Cited by 49Protein Kinase Regulation and GTPase SignalingCellular transport and secretionCalcium signaling and nucleotide metabolism

The Intracellular Distribution of Inositol Polyphosphates in HL60 Promyeloid Cells

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Stuart, J A, Anderson, K L, French, P J, Kirk, C J, Michell, R H·1994·Biochemical Journal

Abstract

1. HL60 promyeloid cells contain high intracellular concentrations of inositol polyphosphates, notably inositol 1,3,4,5,6-pentakisphosphate (InsP5) and inositol hexakisphosphate (InsP6). To determine their intracellular location(s), we studied the release of inositol (poly)phosphates, of ATP, and of cytosolic and granule-enclosed enzymes from cells permeabilized by four different methods. 2. When cells were treated with digitonin, all of the inositol phosphates were released in parallel with the cytosolic constituents. Most of the InsP5 and InsP6 was released before significant permeabilization of azurophil granules. 3. Similar results were obtained from cells preloaded with ethylene glycol and permeabilized by osmotic lysis. 4. Electroporation at approximately 500 V/cm caused rapid release of free inositol. Higher field strengths provoked release of most of the ATP, InsP5 and InsP6, but only slight release of the intracellular enzymes. Multiple discharges released approximately 80-90% of total InsP5 and InsP6. In the absence of bivalent-cation chelators, InsP5 and InsP6 were released less readily than ATP. 5. Treatment of cells with Staphylococcus aureus alpha-toxin caused quantitative release of inositol and ATP, without release of intracellular enzymes. However, inositol phosphates were released much less readily than inositol or ATP. Even after prolonged incubation with a high concentration of alpha-toxin, only approximately 50-70% of InsP2, InsP3 and InsP4 and < or = 20% of InsP5 and InsP6 were released, indicating that the high charge or large hydrated radius of InsP5 and InsP6 might limit their release through small toxin-induced pores. 6. These results indicate that most intracellular inositol metabolites are either in, or in rapid exchange with, the cytosolic compartment of HL60 cells. However, they leave open the possibility that a small proportion of cellular InsP5 and InsP6 (< or = 10-20%) might be in some intracellular bound form.

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Crossref · 10.1042/bj3030517

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  • In mammalian cells, InsP5 and InsP6 are produced in significantly higher concentrations compared to other inositol phosphates.

    “In mammalian cells, InsP5 and InsP6 are produced in significantly higher concentrations compared to other inositol phosphates [39,40], representing the highest products in the HOIP pathway.”

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Authors
Stuart, J. A., Anderson, K. L., French, P. J., Kirk, C. J., & Michell, R. H.
Affiliations
University of Birmingham (GB)
Venue
Biochemical Journal
Published
1994-10-15
Volume
303
Issue
2
Pages
517-525
ISSN
  • 0264-6021 (ISSN-L)
  • 1470-8728
OpenAlex
W140093196
Cited by
49
References
0
Citations by year
2025: 1 · 2024: 4 · 2023: 5 · 2021: 1 · 2020: 2 · 2019: 1 · 2016: 1 · 2015: 3 · 2012: 3
FWCI
0.76
Type
journal article
Language
en
Open access
Locations
  • Biochemical Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • 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
Keywords
inositol polyphosphates, phytic acid, subcellular localization, cell permeabilization, digitonin, osmotic lysis, electroporation, Staphylococcus aureus alpha-toxin, azurophilic granules, ATP release, inositol metabolism
MeSH terms
Adenosine Triphosphate, Bacterial Toxins, beta-Galactosidase, Cell Membrane Permeability, Chelating Agents, Cytosol, Digitonin, Ethylene Glycols, Hemolysin Proteins, Humans, Microscopy, Electron, Osmotic Pressure, Phosphogluconate Dehydrogenase, Phosphoric Monoester Hydrolases, Phytic Acid, Staphylococcus aureus, Tumor Cells, Cultured, Leukemia, Promyelocytic, Acute, Electroporation, Ethylene Glycol

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