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ER - lysosome contacts at a pre-axonal region regulate axonal lysosome availability.

Nazmiye ÖzkanMax KoppersInge van SoestAlexandra van HartenDaphne JurriensNalan LivJudith KlumpermanLukas C KapiteinCasper C HoogenraadGinny G Farías
Published in: Nature communications (2021)
Neuronal function relies on careful coordination of organelle organization and transport. Kinesin-1 mediates transport of the endoplasmic reticulum (ER) and lysosomes into the axon and it is increasingly recognized that contacts between the ER and lysosomes influence organelle organization. However, it is unclear how organelle organization, inter-organelle communication and transport are linked and how this contributes to local organelle availability in neurons. Here, we show that somatic ER tubules are required for proper lysosome transport into the axon. Somatic ER tubule disruption causes accumulation of enlarged and less motile lysosomes at the soma. ER tubules regulate lysosome size and axonal translocation by promoting lysosome homo-fission. ER tubule - lysosome contacts often occur at a somatic pre-axonal region, where the kinesin-1-binding ER-protein P180 binds microtubules to promote kinesin-1-powered lysosome fission and subsequent axonal translocation. We propose that ER tubule - lysosome contacts at a pre-axonal region finely orchestrate axonal lysosome availability for proper neuronal function.
Keyphrases
  • endoplasmic reticulum
  • fluorescent probe
  • living cells
  • spinal cord injury
  • estrogen receptor
  • breast cancer cells
  • optic nerve
  • spinal cord
  • copy number
  • amino acid
  • transcription factor
  • blood brain barrier