Efficient axonal transport of endolysosomes relies on the balanced ratio of microtubule tyrosination and detyrosination

Author:

Konietzny Anja123ORCID,Han Yuhao1245,Popp Yannes126,van Bommel Bas27,Sharma Aditi8,Delagrange Philippe9,Arbez Nicolas9,Moutin Marie-Jo8ORCID,Peris Leticia8ORCID,Mikhaylova Marina12ORCID

Affiliation:

1. Institute of Biology, Humboldt Universität zu Berlin 1 RG Optobiology , , Berlin 10115 , Germany

2. Guest Group ‘Neuronal Protein Transport’, Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf 2 , Hamburg 20251 , Germany

3. Institute of Industrial Science, The University of Tokyo 3 , Tokyo 153-8505 , Japan

4. Centre for Structural Systems Biology 4 , Hamburg 22607 , Germany

5. Structural Cell Biology of Viruses, Leibniz Institute of Virology (LIV) 5 , Hamburg 20251 , Germany

6. Charité – Universitätsmedizin Berlin, Einstein Center for Neurosciences Berlin 6 , 10117 Berlin , Germany

7. Institute for Chemistry and Biochemistry, Freie Universität Berlin 7 , Berlin 14195 , Germany

8. University Grenoble Alpes, Inserm U1216, CNRS, Grenoble Institut Neurosciences 8 , 38000 Grenoble , France

9. Institut de Recherche Servier 9 , Croissy 78290 , France

Abstract

ABSTRACT In neurons, the microtubule (MT) cytoskeleton forms the basis for long-distance protein transport from the cell body into and out of dendrites and axons. To maintain neuronal polarity, the axon initial segment (AIS) serves as a physical barrier, separating the axon from the somatodendritic compartment and acting as a filter for axonal cargo. Selective trafficking is further instructed by axonal enrichment of MT post-translational modifications, which affect MT dynamics and the activity of motor proteins. Here, we compared two knockout mouse lines lacking the respective enzymes for MT tyrosination and detyrosination, and found that both knockouts led to a shortening of the AIS. Neurons from both lines also showed an increased immobile fraction of endolysosomes present in the axon, whereas mobile organelles displayed shortened run distances in the retrograde direction. Overall, our results highlight the importance of maintaining the balance of tyrosinated and detyrosinated MTs for proper AIS length and axonal transport processes.

Funder

Deutsche Forschungsgemeinschaft

Agence National de la Recherche

Leducq Foundation

NeuroCAP-Servier

France Alzheimer

European Molecular Biology Organization

Japan Society for the Promotion of Science

Humboldt University of Berlin

Publisher

The Company of Biologists

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