Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.797701
Title: Developing an alveolar model to test the regenerative potential of placental membrane mesenchymal stem cells in bronchopulmonary dysplasia
Author: Bratt, Jessica A. J.
ISNI:       0000 0004 8504 858X
Awarding Body: Keele University
Current Institution: Keele University
Date of Award: 2019
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Bronchopulmonary dysplasia (BPD) is a neonatal disease affecting the lungs of premature infants. Prematurely born infants have under-developed lungs and require invasive ventilation technologies to provide sufficient oxygen for survival. Artificial ventilation is thought to exacerbate BPD by causing mechanical and oxygen stress on the lung tissue. Despite improvements in paediatric respiratory management, BPD care is limited by a lack of appropriate treatment options and remains a key challenge for clinicians. The pathogenesis of BPD remains poorly understood and currently relies on animal models for investigation. This study looks at developing a hydrogel to provide a human relevant in vitro BPD model to investigate the potential regenerative capabilities of placenta mesenchymal stem cells as a cell-based therapy for BPD. We successfully developed a collagen-elastin hydrogel representative of the human lung alveolus. This allows the co-culture of multiple lung cells in addition to an air-liquid interface which achieves hyperoxygen exposure (equivalent to clinical ventilation interventions) and allows assessment of output measures such as hydrogel contraction, imaging techniques and DNA quantification. We identified a protocol to extract and expand cells from the tracheal suctions of ventilated infants. We cultured these cells within the previously developed model for assessment at hyperoxygen and compared cell function with human adult lung cells. We established that hyperoxygen had a detrimental effect on adult lung cell proliferation and the ability of cells to contract collagen-elastin hydrogels. Hyperoxygen had no observed effect on neonatal lung cells. Finally, placenta derived MSCs (pMSCs) were isolated from the amnion and chorion membrane. We found hyperoxygen exposure has an adverse effect on the expression of MSC cell markers, cell proliferation and cell morphology. This could have implications when developing a cell therapy for the treatment of BPD. When co-cultured with adult lung fibroblast, pMSCs positively influenced the proliferation of adult lung fibroblasts through a paracrine mechanism. These results suggest that pMSCs have the potential to alleviate the oxygen stress that lung cells of BPD infants experience.
Supervisor: Wu, P. ; Forsyth, N. R. ; El Haj, A. J. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.797701  DOI: Not available
Keywords: RM Therapeutics. Pharmacology
Share: