Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639807
Title: Interactions between mitochondria and inflammatory factors during cellular senescence
Author: Correia-Melo, Clara
ISNI:       0000 0004 5365 4737
Awarding Body: University of Newcastle Upon Tyne
Current Institution: University of Newcastle upon Tyne
Date of Award: 2014
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Abstract:
Cellular senescence, the irreversible loss of proliferating capacity of somatic cells, is an important tumour suppressor mechanism but also driver of ageing. These somehow contradictory functions are dependent on the development of the so-called senescent phenotype, which involves over-production of pro-inflammatory and pro-oxidant signals, however the exact mechanisms underlying its induction remain incompletely understood. In this thesis we aimed to understand how mitochondria and pro-inflammatory factors interact during senescence and how they contribute to the senescent phenotype. Firstly, we show that mitochondria are critical for the establishment and maintenance of cell senescence. Elimination of mitochondria rejuvenated senescent human fibroblasts, abrogating the pro-inflammatory phenotype, heterochromatin foci and expression of cyclin-dependent kinase inhibitors p21 and p16. Importantly, a considerable percentage of these cells were able to resume proliferation. Mechanistically, we show that mTORC1 integrates signals from the DNA damage response towards PGC-1β-dependent mitochondrial biogenesis, playing a causal role in the development of senescence. Secondly we show that inhibition of IL-8, a prominent proinflammatory cytokine of the SASP, partially abrogated the senescent phenotype by reducing mTOR-dependent mitochondrial mass and ROS production during senescence. Finally, we demonstrate that inhibition of mitochondrial content in vivo by either rapamycin or PGC-1β deletion prevents age-dependent increase in senescence in mouse liver. Our results suggest mitochondria as an important target for interventions aiming to reduce the load of senescent cells in ageing tissues.
Supervisor: Not available Sponsor: FCT
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.639807  DOI: Not available
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