Calcium sparks

A calcium spark is the microscopic release of calcium (Ca2+) from a store known as the sarcoplasmic reticulum (SR), located within muscle cells.[1] This release occurs through an ion channel within the membrane of the SR, known as a ryanodine receptor (RyR), which opens upon activation.[2] This process is important as it helps to maintain Ca2+ concentration within the cell. It also initiates muscle contraction in skeletal and cardiac muscles and muscle relaxation in smooth muscles. Ca2+ sparks are important in physiology as they show how Ca2+ can be used at a subcellular level, to signal both local changes, known as local control,[3] as well as whole cell changes.

Activation

As mentioned above, Ca2+ sparks depend on the opening of ryanodine receptors, of which there are three types:

  • Type 1 – found mainly in skeletal muscle
  • Type 2 – found mainly in the heart
  • Type 3 – found mainly in the brain

Opening of the channel allows Ca2+ to pass from the SR, into the cell. This increases the local Ca2+ concentration around the RyR, by a factor of 10.[4] Calcium sparks can either be evoked or spontaneous, as described below.

Figure 1: An evoked calcium spark, in a cardiac muscle cell.

Evoked

Electrical impulses, known as action potentials, travel along the cell membrane (sarcolemma) of muscle cells.[5] Located in the sarcolemma of smooth muscle cells are receptors, called dihydropyridine receptors (DHPR). In skeletal and cardiac muscle cells, however, these receptors are located within structures known as T-tubules, that are extensions of the plasma membrane penetrating deep into the cell (see figure 1).[6][7] These DHPRs are located directly opposite to the ryanodine receptors, located on the sarcoplasmic reticulum[8] and activation, by the action potential causes the DHPRs to change shape.[9]

In cardiac and smooth muscle, activation of the DHPR results in it forming an ion channel.[10] This allows Ca2+ to pass into the cell, increasing the local Ca2+ concentration, around the RyR. When four Ca2+ molecules bind to the RyR, it opens, resulting in a larger release of Ca2+, from the SR . This process, of using Ca2+ to activate release of Ca2+ from the SR is known as calcium-induced calcium release.[11]

However, in skeletal muscle the DHPR touches the RyR. Therefore, the shape change of the DHPR activates the RyR directly, without the need for Ca2+ to flood into the cell first. This causes the RyR to open, allowing Ca2+ to be released from the SR.[12]

Spontaneous

Ca2+ sparks can also occur in cells at rest (i.e. cells that have not been stimulated by an action potential). This occurs roughly 100 times every second in each cell[13] and is a result of Ca2+ concentration being too high. An increase in Ca2+ within the SR is thought to bind to Ca2+ sensitive sites on the inside of the RyR causing the channel to open. As well as this, a protein called calsequestrin (found within the SR) detaches from the RyR, when calcium concentration is too high, again allowing the channel to open (see sarcoplasmic reticulum for more details). Similarly, a decrease in Ca2+ concentration within the SR has also proven to lower RyR sensitivity. This is thought to be due to the calsequestrin binding more strongly to the RyR, preventing it from opening and decreasing the likelihood of a spontaneous spark.[14]

Calcium after release

There are roughly 10,000 clusters of ryanodine receptors within a single cardiac cell, with each cluster containing around 100 ryanodine receptors.[13] During a single spontaneous spark, when Ca2+ is released from the SR, the Ca2+ diffuses throughout the cell. As the RyRs in the heart are activated by Ca2+, the movement of the Ca2+ released during a spontaneous spark, can activate other neighbouring RyRs within the same cluster. However, there usually isn't enough Ca2+ present in a single spark to reach a neighbouring cluster of receptors.[13] The calcium can, however, signal back to the DHPR causing it to close and preventing further influx of calcium. This is known as negative feedback.[15]

An increase in Ca2+ concentration within the cell or the production of a larger spark, can lead to a large enough calcium released that the neighbouring cluster can be activated by the first. This is known as spark-induced spark activation and can lead to a Ca2+ wave of calcium release spreading across the cell.[13]

During evoked Ca2+ sparks, all clusters of ryanodine receptors, throughout the cell are activated at almost exactly the same time. This produces an increase in Ca2+ concentration across the whole cell (not just locally) and is known as a whole cell Ca2+ transient. This Ca2+ then binds to a protein, called troponin, initiating contraction, through a group of proteins known as myofilaments.[16]

In smooth muscle cells, the Ca2+ released during a spark is used for muscle relaxation. This is because, the Ca2+ that enters the cell via the DHPR in response to the action potential, stimulates both muscle contraction and calcium release from the SR. The Ca2+ released during the spark, then activates two other ion channels on the membrane. One channel allows potassium ions to exit the cell, whereas the other allows chloride ions to leave the cell. The result of this movement of ions, is that the membrane voltage becomes more negative. This deactivates the DHPR (which was activated by the positive membrane potential produced by the action potential), causing it to close and stopping the flow of Ca2+into the cell, leading to relaxation.[17]

Termination

The mechanism by which SR Ca2+ release terminates is still not fully understood. Current main theories are outlined below:

Local depletion of SR Ca2+

This theory suggests that during a calcium spark, as calcium flows out of the SR, the concentration of Ca2+ within the SR becomes too low. However, this was not thought to be the case for spontaneous sparks as the total release during a Ca2+ spark is small compared to total SR Ca2+ content and researchers have produced sparks lasting longer than 200 milliseconds, therefore showing that there is still enough Ca2+ left within the SR after a 'normal' (200ms) spark.[18] However local depletion in the junctional SR may be much larger than previously thought (see [19]). During the activation of a large number of ryanodine receptors however, as is the case during electrically evoked Ca2+ release , the entire SR is about 50% depleted of Ca2+ and this mechanism will play an important role in repriming of release.

Stochastic attrition

Despite the complicated name, this idea simply suggests that all ryanodine receptors in a cluster, and the associated dihydropyridine receptors happen to randomly close at the same time. This would not only prevent calcium release from the SR, but it would also stop the stimulus for calcium release (i.e. the flow of calcium through the DHPR).[20] However, due to the large numbers of RyRs and DHPRs in a single cell, this theory seems to be unrealistic, as there is a very small probability that they would all close together at exactly the same time.[18]

Inactivation/adaptation

This theory suggests that after activation of the RyR and the subsequent release of Ca2+, the channel closes briefly to recover. During this time, either the channel cannot be reopened, even if calcium is present (i.e. the RyR is inactivated) or the channel can be reopened, however more calcium is required to activate it than usual (i.e. the RyR is in an adaptation phase). This would mean that one-by-one the RyRs would close, thus ending the spark.[20]

Sticky cluster theory

This theory suggests that the above three theories all play a role in preventing calcium release.[21]

Discovery

Spontaneous Ca2+ sparks were discovered in cardiac muscle cells, of rats, in 1992 by Peace Cheng and Mark B. Cannell in Jon Lederer's laboratory at the University of Maryland, Baltimore, U.S.A.

Initially the idea was rejected by the scientific journal, Nature, who believed that the sparks were only present under laboratory conditions (i.e. they were artifacts), and so wouldn't occur naturally within the body. However they were quickly recognised as being of fundamental importance to muscle physiology, playing a huge role in excitation-contraction coupling.

The discovery was made possible due to improvements in confocal microscopes. This allowed for the detection of the release of Ca2+, which were highlighted using a substance known as fluo-3, which caused the Ca2+ to glow. Ca2+ “sparks” were so called because of the spontaneous, localised nature of the Ca2+ release as well as the fact that they are the initiation event of excitation-contraction coupling.

Detection and analysis

Because of the importance of Ca2+ sparks in explaining the gating properties of ryanodine receptors in situ (within the body), many studies have focused on improving their detectability [22][23] in the hope that by accurately and reliably detecting all Ca2+ spark events, their true properties can finally help us to answer the unsolved mystery of spark termination.

See also
  • Calcium-induced calcium release
  • Confocal microscopy
  • Ryanodine receptor

References
  1. Cheng, H.; Lederer, W.J.; Cannell, M.B. (1993). "Calcium sparks: elementary events underlying excitation-contraction coupling in heart muscle". Science. 262 (5134): 740–744. Bibcode:1993Sci...262..740C. doi:10.1126/science.8235594. PMID 8235594.
  2. Lanner, J.T., Georgiou, D.K., Joshi, A.D. and Hamilton, S.L. (2010) 'Ryanodine receptors: Structure, expression, molecular details, and function in calcium release', 2(11)
  3. Cannell, M. and Kong, C. (2011) 'Local control in cardiac E-C coupling', Journal of Molecular and Cellular Cardiology, 52(2), pp. 298–303.
  4. Hoang-Trong, T.M., Ullah, A. and Jafri, S.M. (2015) 'Calcium sparks in the heart: Dynamics and regulation', 6
  5. Lodish, H., Berk, A., Zipursky, L.S., Matsudaira, P., Baltimore, D. and Darnell, J. (2000) The action potential and conduction of electric impulses. Available at: https://www.ncbi.nlm.nih.gov/books/NBK21668/ (Accessed: 11 February 2017)
  6. Brette, F.; Orchard, C. (2003). "T-tubule function in mammalian cardiac myocytes". Circulation Research. 92 (11): 1182–92. doi:10.1161/01.res.0000074908.17214.fd. PMID 12805236.
  7. Cheng, Heping; Lederer, W. J. (2008-10-01). "Calcium Sparks". Physiological Reviews. 88 (4): 1491–1545. doi:10.1152/physrev.00030.2007. ISSN 0031-9333. PMID 18923188.
  8. Scriven, D. R. L.; Dan, P.; Moore, E. D. W. (2000). "Distribution of proteins implicated in excitation-contraction coupling in rat ventricular myocytes". Biophys. J. 79 (5): 2682–2691. Bibcode:2000BpJ....79.2682S. doi:10.1016/s0006-3495(00)76506-4. PMC 1301148. PMID 11053140.
  9. Araya, R.; Liberona, J.; Cárdenas, J.; Riveros, N.; Estrada, M.; Powell, J.; Carrasco, M.; Jaimovich, E. (2003). "Dihydropyridine receptors as voltage sensors for a depolarization-evoked, IP3R-mediated, slow calcium signal in skeletal muscle cells". The Journal of General Physiology. 121 (1): 3–16. doi:10.1085/jgp.20028671. PMC 2217318. PMID 12508050.
  10. Kotlikoff, M (2003). "Calcium-induced calcium release in smooth muscle: The case for loose coupling". Progress in Biophysics and Molecular Biology. 83 (3): 171–91. doi:10.1016/s0079-6107(03)00056-7. PMID 12887979.
  11. Fabiato, A (1983). "Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum". Am. J. Physiol. 245 (1): C1–C14. doi:10.1152/ajpcell.1983.245.1.c1. PMID 6346892.
  12. Meissner, G.; Lu, X. (1995). "Dihydropyridine receptor-ryanodine receptor interactions in skeletal muscle excitation-contraction coupling". Bioscience Reports. 15 (5): 399–408. doi:10.1007/bf01788371. PMID 8825041. S2CID 32810845.
  13. Cheng, H.; Lederer, W. (2008). "Calcium sparks". Physiological Reviews. 88 (4): 1491–545. doi:10.1152/physrev.00030.2007. PMID 18923188.
  14. Bassani, J. W.; Yuan, W.; Bers, D. M. (1995-05-01). "Fractional SR Ca release is regulated by trigger Ca and SR Ca content in cardiac myocytes". American Journal of Physiology. Cell Physiology. 268 (5): C1313–C1319. doi:10.1152/ajpcell.1995.268.5.c1313. ISSN 0363-6143. PMID 7762626.
  15. Sham, J. S. K.; et al. (1998). "Termination of Ca2+ release by a local inactivation of ryanodine receptors in cardiac myocytes". Proc. Natl. Acad. Sci. USA. 95 (25): 15096–15101. Bibcode:1998PNAS...9515096S. doi:10.1073/pnas.95.25.15096. PMC 24581. PMID 9844021.
  16. Herzberg, O.; Moult, J.; James, M. (1986). "Calcium binding to skeletal muscle troponin C and the regulation of muscle contraction". Ciba Foundation Symposium. Novartis Foundation Symposia. 122: 120–44. doi:10.1002/9780470513347.ch8. ISBN 9780470513347. PMID 3792134.
  17. Webb, R (2003). "Smooth muscle contraction and relaxation". Advances in Physiology Education. 27 (4): 201–6. doi:10.1152/advances.2003.27.4.201. PMID 14627618.
  18. Bers, D.M. (2002). "Cardiac excitation-contraction coupling". Nature. 415 (6868): 198–205. Bibcode:2002Natur.415..198B. doi:10.1038/415198a. PMID 11805843. S2CID 4337201.
  19. Kong CHT, Laver DR, Cannell MB (2013). "Extraction of Sub-microscopic Ca Fluxes from Blurred and Noisy Fluorescent Indicator Images with a Detailed Model Fitting Approach". PLOS Comput Biol. 9 (2): e1002931–7. Bibcode:2013PLSCB...9E2931K. doi:10.1371/journal.pcbi.1002931. PMC 3585382. PMID 23468614.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  20. Sham, J. S. K.; et al. (1998). "Termination of Ca2+ release by a local inactivation of ryanodine receptors in cardiac myocytes". Proc. Natl. Acad. Sci. USA. 95 (25): 15096–15101. Bibcode:1998PNAS...9515096S. doi:10.1073/pnas.95.25.15096. PMC 24581. PMID 9844021.
  21. Sobie, E.A., Dilly, K.W., Cruz, J. dos S., Lederer, J.W. and Jafri, S.M. (2002) 'Termination of cardiac ca(2+) sparks: An investigative mathematical model of calcium-induced calcium release', 83(1)
  22. Cheng H, Song LS, Shirokova N, et al. (February 1999). "Amplitude distribution of Ca2+ sparks in confocal images: theory and studies with an automatic detection method". Biophysical Journal. 76 (2): 606–17. doi:10.1016/S0006-3495(99)77229-2. PMC 1300067. PMID 9929467.
  23. Sebille S, Cantereau A, Vandebrouck C, et al. (January 2005). "Ca2+ sparks in muscle cells: interactive procedures for automatic detection and measurements on line-scan confocal images series". Computer Methods and Programs in Biomedicine. 77 (1): 57–70. doi:10.1016/j.cmpb.2004.06.004. PMID 15639710.

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