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TRPM2

From Wikipedia, the free encyclopedia
TRPM2
Identifiers
AliasesTRPM2,Trpm2, 9830168K16Rik, C79133, LTRPC2, TRPC7, Trp7, Trrp7, EREG1, KNP3, NUDT9H, NUDT9L1, LTrpC-2, transient receptor potential cation channel subfamily M member 2
External IDsOMIM:603749;MGI:1351901;HomoloGene:20709;GeneCards:TRPM2;OMA:TRPM2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001001188
NM_003307
NM_001320350
NM_001320351
NM_001320352

NM_138301

RefSeq (protein)

NP_001307279
NP_001307280
NP_001307281
NP_003298

NP_612174

Location (UCSC)Chr 21: 44.35 – 44.44 MbChr 10: 77.91 – 77.97 Mb
PubMedsearch[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Transient receptor potential cation channel, subfamily M, member 2,also known asTRPM2,is aproteinthat in humans is encoded by theTRPM2gene.

Structure[edit]

The protein encoded by this gene is a non-selective calcium-permeablecation channeland is part of theTransient Receptor Potentialion channel super family. The closest relative is the cold andmentholactivatedTRPM8ion channel. While TRPM2 is not cold sensitive it is activated by heat.[5]The TRPM2 ion channel is activated by free intracellularADP-ribosein synergy with free intracellularcalcium.[6]ADP-Ribose is produced to by the enzymePARPin response to oxidative stress and confers susceptibility tocell death.Several alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known.[7]

Function[edit]

TheTRPM2gene is highly expressed in the brain and was implicated by both genetic linkage studies in families[8]and then by case control or trio allelic association studies in the genetic aetiology ofbipolar affective disorder(Manic Depression).[9][10]

The physiological role of TRPM2 is not well understood. It was shown to be involved ininsulinsecretion.[5][11]In theimmune cellsit mediates parts of the responses toTNF- Alpha.[12]A role has been suggested for TRPM2 in activation ofNLRP3inflammasome,the dysregulation of which is strongly associated with a number of auto inflammatory and metabolic diseases, such as gout, obesity and diabetes.[13]In the brain it is involved in the toxicity ofamyloid beta,a protein associated withAlzheimer's disease.[14]In 2016, TRPM2 channel was strongly implicated in the detection of non-painful warm stimuli. Chun-Hsiang Tan and Peter McNaughton studied the responses of actualsensory neuronsto thermal stimuli, then used an RNA-sequencing strategy to identify TRPM2 as genetically required for warmth detection in the non-noxious range of 33–38 °C.[15]

Clinical significance[edit]

TRPM2 expression and function help preserve cancer cell viability.[16]TRPM2 channels are highly expressed in many cancers, notablyneuroblastoma.[16]

See also[edit]

References[edit]

  1. ^abcGRCh38: Ensembl release 89: ENSG00000142185Ensembl,May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000009292Ensembl,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. ^abTogashi K, Hara Y, Tominaga T, Higashi T, Konishi Y, Mori Y, Tominaga M (2006)."TRPM2 activation by cyclic ADP-ribose at body temperature is involved in insulin secretion".The EMBO Journal.25(9): 1804–15.doi:10.1038/sj.emboj.7601083.PMC1456947.PMID16601673.
  6. ^Csanády L, Törocsik B (2009)."Four Ca2+ ions activate TRPM2 channels by binding in deep crevices near the pore but intracellularly of the gate".The Journal of General Physiology.133(2): 189–203.doi:10.1085/jgp.200810109.PMC2638199.PMID19171771.
  7. ^"Entrez Gene: TRPM2 transient receptor potential cation channel, subfamily M, member 2".
  8. ^Gurling H (1998). "Chromosome 21 workshop".Psychiatric Genetics.8(2): 109–13.doi:10.1097/00041444-199800820-00015.PMID9686433.
  9. ^McQuillin A, Bass NJ, Kalsi G, Lawrence J, Puri V, Choudhury K, Detera-Wadleigh SD, Curtis D, Gurling HM (2006). "Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3".Molecular Psychiatry.11(2): 134–42.doi:10.1038/sj.mp.4001759.PMID16205735.S2CID22030624.
  10. ^Xu C, Macciardi F, Li PP, Yoon IS, Cooke RG, Hughes B, Parikh SV, McIntyre RS, Kennedy JL, Warsh JJ (2006). "Association of the putative susceptibility gene, transient receptor potential protein melastatin type 2, with bipolar disorder".American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics.141B(1): 36–43.doi:10.1002/ajmg.b.30239.PMID16252251.S2CID6439507.
  11. ^Bari MR, Akbar S, Eweida M, Kühn FJ, Gustafsson AJ, Lückhoff A, Islam MS (2009)."H2O2-induced Ca2+ influx and its inhibition by N-(p-amylcinnamoyl) anthranilic acid in the beta-cells: involvement of TRPM2 channels".Journal of Cellular and Molecular Medicine.13(9B): 3260–7.doi:10.1111/j.1582-4934.2009.00737.x.PMC4516483.PMID19382906.
  12. ^Yamamoto S, Shimizu S, Kiyonaka S, Takahashi N, Wajima T, Hara Y, Negoro T, Hiroi T, Kiuchi Y, Okada T, Kaneko S, Lange I, Fleig A, Penner R, Nishi M, Takeshima H, Mori Y (2008)."TRPM2-mediated Ca2+influx induces chemokine production in monocytes that aggravates inflammatory neutrophil infiltration".Nature Medicine.14(7): 738–47.doi:10.1038/nm1758.PMC2789807.PMID18542050.
  13. ^Zhong Z, Zhai Y, Liang S, Mori Y, Han R, Sutterwala FS, Qiao L (2013)."TRPM2 links oxidative stress to NLRP3 inflammasome activation".Nature Communications.4:1611.Bibcode:2013NatCo...4.1611Z.doi:10.1038/ncomms2608.PMC3605705.PMID23511475.
  14. ^Miller BA (2006). "The role of TRP channels in oxidative stress-induced cell death".The Journal of Membrane Biology.209(1): 31–41.doi:10.1007/s00232-005-0839-3.PMID16685599.S2CID23311452.
  15. ^Tan CH, McNaughton PA (2016)."The TRPM2 ion channel is required for sensitivity to warmth".Nature.536(7617): 460–3.Bibcode:2016Natur.536..460T.doi:10.1038/nature19074.PMC5720344.PMID27533035.
  16. ^abYu P, Cai X, Liang Y, Yang W (2019)."Roles of NAD + and Its Metabolites Regulated Calcium Channels in Cancer".Molecules.25(20): 4826.doi:10.3390/molecules25204826.PMC7587972.PMID33092205.

Further reading[edit]

External links[edit]

This article incorporates text from theUnited States National Library of Medicine,which is in thepublic domain.