Microfilaments and microtubules in calcium ionophore-induced secretion of lysosomal enzymes from human
Abstract:
Human peripheral blood leukocytes (PMN) are induced to release lysosomal enzymes by the calcium ionophore A23187 in the presence but not the absence of extracellular Ca++. Whereas secretion induced by particulate or immune stimuli is accompanied by an increase in visible microtubules and is inhibitable by colchicine, secretion induced by A23187 and Ca++ was not accompanied by an increase in microtubule numbers and was not inhibited by colchicine. Ca++ did not appear to regulate microtubule assembly in these cells since resting PMN had a mean of 22.3 +/- 2.0 microtubules in the centriolar region as compared to 22.3 +/- 1.1 in ionophore-treated cells and 24.9 +/- 1.5 in cells exposed to ionophore and 1 mM Ca++. Bipolar filaments, 10 nm thick and 300--400 nm long, were numerous in the pericortical cytoplasm of cells exposed to both reagents. Microtubules in these cells were decorated with an electron-opaque fibrillar material. PMN exposed to A23187 and Ca++ were contracted in two directions at right angles to each other: (a) Contractions parallel to the plasma membrane resulted in extensive plication of the cell membrane. The cytoplasm subjacent to the plicae contained dense filamentous webs. Plication was prevented by cytochalasin B or reversed by subsequent exposure to an endocytic stimulus such as zymosan. (b) Contractions perpendicular to the plasma membrane, toward the cytocenter, resulted in the formation of vacuoles in normal PMN and of membrane invaginations in cytochalasin B-treated PMN. Whereas contractions parallel to the plasma membrane could occur in the absence of enzyme release (ionophore alone) and enzyme release could occur in the absence of such contractions (ionophore plus calcium plus cytochalasin B), contraction toward the cytocenter occurred in all experimental conditions in which significant enzyme release was obtained. Thus, lysosomal enzyme secretion in PMN involves contractile movements in the plasma membrane toward the lysosomes rather than the reverse. These calcium-mediated contractile events are mediated by cytochalasin B-insensitive microfilaments but not by microtubule assembly.
Insights
Calcium and ionophore A23187 trigger human peripheral blood leukocyte (PMN) enzyme release via microfilament-mediated contractions, not microtubule assembly. This process involves inward cell membrane movements towards lysosomes.
Area of Science:
- Cell Biology
- Immunology
- Biochemistry
Background:
- Human peripheral blood leukocytes (PMN) release lysosomal enzymes in response to various stimuli.
- Secretion pathways can involve cytoskeletal rearrangements, including microtubule and microfilament dynamics.
- The specific role of calcium and cytoskeletal elements in PMN degranulation requires further elucidation.
Purpose of the Study:
- To investigate the role of extracellular calcium (Ca++) and the ionophore A23187 in inducing lysosomal enzyme release from human PMN.
- To determine the involvement of microtubules and microfilaments in calcium-dependent PMN secretion.
- To elucidate the mechanical events underlying calcium-mediated degranulation in PMN.
Main Methods:
- Stimulation of human peripheral blood leukocytes (PMN) with calcium ionophore A23187 in the presence and absence of extracellular Ca++.
- Microscopic analysis of microtubule and microfilament structures using electron microscopy.
- Assessment of lysosomal enzyme release and cellular contractions under various experimental conditions, including treatment with colchicine and cytochalasin B.
Main Results:
- Calcium ionophore A23187 induced lysosomal enzyme release in PMN only in the presence of extracellular Ca++.
- Unlike secretion induced by other stimuli, A23187- and Ca++-induced release was not associated with increased microtubules and was insensitive to colchicine.
- Ca++-mediated secretion involved contractions of the plasma membrane towards the cell interior, mediated by cytochalasin B-insensitive microfilaments, not microtubule assembly.
Conclusions:
- Calcium-mediated lysosomal enzyme secretion in human PMN is driven by microfilament-dependent contractile events, not microtubule polymerization.
- The observed contractions involve inward movement of the plasma membrane and associated structures towards lysosomes.
- These findings reveal a distinct mechanism for calcium-induced degranulation in PMN, highlighting the role of microfilaments in this process.
Related Concept Videos
Studying the Cytoskeleton
Overview of Secretory Vesicles
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Fusion of Secretory Vesicles with the Plasma Membrane
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
Mechanism of Filopodia Formation
Their main function is to guide migrating cells during normal tissue morphogenesis or cancer metastasis by recognizing and making initial contacts with the extracellular matrix. However, they can also act as stationary cell anchors or help to establish communication...
Feedback Regulation of Calcium Concentration
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
Calmodulin-dependent Signaling
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...


