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Mechanisms and functions of lysosome positioning
Abstract
Lysosomes have been classically considered terminal degradative organelles, but in recent years they have been found to participate in many other cellular processes, including killing of intracellular pathogens, antigen presentation, plasma membrane repair, cell adhesion and migration, tumor invasion and metastasis, apoptotic cell death, metabolic signaling and gene regulation. In addition, lysosome dysfunction has been shown to underlie not only rare lysosome storage disorders but also more common diseases, such as cancer and neurodegeneration. The involvement of lysosomes in most of these processes is now known to depend on the ability of lysosomes to move throughout the cytoplasm. Here, we review recent findings on the mechanisms that mediate the motility and positioning of lysosomes, and the importance of lysosome dynamics for cell physiology and pathology.
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Intracellular localization of lysosomes regulates their ability to interact and fuse with vesicles such as autophagosomes or endosomes.
“Notably, intracellular localization of lysosomes regulates their ability to interact and fuse with vesicles such as autophagosomes or endosomes31, 32, 47, 48.”
From Phosphatidylinositol-(4,5)-Bisphosphate Regulates Plasma Cholesterol Through LDL (Low-Density Lipoprotein) Receptor Lysosomal Degradation (2020) · cites this paper as [32]
The Autophagy section states that juxtanuclear lysosome positioning facilitates fusion with autophagosomes and that disrupting this positioning reduces the probability of fusion. Figure 1 links lysosome movement to endocytic degradation, but the passages do not establish that positioning regulates lysosome fusion with endosomes specifically. Page numbers were not available in our copy. (LLM, conf=0.82)
Experimental — accuracy not yet measuredLysosome activity depends on its position within the cell.
“Lysosome activity is dependent on its position within the cell31, 32.”
From Phosphatidylinositol-(4,5)-Bisphosphate Regulates Plasma Cholesterol Through LDL (Low-Density Lipoprotein) Receptor Lysosomal Degradation (2020) · cites this paper as [32]
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Metadata
- Authors
- Pu, J., Guardia, C. M., Keren-Kaplan, T., & Bonifacino, J. S.
- Affiliations
- Cell Biology and Neurobiology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health , Bethesda, MD 20892 , USA
- ORCID
- Bonifacino, Juan S.
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2016-12-01
- Volume
- 129
- Issue
- 23
- Pages
- 4329-4339
- ISSN
- 1477-9137
- 0021-9533
- Cited by
- 570
- References
- 13
- Language
- en
- Funders
- National Institute of Child Health and Human Development (ZIA HD001607)
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