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Grant: Master's Award: Canada Graduate Scholarships

Queen's University (Kingston, Ontario)

$27,000.00

Spatio-temporal and transcriptional profiling of monocyte-derived macrophages in spinal cord injury

FY 2024-25

Summary
TitleSpatio-temporal and transcriptional profiling of monocyte-derived macrophages in spinal cord injuryLay TitleUnderstanding how and when specific immune cells affect spinal cord injuryLay AbstractSpinal cord injury (SCI) is a life-altering condition caused by damage to the spinal cord, often caused by car accidents, falls, or violence. The immune system response to SCI has been well-characterized. Although the immune system is thought to support SCI recovery, it can often become overactivated and cause even greater damage, known as secondary injury. It is hypothesized that some of this secondary injury can be attributed to monocyte-derived macrophages (MDMs), which are a specific type of immune cell. Previous research has shown that most MDMs in the spinal cord after injury migrated there from the spleen. However, removing the spleen doesnt change SCI recovery, but removing all the MDMs improves recovery. This indicates that there is a population of MDMs outside of the spleen that are generating the majority of the secondary injury. We hypothesize that these harmful MDMs are migrating to the spinal cord from the small intestine. To test this hypothesis, we are going to use a mouse model with photoconvertible cells. This means all the cells in the body express a green protein that can be changed to red when exposed to a violet laser. We will shine the laser on the small intestine and then perform a spinal cord injury using a standardized impactor. Since the laser will only convert the intestinal cells, we will know that any red cells found in the spinal cord migrated there from the intestine. We will duplicate this process in the spleen and liver to measure the degree of MDM migration from each tissue type.
Program
Master's Award: Canada Graduate Scholarships
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
530101
Name
Wilcox Natalie C
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Special Cases - Awards Programs
Projecttitle
Spatio-temporal and transcriptional profiling of monocyte-derived macrophages in spinal cord injury
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$27,000
Cihrequipment2
$0
Programname2
Master's Award: Canada Graduate Scholarships
Keyworddelim
Central Nervous System Injury; Marginal Pool; Monocyte-Derived Macrophages (Mdms); Neuroimmune; Photoconversion; Spinal Cord Injury; Tissue-Specific Migration
Abstract
TitleSpatio-temporal and transcriptional profiling of monocyte-derived macrophages in spinal cord injuryLay TitleUnderstanding how and when specific immune cells affect spinal cord injuryLay AbstractSpinal cord injury (SCI) is a life-altering condition caused by damage to the spinal cord, often caused by car accidents, falls, or violence. The immune system response to SCI has been well-characterized. Although the immune system is thought to support SCI recovery, it can often become overactivated and cause even greater damage, known as secondary injury. It is hypothesized that some of this secondary injury can be attributed to monocyte-derived macrophages (MDMs), which are a specific type of immune cell. Previous research has shown that most MDMs in the spinal cord after injury migrated there from the spleen. However, removing the spleen doesnt change SCI recovery, but removing all the MDMs improves recovery. This indicates that there is a population of MDMs outside of the spleen that are generating the majority of the secondary injury. We hypothesize that these harmful MDMs are migrating to the spinal cord from the small intestine. To test this hypothesis, we are going to use a mouse model with photoconvertible cells. This means all the cells in the body express a green protein that can be changed to red when exposed to a violet laser. We will shine the laser on the small intestine and then perform a spinal cord injury using a standardized impactor. Since the laser will only convert the intestinal cells, we will know that any red cells found in the spinal cord migrated there from the intestine. We will duplicate this process in the spleen and liver to measure the degree of MDM migration from each tissue type.
Competitiondate
202412
Approvedterm2
1 yr 0 mth
Pinamesdelim
Wilcox, Natalie C
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $27,000~ $0~