# TBK1 activity regulates the directionality of axonal transport of signalling endosomes

## TL;DR

This study shows that the TBK1 kinase controls the one-way movement of signaling endosomes in neurons, which is crucial for nerve cell survival and may be disrupted in ALS.

## Contribution

The paper identifies TBK1 as a novel regulator of unidirectional signaling endosome transport via Rab7 phosphorylation.

## Key findings

- TBK1 phosphorylates Rab7 at S72, affecting its binding to dynein adaptors.
- TBK1 knockdown or Rab7 S72E mutation causes bidirectional movement of signaling endosomes.
- Transport of lysosomes and mitochondria remains unaffected by these changes.

## Abstract

Neurotrophin-containing signalling endosomes travel from the distal axon to the soma. ALS-linked kinase TBK1 governs the directionality of their transport in motor neurons by phosphorylating Rab7.

The polarised and complex morphology of neurons poses massive challenges for efficient cargo delivery between the axon and soma, a process termed axonal transport. We have previously shown that the retrograde axonal transport of pro-survival, neurotrophic signalling endosomes relies on Rab7 in motor neurons, and that their trafficking is impaired in the early stages of amyotrophic lateral sclerosis (ALS) pathogenesis. Here, we report the effect of Rab7 phosphorylation on the transport of these signalling endosomes. We show that the ALS-linked kinase TBK1 phosphorylates Rab7 at S72 in neurons, altering its binding to cytoplasmic dynein adaptors. Accordingly, both TBK1 knockdown and the expression of a loss-of-function Rab7 mutant (S72E) induce aberrant bidirectional movement of signalling endosomes without modifying neuronal polarity or endosomal sorting. This alteration is specific for signalling endosomes, as axonal transport of lysosomes and mitochondria remains unaffected. We have therefore discovered a new TBK1 function that ensures the unidirectional transport of signalling endosomes, suggesting that reduced TBK1 activity determines retrograde transport dysfunctions and long-range signalling impairments.