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Guinea-pig megakaryocytes can respond to external ADP by activating Ca2(+)-dependent potassium conductance
1Department of Pharmacology, Gunma University School of Medicine, Maebashi, Japan.
Abstract:
1. The responses of megakaryocytes to adenosine diphosphate (ADP) were studied using whole-cell patch electrodes and a Ca2(+)-sensitive fluorescent dye, Fura-2. Megakaryocytes (diameter, 17-42 microns) were mechanically dissociated from the bone marrow of adult guinea-pigs and ADP (1-10 microM) was pressure-applied to megakaryocytes under recording. 2. In megakaryocytes immersed in standard saline, ADP evoked an obvious outward current at a membrane potential of -63 mV. The current was identified as a K(+)-carried current, since the reversal potential depended distinctly on the external K+ concentration, but it showed no changes after removal of external Na+. The amplitude of evoked K+ currents showed considerable intercell variation, which is presumably due to differences of current density in the membrane. 3. During application of ADP, the evoked K+ current was not sustained but slowly decayed to become negligible within 10-20 s, suggesting the appearance of desensitization. The response of the megakaryocyte to ADP recovered slowly and returned to an original level after 4-5 min of continuous washing. 4. When the intracellular free Ca2+ concentration ([Ca2+]i) was measured using the Ca2(+)-sensitive fluorescent dye, Fura-2, application of 10 microM-ADP induced an increase of [Ca2+]i by about 5-fold, which was followed by a gradual decay to the original level within 30-50 s. Roles of internal Ca2+ for activating the K+ current were confirmed by observing (1) enhancement of evoked currents by the use of internal saline containing no Ca2+ chelators and (2) generation of prolonged K+ current by application of a Ca2+ ionophore, A23187, to the megakaryocyte. 5. In a fraction of the megakaryocytes, spontaneous hyperpolarization of the resting membrane potential was observed. The hyperpolarization seemed to result from the activation of K+ channels in the membrane, which was caused by spontaneous release of Ca2+ from the internal storage site. 6. It was concluded that megakaryocytes of the guinea-pig can respond to external ADP by increasing [Ca2+]i and consequently by activating Ca2(+)-dependent K+ channels in the membrane.
Insights
Adenosine diphosphate (ADP) activates potassium (K+) channels in guinea-pig megakaryocytes by increasing intracellular calcium. This calcium-dependent potassium current is crucial for megakaryocyte function and response to ADP signaling.
Area of Science:
- Cellular Physiology
- Hematology
- Ion Channel Biology
Background:
- Megakaryocytes are essential for platelet production.
- Adenosine diphosphate (ADP) is a key signaling molecule in platelet biology.
- The electrophysiological responses of megakaryocytes to ADP are not fully understood.
Purpose of the Study:
- To investigate the electrophysiological and calcium signaling responses of guinea-pig megakaryocytes to ADP.
- To elucidate the role of intracellular calcium in mediating ADP-induced currents in megakaryocytes.
- To identify the ion channels involved in the megakaryocyte response to ADP.
Main Methods:
- Whole-cell patch-clamp electrophysiology was used to record membrane currents.
- Fura-2 fluorescent dye was employed to measure intracellular free calcium concentration ([Ca2+]i).
- Megakaryocytes were mechanically dissociated from guinea-pig bone marrow.
Main Results:
- ADP evoked an outward, potassium (K+)-carried current in megakaryocytes.
- ADP application led to a rapid, approximately 5-fold increase in intracellular calcium ([Ca2+]i).
- Intracellular calcium elevation was confirmed to activate these potassium currents, and spontaneous calcium release also activated K+ channels.
Conclusions:
- Guinea-pig megakaryocytes respond to external ADP by increasing intracellular calcium.
- This calcium increase subsequently activates calcium-dependent potassium (K+) channels in the megakaryocyte membrane.
- ADP-induced calcium signaling and K+ channel activation are significant mechanisms in megakaryocyte physiology.