Functional Exploration Of T-Type Calcium Channels (Cav3.2 And Cav3.3) And Their Sensitivity To Zinc
Tahar Hazzaz Abouamal*, Zineb Choukairi, Fechtali Taoufiq
Identifiers and Pagination:Year: 2018
First Page: 280
Last Page: 287
Publisher Id: TOMICROJ-12-280
Article History:Received Date: 30/3/2018
Revision Received Date: 28/6/2018
Acceptance Date: 2/7/2018
Electronic publication date: 31/7/2018
Collection year: 2018
open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: (https://creativecommons.org/licenses/by/4.0/legalcode). This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
T-type Ca2+ channels (TTCC) are low Voltage-gated calcium channels, expressed in various tissues such as the brain and heart, and contribute to a variety of physiological functions including neuronal excitability, hormone secretion, muscle contraction, and pacemaker activity. At high concentrations, Zinc (Zn2+) is naturally attached to cell membranes and is therefore considered a reversible inhibitor of calcium. Zinc is also involved in the kinetics of sodium and potassium currents. Zinc is essential for many functions. A low zinc tenor is associated with emotional instability, digestive disorders, slow-growing and alteration of protein synthesis.
Material and Methods:
For the Cell Culture we used HEK-293/tsA-201, and for transfection, the pCDNA3 plasmid constructs encoding human CaV3.2, and CaV3.3 subunits. Electrophysiological experiments were performed using the whole cell configuration of the patch-clamp technique. T-type currents were recorded using a test pulse from a holding potential at (-100mV) to (-30 mV), data Acquisition and Analysis for Current-voltage relationships (I-V curves) were recorded for the two cloned T-type Ca2+ channels (Cav3.2, Cav3.3).
Our studies describe the behavior of these channels Cav3.2 and Cav3.3 and also their current sensitivity to Zinc (Zn2+) in transfected HEK-293/tsA-201cells. Our results show that Zn2+ applies a modulatory effect on T-type calcium channels. We observe that Zn2+ differentially modulates the CaV3.2 and CaV3.3 channels. Zn2+ preferably inhibits Cav3.2.
We have demonstrated that Zn2+ differentially modulates two CaV3 channels (Cav3.2 and Cav3.3): It is a preferential blocker of CaV3.2 channels and it alters the gating behaviour of CaV3.3 channels.
Gated calcium channels are present in various cells of the human body and their pharmacological properties are independent of cell type where they reside .
T-type channels have distinct functional properties compared to L-type channels: Faster kinetics of inactivation and activation, and slower deactivation kinetics. Since T channels are able to activate by low depolarization near resting potential of the membrane, their functions are also related to the control of neuronal excitability [2-6]. T-type Ca2+ channels (TTCC) are low Voltage-gated calcium channels, expressed in various tissues such as the brain and heart, and contribute to a variety of physiological functions including neuronal excitability, hormone secretion, muscle contraction, and pacemaker activity. In addition, an increasing body of evidence shows that TTCC can trigger fast and low-threshold exocytosis [7-14].
On the other hand, Zinc is essential for all mammals because it has various actions on nerve cells. However, it is widely reported that zinc can be very toxic to neurons in small amounts. At high concentrations, zinc (Zn2+) is naturally attached to cell membranes and is therefore considered a reversible inhibitor of calcium.
Zinc is also involved in the kinetics of sodium and potassium currents. Zinc is essential for many functions. A low zinc tenor is associated with emotional instability, digestive disorders, slow-growing and alteration of protein synthesis.
Despite the fact that Zn2+ is related to proteins in biological systems, it is also involved in some neurodegenerative diseases such as Alzheimer's disease , and synaptic plasticity , amyotrophic lateral sclerosis  and Parkinson's disease . Zinc is also involved in some neuropathology [19-23].
Cell Culture and Transfection - HEK-293/tsA-201 cells were cultivated in Dulbecco’s modified Eagle’s medium supplemented with glutamax and 10% fetal bovine serum (Life technologies) using standard techniques.
For transfection, we use pCDNA3 plasmid constructs encoding human CaV3.2 , and CaV3.3 subunits . We also use NaCl (150 mM) and the transfection agent Jet-PEI (QBiogen, Illkirch, France). The green fluorescent protein (GFP) was co-transfected to monitor cells.Cells were grown to 90% confluence in 35-mm Petri dishes. 36-48h after transfection, GFP - positive cells expressing sufficient levels of the Ca2+ channels were examined for electrophysiological recordings. To this end, cells were split by trypsin, plated on petri dishes at 510% confluence with 2 ml of mix (SVF + DMEM), and given 2 - 3 h to settle before starting the patch clamp.
2.1. Preparation of Intracellular and Extracellular Media
The preparation of the intracellular and extracellular media are necessary to start the patch clamp experiments. The extracellular solution contained (in mM): 135 NaCl, 20 TEA-Cl and 2 CaCh, 1 MgCl2, 10 HEPES pH to 7, 4 The internal pipette solution contained (in mM): 140 CsCl, 10 EGTA, 3 CaCh, and 10 HEPES ph to 7,2.
Electrophysiological experiments were performed using the wholecell configuration of the patch-clamp technique. Recordings were obtained using an Axopatch 200 and pCLAMP data acquisition software (Axon Instruments, Inc., Union City, CA, USA). The sampling frequency for acquisition was 10 kHz and data were filtered at 2 kHz. Zinc chloride (ZnCl2) was purchased from Sigma-Aldrich (France), and was dissolved in extracellular medium at 1 M as a stock solution, kept at 4°C and applied at final concentrations to recorded cells by a gravity-driven perfusion device controlled by solenoid valves.
2.3. Patch Clamp Recordings on Cultured Cells
In HEK-293 cells, T-type whole-cell patch clamp recordings were performed 2-3 days after transfection. T-type currents were recorded using a test pulse from a holding potential at (-100mV) to (-30 mV) and using 2 mM Ca2+ at room temperature. The current density was calculated according to the capacitance of the cell and expressed in pA/picofarad.
2.4. Data Acquisition and Analysis
Current-voltage relationships (I-V curves) were recorded for the two cloned T-type Ca2+ channels (Cav3.2, Cav3.3), The protocol stepped the cell membrane potential from -100 mV to test potentials starting at -100 and increasing to +70 mV in 10 mV or 5 mV increments. For Zn2+, we use the protocol Test potential from -100 mV to -30 mV and 10 step for each concentration between (0pM and 100pM).
3.1. Records of Calcium T-type Ca2+ Channels
3.1.1. For Cav 3.2
The results obtained in this studyfor CaV3.2 showed that the biophysical behavior T-type calcium channel varies with the applied voltage. We obtained values from the software pCLAMP™ and Clampfit 10.7.0 for data analysis.
The potential values are going from -80mV to +70 mV and a current: From -30.639 pA at (-80mV) to - 786.132pA at (-35 mV) and then to 26.489pA at (+70mV), the Fig. (1A) shows the currents of calcium channels CaV3.2, The red line show the first Sweep (recording 1), All data from recording are summarized in (Table 1). below:
3.1.2. For Cav 3.3
The results obtained in this study, for CaV3.3 showed that the biophysical behavior T-type calcium channel varies with the applied voltage. We obtained values from the software pCLAMP™ and Clampfit 10.7.0 for data analysis.
The potential values are going from -100mV to +70 mV and a current: From -15.136718pA at(-100mV) to -515.86pA at (-30 mV) and then to 44.67pA at (+70mV), the Fig. (1B) shows the currents of calcium channels CaV3.3, The red line show the first Sweep (recording 1), all data from recording are summarized in (Table 2). below:
3.2. Zn2+ Inhibition of T-Type Calcium Channels
To determine the molecular consequences of the Zinc (Zn2+) on channel function. The biophysical properties of the channels were characterized by standard whole-cell patch clamp techniques.We recorded macroscopic Ca2+ current in the whole-cell configuration to define the effect of Zinc (Zn2+) on cloned channels (Cav3.2 and Cav3.3).
Fig. (2A-2B) shows the recording of zinc on calcium channels 3.2 and 3.3, The space between the bold curves represents the change in concentration between each 10 sweeps, The level of inhibition is proportional to the concentration of Zn2+. When zinc concentration is increased, the level of inhibition also increases.
The red line in Fig. (2A show the Sweep 26 with voltage of: -35.2783 pA and 100 uM of Zn2+ Concentration.
The red line in Fig. (2B) show the Sweep 26 with voltage of: -542.236 pA that represent the first sweep after washout.
The error bars in Fig. (2C and 2D) represent the SE (standard error); For exemple for CAV3.2 the I/Ictrl is between 0,724971 and 0,9652457 for Log [Zn2+] = -7 (0,1 µM) with n = 10 and between 0,504065 and 0,7732869 for Log[Zn2+] = - 6 (1µM) with n = 8.For CAV3.3 the I/Ictrl is between 0,876818 and 0,9874821 for Log [Zn2+] = -6 (1 µM) with n = 10 and between 0,8043191 and 0,9179184 for Log [Zn2+] = - 5 (10 µM) with n = 10.
For CAV3.3 the I/Ictrl is between 0,876818 and 0,9874821 for Log [Zn2+] = -6 (1 µM) with n = 10 and between 0,8043191 and 0,9179184 for Log [Zn2+] = - 5 (10 µM) with n = 10.
The Fig. (2E) shows a bar graph of the average inhibition of CaV3.2 and CaV3.3 currents with 1 µM Zn+.
Fig. (2F) shows the dose response relationships for Zn2+ inhibition of CaV3.2 and CaV3.3 currents. The fraction of unblocked peak current (I/ICtrl) is plotted against Zn2+ concentration. The IC50 values were obtained from fitted data using a sigmoidal dose response with variable Hill slope equation with results for CAV3.2 (IC50 = 0.7648) and for CAV3.3 (IC50 = 0.5097)
The detailed data for the sigmoidal dose-response are present in (Table 3) below:
|Sigmoidal Dose-Response||Cav 3.2
|Sigmoidal, 4PL, X is log(concentration)||–||–|
|95% Confidence Intervals|
|Top||0,9061 to 0,9841||0,9645 to 1,010|
|Bottom||-0,06980 to 0,05246||-1,078 to -0,005667|
|LogIC50||-5,958 to -5,679||-3,764 to -2,704|
|HillSIope||-0,9421 to -0,6137||-0,7447 to -0,4520|
|IC50||1,101e-006 to 2,094e-006||0,0001720 to 0,001979|
|Span||0,8739 to 1,034||0,9799 to 2,078|
In the present study, we observe that Zn2+ differentially modulates the CaV3.2 and CaV3.3 channels. Zn2+ preferably inhibits Cav3.2 channels with an IC50 in the submicromolar range (~ 0.8 pm), which is 100 to 200 times lower than that of CaV3.3 channels. Zn2+ inhibition of CaV3 channels is related to a negative change in steady state activation and inactivation properties, except CaV3.2 steady state activation properties which remain the same.
What we can conclude from our study is that Zn2+ involves a significant slowdown in the inactivation kinetics of the CaV3.3 currents, as well as a very apparent slowdown in CaV3.3 current deactivation kinetics. As a result, it has been found through action potential clamping experiments in cells that express CaV3.3, that Zn2+ can cause a significant increase in Ca2 + input, especially during the potential range of post depolarizing.
In conclusion, we have demonstrated that Zn2+ differentially modulates two CaV3 channels (Cav3.2 and Cav3.3): it is a preferential blocker of CaV3.2 channels and it alters the gating behaviour of CaV3.3 channels.
ETHICS APPROVAL AND CONSENT TO PARTICIPATE
HUMAN AND ANIMAL RIGHTS
No animals/humans were used for studies that are the basis of this review.
CONSENT FOR PUBLICATION
CONFLICT OF INTEREST
The authors declare no conflict of interest, financial or otherwise.