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dc.contributor.advisorMcCullagh, Karl
dc.contributor.authorBahri, Ola Abdulsamad
dc.date.accessioned2018-07-24T08:22:19Z
dc.date.issued2019-07-05
dc.identifier.urihttp://hdl.handle.net/10379/7423
dc.description.abstractDuchenne Muscular Dystrophy (DMD) is a progressive X-linked fatal muscle degenerative disorder caused by the absence of the sarcolemmal associated dystrophin-glycoprotein complex (DGC) that connects the intracellular cytoskeleton to the extracellular matrix. DMD has an incidence of 1:3,500 in males. Females can be carriers of DMD mutations and asymptomatically affected at later ages. This thesis encompasses three main studies focussed on different therapeutic targets for DMD. The first study examines the therapeutic potential of using gene therapy in correcting calcium dysregulation in the pre-clinical mdx mouse model of DMD. Adeno-associated virus 2/9 (AAV2/9) carrying the green fluorescent protein (GFP) showed robust transduction in gastrocnemius of mdx mice. Intramuscular injection of AAV-hSERCA2a (sarco/endoplasmic reticulum Ca2+-ATPase) demonstrated some amelioration in the dystrophic phenotype including a reduction in the percentage of central nucleated fibres (CNFs) and enhanced gene expression of [Ca2+]-buffering proteins. However, striking elevations in the expression of genes encoding SERCA-inhibitors, inflammatory and proteolytic related proteins were also observed. Hence, we conclude that elevation in the aforementioned genes can present a challenge to the benefits of AAV-hSERCA2a gene therapy in mdx mice. The second part of this thesis is mostly dedicated to characterising the dermal associated panniculus carnosus (PC) skeletal muscle in wild-type and mdx mice. Histological and morphological hallmarks of dystrophy were assessed in PC at different age time-points. We next chose to study the myogenicity of the PC by isolating the PC satellite cells (SCs) from wild-type and mdx mice of both genders and differentiated them in vitro. Finally, we examined the hypothesis of Ca2+ dysregulation in the differentiated PC cells. PC muscle demonstrated a high turnover that increased with dystrophy and further augmented with age. We found that PC exemplified gender dimorphism in muscular dystrophy demonstrated by high myogenic activity in male mdx PC-derived cells in contrast to females. In conclusion, we propose that PC is a unique muscle model to study cellular mechanisms impinging on muscle regeneration in healthy and diseased mice that may reveal new therapeutic targets for DMD. Finally, we examined gender dimorphism in muscle regeneration by analysing morphology, myogenic and calcium-handling genes. This was facilitated by studying the histological and morphological hallmarks of dystrophy and measuring mRNA levels of selected genes including sex-hormone receptors, myogenic factors, MyHC isoforms and Ca2+-handling proteins. Demonstrated by the percentage of CNF, dystrophic gastrocnemius muscles regenerated more than dystrophic PC muscles. Male PC muscles of mdx mice demonstrated a higher turnover compared to their female counterparts. In addition, while dystrophic gastrocnemius muscles underwent hypertrophy, dystrophic PC remained at similar size to healthy counterparts. Furthermore, while dystrophy displayed no effect on capillarization in gastrocnemius, PC muscles had variable responses between genders. In summary, we propose that female PC muscles had the highest capability in managing muscular dystrophy and, hence, by further investigating it, this may lead to promising therapeutic approach for DMD.en_IE
dc.publisherNUI Galway
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectDuchenneen_IE
dc.subjectMuscular Dystrophyen_IE
dc.subjectPanniculus Carnosusen_IE
dc.subjectSERCAen_IE
dc.subjectCalcium dysregulationen_IE
dc.subjectDMDen_IE
dc.subjectGender Dimorphismen_IE
dc.subjectSkeletal Muscleen_IE
dc.subjectPhysiologyen_IE
dc.subjectMedicineen_IE
dc.titleTherapeutic targets for duchenne muscular dystrophyen_IE
dc.typeThesisen
dc.contributor.funderMinistry of Higher Education, Kingdom of Saudi Arabiaen_IE
dc.local.noteAfter I received my Bachelor’s degree in Biology from Umm Al-Qura University, I was honoured to be awarded a scholarship by KASP (King Abdullah Scholarship Program) to pursue a Master degree in Biomedical Science at National university of Ireland – Galway where I received the degree in 2012. I was then awarded another scholarship by KASP to do a Ph.D. in a relative field. I passed my PhD defense on the 21st of May 2018.I performed my Ph.D. research in the Regenerative Medicine Institute in National university of Ireland - Galway in the laboratory of Dr. Karl McCullagh at the Department of Physiology, NUIG. As a graduate student, my research was aimed at investigating different therapeutic targets for ameliorating the genetic disorder of Duchenne muscular dystrophy.en_IE
dc.description.embargo2019-10-03
dc.local.finalYesen_IE
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