemic muscle injury associated with smooth muscle spasm, and vasculopathy in the subject.

11. The method of claim 3 wherein the method is used to inhibit intimal hyperplasia.

12. The method of claim 4 wherein the method is used to inhibit intimal hyperplasia.

Assignments (3)
LICENSE Recorded Nov 6, 2024
From: ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 069295/0303 →
CONFIRMATORY LICENSE Recorded May 13, 2019
From: ARIZONA STATE UNIVERSITY - TEMPE CAMPUS
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 049158/0679 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2008
From: BROPHY, COLLEEN; KOMALAVILAS, PADMINI; PANITCH, ALYSSA; SEAL, BRANDON; JOSHI, LOKESH
To: ARIZONA BOARD OF REGENTS
Reel/Frame 020851/0296 →
Continuity (1)
Related Publication 20090258819A1 · Oct 15, 2009