Maintains internal cell environment.
Allows movement of substances in and out of the cell.
Recognition and communication through cells.
Hydrophobic molecules, eg:
water
alcohol
oxygen
Hydrophilic molecules, eg:
ions
large molecules
Simple diffusion
Facilitated diffusion
Osmosis
Active transport
Distance
Concentration gradient
Physical barriers
Surface area
Molecular signals: contact with other cells, tumours release signalling molecules, hormones promote cell division in tissue.
Environmental conditions: pH levels, temperature, nutrients.
Faster division
Less specialised
Develop their own blood supply
DNA mutations occur
No limited number of divisions
Can spread to other parts of the body.
Mutations to proto-oncogenes: mutation turns them to oncogenes that promote uncontrolled cell division
Mutations to tumour suppressor genes
Hereditary cancers: when someone inherits mutated genes.
Chemical: tobacco, air pollution
Physical: X-Rays, UV light
Biological: Viruses
Cells which are damaged or defective must be eliminated.
During fetal development, the removal of excess cells.
Activation of caspases and begin breakdown of cell contents.
Cell shrinks and blebs begin to form.
Cells continue to shrink and package themselves into apoptotic bodies.
Phagocytosis.
In necrosis, external factors cause internal tissue damage and cell disfunction.
Apoptosis is pre-planned, and required for smooth bodily functioning..
Necrosis is cellular death when exposed to extreme conditions.
Mitochondrial Pathway (Intracellular): Triggered when cell components, DNA, is damaged. Proteins signal for beginning of cascade reactions.
Death Receptor Pathway (Extracellular): Triggered by immune cells outside the target cell. Cells under stress can all trigger this pathway.
Too much apoptosis can lead to degenerative diseases such as Alzheimerās or Parkinsonās.
Too little apoptosis is seen in Syndactyly, where the skin between digits is not removed during embryonic development.
Due to apoptosis not occurring when it should:
Genetic mutations that increase cell division rate.
Caspases mutations that prevent function.
Defects in proteins leading to caspases activation
Defects in signal reception of apoptosis triggers.
Embryonic stem cells
Adult (somatic) stem cells
Induced pluripotent stem cells
Totipotent
Pluripotent
Multipotent
Unipotent
Does harvesting embryotic stem cells kill embryos? Taking lives?
Why use embryos when IPSCs exist?