Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
University of Manitoba
$105,000.00
The effects of Chlamydia pneumoniae infection on nuclear protein import
EF 2009-10
Résumé
The leading cause of death in developed countries is heart attack. Heart attacks occur when plaque (atherosclerosis) blocks the blood vessels. There are many environmental causes of heart attacks and atherosclerosis, including diet, exercise, and high blood cholesterol. However, these factors alone cannot account for all incidence of heart disease. Recently, infection has been associated in clinical research with the development of atherosclerosis. The human body comes into contact with harmful germs every day of our lives. One such common infection is the bacteria, Chlamydia pneumoniae (Cpn). By the age of 65, Cpn will have infected 75% of the population. Cpn has been found directly in plaques of heart attack patients.
Cpn can live inside of the cells found in the blood vessel walls. In the development of a plaque, cells send and receive signals, resulting in the harmful changes. The nucleus is the central command centre of the cell, in charge of interpreting and responding to these signals. Previously, our lab has found that bad cholesterol (LDL) can affect transport of signals into the nucleus, leading to plaque development. It is possible, that as Cpn hijacks cell function, it alters the transport of normal, healthy signals to the nucleus. This change would then lead to the unhealthy characteristics of a blood vessel cell in an atherosclerotic plaque. We will measure changes in the movement of signals into the nucleus after Cpn infection, in order to understand the way Cpn can control cell activity.
This study will provide us with a better understanding of the role of Cpn in heart disease. Since such a large portion of the population has been exposed to Cpn by late adulthood, it is important to understand its contribution, for both treatment and prevention of heart attacks. If Cpn can be proven as a risk factor, early treatment options could be used to save many Canadian lives.
Programme
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Bénéficiaire
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
206106
Name
Deniset Justin F
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
The effects of Chlamydia pneumoniae infection on nuclear protein import
Programtype2
Studentship Programs
Orgnameinp2
University of Manitoba
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Atherosclerosis; Chlamydia Pneumoniae; Infection; Microinjection; Nuclear Protein Import; Smooth Muscle Cell Proliferation
Abstract
The leading cause of death in developed countries is heart attack. Heart attacks occur when plaque (atherosclerosis) blocks the blood vessels. There are many environmental causes of heart attacks and atherosclerosis, including diet, exercise, and high blood cholesterol. However, these factors alone cannot account for all incidence of heart disease. Recently, infection has been associated in clinical research with the development of atherosclerosis. The human body comes into contact with harmful germs every day of our lives. One such common infection is the bacteria, Chlamydia pneumoniae (Cpn). By the age of 65, Cpn will have infected 75% of the population. Cpn has been found directly in plaques of heart attack patients.
Cpn can live inside of the cells found in the blood vessel walls. In the development of a plaque, cells send and receive signals, resulting in the harmful changes. The nucleus is the central command centre of the cell, in charge of interpreting and responding to these signals. Previously, our lab has found that bad cholesterol (LDL) can affect transport of signals into the nucleus, leading to plaque development. It is possible, that as Cpn hijacks cell function, it alters the transport of normal, healthy signals to the nucleus. This change would then lead to the unhealthy characteristics of a blood vessel cell in an atherosclerotic plaque. We will measure changes in the movement of signals into the nucleus after Cpn infection, in order to understand the way Cpn can control cell activity.
This study will provide us with a better understanding of the role of Cpn in heart disease. Since such a large portion of the population has been exposed to Cpn by late adulthood, it is important to understand its contribution, for both treatment and prevention of heart attacks. If Cpn can be proven as a risk factor, early treatment options could be used to save many Canadian lives.
Competitiondate
200910
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Deniset, Justin F
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~