TRPM7 silencing attenuates Mg2+ influx in cardiac myoblasts, H9c2 cells
TRPM7, a member of the melastatin subfamily of transient receptor potential channels, is suggested to be a potential candidate for a physiological Mg 2+ channel. However, there is no direct evidence of Mg 2+ permeation through endogenous TRPM7. To determine the physiological roles of TRPM7 in intrac...
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Published in | The journal of physiological sciences Vol. 70; no. 1; pp. 1 - 47 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Springer
07.10.2020
BioMed Central |
Subjects | |
Online Access | Get full text |
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Summary: | TRPM7, a member of the melastatin subfamily of transient receptor potential channels, is suggested to be a potential candidate for a physiological Mg
2+
channel. However, there is no direct evidence of Mg
2+
permeation through endogenous TRPM7. To determine the physiological roles of TRPM7 in intracellular Mg
2+
homeostasis, we measured the cytoplasmic free Mg
2+
concentration ([Mg
2+
]
i
) in TRPM7-silenced H9c2 cells. [Mg
2+
]
i
was measured in a cluster of 8–10 cells using the fluorescent indicator, furaptra. TRPM7 silencing did not change [Mg
2+
]
i
in Ca
2+
-free Tyrode’s solution containing 1 mM Mg
2+
. Increasing the extracellular Mg
2+
to 92.5 mM raised [Mg
2+
]
i
in control cells (1.56 ± 0.19 mM) at 30 min, while this effect was significantly attenuated in TRPM7-silenced cells (1.12 ± 0.07 mM). The Mg
2+
efflux driven by Na
+
gradient was unaffected by TRPM7 silencing. These results suggest that TRPM7 regulates the rate of Mg
2+
influx in H9c2 cells, although cytoplasmic Mg
2+
homeostasis at basal conditions is unaffected by TRPM7 silencing. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1880-6546 1880-6562 |
DOI: | 10.1186/s12576-020-00772-z |