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TRPV2

From Wikipedia, the free encyclopedia
TRPV2
Available structures
PDBOrtholog search:PDBeRCSB
Identifiers
AliasesTRPV2,VRL, VRL-1, VRL1, transient receptor potential cation channel subfamily V member 2
External IDsOMIM:606676;MGI:1341836;HomoloGene:7993;GeneCards:TRPV2;OMA:TRPV2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

51393

22368

Ensembl

ENSG00000187688

ENSMUSG00000018507

UniProt

Q9Y5S1

Q9WTR1

RefSeq (mRNA)

NM_016113

NM_011706
NM_001382489
NM_001382490
NM_001382491
NM_001382492

RefSeq (protein)

NP_057197

NP_035836
NP_001369418
NP_001369419
NP_001369420
NP_001369421

Location (UCSC)Chr 17: 16.42 – 16.44 MbChr 11: 62.47 – 62.49 Mb
PubMedsearch[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Transient receptor potential cation channel subfamily V member 2is aproteinthat in humans is encoded by theTRPV2gene.[5][6]TRPV2 is a nonspecific cation channel that is a part of the TRP channel family. This channel allows the cell to communicate with its extracellular environment through the transfer of ions, and responds to noxious temperatures greater than 52 °C. It has a structure similar to that ofpotassium channels,and has similar functions throughout multiple species; recent research has also shown multiple interactions in the human body.

TRP subfamily

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The vanilloid TRP subfamily (TRPV) named after the vanilloid receptor 1 consist of six members, four of them (TRPV1-TRPV4) have been related to thermal sensation. TRPV2 shares 50% of its homology with TRPV1. Compared to TRPV1 channels, TRPV2 channels do not open in response to vanilloids likecapsaicinor thermal stimuli around 43 °C.[7]This may be due to the composition of the ankyrin repeat domains in TRPV2, which are different than those in TRPV1. However, TRPV2 channels can open by noxious temperatures greater than 52 °C.[7]TRPV2 initially was characterized as a noxious heat sensor channel, but more evidence suggest its importance in various osmosensory and mechanosensory mechanisms. The channel can open in response to a variety of stimuli includinghormones,growth factors,mechanical stretching,heat,osmotic swelling, lysophospholipids, andcannabinoids.These channels are expressed in medium to large diameter neurons,motor neurons,and other non-neuronal tissues like theheartandlungs,which indicates its versatile function. The channel has an important role for basic cell function including contraction,cell proliferation,andcell death.The same channel can have different functions depending on the type of tissue. Other roles of TRPV2 continue to be explored in an attempt to define the role of translocation of TRPV2 by growth factors.SET2is a TRPV2 selective antagonist.[8]

Discovery

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TRPV2 was independently discovered by two research groups and described in 1999. It was identified in the lab ofDavid Juliusas a close homolog of TRPV1, known as the first identified thermosensitive ion channel.[5]Itaru Kojima from Gunma University was looking for a protein which is responsible for the entry of calcium into cells in response toinsulin-like growth factor-1(IGF-1). Upon stimulation of cells with IGF-1, it was discovered that TRPV2 translocates towards and integrates into the cell membrane and increases intracellular calcium concentrations.

Structure

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TRPV2 channel has a similar structure topotassium channels,which are the largestion channelfamily. This channel is composed of six transmembrane spanning regions (S1-S6) with a pore forming loop between S5 and S6.[9]The pore forming loop also defines the selectivity filter, which determines the ions that are able to enter the channel. The S1-S4 region, as well as the N and C terminals of the protein, is important in reference to the gating of the channel. Although TRPV2 is a nonspecific cation channel, it is more permeable to calcium ions; calcium is an intracellular messenger and plays a very important role in a variety of different cellular processes. At rest, the pore channel is closed; in the activated state, the channel opens, allowing the influx of sodium and calcium ions that initiates anaction potential.

Species homology

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Orthologoues between rat and mouse aligned with humans

The TRPV subfamily of channels of 1 through 4 have unique functions. One important variation is that these channels trigger cellular signaling pathways via non-selective cation flux, making them unique. Specifically, the TRPV2 channel has structural similarities amongst the other members of the TRPV family. For instance, the channel consists of sixtransmembrane domainsand a pore forming loop between S5 and S6.[9]Within the human genome, putative homologs can be found. This suggests that theamino acidsandproteinscoded come from a common ancestor where their structures are conserved in function.

Among the subfamily, TRPV2 and TRPV1 share 50% of their sequence identity not only in humans, but in rats as well. The rat TRPV2 can be comparable to that of humans because they exhibit similar surface localization among one another. Each channel possessesATPbinding regions and the 50% sequence identity between TRPV1 and TRPV2 suggests that both channel'sAnkyrin repeatdomain (ARD) bind to different regulatory ligands as well.[9]The channels structure can be observed as similar to that ofpotassium channels.In knockout mice, the physiological thermal responses show similar activation to wild-type mice. On top of that, humans, rats, and mice are consideredorthologues.

Tissue distribution

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Homo sapiens

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Inhomo sapiens,there is broad expression of TRPV2 in thelymph nodes,spleen,lung,appendix,andplacenta;it is mostly expressed in the lungs.[10]TRPV2 is majorly in a sub population of medium to largesensory neurons,as well as being distributed in thebrainandspinal cord.[11]The mRNA expression of TRPV2 is also found in human pulmonary and umbilical veinendothelial cells.[11]Based onmRNAexpression of TRPV2 in mice, it is also speculated that it is expressed in arterial muscle cells, which can then be influenced by blood pressure; though it was evident that TRPV2 expression was localized in the intracellular area, some growth factors localized it to the plasmacell membrane.[11]In circulatory organs, studies and data suggest that TRPV2 may be a mechanosensor, meaning that it can sense changes in external stimuli; the mechanisms involved in opening TRPV2 by membrane stretching or hypoosmotic cell swelling have not yet been determined.[11]

Mus musculus

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Mus Musculus-huismuis2

Inmus musculus(house mouse), TRPV2 functions as a protein coding gene. There is broad expression of TRPV2 in thethymus,placenta,cerebellum,andspleen;it is most commonly expressed in the thymus.[12]Thethymusis a lymphoid organ involved in the function of the immune system, whereT cellsmature. T cells are an important component to the adaptive immune system, because it is where the body adapts to foreign substances; this demonstrates TRPV2's importance in the immune system. TRPV2 in mus musculus is also activated by hypo-osmolarity and cell stretching, indicating that TRPV2 plays a role inmechanotransductionin mice as well.[12]In experiments with knockout mice (TRPV2KO mice), it was found that TRPV2 is expressed in brownadipocytesand inbrown adipose tissue(BAT). It can be concluded that TRPV2 plays a role in BATthermogenesisin mice, since it was found that a lack of TRPV2 impairs this thermogenesis in BAT; given these results, this could be a target for human obesity therapy.[13]

Rattus norvegicus

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Inrattus norvegicus(Norway rat), there is broad expression of TRPV2 in theadrenal glandsand the lungs, being most present in the adrenal glands. TRPV2 is also present in thethymusandspleen,but not in high amounts. Without using any external growth factors, TRPV2 is highly specific to the plasmacell membranein rat adult dorsal root ganglions,cerebral cortex,and arterial muscle cells.[11]

Clinical significance

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Cancer

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TRPV2 plays a role in negative homeostatic control of excess cell proliferation by inducingapoptosis(programmed cell death).[9]This is accomplished predominantly through theFas pathway,also known as the death-inducing signaling complex. Activation of TRPV2 by growth factors and hormones induces the receptor to translocate from intracellular compartments to the plasma membrane, which initiates the development of death signals.[14]An example of the role of TRPV2 in apoptosis is its expression in the bladder cancer t24 cell line. TRPV2 in bladder cancer leads to apoptosis through the influx of calcium ions through the TPRV2 channel. In some tumors, the over-expression of TRPV2 can lead to abnormal signaling pathways that drives unchecked cell proliferation and resistance to apoptotic stimuli. The over-expression of TRPV2 has been linked to several cancer types and cell lines.[15][16]TRPV2 is expressed in humanHepG2 cells,a cell line containing human liver carcinogenic cells. Heat allows for calcium entry into these cells through TRPV2 channels, which aid in the maintenance of these cells.[17]TRPV2 also negatively affects patients withgliomas.TRPV2 in carcinogenicglial cellsleads to resistance toapoptotic cell death,leading to harmful, carcinogenic cell survival.[18]

Immunity

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Antigens presentation

TRPV2 is expressed in the spleen,lymphocytes,andmyeloid cellsincludinggranulocytes,macrophagesandmast cells.Among these cell types, TRPV2 mediates cytokine release,phagocytosis,endocytosis,podosomeassembly, and inflammation.[19]The influx of calcium seems to play an important role in these functions.Mast cellsareleukocytes(white blood cells) rich in histamine which are able to respond to a variety of stimuli, often initiating inflammatory and/or allergic responses. The responses generated by mast cells rely on the calcium influx in the plasma membrane with the help of channels. Surface localization of the TRPV2 protein along with coupling of the protein to calcium and proinflammatorydegranulationhave been found in mast cells. The activation of TRPV2 in high temperatures permits calcium ion influx, inducing the release of proinflammatory factors. Therefore, TRPV2 is essential in mast cell degranulation as a result of its response to heat.[20] Immune cells are also able to kill pathogens by binding to them and engulfing them in a process known asphagocytosis.In macrophages TRPV2 recruitment toward the phagosome is regulated byPI3k signaling,protein kinase C,akt kinase, andSrc kinases.[9]They are able to locate these microbes throughchemotaxiswhich is TRPV2 mediated. When the pathogen is endocytosed it is degraded then presented on the membrane of antigen presenting cells (i.e. macrophages). Macrophages present these antigens to T cells via amajor histocompatibility complex(MHC). The region between the MHC-peptide and the T cell receptor is known as theimmunosynapse.TRPV2 channels are highly concentrated in this region. When these two cells interact, it allows calcium to diffuse through the TRPV2 channel. TRPV2mRNAhas been detected inCD4+andCD8+T cells as well as in human B lymphocytes. TRPV2 is one type of ion channel that directs T cell activation, proliferation, and defense mechanisms. If the TRPV2 channel were absent or not functioning properly in T cells, T cell receptor signaling would not be optimal. TRPV2 also acts as a transmembrane protein on the surface of B cells, negatively controlling B cell activation.[20]Abnormal TRPV2 expression has been reported inhematologicaldiseases includingmultiple myeloma,myelodysplastic syndrome,Burkitt lymphoma,andacute myeloid leukemia.[19]

Metabolic

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TRPV2 seems to be essential in glucosehomeostasis.It is highly expressed in MIN6 cells, which is aβ-cell.These cell types are known for releasinginsulin,a molecule that functions to keep glucose levels low. Under unstimulated conditions, TRPV2 is localized in thecytoplasm.Activation causes the channel to translocate to theplasma membrane.This triggers the influx ofcalciumresulting in insulin secretion.[7]

Cardiovascular

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TRPV2 is very important in the structure and function ofcardiomyocytes(heart cells). Compared to skeletal muscles, TRPV2 is expressed 10 times as high in cardiomyocytes[21]and is important in current conduction. TRPV2 has been shown to be involved in stretch-dependent responses in heart cells. TRPV2 expression is concentrated inintercalated discswhich allows the synchronous contraction of cardiomyocytes. Abnormal expression of TRPV2 results in reduced shortening length, shortening rate, and lengthening rate which ultimately compromise cardiac contractile function.

Ligands

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Agonist

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Agonists include:[22]

See also

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References

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  1. ^abcGRCh38: Ensembl release 89: ENSG00000187688–Ensembl,May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000018507–Ensembl,May 2017
  3. ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^abCaterina MJ, Rosen TA, Tominaga M, Brake AJ, Julius D (April 1999)."A capsaicin-receptor homologue with a high threshold for noxious heat".Nature.398(6726): 436–41.Bibcode:1999Natur.398..436C.doi:10.1038/18906.PMID10201375.S2CID4415522.
  6. ^Clapham DE, Julius D, Montell C, Schultz G (December 2005). "International Union of Pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels".Pharmacological Reviews.57(4): 427–50.doi:10.1124/pr.57.4.6.PMID16382100.S2CID17936350.
  7. ^abcShibasaki K (September 2016)."Physiological significance of TRPV2 as a mechanosensor, thermosensor and lipid sensor".The Journal of Physiological Sciences.66(5): 359–65.doi:10.1007/s12576-016-0434-7.PMC10717341.PMID26841959.S2CID582291.
  8. ^Chai H, Cheng X, Zhou B, Zhao L, Lin X, Huang D, et al. (February 2019). "Structure-Based Discovery of a Subtype-Selective Inhibitor Targeting a Transient Receptor Potential Vanilloid Channel".Journal of Medicinal Chemistry.62(3): 1373–1384.doi:10.1021/acs.jmedchem.8b01496.PMID30620187.S2CID58543255.
  9. ^abcdePerálvarez-Marín A, Doñate-Macian P, Gaudet R (November 2013)."What do we know about the transient receptor potential vanilloid 2 (TRPV2) ion channel?"(PDF).The FEBS Journal.280(21): 5471–87.doi:10.1111/febs.12302.PMC3783526.PMID23615321.
  10. ^"TRPV2: transient receptor potential cation channel subfamily V member 2 [Homo sapiens (human)]".NCBI.
  11. ^abcdeKatsuhiko M, Shigekawa M, Imaizumi Y (2007). "Chapter 28A: New Insight into the Function of TRPV2 in Circulatory Organs". In Liedtke WB, Heller S (eds.).TRP Ion Channel Function in Sensory Transduction and Cellular Signaling Cascades.Frontiers in Neuroscience. Boca Raton (FL): CRC Press/Taylor & Francis.ISBN978-0-8493-4048-2.PMID21204489.
  12. ^ab"TRPV2: transient receptor potential cation channel, subfamily V, member 2 [Mus musculus (house mouse)]".NCBI.
  13. ^Sun W, Uchida K, Suzuki Y, Zhou Y, Kim M, Takayama Y, et al. (March 2016)."Lack of TRPV2 impairs thermogenesis in mouse brown adipose tissue".EMBO Reports.17(3): 383–99.doi:10.15252/embr.201540819.PMC4772987.PMID26882545.
  14. ^Liberati S, Morelli MB, Amantini C, Santoni M, Nabissi M, Cardinali C, Santoni G (2014). "Advances in transient receptor potential vanilloid-2 channel expression and function in tumor growth and progression".Current Protein & Peptide Science.15(7): 732–7.doi:10.2174/1389203715666140704115913.hdl:11581/359381.PMID25001513.
  15. ^Santoni G, Amantini C, Maggi F, Marinelli O, Santoni M, Nabissi M, Morelli MB (February 2020)."The TRPV2 cation channels: from urothelial cancer invasiveness to glioblastoma multiforme interactome signature".Laboratory Investigation; A Journal of Technical Methods and Pathology.100(2): 186–198.doi:10.1038/s41374-019-0333-7.PMID31653969.S2CID204887121.
  16. ^Siveen KS, Nizamuddin PB, Uddin S, Al-Thani M, Frenneaux MP, Janahi IA, et al. (2020)."TRPV2: A Cancer Biomarker and Potential Therapeutic Target".Disease Markers.2020:8892312.doi:10.1155/2020/8892312.PMC7746447.PMID33376561.
  17. ^Lehen'kyi V, Prevarskaya."TRPV2 (transient potential cation channel, subfamily V, member 2)".Atlas of Genetics and Cytogenetic in Oncology and Haematology.
  18. ^Nabissi M, Morelli MB, Amantini C, Farfariello V, Ricci-Vitiani L, Caprodossi S, et al. (May 2010)."TRPV2 channel negatively controls glioma cell proliferation and resistance to Fas-induced apoptosis in ERK-dependent manner".Carcinogenesis.31(5): 794–803.doi:10.1093/carcin/bgq019.PMID20093382.
  19. ^abCaterina MJ, Pang Z (December 2016)."TRP Channels in Skin Biology and Pathophysiology".Pharmaceuticals.9(4): 77.doi:10.3390/ph9040077.PMC5198052.PMID27983625.
  20. ^abSantoni G, Farfariello V, Liberati S, Morelli MB, Nabissi M, Santoni M, Amantini C (2013-02-14)."The role of transient receptor potential vanilloid type-2 ion channels in innate and adaptive immune responses".Frontiers in Immunology.4:34.doi:10.3389/fimmu.2013.00034.PMC3572502.PMID23420671.
  21. ^Aguettaz E, Bois P, Cognard C, Sebille S (November 2017). "Stretch-activated TRPV2 channels: Role in mediating cardiopathies".Progress in Biophysics and Molecular Biology.130(Pt B): 273–280.doi:10.1016/j.pbiomolbio.2017.05.007.PMID28546113.
  22. ^Muller C, Morales P, Reggio PH (2019-01-15)."Cannabinoid Ligands Targeting TRP Channels".Frontiers in Molecular Neuroscience.11:487.doi:10.3389/fnmol.2018.00487.PMC6340993.PMID30697147.
  23. ^Laragione T, Harris C, Gulko PS. Combination therapy of a TRPV2 agonist with a TNF inhibitor achieves sustained suppression of disease severity and reduced joint damage.Clin Exp Immunol.2023 Mar 24;211(3):233-238.doi:10.1093/cei/uxac124PMID36571199
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This article incorporates text from theUnited States National Library of Medicine,which is in thepublic domain.

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