Absence of ATG9A and synaptophysin demixing on Rab5 mutation-induced giant endosomes

ATG9A is the only integral membrane protein among core autophagy-related (ATG) proteins. We previously found that ATG9A does not co-assemble into synaptophysin-positive vesicles, but rather, localizes to a distinct pool of vesicles within synapsin condensates in both fibroblasts and nerve terminals. The endocytic origin of these vesicles further suggests the existence of different intracellular sorting or segregation mechanisms for ATG9A and synaptophysin in cells. However, the precise underlying mechanism remains largely unknown. In this follow-up study, we investigated the endosomal localization of these two proteins by exploiting the advantages of a Rab5 mutant that induces the formation of enlarged endosomes. Notably, ATG9A and synaptophysin intermix perfectly and do not segregate on giant endosomes, indicating that the separation of these two proteins is not solely caused by the inherent properties of the proteins, but possibly by other unknown factors.

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Publication Details

Journal
Molecular Brain
Published
2024-09-02
DOI
https://doi.org/10.1186/s13041-024-01132-3
Citations
1
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
0.33

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article

Absence of ATG9A and synaptophysin demixing on Rab5 mutation-induced giant endosomes

Yumei Wu, Ji-Young Choi, Daehun Park
1 citations
Molecular Brain
Cellular transport and secretion
0.33
article

Absence of ATG9A and synaptophysin demixing on Rab5 mutation-induced giant endosomes

Yumei Wu, Ji-Young Choi, Daehun Park
article en
1 citations

Abstract

ATG9A is the only integral membrane protein among core autophagy-related (ATG) proteins. We previously found that ATG9A does not co-assemble into synaptophysin-positive vesicles, but rather, localizes to a distinct pool of vesicles within synapsin condensates in both fibroblasts and nerve terminals. The endocytic origin of these vesicles further suggests the existence of different intracellular sorting or segregation mechanisms for ATG9A and synaptophysin in cells. However, the precise underlying mechanism remains largely unknown. In this follow-up study, we investigated the endosomal localization of these two proteins by exploiting the advantages of a Rab5 mutant that induces the formation of enlarged endosomes. Notably, ATG9A and synaptophysin intermix perfectly and do not segregate on giant endosomes, indicating that the separation of these two proteins is not solely caused by the inherent properties of the proteins, but possibly by other unknown factors.

Molecular BrainVol. 17(1)
Yale University (US), Catholic University of Korea (KR)
Catholic University of Korea
Openalex Percentile: Top 42%
Cellular transport and secretion
0.33
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Absence of ATG9A and synaptophysin demixing on Rab5 mutation-induced giant endosomes — Yumei Wu, Ji-Young Choi, et al. · Molecular Brain (2024) | TGRS Research Map | TGRS