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

  • Nazmiye Özkan
  • , Max Koppers
  • , Inge van Soest
  • , Alexandra van Harten
  • , Daphne Jurriens
  • , Nalan Liv
  • , Judith Klumperman
  • , Lukas C. Kapitein
  • , Casper C. Hoogenraad
  • , Ginny G. Farías

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

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.
Original languageEnglish
Article number4493
Pages (from-to)1-18
Number of pages18
JournalNature Communications
Volume12
Early online date23 Jul 2021
DOIs
Publication statusPublished - 2021
Externally publishedYes

Funding

We thank Dr. Juan Bonifacino (NIH) for sharing the GFP-KIF5A-rigor and mCh-KIF5A-Strep constructs. We acknowledge C. de Heus and T. Veenendaal of the Cell Microscopy Center UMC Utrecht for their valuable assistance with CLEM experiments. We thank Dr. Anna Akhmanova for critically reading the manuscript. This work was supported by the Netherlands Organization for Scientific Research (NWO) through a VIDI grant (016.VIDI.189.019) to G.G.F., a KLEIN grant (OCENW.KLEIN.236) to G.G. F. and J.K., a VENI grant (VI.VENI.202.113) to M.K., a NWO Roadmap on Netherlands Electron Microscopy infrastructure NEMI (project 184.034.014) to J.K., a ZonMW-TOP grant (91216006) to J.K., and a ZonMW-TOP (91217002) grant to L.C.K. Additional support came from the European Research Council (ERC-StG 950617 to G.G.F., ERC-CoG 819219 to L.C.K), Alzheimer Nederland (WE. 15045 to C.C.H., WE.03-2019-10 to J. K.), and the Deutsche Forschungs Gemeinschaft (DFG FOR2625 to J.K.).

FundersFunder number
FP7 Ideas: European Research Council
ZonMw
European Research CouncilERC-CoG 819219
Alzheimer NederlandWE.03-2019-10, WE. 15045
Nederlandse Organisatie voor Wetenschappelijk Onderzoek91217002, VI.VENI.202.113, 91216006, OCENW.KLEIN.236, 184.034.014
Horizon 2020 Framework Programme950617
Deutsche ForschungsgemeinschaftDFG FOR2625

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