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Lecture notes Cells and Immunity Why We Can't Live Forever (BI2BC45) $10.38   Add to cart

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Lecture notes Cells and Immunity Why We Can't Live Forever (BI2BC45)

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The seventh lecture in a series for the module Cells and Immunity. This lecture covers aging, parabiosis, DNA damage/repair and more. A great way to start your understanding of the module or to miss a lecture or two.

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  • August 6, 2022
  • 4
  • 2019/2020
  • Class notes
  • Dr phil baker
  • All classes
  • Unknown
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27.11.19


L7 – Why we can’t live forever?


Lecture:
 Process of aging
o Subclinical age (part of life when starts getting ill)
o Age-related diseases w/ medical intervention and anti-aging therapies (↑subclinical
age)
o ↑ susceptibility as cells don’t function properly
 Parabiosis
o Join vascular system of young and old mice
 Young mice affected = ↓ neurogenesis, ↓ synaptic plasticity and ↓
cognition
 Opposite (rejuvenation) in older
 Balance systems
 What factors play a role in aging?
o ↓ cell prolif (don’t ↑ or cancer!) then ↑ cell replacement
o DNA damage/repair occur
 ↑ mutagens and damaging chemicals = rapid prolif = cancer
o Post-mitotic cells = Nerve cells/erythrocytes do not divide when mature
 Nerve cell replacement = memory ∆/loss
 Stem cells
o Compartments of stem cells (protection of damaging agents)
o Stem cell → stem cell + precursor cells/transit-amplifying cells → post-mitotic cells
→ cell death
o Do slowly reduce telomere length (different)
 Cell prolif
o Regenerate liver via prolif by losing surrounding cells (replacing)
 Primary cells can divide for 30-50 cells
o Hayflick limit = Stop bc loss of telomere
o Culture becomes senescent
 Demoralized by switching on telomerase expression = rebuilding telomeres
(found in cancer cells)
 Tumor suppressing mechanisms
o Telomerase is a reverse transcriptase (using RNA template
to extend the ends)
o Human hTERT gene switched on = immortality
 Senescence should be cleared, or cell recycled?
 Telomeres keep length that they are immortalized at
 Low telomerase activity = chromosomal activity, genome instability, growth
arrest and apoptosis
 Telomere length/activity are longer in females, determined by
enviro/genetic and are variable amongst individuals
o Age of cells = effects rate or efficiency of cell prolif
 Human premature aging syndromes have a very low telomere length
 Germ line cells have a fixed length genome
 Telomere structure

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