TBK1 orchestrates autophagy and endo-lysosomal pathways in human neurons

Haploinsufficiency of TBK1 causes familial ALS and frontotemporal dementia (FTD), yet the mechanisms by which TBK1 loss leads to neurodegeneration remain unclear. Using deep proteomics and phospho-proteomics, we demonstrate that TBK1 regulates select macroautophagy/autophagy factors, targeting cargo receptors and autophagy initiation factors, and also sustains the phosphorylation of the late endosomal marker RAB7A in stem cells and stem cell-derived excitatory neurons. We further uncovered novel TBK1-dependent phosphorylation sites in the key autophagy protein SQSTM1/p62. Loss of TBK1 function results in a cell-autonomous neurodegenerative phenotype characterized by impaired neurite outgrowth and lysosomal dysfunction.

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Publication Details

Journal
Autophagy
Published
2026-01-04
DOI
https://doi.org/10.1080/15548627.2025.2609924
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
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article

TBK1 orchestrates autophagy and endo-lysosomal pathways in human neurons

Julie Smeyers, Daniel A. Mordes
Autophagy
Amyotrophic Lateral Sclerosis Research
article

TBK1 orchestrates autophagy and endo-lysosomal pathways in human neurons

Julie Smeyers, Daniel A. Mordes
article en

Abstract

Haploinsufficiency of TBK1 causes familial ALS and frontotemporal dementia (FTD), yet the mechanisms by which TBK1 loss leads to neurodegeneration remain unclear. Using deep proteomics and phospho-proteomics, we demonstrate that TBK1 regulates select macroautophagy/autophagy factors, targeting cargo receptors and autophagy initiation factors, and also sustains the phosphorylation of the late endosomal marker RAB7A in stem cells and stem cell-derived excitatory neurons. We further uncovered novel TBK1-dependent phosphorylation sites in the key autophagy protein SQSTM1/p62. Loss of TBK1 function results in a cell-autonomous neurodegenerative phenotype characterized by impaired neurite outgrowth and lysosomal dysfunction.

AutophagyVol. 22(3)
University of California System (US)
Life below water
Openalex Percentile: Top 98%
Amyotrophic Lateral Sclerosis Research
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