The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Dynein-dependent Movement of Autophagosomes Mediates Efficient Encounters with Lysosomes
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Under starvation conditions, autophagosomes and lysosomes move toward the cell center, facilitating fusion and degradation of autophagosomal content.
“under starvation conditions, autophagosomes and lysosomes move toward the cell center, facilitating the fusion between both organelles and degradation of the autophagosomal content9,10.”
From TFEB regulates lysosomal positioning by modulating TMEM55B expression and JIP4 recruitment to lysosomes (2017) · cites this paper as [9]
The sections “Autophagosomes move toward the cell center” and “Significance of the rapid vectorial movement for autophagy” support movement of autophagosomes toward centrally clustered lysosomes and its role in efficient targeting. But “Anti-LC3 antibody microinjection inhibits autophagosome movement” says lysosome localization did not significantly change under starvation; the paper does not support the claim that lysosomes also move toward the cell center under those conditions. Page numbers are unavailable in our copy. (LLM, conf=0.90)
Experimental — accuracy not yet measuredLysosomal positioning, modulated by cellular stimuli, regulates autophagic flux, and starvation-induced perinuclear lysosome-autophagosome fusion is critical for cargo degradation.
“Lysosomal positioning, modulated by cellular stimuli, regulates autophagic flux, and starvation-induced perinuclear lysosome-autophagosome fusion is critical for cargo degradation (Kimura et al. 2008), (Korolchuk et al. 2011).”
From TMEM55B downregulation promotes neurodegeneration in Alzheimer’s disease models (2026) · cites this paper as Kimura et al. 2008
In “Anti-LC3 antibody microinjection inhibits autophagosome movement” (page unavailable), the paper reports faster delivery of autophagosome markers to perinuclear lysosomes during starvation and shows that inhibiting autophagosome movement impairs that delivery. It does not establish that stimulus-modulated lysosomal positioning regulates autophagic flux: it explicitly reports that starvation did not significantly change lysosome localization. The experiment measures delivery, not cargo degradation directly. (LLM, conf=0.88)
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Metadata
- Authors
- Kimura, S., Noda, T., & Yoshimori, T.
- Venue
- Cell Structure and Function
- Publisher
- Japan Society for Cell Biology
- Published
- 2008
- Volume
- 33
- Issue
- 1
- Pages
- 109-122
- ISSN
- 0386-7196
- 1347-3700
- Cited by
- 438
- References
- 6
- Language
- en
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