Grant: Travel Awards - Institute Community Support
Ottawa Hospital Research Institute
$1,000.00
Altered Repair Potential And Gene Expression Profile Of CD146+ Endogenous Lung Mesenchymal Stromal Cells in Experimental Bronchopulmonary Dysplasia
EF 2015-16
Résumé
In Canada 8% of all babies are born preterm (before 37 weeks of gestational age). One of the most common complications seen in these children is bronchopulmonary dysplasia (BPD), a long lasting lung disease. These babies need a breathing machine and supplemental oxygen to stay alive; unfortunately, this also damages the still growing lung. Currently there is no treatment for BPD. Babies with BPD are often sent home with oxygen and continue to have lung problems such as asthma or emphysema ("smoker lung" even without smoking) later in life. We found a possible new treatment: our body contains stem cells, a pool of cells that can become any type of cell in the body. Stem cells help organs to grow and to repair. Previously, we found that a particular type of stem cell from the cord blood (mesenchymal stromal cell or MSC) can heal the lung of newborn rats exposed to high oxygen (BPD model). But babies that have BPD have more MSCs in their breathing tube indicating that the lung MSCs don't do their job in BPD. In the research presented here, we found that in newborn rats exposed to high oxygen the MSCs from their lungs impair the formation of blood vessels, which is necessary for the growing lung. Moreover, they are no longer expressing the right genes to support the growing lung or to control the immune system. In conclusion, in our model the MSCs likely contribute to the development of BPD. It is important to understand the good and bad things these MSCs can do because it may delay the use of MSCs as a new and desperately needed treatment for babies with BPD.
Programme
Travel Awards - Institute Community Support
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
331818
Name
Collins Jennifer J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Institute of Circulatory and Respiratory Health
Projecttitle
Altered Repair Potential And Gene Expression Profile Of CD146+ Endogenous Lung Mesenchymal Stromal Cells in Experimental Bronchopulmonary Dysplasia
Programtype2
Undefined
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Bronchopulmonary Dysplasia; Functional Analysis; Hyperoxia; Mesenchymal Stromal Cells; Microarray; Primary Cell Isolation & Culture; Rat Pups
Abstract
In Canada 8% of all babies are born preterm (before 37 weeks of gestational age). One of the most common complications seen in these children is bronchopulmonary dysplasia (BPD), a long lasting lung disease. These babies need a breathing machine and supplemental oxygen to stay alive; unfortunately, this also damages the still growing lung. Currently there is no treatment for BPD. Babies with BPD are often sent home with oxygen and continue to have lung problems such as asthma or emphysema ("smoker lung" even without smoking) later in life. We found a possible new treatment: our body contains stem cells, a pool of cells that can become any type of cell in the body. Stem cells help organs to grow and to repair. Previously, we found that a particular type of stem cell from the cord blood (mesenchymal stromal cell or MSC) can heal the lung of newborn rats exposed to high oxygen (BPD model). But babies that have BPD have more MSCs in their breathing tube indicating that the lung MSCs don't do their job in BPD. In the research presented here, we found that in newborn rats exposed to high oxygen the MSCs from their lungs impair the formation of blood vessels, which is necessary for the growing lung. Moreover, they are no longer expressing the right genes to support the growing lung or to control the immune system. In conclusion, in our model the MSCs likely contribute to the development of BPD. It is important to understand the good and bad things these MSCs can do because it may delay the use of MSCs as a new and desperately needed treatment for babies with BPD.
Competitiondate
201505
Approvedterm2
1 yr 0 mth
Pinamesdelim
Collins, Jennifer J
Approvedterm
1 an 0 mois
Cihrcontribution2
Inst of Circ &Respiratory Hlth~ $1,000~ $0~