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A major interspecies difference in the ionic selectivity of megakaryocyte Ca 2+ -activated channels sensitive to the TMEM16F inhibitor CaCCinh-A01

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posted on 2019-06-17, 15:07 authored by Kirk A. Taylor, Martyn P. Mahaut-Smith
TMEM16F is a surface membrane protein critical for platelet procoagulant activity, which exhibits both phospholipid scramblase and ion channel activities following sustained elevation of cytosolic Ca 2+ . The extent to which the ionic permeability of TMEM16F is important for platelet scramblase responses remains controversial. To date, only one study has reported the electrophysiological properties of TMEM16F in cells of platelet/megakaryocyte lineage, which observed cation-selectivity within excised patch recordings from murine marrow-derived megakaryocytes. This contrasts with reports using whole-cell recordings that describe this channel as displaying either selectivity for anions or being relatively non-selective amongst the major physiological monovalent ions. We have studied TMEM16F expression and channel activity in primary rat and mouse megakaryocytes and the human erythroleukemic (HEL) cell line that exhibits megakaryocytic surface markers. Immunocytochemical analysis was consistent with surface TMEM16F expression in cells from all three species. Whole-cell recordings in the absence of K + -selective currents revealed an outwardly rectifying conductance activated by a high intracellular Ca 2+ concentration in all three species. These currents appeared after 5–6 minutes and were blocked by CaCC inh -A01, properties typical of TMEM16F. Ion substitution experiments showed that the underlying conductance was predominantly Cl – -permeable in rat megakaryocytes and HEL cells, yet non-selective between monovalent anions and cations in mouse megakaryocytes. In conclusion, the present study further highlights the difference in ionic selectivity of TMEM16F in platelet lineage cells of the mouse compared to other mammalian species. This provides additional support for the ionic “leak” hypothesis that the scramblase activity of TMEM16F does not rely upon its ability to conduct ions of a specific type.

Funding

This work was supported by the Medical Research Council [DTG].

History

Citation

Platelets, 2019

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/Biological Sciences/Molecular & Cell Biology

Version

  • VoR (Version of Record)

Published in

Platelets

Publisher

Taylor & Francis

issn

0953-7104

eissn

1369-1635

Acceptance date

2019-03-04

Copyright date

2019

Available date

2019-06-17

Publisher version

https://www.tandfonline.com/doi/full/10.1080/09537104.2019.1595560

Notes

Color versions of one or more of the figures in the article can be found online at www.tandfonline.com/iplt

Language

en

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