Usage
  • 36 views
  • 152 downloads

Endothelial Colony Forming Cells: Role in Bronchopulmonary Dysplasia and evaluation of new therapeutic strategies

  • Author / Creator
    Rajabali, Saima Nasiruddin
  • Bronchopulmonary dysplasia (BPD), a chronic lung disease of prematurity, results in alveolar simplification and respiratory distress in the newborn. Vascular component is implicated. Lung damage involves a deficiency in the number and function of progenitor cells. We hypothesize that endothelial colony forming cells (ECFCs) exist in the developing human lung, are impaired in hyperoxia and secrete exosomes. ECFCs from human fetal lung expressed CD31, CD105, CD144, CD146 and were negative for CD14 and CD45. In hyperoxic conditions, cord formation and clonogenic potential was impaired. Mesenchymal stem cell conditioned media (MSC CdM) improved clonogenic potential. Exosomes were isolated from human cord blood derived ECFC CdM and characterized using electron microscopy and protein expression. This study provides novel finding that ECFCs exist in human fetal lung and their function is impaired in hyperoxia. They may exert their effect by exosomes. This provides a rationale for use of exogenous stem cells in BPD.

  • Subjects / Keywords
  • Graduation date
    2013-11
  • Type of Item
    Thesis
  • Degree
    Master of Science
  • DOI
    https://doi.org/10.7939/R30R9MB0S
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
  • Language
    English
  • Institution
    University of Alberta
  • Degree level
    Master's
  • Department
    • Medical Sciences-Paediatrics
  • Supervisor / co-supervisor and their department(s)
    • Dr. Bernard Thebaud, Department of Pediatrics
  • Examining committee members and their departments
    • Dr. John Greer, Department of Physiology
    • Dr. Jason Dyck, Department of Pediatrics
    • Dr. Gary Lopaschuk, Department of Pediatrics