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Lecture Notes

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Lecture notes of 13 pages for the course Cell Biology and developmental genetics at QMUL

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  • March 7, 2021
  • 13
  • 2020/2021
  • Class notes
  • Kermorgant
  • All classes

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By: betulalm • 3 year ago

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Interplay between growth factor receptor trafficking and signalling
Learning objective

1. C-Met signals from the endosome
2. C-Met signalling on endosome promotes tumorigenesis
3. The endosome: a signalling platform

Explain 2 reasons why a receptor signals on endosome rather than only on plasma membrane, which are the following:

4. Signalling en endosome: protection against phosphatases
5. Signalling en endosome: access to specific signals

c-Met/HGF

 Example used is c-Met and will always hear about c-Met
 Text book shows C-Met receptor found at the plasma membrane or surface of the cell and ligand binds to receptor
 The binding of ligand will trigger c-Met activation and signalling, which occurs at the plasma membrane as shown in
the image.




Receptor compartmental signalling

 Another consequence of ligand binding is internalisation of receptor (RTK), which occurs in sec/min (rapid).
 Endocytosis and signalling mechanism are complex and scientist do not completely understand or know which occurs
first but may require each other.
 The receptor does not only signal at the plasma membrane but also inside the cell in endosome
 There is literature showing that signalling also occurs on the ER and not always on the endosome. In this module, will
only speak about signalling in endosome.
 The receptor enters cell while still being bound to its ligand however this is not shown in the image.
- Red oval= receptor
- Red circle = ligand
 In the endosome, the ligand bound active receptor can still be associated to signalling molecules and adaptors
 There are not many pathways known to be activated on structures, such as endosome. Therefore, this is just the
beginning.
 So far only believe that the signalling cascade occurs at the PM but the same signalling cascade may be occurring on
organelles/compartments.
 The following can be a possibility, currently there is no consensus but both could happen
- It may be that some of the signalling starts at the plasma membrane and once the receptor enters the cell the
signalling is sustained on the receptor
- Some signalling pathways may only occur on the endosome

, l- c-Met signals from the endosome

 Once the receptor enters the cell it will go into the early endosome followed by late endosome and the get degraded
 ERK is a protein in the MAPK/ERK pathway (also known as ras-raf-MEK-ERK pathway) is a chain of proteins in the cell
that communicates a signal from a receptor on the surface of the cell to the DNA in the nucleus
 Image showing c-Met receptor at the plasma membrane, the ligand, HGF binds to c-Met and enters the early
endosome and traffics along microtubules to the late endosome.
 ERK (protein) gets phosphorylated
 ETK can signal on an endosome




 Internalisation of the c-Met receptor
- Once the receptor enters the cell, the receptor goes on the early endosome followed by MVB/late endosome
and then degraded.
- This is still true as after 2 hours, 50% of the c-Met has been degraded and the other 50% is still inside the cell
- The remaining 50% c-Met receptor may have been recycled back to the PM
 Most of receptor tyrosine kinases get endocytosed and then degraded. In certain situation, RTK gets recycled but
usually endocytosis pathway is preferred.
 Between the time the receptor gets in the cell and degrades, the receptor is bound to ligand and signalling molecules
and can activate signalling pathways.

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