GENE-TARGETED MINIATURE SWINE MODELS OF ATHEROSCLEROSIS

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$118,125.00
Award Year:
2006
Program:
SBIR
Phase:
Phase I
Contract:
1R43HL083555-01
Award Id:
80738
Agency Tracking Number:
HL083555
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
419 VENTURE CT, VERONA, WI, 53593
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
n/a
Principal Investigator:
JOHNDOBRINSKY
() -
Business Contact:
LUDWIGSIMMET
(608) 845-1502
simmet@minitube.com
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): Minitube of America will use SBIR funds to develop porcine models of atherosclerosis. Cardiovascular disease is the leading cause of morbidity and mortality in the United States and coronary artery disease accounts for a majority of the deaths. Research to uncover the etiology of atherosclerosis and to develop new therapies has relied heavily on the use of animal models. Most of these studies point to hypercholesterolemia as the principal cause of atherosclerosis. Rabbits, swine and rhesus monkeys with genetic mutations linked to hypercholesterolemia have been used to study atherosclerosis but recent research has focused on genetically modified mice. However, genetically modified mice that manifest hypercholesterolemia do not exhibit lesions typical of atherosclerosis in humans. In contrast, swine pedigrees that develop hypercholesterolemia as a result of naturally occurring genetic mutations manifest arterial lesions similar to those seen in human. The goal of this project is to introduce specific genetic alterations in miniature swine that reproduce the genetic and pathological characteristics of human atherosclerosis. Studies in humans, mice and swine indicate that alterations in the low-density lipoprotein gene (Ldlr) can produce hypercholesterolemia and early onset atherosclerotic lesions in coronary and other arteries. The approach in this project will be to use traditional and/or novel gene targeting methods to knockout both alleles of Ldlr in male and female miniature swine cells. These Ldlr-/- cells will be used in nuclear transfer to produce Ldlr-/- founder animals that will be analyzed for their propensity to develop atherosclerosis. These genetically modified miniature swine will be expanded through breeding and then sold to meet a growing need of medical device and pharmaceutical companies for uniform animal models of human pathologies that can help predict the outcome of human therapeutic interventions.

* information listed above is at the time of submission.

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