Journal
METALLOMICS
Volume 15, Issue 6, Pages -Publisher
OXFORD UNIV PRESS
DOI: 10.1093/mtomcs/mfad031
Keywords
ZnT-1; T-type calcium channel; voltage-gated calcium channel auxiliary beta subunit; Erk1; 2; L-type calcium channel; Raf-1
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ZnT1 is a zinc transporter that plays a crucial role in maintaining cellular zinc balance. In addition to its role in zinc transport, ZnT1 also inhibits the L-type calcium channel (LTCC) and activates the Raf-ERK signaling to enhance the activity of T-type calcium channel (TTCC). The presence of the voltage-gated calcium channel (VGCC) beta-subunit inhibits the ZnT1-induced augmentation of TTCC function, possibly through the reduction of ZnT1-induced activation of Ras-ERK signaling.
ZnT1 is a major zinc transporter that regulates cellular zinc homeostasis. We have previously shown that ZnT1 has additional functions that are independent of its activity as a Zn2+ extruder. These include inhibition of the L-type calcium channel (LTCC) through interaction with the auxiliary beta-subunit of the LTCC and activation of the Raf-ERK signaling leading to augmented activity of the T-type calcium channel (TTCC). Our findings indicate that ZnT1 increases TTCC activity by enhancing the trafficking of the channel to the plasma membrane. LTCC and TTCC are co-expressed in many tissues and have different functions in a variety of tissues. In the current work, we investigated the effect of the voltage-gated calcium channel (VGCC) beta-subunit and ZnT1 on the crosstalk between LTCC and TTCC and their functions. Our results indicate that the beta-subunit inhibits the ZnT1-induced augmentation of TTCC function. This inhibition correlates with the VGCC beta-subunit-dependent reduction in ZnT1-induced activation of Ras-ERK signaling. The effect of ZnT1 is specific, as the presence of the beta-subunit did not change the effect of endothelin-1 (ET-1) on TTCC surface expression. These findings document a novel regulatory function of ZnT1 serving as a mediator in the crosstalk between TTCC and LTCC. Overall, we demonstrate that ZnT1 binds and regulates the activity of the beta-subunit of VGCC and Raf-1 kinase and modulates surface expression of the LTCC and TTCC catalytic subunits, consequently modulating the activity of these channels.
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