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Printable Handouts
Navigable Slide Index
- Introduction
- Mitochondria, the powerplant of the cell
- Mitochondrial functions
- Mitochondria utilize both mtDNA & nDNA
- Mitochondrial genome
- Mitochondrial diseases
- Mitochondrial diseases (mtDNA)
- Mitochondria in ageing (observations)
- Role of mitochondria in ageing
- Metabolic rate theory of aging
- Rate of living hypothesis
- Metabolic rate theory of aging (examples)
- Mitochondria dysfunction can extend life span
- Mitochondria dysfunction extends lifespan in mice
- Various effects of partial mitochondrial deficiency
- Metabolic rate theory of aging (Cons)
- Caloric restriction (CR)
- Mitochondrial ROS production
- Main sites of mitochondrial ROS production
- Oxygen is a potent source of damage
- Increased ROS production ≠ oxidative stress
- Correlative studies vs.."intervention" studies
- New evidence for the theory of the stork
- ROS, oxidative damage and ageing
- Oxidative damage and dietary supplementation
- Oxidative stress in lifespan determination
- ROS as signaling molecule and mitohormesis
- Mitochondrial DNA mutations
- mtDNA mutations and ageing
- Heteroplasmy vs. Homoplasmy
- Relaxed replication of mtDNA
- Mitochondrial/Free radical theory of aging
- The vicious cycle
- mtDNA mutator mice
- mtDNA mutator mice survival curve
- Aging phenotypes in mtDNA mutator mice
- Obvious phenotypes of mtDNA mutator mice
- Progression of alopecia
- Osteoporosis, loss of fat and muscle mass
- Skin changes
- Cardiomyopathy in mtDNA mutator mice
- Fertility problems (ovaries)
- Progressive hearing loss
- Progressive hearing loss (spiral ganglia neurons)
- Increased apoptosis in mtDNA mutator mice
- Aging phenotypes in old control mice
- Massive mitochondrial dysfunction
- No change in ROS production
- Increased turnover of mitochondrial transcripts
- Premature aging of mtDNA mutator mice
- Is there a role for mitochondria in aging?
- The signaling role of mitochondria in ageing
- Role of mtDNA mutations in ageing
- Conclusions
- Final remark
- Acknowledgements
Topics Covered
- Mitochondria function/dysfunction and related outcomes
- Metabolic rate theory of aging
- Beneficial effects of caloric restriction
- ROS production and oxidative stress effect on aging
- Free radical theory of aging
- Mitochondrial DNA mutations phenotypes
Talk Citation
Trifunovic, A. (2018, February 28). Mitochondria and ageing in model systems [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/RQLE3920.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Aleksandra Trifunovic has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: Mitochondria in Health and Disease
Transcript
Please wait while the transcript is being prepared...
0:00
My name is Aleksandra Trifunovic,
I'm a professor of mitochondria genetics in disease and aging at
the University of Cologne in Germany and
the title of talk is Mitochondria and Ageing in Model Systems.
0:14
The Mitochondria are the powerplants of the cells.
Without them we would not be able to sustain any kinds of multicellular life on earth.
To function properly, our body in each
second needs around three times 10 to the power of 18 molecules of ATP,
and that means that our mitochondria produce roughly around 70 kilos of ATP every day.
Most of this ATP is consumed by central nervous system and brain in our bodies.
0:47
So, although mitochondria is considered as
this extremely powerful electric centrals of our body,
they actually produce and harbor
many other different processes that are
essential for our body functioning and homeostasis.
So among those, we have fatty acid oxidation,
TCA cycle, production of different intermediates like for example,
iron-sulphur cluster assembly intermediates or heme synthesis intermediates,
also some parts of amino acid synthesis are located inside mitochondria.
1:25
So, mitochondria are unique in
animal cells in the way that they have their own mitochondrial DNA,
and this is the leftover of the fact that mitochondria used to be
a bacteria that once upon a time invaded a primordial eukaryotic cells.
Today, they rely on two different genomes,
ones is in the nucleus and is called nuclear genome and one is mitochondrial genome,
and in order to function properly they need to
coordinate expression of genes in both of these places,
and they have to assemble different parts of mitochondria in a very coordinated way.
This can be very demanding and very tricky.
So, mitochondrial DNA is actually a very small DNA molecule.