PIKfyve Regulates Vacuole Maturation and Nutrient Recovery following Engulfment
Open accessAbstract
The scavenging of extracellular macromolecules by engulfment can sustain cell growth in a nutrient-depleted environment. Engulfed macromolecules are contained within vacuoles that are targeted for lysosome fusion to initiate degradation and nutrient export. We have shown that vacuoles containing engulfed material undergo mTORC1-dependent fission that redistributes degraded cargo back into the endosomal network. Here we identify the lipid kinase PIKfyve as a regulator of an alternative pathway that distributes engulfed contents in support of intracellular macromolecular synthesis during macropinocytosis, entosis, and phagocytosis. We find that PIKfyve regulates vacuole size in part through its downstream effector, the cationic transporter TRPML1. Furthermore, PIKfyve promotes recovery of nutrients from vacuoles, suggesting a potential link between PIKfyve activity and lysosomal nutrient export. During nutrient depletion, PIKfyve activity protects Ras-mutant cells from starvation-induced cell death and supports their proliferation. These data identify PIKfyve as a critical regulator of vacuole maturation and nutrient recovery during engulfment.
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Lysosomal degradation of internalized entotic cells generates nutrients recovered by engulfing cells via a mechanism involving PIKFYVE.
“the lysosomal degradation of internalized entotic cells generates nutrients that are recovered by engulfing cells, via a mechanism that reportedly involves phosphoinositide kinase, FYVE-type zinc finger containing (PIKFYVE) [704, 707, 708].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [708]
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References 47 · Cited by 140
- Authors
- Krishna, S., Palm, W., Lee, Y., Yang, W., Bandyopadhyay, U., Xu, H., Florey, O., Thompson, C. B., & Overholtzer, M.
- Affiliations
- Memorial Sloan Kettering Cancer Center (US)
- University of Michigan (US)
- Babraham Institute (GB)
- Corresponding author
- Overholtzer, Michael
- ORCID
- Venue
- Developmental Cell
- Publisher
- Elsevier BV
- Published
- 2016-09
- Volume
- 38
- Issue
- 5
- Pages
- 536-547
- ISSN
- 1534-5807 (ISSN-L)
- PMC
- PMC5046836
- OpenAlex
- W2519911943
- Cited by
- 140
- References
- 47
- Citations by year
- 2026: 9 · 2025: 14 · 2024: 14 · 2023: 18 · 2022: 15 · 2021: 21 · 2020: 10 · 2019: 12 · 2018: 15 · 2017: 12
- FWCI
- 8.95
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Developmental Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (RO1GM111350-01)
- National Cancer Institute (PO1 CA104838)
- MSK Cancer Center (P30 CA008748)
- Benjamin Friedman Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- PIKfyve, engulfment, macropinocytosis, entosis, phagocytosis, TRPML1, nutrient recovery, mTORC1, nutrient deprivation, endosomal trafficking
- MeSH terms
- Mechanistic Target of Rapamycin Complex 1, Animals, Humans, Lysosomes, Phagocytosis, Endosomes, Starvation, Vacuoles, Caenorhabditis elegans, Phosphatidylinositol 3-Kinases, Cell Line, Tumor, Multiprotein Complexes, Transient Receptor Potential Channels, TOR Serine-Threonine Kinases
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