Grant: Operating Grant
University of British Columbia
$337,447.00
Characterization of Functional L-Type Calcium Channels in Lymphocytes
FY 2009-10
Summary
The immune system is a complex network that consists of many cell types. Lymphocytes are one particular cell type of the immune system that becomes activated when the body is infected to kill off the invading pathogen. However, sometimes lymphocytes can become inappropriately activated when the body is not infected and this can result in an autoimmune disorder. The way that lymphocytes become activated is not completely known. The element, calcium, is one component in these cells that is required for their activation. However, the means by which calcium gains entry into lymphocytes remains unknown. We have recently identified two variations of a protein which form a "channel" that is found on the surface of lymphocytes, which may allow calcium to enter them. We predict that these calcium channels play a role in lymphocyte activation and may be responsible for the inappropriate immune responses that lead to autoimmune diseases, such as arthritis. We will test this idea by comparing a mouse that has the calcium channel deleted to normal mice. We will look for any reduction in immune strength in the absence of the calcium channel and this will help us further understand the role of the calcium channel. Identifying calcium channels responsible for calcium movement into lymphocytes may lead to the generation of novel drug targets that would allow investigators to block the immune activation that causes diseases such as arthritis and diabetes.
Department
Program
Operating Grant
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
190775
Name
Jefferies Wilfred A
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Immunology & Transplantation
Projecttitle
Characterization of Functional L-Type Calcium Channels in Lymphocytes
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$337,447
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Arthritis; Cacna1f; Diabetes; Mouse Models; T-Lymphocyte; Voltage-Gated Calcium Channel
Abstract
The immune system is a complex network that consists of many cell types. Lymphocytes are one particular cell type of the immune system that becomes activated when the body is infected to kill off the invading pathogen. However, sometimes lymphocytes can become inappropriately activated when the body is not infected and this can result in an autoimmune disorder. The way that lymphocytes become activated is not completely known. The element, calcium, is one component in these cells that is required for their activation. However, the means by which calcium gains entry into lymphocytes remains unknown. We have recently identified two variations of a protein which form a "channel" that is found on the surface of lymphocytes, which may allow calcium to enter them. We predict that these calcium channels play a role in lymphocyte activation and may be responsible for the inappropriate immune responses that lead to autoimmune diseases, such as arthritis. We will test this idea by comparing a mouse that has the calcium channel deleted to normal mice. We will look for any reduction in immune strength in the absence of the calcium channel and this will help us further understand the role of the calcium channel. Identifying calcium channels responsible for calcium movement into lymphocytes may lead to the generation of novel drug targets that would allow investigators to block the immune activation that causes diseases such as arthritis and diabetes.
Competitiondate
200909
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Jefferies, Wilfred A
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $337,447~ $0~