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Elife ; 72018 12 18.
Artigo em Inglês | MEDLINE | ID: mdl-30560783

RESUMO

Although it has been known for over a decade that the inflammatory mediator NGF sensitizes pain-receptor neurons through increased trafficking of TRPV1 channels to the plasma membrane, the mechanism by which this occurs remains mysterious. NGF activates phosphoinositide 3-kinase (PI3K), the enzyme that generates PI(3,4)P2 and PIP3, and PI3K activity is required for sensitization. One tantalizing hint came from the finding that the N-terminal region of TRPV1 interacts directly with PI3K. Using two-color total internal reflection fluorescence microscopy, we show that TRPV1 potentiates NGF-induced PI3K activity. A soluble TRPV1 fragment corresponding to the N-terminal Ankyrin repeats domain (ARD) was sufficient to produce this potentiation, indicating that allosteric regulation was involved. Further, other TRPV channels with conserved ARDs also potentiated NGF-induced PI3K activity. Our data demonstrate a novel reciprocal regulation of PI3K signaling by the ARD of TRPV channels.


Assuntos
Membrana Celular/efeitos dos fármacos , Fator de Crescimento Neural/farmacologia , Fosfatidilinositol 3-Quinase/metabolismo , Animais , Linhagem Celular , Membrana Celular/metabolismo , Ativação Enzimática/efeitos dos fármacos , Células Híbridas , Camundongos , Microscopia de Fluorescência/métodos , Fosfatidilinositol 3-Quinase/genética , Fosfatidilinositóis/metabolismo , Ligação Proteica/efeitos dos fármacos , Ratos , Canais de Cátion TRPV/genética , Canais de Cátion TRPV/metabolismo
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