A multi PDZ-domain protein Pdzd2 contributes to functional expression of sensory neuron-specific sodium channel NaV1.8

The voltage-gated sodium channel NaV1.8 is expressed exclusively in nociceptive sensory neurons and plays an important role in pain pathways. NaV1.8 cannot be functionally expressed in non-neuronal cells even in the presence of β-subunits. We have previously identified Pdzd2, a multi PDZ-domain prot...

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Veröffentlicht in:Molecular and cellular neuroscience 2009-10, Vol.42 (3), p.219-225
Hauptverfasser: Shao, Dongmin, Baker, Mark D., Abrahamsen, Bjarke, Rugiero, Francois, Malik-Hall, Misbah, Poon, W.-Y. Louisa, Cheah, Kathryn S.E., Yao, Kwok-Ming, Wood, John N., Okuse, Kenji
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Sprache:eng
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Zusammenfassung:The voltage-gated sodium channel NaV1.8 is expressed exclusively in nociceptive sensory neurons and plays an important role in pain pathways. NaV1.8 cannot be functionally expressed in non-neuronal cells even in the presence of β-subunits. We have previously identified Pdzd2, a multi PDZ-domain protein, as a potential interactor for NaV1.8. Here we report that Pdzd2 binds directly to the intracellular loops of NaV1.8 and NaV1.7. The endogenous NaV1.8 current in sensory neurons is inhibited by antisense- and siRNA-mediated downregulation of Pdzd2. However, no marked change in pain behaviours is observed in Pdzd2-decificent mice. This may be due to compensatory upregulation of p11, another regulatory factor for NaV1.8, in dorsal root ganglia of Pdzd2-deficient mice. These findings reveal that Pdzd2 and p11 play collaborative roles in regulation of NaV1.8 expression in sensory neurons.
ISSN:1044-7431
1095-9327
DOI:10.1016/j.mcn.2009.07.003