The Ultrastructural and Abnormal Calcium Handling in Pulmonary Vein Sleeve Cells, Atrial and Ventricular Myocytes During Ageing

Masoud, Said (2018). The Ultrastructural and Abnormal Calcium Handling in Pulmonary Vein Sleeve Cells, Atrial and Ventricular Myocytes During Ageing. PhD thesis The Open University.

DOI: https://doi.org/10.21954/ou.ro.0000e0ab

Abstract

Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia, with age being a significant risk factor. It is well established now that electric activities originating from pulmonary vein sleeve cells (PVCs) initiate AF. Factors that are involved in maintaining AF include structural remodelling and abnormal Ca²⁺ handling in PVCs and atrial myocytes. Whilst structural changes and alterations in the Ca²⁺ homeostasis have been described previously in atrial myocytes, similar studies are still lacking in PVCs. Thus, this thesis investigated structural remodelling and Ca²⁺ handling, particularly in PVCs from 3- and 24month-old mice.

Using immunohistochemical and electron microscopy (EM) studies, this thesis revealed that PVCs just like atrial and ventricular myocytes, express RyR2, Cx40, and Cx43. Whilst RyR2 and Cx43 expressions did not change with age, Cx40 expression was found to deteriorate during ageing. Additionally, EM studies showed significant alterations in mitochondria which increased in size and numbers during ageing. Unlike PVCs, mitochondria in atrial myocytes were enlarged but did not increase in numbers during ageing. Mitochondria in ventricular myocytes did not deteriorate with age.

This study also showed that Ca²⁺ homeostasis in PVCs is disrupted during ageing. PVCs from aged mice had an increased frequency and duration of spontaneous Ca²⁺ waves, with reduced amplitude, less able to follow electrical pacing and had higher basal ROS levels compared to PVCs from young mice.

Additional studies attempted to induce ageing chemically with hydroxyurea (HU) in neonatal rat ventricular myocytes (NRVMs). HU inhibited pacing ability, induced autophagy and increased inducible ROS. Although some changes in chemically ageing model were similar to those in aged PVCs, further studies are needed to fully establish whether HU can induce ageing in NRVMs.

In conclusion, this study showed that structural remodelling and Ca²⁺ homeostasis differs in PVCs during ageing which may facilitate the occurrence of arrhythmias.

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About

• Item ORO ID
• 57515
• Item Type
• PhD Thesis
• Project Funding Details

• Funded Project Name	Project ID	Funding Body
  The Open	Not Set	The Open University (OU)

• Keywords
• atrial fibrillation; atrial arrhythmias; cell interaction; blood-vessels; calcium; myocardium; cardiovascular diseases in old age; heart; veins
• Academic Unit or School
• Faculty of Science, Technology, Engineering and Mathematics (STEM)
  Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
• Research Group
• Institute for Innovation Generation in the Life Sciences (Innogen)
  Cardiovascular Research Cluster
• Copyright Holders
• © 2018 The Author
• Depositing User
• Said Masoud