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干细胞因子/c-Kit信号传导对伤害性感受的调节

Nociceptive tuning by stem cell factor/c-Kit signaling.

作者信息

Milenkovic Nevena, Frahm Christina, Gassmann Max, Griffel Carola, Erdmann Bettina, Birchmeier Carmen, Lewin Gary R, Garratt Alistair N

机构信息

Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13092 Berlin, Germany.

出版信息

Neuron. 2007 Dec 6;56(5):893-906. doi: 10.1016/j.neuron.2007.10.040.

Abstract

The molecular mechanisms regulating the sensitivity of sensory circuits to environmental stimuli are poorly understood. We demonstrate here a central role for stem cell factor (SCF) and its receptor, c-Kit, in tuning the responsiveness of sensory neurons to natural stimuli. Mice lacking SCF/c-Kit signaling displayed profound thermal hypoalgesia, attributable to a marked elevation in the thermal threshold and reduction in spiking rate of heat-sensitive nociceptors. Acute activation of c-Kit by its ligand, SCF, resulted in a reduced thermal threshold and potentiation of heat-activated currents in isolated small-diameter neurons and thermal hyperalgesia in mice. SCF-induced thermal hyperalgesia required the TRP family cation channel TRPV1. Lack of c-Kit signaling during development resulted in hypersensitivity of discrete mechanoreceptive neuronal subtypes. Thus, c-Kit can now be grouped with a small family of receptor tyrosine kinases, including c-Ret and TrkA, that control the transduction properties of sensory neurons.

摘要

调节感觉神经回路对环境刺激敏感性的分子机制目前仍知之甚少。我们在此证明干细胞因子(SCF)及其受体c-Kit在调节感觉神经元对自然刺激的反应性中起核心作用。缺乏SCF/c-Kit信号传导的小鼠表现出明显的热痛觉减退,这归因于热敏伤害性感受器的热阈值显著升高和放电率降低。其配体SCF对c-Kit的急性激活导致分离的小直径神经元的热阈值降低和热激活电流增强,以及小鼠出现热痛觉过敏。SCF诱导的热痛觉过敏需要TRP家族阳离子通道TRPV1。发育过程中c-Kit信号的缺失导致离散的机械感受神经元亚型出现超敏反应。因此,c-Kit现在可以与一小类受体酪氨酸激酶归为一类,包括c-Ret和TrkA,它们控制感觉神经元的转导特性。

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