ArticleThe Journal of physiology1990
Voltage-gated calcium and potassium currents in megakaryocytes dissociated from guinea-pig bone marrow.
Article in The Journal of physiology, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 26 citations in OpenAlex.
- The voltage-gated KPlatelets · 2022Article
- Why do platelets express KPlatelets · 2021Review
- Kv1.3 is the exclusive voltage-gated K+ channel of platelets and megakaryocytes: roles in membrane potential, Ca2+ signalling and platelet count.The Journal of physiology · 2010Article
- Acetylsalicylic acid enhances purinergic receptor-mediated outward currents in rat megakaryocytes.American journal of physiology. Cell physiology · 2010Article
- ADP and inositol trisphosphate evoke oscillations of a monovalent cation conductance in rat megakaryocytes.The Journal of physiology · 1998Article
- ADP-induced rapid inward currents through Ca(2+)-permeable cation channels in mouse, rat and guinea-pig megakaryocytes: a patch-clamp study.The Journal of physiology · 1996Article
- Three cation influx currents activated by purinergic receptor stimulation in rat megakaryocytes.The Journal of physiology · 1994Article
- Cyclic nucleotide-dependent regulation of agonist-induced calcium increases in mouse megakaryocytes.The Journal of physiology · 1992Article
- Guinea-pig megakaryocytes can respond to external ADP by activating Ca2(+)-dependent potassium conductance.The Journal of physiology · 1990Article
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. The electrophysiological properties of the cell membrane of guinea-pig megakaryocytes were studied using the whole-cell patch-clamp technique. The megakaryocytes (diameter, 17-42 microns) were dissociated mechanically from the bone marrow of adult guinea-pigs. 2. In a proportion of cells, spike-like action potentials were generated in response to depolarization when the cells were immersed in standard saline containing 10 mM-Ca2+. Under voltage clamping, a transient inward current followed by a slowly Ca2+. Under voltage clamping, a transient inward current followed by a slowly developing outward current was produced when the membrane potential was made more positive than -55 mV. 3. The inward currents were identified as Ca2(+)-carried current, since the amplitude depended distinctly on external Ca2+ concentration and since replacement of external Ca2+ with Mn2+ reversibly diminished the current. The Ca2+ channels involved are most probably of the transient type (T-type). 4. The reversal potential of the outward current changed from -87 to -46 and -7 mV when the external K+ concentration was raised from 5 to 25 and 125 mM. 5. The outward current was insensitive to chelation of internal Ca2+ but was blocked by external application of quinine, 4-aminopyridine and tetraethylammonium, and was thus very probably a membrane potential-dependent K+ current. The dependence of the current activation and inactivation on the membrane potential was consistent with that of a delayed K+ rectifier. 6. The amplitudes of the Ca2+ currents and K+ currents showed considerable intercell variation. However, the density of the Ca2+ current showed a tendency to increase with megakaryocyte size, presumably accompanying maturation. The roles of these currents in cellular function remain to be elucidated.
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