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Evidence for the involvement of ASIC3 in sensory mechanotransduction in proprioceptors

机译:ASIC3参与本体感受器感觉机械转导的证据

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Acid-sensing ion channel 3 (ASIC3) is involved in acid nociception, but its possible role in neurosensory mechanotransduction is disputed. We report here the generation of Asic3-knockout/eGFPf-knockin mice and subsequent characterization of heterogeneous expression of ASIC3 in the dorsal root ganglion (DRG). ASIC3 is expressed in parvalbumin (Pv+) proprioceptor axons innervating muscle spindles. We further generate a floxed allele of Asic3 ( Asic3 f/f ) and probe the role of ASIC3 in mechanotransduction in neurite-bearing Pv+ DRG neurons through localized elastic matrix movements and electrophysiology. Targeted knockout of Asic3 disrupts spindle afferent sensitivity to dynamic stimuli and impairs mechanotransduction in Pv+ DRG neurons because of substrate deformation-induced neurite stretching, but not to direct neurite indentation. In behavioural tasks, global knockout ( Asic3 ?/? ) and Pv-Cre::Asic3 f/f mice produce similar deficits in grid and balance beam walking tasks. We conclude that, at least in mouse, ASIC3 is a molecular determinant contributing to dynamic mechanosensitivity in proprioceptors.
机译:酸敏感离子通道3(ASIC3)参与酸伤害感受,但其在神经感觉机械转导中的可能作用受到争议。我们在这里报告了Asic3-基因敲除/ eGFPf基因敲除小鼠的产生,以及在背根神经节(DRG)中ASIC3异种表达的表征。 ASIC3在支配肌肉纺锤体的小白蛋白(Pv +)本体感受器轴突中表达。我们还生成了Asic3的一个等位基因(Asic3 f / f ),并通过局部弹性基质运动和电生理学研究了ASIC3在神经突携带Pv + DRG神经元的机械转导中的作用。定向敲除Asic3会破坏纺锤体对动态刺激的传入敏感性,并由于底物变形诱导的神经突伸展而损害Pv + DRG神经元的机械传导,但不能直接诱导神经突入。在行为任务中,整体敲除(Asic3 ?/?)和Pv-Cre :: Asic3 f / f 小鼠在网格和平衡木行走任务中产生类似的缺陷。我们得出的结论是,至少在小鼠中,ASIC3是促成本体感受器动态机械敏感性的分子决定因素。

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