Key result
Kv1.3 forms the exclusive voltage-gated K+ channel of platelets and megakaryocytes, and its deletion in mice significantly increased platelet counts compared to wild-type controls.
Why the study?
Does Kv1.3 blockade or genetic deletion alter membrane potential, Ca2+ signaling, and platelet count in megakaryocytes and platelets?
Does Kv1.3 blockade or genetic deletion alter membrane potential, Ca2+ signaling, and platelet count in megakaryocytes and platelets?
Absolute Event Rate: 1.47% vs 1.12%
p-value: p=<0.005
Kv1.3 is the exclusive voltage-gated K+ channel in platelets and megakaryocytes, playing a critical role in setting resting membrane potential, regulating agonist-evoked Ca2+ signaling, and influencing circulating platelet numbers.
Kv1.3 may offer a novel target to modulate platelet counts; leaves open clinical translation from murine models.
A delayed rectifier voltage-gated K(+) channel (Kv) represents the largest ionic conductance of platelets and megakaryocytes, but is undefined at the molecular level. Quantitative RT-PCR of all known Kv alpha and ancillary subunits showed that only Kv1.3 (KCNA3) is substantially expressed in human platelets. Furthermore, megakaryocytes from Kv1.3(/) mice or from wild-type mice exposed to the Kv1.3 blocker margatoxin completely lacked Kv currents and displayed substantially depolarised resting membrane potentials. In human platelets, margatoxin reduced the P2X(1)- and thromboxaneA(2) receptor-evoked [Ca(2+)](i) increases and delayed the onset of store-operated Ca(2+) influx. Megakaryocyte development was normal in Kv1.3(/) mice, but the platelet count was increased, consistent with a role of Kv1.3 in apoptosis or decreased platelet activation. We conclude that Kv1.3 forms the Kv channel of the platelet and megakaryocyte, which sets the resting membrane potential, regulates agonist-evoked Ca(2+) increases and influences circulating platelet numbers.
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McCloskey et al. (2010) studied this question. Kv1.3 deletion or margatoxin vs. Wild-type or untreated controls was evaluated on Platelet count (x 10^6 / μl) (p=<0.005). Kv1.3 forms the exclusive voltage-gated K+ channel of platelets and megakaryocytes, and its deletion in mice significantly increased platelet counts compared to wild-type controls.
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