Objective To assess the functional effects of a variant, c.89 G > A (p.Arg30Gln), in the transient receptor potential melastatin 8 (TRPM8) cold-sensing, nonselective cation channel, which we have previously identified in a patient with familial trigeminal neuralgia. Methods We carried out Ca2+ imaging and whole-cell patch-clamp recording. Results The TRPM8 mutation enhances channel activation, increases basal current amplitude and intracellular [Ca2+] in cells carrying the mutant channel, and enhances the response to menthol. Conclusions We propose that Arg30Gln confers gain-of-function attributes on TRPM8, which contribute to pathogenesis of trigeminal neuralgia in patients carrying this mutation.

Trigeminal neuralgia TRPM8 mutation: Enhanced activation, basal [Ca2+]i and menthol response / Gualdani, R., Yuan, J.-H., Effraim, P.R., Di Stefano, G., Truini, A., Cruccu, G., Dib-Hajj, S.D., Gailly, P., Waxman, S.G.. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - 7:1(2021). [10.1212/NXG.0000000000000550]

Trigeminal neuralgia TRPM8 mutation: Enhanced activation, basal [Ca2+]i and menthol response

Di Stefano G.;Truini A.;Cruccu G.;
2021

Abstract

Objective To assess the functional effects of a variant, c.89 G > A (p.Arg30Gln), in the transient receptor potential melastatin 8 (TRPM8) cold-sensing, nonselective cation channel, which we have previously identified in a patient with familial trigeminal neuralgia. Methods We carried out Ca2+ imaging and whole-cell patch-clamp recording. Results The TRPM8 mutation enhances channel activation, increases basal current amplitude and intracellular [Ca2+] in cells carrying the mutant channel, and enhances the response to menthol. Conclusions We propose that Arg30Gln confers gain-of-function attributes on TRPM8, which contribute to pathogenesis of trigeminal neuralgia in patients carrying this mutation.
2021
pain; trigeminal neuralgia
01 Pubblicazione su rivista::01a Articolo in rivista
Trigeminal neuralgia TRPM8 mutation: Enhanced activation, basal [Ca2+]i and menthol response / Gualdani, R., Yuan, J.-H., Effraim, P.R., Di Stefano, G., Truini, A., Cruccu, G., Dib-Hajj, S.D., Gailly, P., Waxman, S.G.. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - 7:1(2021). [10.1212/NXG.0000000000000550]
File allegati a questo prodotto
File Dimensione Formato  
Gualdani_TRPM8_2021.pdf

accesso aperto

Tipologia: Documento in Post-print (versione successiva alla peer review e accettata per la pubblicazione)
Licenza: Creative commons
Dimensione 423.91 kB
Formato Adobe PDF
423.91 kB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1572538
Citazioni
  • ???jsp.display-item.citation.pmc??? 19
  • Scopus 22
  • ???jsp.display-item.citation.isi??? 23
social impact