Key result
The patch-clamp technique was successfully used to record single-channel events and membrane potential in human platelets activated with thrombin and ionomycin.
Why the study?
Existing patch-clamp methodologies required revisiting to suggest new approaches for measuring single ion channel activity and membrane potential in human platelets.
This study introduces new patch-clamp approaches for investigating the role of ion channels and membrane potential in platelet physiological and pathophysiological responses.
Answers are grounded in this paper and cite their sources.
Facilitates platelet ion channel research; leaves open clinical translation to thrombosis management.
In this study, we have revisited the existing and suggested new approaches to the use of patch-clamp methodology for measuring the activity of single ion channels and membrane potential of human platelets in the cell-attached configuration. We recorded single-channel events of platelets in the cell-attached configuration after activation with potent agonists: thrombin and ionomycin. The feasibility of platelet membrane potential measurement in cell-attached mode was investigated both experimentally and with the help of simple electrical circuits, revealing that the single-channel events can alter the recorded potential by invoking oscillations. Here, the simple approach to obtain inside-out configuration was described and calcium-dependent single-channel ion currents were recorded. Taken together, this study introduces new approaches for further investigations of the role of ion channels and membrane potential in platelet physiological and pathophysiological response.
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Kokhan et al. (2021) studied Human platelets. Patch-clamp technique was evaluated on Measurement of single ion channel activity and membrane potential. The patch-clamp technique was successfully used to record single-channel events and membrane potential in human platelets activated with thrombin and ionomycin.
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