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Monitoring Neutrophil Elastase and Cathepsin G Activity in Human Sputum Samples
Published on: May 21, 2021
Monensin disruption of neutrophil granule genesis
R T Parmley1, J M Kinkade, D T Akin
1Department of Pediatrics, University of Texas Health Science Center, San Antonio, Texas 78284-7810.
Abstract:
The Na+/H+ ionophore monensin (M) has been used widely to study intracellular pH gradients and acidic subcellular compartments. In the present study, cultured myeloid leukemia HL60 cells, directly sampled bone marrow cells, and peripheral blood neutrophils were exposed to 1-5 microM monensin for 0.5-20 hours. The effects were evaluated using ultrastructural, cytochemical, and biochemical methods. In HL60 cells and marrow promyelocytes treated with monensin, progressive vacuolation of the trans then the cis Golgi was observed. These vacuoles lacked diaminobenzidine (DAB) reactive peroxidase, high iron diamine (HID) reactive sulfated glycoconjugates, and periodate-thiocarbohydrazide-silver proteinate (PA-TCH-SP) reactive vicinal glycol containing complex carbohydrates, but some cis Golgi elements retained osmium zinc iodide reactive reducing groups. The number of normal intensely stained HID reactive granules decreased and an incomplete granule that was DAB-positive/HID-negative, PA-TCH-SP-negative with flocculent matrix density increased in frequency as a function of time and concentration of monensin. Treatment of HL60 cells with monensin markedly reduced 35SO4 incorporation but myeloperoxidase labeling and activity per cell remained constant, although it shifted to lower density granule fractions consistent with the persistent DAB staining of endoplasmic reticulum and synthesis of a DAB-positive, HID-negative granule in intact HL60 cells. The Golgi complex of monensin-treated myelocytes and segmented neutrophils was also vacuolated. A subpopulation of preformed primary granules in promyelocytes, myelocytes, and segmented neutrophils appeared to increase in size and peripheral or central electron lucency. These selective effects of monensin indicate that granule components may be packaged into DAB-positive organelles that are deficient in trans Golgi-derived elements (HID- and PA-TCH-SP-negative) and that some preformed primary granules contain a monensin sensitive Na+/H+ gradient.
Insights
Monensin disrupts intracellular pH gradients, affecting Golgi and granule formation in myeloid cells. This ionophore reveals insights into granule packaging and monensin-sensitive Na+/H+ gradients within these cells.
Area of Science:
- Cell Biology
- Hematology
- Biochemistry
Background:
- The Na+/H+ ionophore monensin is a tool for studying intracellular pH and acidic compartments.
- Understanding monensin's effects on myeloid cells is crucial for interpreting its use in cellular research.
Purpose of the Study:
- To investigate the ultrastructural, cytochemical, and biochemical effects of monensin on myeloid leukemia HL60 cells, bone marrow cells, and neutrophils.
- To elucidate the impact of monensin on Golgi complex function and granule biogenesis in these cell types.
Main Methods:
- Exposure of cultured HL60 cells, bone marrow cells, and neutrophils to varying concentrations and durations of monensin.
- Evaluation using transmission electron microscopy (TEM), cytochemical staining (DAB, HID, PA-TCH-SP, Osmium-Zinc-Iodide), and biochemical assays (35SO4 incorporation).
Main Results:
- Monensin induced progressive vacuolation of the Golgi complex (trans then cis) in HL60 cells and promyelocytes.
- Vacuoles and altered granules showed differential reactivity for cytochemical markers, indicating defects in glycosylation and protein packaging.
- Monensin reduced 35SO4 incorporation but maintained myeloperoxidase activity, suggesting altered proteoglycan synthesis and granule composition.
Conclusions:
- Monensin selectively affects granule component packaging, leading to DAB-positive organelles deficient in trans-Golgi-derived elements.
- The study demonstrates that some primary granules contain a monensin-sensitive Na+/H+ gradient, impacting their maturation and content.
- Monensin's distinct effects provide insights into the dynamic processes of granule formation and intracellular transport in myeloid cells.
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