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KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects
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International audience. Loss-of-function mutations in the potassium-chloride cotransporter KCC3 lead to Andermann syndrome, a severe sensorimotor neuropathy characterized by areflexia, amyotrophy and locomotor abnormalities. The molecular events responsible for axonal loss remain poorly understood. Here, we establish that global or neuron-specific KCC3 loss-of-function in mice leads to early neuromuscular junction (NMJ) abnormalities and muscular atrophy that are consistent with the pre-synaptic neurotransmission defects observed in patients. KCC3 depletion does not modify chloride handling, but promotes an abnormal electrical activity among primary motoneurons and mislocalization of Na$^+$/K$^+$-ATPase $\alpha$1 in spinal cord motoneurons. Moreover, the activity-targeting drug carbamazepine restores Na$^+$/K$^+$-ATPase $\alpha$1 localization and reduces NMJ denervation in $Slc12a6^{-/-}$ mice. We here propose that abnormal motoneuron electrical activity contributes to the peripheral neuropathy observed in Andermann syndrome.
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