Biology:TRPC3

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Short description: Protein and coding gene in humans


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Short transient receptor potential channel 3 (TrpC3) also known as transient receptor protein 3 (TRP-3) is a protein that in humans is encoded by the TRPC3 gene. The TRPC3/6/7 subfamily are implicated in the regulation of vascular tone, cell growth, proliferation and pathological hypertrophy.[1] These are diacylglycerol-sensitive cation channels known to regulate intracellular calcium via activation of the phospholipase C (PLC) pathway and/or by sensing Ca2+ store depletion.[2] Together, their role in calcium homeostasis has made them potential therapeutic targets for a variety of central and peripheral pathologies.[3]

Function

Non-specific cation conductance elicited by the activation of TrkB by BDNF is TRPC3-dependent in the CNS.[4] TRPC channels are almost always co-localized with mGluR1-expressing cells and likely play a role in mGluR-mediated EPSPs.[5]

The TRPC3 channel has been shown to be preferentially expressed in non-excitable cell types, such as oligodendrocytes.[2] However, evidence suggests that active TRPC3 channels in basal ganglia (BG) output neurons are responsible for maintaining a tonic inward depolarizing current that regulates resting membrane potential and promotes regular neuronal firing.[6] Conversely, inhibiting TRPC3 promotes cellular hyperpolarization, which can lead to slower and more irregular neuronal firing. While it's unclear if TRPC3 channels have equal expression, other members of the TRPC family have been localized to the axon hillock, cell body, and dendritic processes of dopamine-expressing cells.[7]

The neuromodulator, substance P, activates TRPC3/7 channels inducing cellular currents that underlie rhythmic pacemaker activity in the brainstem, enhancing the regularity and frequency of respiratory rhythms,[8] showing homology to the mechanism described in BG neurons. Transgenic cardiomyocytes expressing TRPC3 show prolonged action potential duration when exposed to a TRPC3 agonist.[9] The same cardiomyocytes also increase their firing rate with agonist exposure under a current-clamp tetanus protocol suggesting that they may play a role in cardiac arrhythmogenesis.

Modulators

A small molecule agonist is GSK1702934A and antagonists are GSK417651A and GSK2293017A.[1] A commercially available inhibitor is available in the form of a pyrazole compound, Pyr3[10] TRPC3 has been shown to specifically interact with TRPC1[11][12] and TRPC6.[13]

See also

References

  1. 1.0 1.1 Xu, Xiaoping; Lozinskaya, Irina; Costell, Melissa; Lin, Zuojun; Ball, Jennifer A.; Bernard, Roberta; Behm, David J.; Marino, Joseph P. et al. (2013-01-29). "Characterization of Small Molecule TRPC3 and TRPC6 agonist and Antagonists". Biophysical Journal 104 (2, Supplement 1): 454a. doi:10.1016/j.bpj.2012.11.2513. Bibcode2013BpJ...104..454X. 
  2. 2.0 2.1 "Cellular localization of TRPC3 channel in rat brain: preferential distribution to oligodendrocytes". Neuroscience Letters 365 (2): 137–42. July 2004. doi:10.1016/j.neulet.2004.04.070. PMID 15245795. 
  3. "TRP channels as therapeutic targets". Current Topics in Medicinal Chemistry 13 (3): 241–3. 2013-01-01. doi:10.2174/1568026611313030001. PMID 23432057. 
  4. "Activation of a TRPC3-dependent cation current through the neurotrophin BDNF". Neuron 24 (1): 261–73. 1999. doi:10.1016/S0896-6273(00)80838-7. PMID 10677043. 
  5. "Immunohistochemical localization of TRPC6 in the rat substantia nigra". Neuroscience Letters 424 (3): 170–4. September 2007. doi:10.1016/j.neulet.2007.07.049. PMID 17723267. 
  6. "Constitutively active TRPC3 channels regulate basal ganglia output neurons". The Journal of Neuroscience 28 (2): 473–82. January 2008. doi:10.1523/JNEUROSCI.3978-07.2008. PMID 18184790. 
  7. Zhu, Michael X., ed (2011). "TRPC Channels in Neuronal Survival". TRPC Channels in Neuronal Surviva. Boca Raton (FL): CRC Press/Taylor & Francis. ISBN 978-1-4398-1860-2. https://www.ncbi.nlm.nih.gov/books/NBK92826/. 
  8. "Substance P modulation of TRPC3/7 channels improves respiratory rhythm regularity and ICAN-dependent pacemaker activity". The European Journal of Neuroscience 31 (7): 1219–32. April 2010. doi:10.1111/j.1460-9568.2010.07156.x. PMID 20345918. 
  9. "TRPC3 contributes to regulation of cardiac contractility and arrhythmogenesis by dynamic interaction with NCX1". Cardiovascular Research 106 (1): 163–73. April 2015. doi:10.1093/cvr/cvv022. PMID 25631581. 
  10. "Selective and direct inhibition of TRPC3 channels underlies biological activities of a pyrazole compound". Proceedings of the National Academy of Sciences of the United States of America 106 (13): 5400–5. March 2009. doi:10.1073/pnas.0808793106. PMID 19289841. Bibcode2009PNAS..106.5400K. 
  11. "Formation of novel TRPC channels by complex subunit interactions in embryonic brain". The Journal of Biological Chemistry 278 (40): 39014–9. October 2003. doi:10.1074/jbc.M306705200. PMID 12857742. 
  12. "Coassembly of TRP and TRPL produces a distinct store-operated conductance". Cell 89 (7): 1155–64. June 1997. doi:10.1016/S0092-8674(00)80302-5. PMID 9215637. 
  13. "Subunit composition of mammalian transient receptor potential channels in living cells". Proceedings of the National Academy of Sciences of the United States of America 99 (11): 7461–6. May 2002. doi:10.1073/pnas.102596199. PMID 12032305. Bibcode2002PNAS...99.7461H. 

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.