| Autor: |
Jeanne M. Nerbonne, David M. Ornitz, Ann Marie Craig, Fernanda Laezza, Jun Yang Lou, Kathryn A. Yamada, Benjamin R. Gerber, Maolei Xiao, Hali Hartmann |
| Rok vydání: |
2005 |
| Předmět: |
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| Zdroj: |
The Journal of Physiology. 569:179-193 |
| ISSN: |
0022-3751 |
| Popis: |
Genetic ablation of the fibroblast growth factor (Fgf) 14 gene in mice or a missense mutation in Fgf14 in humans causes ataxia and cognitive deficits. These phenotypes suggest that the neuronally expressed Fgf14 gene is essential for regulating normal neuronal activity. Here, we demonstrate that FGF14 interacts directly with multiple voltage-gated Na + (Nav) channel α subunits heterologously expressed in non-neuronal cells or natively expressed in a murine neuroblastoma cell line. Functional studies reveal that these interactions result in the potent inhibition of Nav channel currents (I Na) and in changes in the voltage dependence of channel activation and inactivation. Deletion of the unique amino terminus of the splice variant of Fgf14, Fgf14-1b ,o rexpression of the splice variant Fgf14-1a modifies the modulatory effects on I Na, suggesting an important role for the amino terminus domain of FGF14 in the regulation of Nav channels. To investigate the function of FGF14 in neurones, we directly expressed Fgf14 in freshly isolated primary rat hippocampal neurones. In these cells, the addition of FGF14-1a‐GFP or FGF14-1b‐GFP increased I Na density and shifted the voltage dependence of channel activation and inactivation. In fully differentiated neurones, FGF14-1a‐GFP or FGF14-1b‐GFP preferentially colocalized with endogenous Nav channels at the axonal initial segment, a critical region for action potential generation. Together, these findings implicate FGF14 as a unique modulator of Nav channel activity in the CNS and provide a possible mechanism to explain the neurological phenotypes observed in mice and humans with mutations in Fgf14. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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