Biology:T-type calcium channel

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Short description: Family of transport proteins

T-type calcium channels are low voltage activated calcium channels that become inactivated during cell membrane hyperpolarization but then open to depolarization. The entry of calcium into various cells has many different physiological responses associated with it. Within cardiac muscle cell and smooth muscle cells voltage-gated calcium channel activation initiates contraction directly by allowing the cytosolic concentration to increase. Not only are T-type calcium channels known to be present within cardiac and smooth muscle, but they also are present in many neuronal cells within the central nervous system. Different experimental studies within the 1970s allowed for the distinction of T-type calcium channels (transient opening calcium channels) from the already well-known L-type calcium channels (Long-Lasting calcium channels). The new T-type channels were much different from the L-type calcium channels due to their ability to be activated by more negative membrane potentials, had small single channel conductance, and also were unresponsive to calcium antagonist drugs that were present.[1] These distinct calcium channels are generally located within the brain, peripheral nervous system, heart, smooth muscle, bone, and endocrine system.[2]

The distinct structures of T-type calcium channels are what allow them to conduct in these manners, consisting of a primary α1 subunit. The α1 subunit of T-type channels is the primary subunit that forms the pore of the channel, and allows for entry of calcium.

T-type calcium channels function to control the pace-making activity of the SA Node within the heart and relay rapid action potentials within the thalamus. These channels allow for continuous rhythmic bursts that control the SA Node of the heart.[3]

Pharmacological evidence of T-type calcium channels suggest that they play a role in several forms of cancer,[4] absence epilepsy,[5] pain,[6] and Parkinson's disease.[7] Further research is continuously occurring to better understand these distinct channels, as well as to create drugs to selectively target these channels.

Calcium channel, voltage-dependent, T-type, alpha 1G subunit
Identifiers
SymbolCACNA1G
IUPHAR535
HGNC1394
OMIM604065
RefSeqNM_018896
UniProtO43497
Other data
LocusChr. 17 q22
Calcium channel, voltage-dependent, T-type, alpha 1H subunit
Identifiers
SymbolCACNA1H
IUPHAR536
NCBI gene8912
HGNC1395
OMIM607904
RefSeqNM_001005407
UniProtO95180
Other data
LocusChr. 16 p13.3
Calcium channel, voltage-dependent, T-type, alpha 1I subunit
Identifiers
SymbolCACNA1I
IUPHAR537
NCBI gene8911
HGNC1396
OMIM608230
RefSeqNM_001003406
UniProtQ9P0X4
Other data
LocusChr. 22 q13.1

Function

Like any other channel in a cell membrane, the primary function of the T-type voltage gated calcium channel is to allow passage of ions, in this case calcium, through the membrane when the channel is activated. When membrane depolarization occurs in a cell membrane where these channels are embedded, they open and allow calcium to enter the cell, which leads to several different cellular events depending on where in the body the cell is found. As a member of the Cav3 subfamily of voltage-gated calcium channels, the function of the T-type channel is important for the repetitive firing of action potentials in cells with rhythmic firing patterns such as cardiac muscle cells and neurons in the thalamus of the brain.[1] T-type calcium channels are activated in the same range as voltage-gated sodium channels, which is at about -55 mV. Because of this very negative value at which these channels are active, there is a large driving force for calcium going into the cell. The T-type channel is regulated by both dopamine and other neurotransmitters, which inhibit T-type currents. Additionally, in certain cells angiotensin II enhances the activation of T-type channels.[1]

Heart

This is important in the aforementioned depolarization events in the pace-making activity of the sinoatrial (SA) Node in the heart and in the neuron relays of the thalamus so that quick transmission of action potentials can occur. This is very important for the heart when stimulated by the sympathetic nervous system that causes the heart rate to increase, in that not only does the T-type calcium channel provide an extra depolarization punch in addition to the voltage gated sodium channels to cause a stronger depolarization, but it also helps provide a quicker depolarization of the cardiac cells.[1][3]

Fast-acting

Another important facet of the T-type voltage gated calcium channel is its fast voltage-dependent inactivation compared to that of other calcium channels. Therefore, while they help provide stronger and quicker depolarization of cardiac muscle cells and thalamus nerve cells, T-type channels also allow for more frequent depolarization events. This is very important in the heart in the simple fact that the heart is better apt to increase its rate of firing when stimulated by the sympathetic nervous system innervating its tissues. Although all of these functions of the T-type voltage gated calcium channel are important, quite possibly the most important of its functions is its ability to generate potentials that allow for rhythmic bursts of action potentials in cardiac cells of the sinoatrial node of the heart and in the thalamus of the brain.[1] Because the T-type channels are voltage dependent, hyperpolarization of the cell past its inactivation voltage will close the channels throughout the SA node, and allow for another depolarizing event to occur. The voltage dependency of the T-type channel contributes to the rhythmic beating of the heart.[3]

Structure

Voltage-gated calcium channels are made up of several subunits. The α1 subunit is the primary subunit that forms the transmembrane pore of the channel.[1] The α1 subunit also determines the type of calcium channel. The β, α2δ, and γ subunits, present in only some types of calcium channels, are auxiliary subunits that play secondary roles in the channel.[2]

α1 Subunit

The α1 subunit of T-type calcium channels is similar in structure to the α subunits of K+(potassium ion) channels, Na+(sodium ion) channels, and other Ca2+(calcium ion) channels. The α1 subunit is composed of four domains (I-IV), with each domain containing 6 transmembrane segments (S1-S6). The hydrophobic loops between the S5 and S6 segments of each domain form the pore of the channel.[1][3] The S4 segment contains a high quantity of positively charged residues and functions as the voltage sensor of the channel opening or closing based on the membrane potential.[3] The exact method by which the S4 segment controls the opening and closing of the channel is currently unknown.

Auxiliary subunits

The β, α2δ, and γ subunits are auxiliary subunits that affect channel properties in some calcium channels. The α2δ subunit is a dimer with an extracellular α2 portion linked to a transmembrane δ portion. The β subunit is an intracellular membrane protein. The α2δ and β subunits have an effect on the conductance and kinetics of the channel.[8] The γ subunit is a membrane protein that has an effect on the voltage sensitivity of the channel.[8] Current evidence shows that isolated T-type α1 subunits have similar behavior to natural T-type channels, suggesting that the β, α2δ, and γ subunits are absent from T-type calcium channels and the channels are made up of only an α1 subunit.[3]

Variation

There are three known types of T-type calcium channels, each associated with a specific α1 subunit.

Designation α1 Subunit Gene
Cav3.1 α1G (CACNA1G)
Cav3.2 α1H (CACNA1H)
Cav3.3 α1I (CACNA1I)

Pathology

When these channels are not functioning correctly, or are absent from their usual domains, several issues can result.

Cancer

T-type Calcium channels are expressed in different human cancers such as breast, colon, prostate, insulinoma, retinoblastoma, leukemia, ovarian, and melanoma, and they also play key roles in proliferation, survival, and the regulation of cell cycle progression in these forms of cancer . This was demonstrated through studies that showed that down regulating T-type channel isoforms, or just blocking the T-type calcium channels caused cytostatic effects in cancer cells such as gliomas, breast, melanomas, and ovarian, esophageal, and colorectal cancers . Some of the most notorious forms of cancer tumors contain cancer stem cells (CSC), which makes them particularly resistant to any cancer therapy . Furthermore, there is evidence that suggests that the presence of the CSC in human tumors may be associated with the expression of T-type calcium channels in the tumors.[6]

Epilepsy

The major disease that involves the T-type calcium channel is absence epilepsy. This disease is caused by mutations of T-type calcium channel itself. Individuals with absence seizures have brief periods of behavioral arrest and unresponsiveness.[1] Experiments on the Genetic Absence Epilepsy Rat of Strasbourg (GAERS) suggested that absence epilepsy in the rat was linked to T-type channel protein expression.[5] In fact, neurons isolated from the reticular nucleus of the thalamus of the GAERS showed 55% greater T-type currents, and these currents were attributed to an increase in the Cav3.2 mRNA, according to Tally et al.[5] suggesting that T-type protein expression was up regulated in the GAERS. Further experiments on the GAERS showed that, indeed, the expression of T-type calcium channels play a key role in seizures caused by absence epilepsy in the GAERS.[5] Also, other evidence suggest that T-type calcium channel expression is not only up regulated in absence epilepsy, but also in other forms of epilepsy as well.[5] The first-line treatments for childhood absence epilepsy, valproate and ethosuximide, are both blockers of T-type calcium channels; the second-line treatment, lamotrigine, although not a T-type calcium channel blocker, does inhibit high-voltage activated calcium channels.[9]

Pain

The Cav3.2 isoform of T-type calcium channels has been found to involve in pain in animal models with acute pain[10] and chronic pain: neuropathic pain[4][11] (PDN), inflammatory pain[12] and visceral pain.[13]

Parkinson's disease

Increased neuronal bursting occurs throughout the central motor system in both human forms and animals models of Parkinson's disease.[14] T-type calcium channels are highly expressed in basal ganglia structures as well as neurons in the motor areas of the thalamus and are thought to contribute to normal and pathological bursting by means of low-threshold spiking.[15] Basal ganglia recipient neurons in the thalamus are particularly interesting because they are directly inhibited by the basal ganglia output.[16] Consistent with the standard rate model of the basal ganglia, the increased firing in basal ganglia output structures observed in Parkinson's disease would exaggerate the inhibitory tone in thalamocortical neurons. This may provide the necessary hyperpolarization to de-inactivate T-type calcium channels, which can result in rebound spiking. In normal behavior, bursting likely plays a role in increasing the likelihood of synaptic transmission, initiating state changes between rest and movement, and might signal neural plasticity due to the intracellular cascades brought on by the rapid influx of calcium.[17] While these roles are not mutually exclusive, most attractive is the hypothesis that persistent bursting promotes a motor state resistant to change, potentially explaining the akinetic symptoms of Parkinson's disease.[18]

As a drug target

Calcium channel blockers (CCB) such as mibefradil can also block L-type calcium channels, other enzymes, as well as other channels.[4] Consequently, research is still being conducted to design highly selective drugs that can target T-type calcium channels alone.[4]

Cancer

Furthermore, since T-type calcium channels are involved in proliferation, survival and cell cycle progression of these cells, they are potential targets for anticancer therapy.[4] As mentioned above, blockage or down regulation of the T-type calcium channels causes cytostasis in tumors; but this blockage or down regulation of the T-channels may also induce cytotoxic effects. Consequently, it is not yet clear what the benefits or disadvantages of targeting T-type calcium channels in anticancer therapy are.[4] On the other hand, a combined therapy involving administration of a T-type channel antagonist followed by cytotoxic therapy is currently in its clinical trial phase.[4]

Painful Diabetic Neuropathy (PDN)

In addition, drugs used for treating PDN are associated with serious side effects and target specifically the CaV3.2 isoform (responsible for development of neuropathic pain in PDN) could reduce side effects.[6] As a result, research to improve or design new drugs is currently on-going.[6]

Parkinson's disease

T-type calcium channels represent an alternative approach to Parkinson's disease treatment as their primary influence is not concerning the central dopaminergic system. For example, they offer great potential in reducing side effects of dopamine replacement therapy, such as levodopa-induced dyskinesia. The co-administration of T-type calcium channel blockers with standard Parkinson's disease medications is most popular in Japan, and several clinical studies have shown significant efficacy.[7] However, most of these drugs are experimental and operate in a non-specific manner, potentially influencing sodium channel kinetics as well as dopamine synthesis. Novel T-type calcium channel inhibitors have recently been discovered which more selectively target the CaV3.3 channel sub-type expressed in central motor neurons, showing robust modulation in a rodent and primate models of Parkinson's disease.[15][19]

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 "Voltage-gated calcium channels". Cold Spring Harbor Perspectives in Biology 3 (8): a003947. August 2011. doi:10.1101/cshperspect.a003947. PMID 21746798. 
  2. ↑ 2.0 2.1 "Neuronal T-type calcium channels: what's new? Iftinca: T-type channel regulation". Journal of Medicine and Life 4 (2): 126–138. May 2011. PMID 21776294. 
  3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 "Molecular physiology of low-voltage-activated t-type calcium channels". Physiological Reviews 83 (1): 117–161. January 2003. doi:10.1152/physrev.00018.2002. PMID 12506128. 
  4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 "T-type calcium channels blockers as new tools in cancer therapies". Pflügers Archiv 466 (4): 801–810. April 2014. doi:10.1007/s00424-014-1444-z. PMID 24449277. 
  5. ↑ 5.0 5.1 5.2 5.3 5.4 "The role of T-type calcium channels in epilepsy and pain". Current Pharmaceutical Design 12 (18): 2189–2197. 2006. doi:10.2174/138161206777585184. PMID 16787249. 
  6. ↑ 6.0 6.1 6.2 6.3 "Targeting of CaV3.2 T-type calcium channels in peripheral sensory neurons for the treatment of painful diabetic neuropathy". Pflügers Archiv 466 (4): 701–706. April 2014. doi:10.1007/s00424-014-1452-z. PMID 24482063. 
  7. ↑ 7.0 7.1 "A review of the use of zonisamide in Parkinson's disease". Therapeutic Advances in Neurological Disorders 2 (5): 313–317. September 2009. doi:10.1177/1756285609338501. PMID 21180621. 
  8. ↑ 8.0 8.1 From neuron to brain (5th ed.). Sunderland, Mass.: Sinauer Associates. 2012. pp. 87–88. ISBN 9780878936090. 
  9. ↑ "A Practical Guide to Treatment of Childhood Absence Epilepsy". Paediatric Drugs 21 (1): 15–24. February 2019. doi:10.1007/s40272-019-00325-x. PMID 30734897. 
  10. ↑ "Attenuated pain responses in mice lacking Ca(V)3.2 T-type channels". Genes, Brain and Behavior 6 (5): 425–431. July 2007. doi:10.1111/j.1601-183X.2006.00268.x. PMID 16939637. 
  11. ↑ "T-type calcium channels in neuropathic pain". Pain 157 (Suppl 1): S15–S22. February 2016. doi:10.1097/j.pain.0000000000000469. PMID 26785151. https://hal.archives-ouvertes.fr/hal-02356330/file/Review%20Pain%20-%20Bourinet%20et%20al%20-%20final.pdf. 
  12. ↑ "Ca(v)3.2 calcium channels: the key protagonist in the supraspinal effect of paracetamol". Pain 155 (4): 764–772. April 2014. doi:10.1016/j.pain.2014.01.015. PMID 24447516. https://hal.archives-ouvertes.fr/hal-02356344/file/Kerckhove%20et%20al%20%282014%29%20Pain%20-%20Paracetamol%20and%20Cav3.2.pdf. 
  13. ↑ "T-type calcium channels contribute to colonic hypersensitivity in a rat model of irritable bowel syndrome". Proceedings of the National Academy of Sciences of the United States of America 108 (27): 11268–11273. July 2011. doi:10.1073/pnas.1100869108. PMID 21690417. Bibcode: 2011PNAS..10811268M. 
  14. ↑ "Basal ganglia activity patterns in parkinsonism and computational modeling of their downstream effects". The European Journal of Neuroscience 36 (2): 2213–2228. July 2012. doi:10.1111/j.1460-9568.2012.08108.x. PMID 22805066. 
  15. ↑ 15.0 15.1 "Anatomical localization of Cav3.1 calcium channels and electrophysiological effects of T-type calcium channel blockade in the motor thalamus of MPTP-treated monkeys". Journal of Neurophysiology 115 (1): 470–485. January 2016. doi:10.1152/jn.00858.2015. PMID 26538609. 
  16. ↑ "The functional anatomy of basal ganglia disorders". Trends in Neurosciences 12 (10): 366–375. October 1989. doi:10.1016/0166-2236(89)90074-X. PMID 2479133. 
  17. ↑ "Motor thalamus integration of cortical, cerebellar and basal ganglia information: implications for normal and parkinsonian conditions". Frontiers in Computational Neuroscience 7: 163. 2013-01-01. doi:10.3389/fncom.2013.00163. PMID 24273509. 
  18. ↑ "Basal ganglia beta oscillations accompany cue utilization". Neuron 73 (3): 523–536. February 2012. doi:10.1016/j.neuron.2011.11.032. PMID 22325204. 
  19. ↑ "The Discovery and Characterization of ML218: A Novel, Centrally Active T-Type Calcium Channel Inhibitor with Robust Effects in STN Neurons and in a Rodent Model of Parkinson's Disease". ACS Chemical Neuroscience 2 (12): 730–742. December 2011. doi:10.1021/cn200090z. PMID 22368764. 



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