Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763340
Title: The analysis of exosomal Tau release and its regulation
Author: Bradshaw, Aaron
ISNI:       0000 0004 7661 3057
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2018
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
The secretion of Tau protein from cells combined with its trans-cellular uptake has been hypothesised as a central component in the progression of Tauopathic neurodegenerative diseases. Exosomes, small (30 - 140 nm) vesicles released from cells, may represent a privileged route for secretion and transmission of neurodegenerative proteins. We hypothesised that 1) Tau protein may be released from cells in exosomes 2) that this process may be regulated by the interaction of Tau with the chaperone network and SUMOylation of Tau and 3) exosomes may transmit Tau to naïve cells. We established and characterised the exosomal release of Tau from SH-SY5Y cells; all isoforms of Tau studied, including endogenous SH-SY5Y Tau, were detected in exosomal fractions. Exosomal 2N4R-Tau was C-terminally truncated and intra-luminal. We investigated the role of Tau-Hsc70 interaction in its exosomal release and identified the co-chaperone DNAjC5 as a key mediator in this process. SUMOylation of Tau protein was also identified as a key process regulating its exosomal release. We furthermore gathered evidence connecting Tau protein dysfunction (P301L-Tau; oligomerisation) and exosomal release, implicating exosomal Tau release as a potentially disease relevant process. In order to model the transmission of Tau between cells, we studied the uptake of a) Tau recovered from cells and b) Tau secreted from cells. However, naïve SH-SY5Y cells were able to internalise extracellular Tau only to a low extent. When co-cultured, Tau protein transferred efficiently between cells. This process was potentiated by lysosomal compromise and dependent upon cell density. Finally, we determined that exosomes isolated from SH-SY5Y cells with ectopic expression of P301L-Tau were selectively toxic to primary mouse cortical neurons. Overall the work presented here confirms the exosomal release of Tau protein and links this process to pathological Tau. Our work identifies key cellular mechanisms governing the exosomal release of Tau that may serve as points of departure for future studies investigating the release and transmission of Tau, and the role of exosomes therein.
Supervisor: Cooper, J. M. ; de Silva, R. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.763340  DOI: Not available
Share: