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smoothened 受体信号调节大鼠体感皮层 GABA 极性的发育转变。

Smoothened receptor signaling regulates the developmental shift of GABA polarity in rat somatosensory cortex.

机构信息

Aix-Marseille University, Parc Scientifique de Luminy, 13273, Marseille, France.

INSERM (Institut National de la Santé et de la Recherche Médicale) Unité 1249, Marseille, Parc Scientifique de Luminy, 13273 Marseille, France.

出版信息

J Cell Sci. 2020 Oct 23;133(20):jcs247700. doi: 10.1242/jcs.247700.

Abstract

Sonic hedgehog (Shh) and its patched-smoothened receptor complex control a variety of functions in the developing central nervous system, such as neural cell proliferation and differentiation. Recently, Shh signaling components have been found to be expressed at the synaptic level in the postnatal brain, suggesting a potential role in the regulation of synaptic transmission. Using electroporation of constitutively active and negative-phenotype forms of the Shh signal transducer smoothened (Smo), we studied the role of Smo signaling in the development and maturation of GABAergic transmission in the somatosensory cortex. Our results show that enhancing Smo activity during development accelerates the shift from depolarizing to hyperpolarizing GABA in a manner dependent on functional expression of potassium-chloride cotransporter type 2 (KCC2, also known as SLC12A5). On the other hand, blocking Smo activity maintains the GABA response in a depolarizing state in mature cortical neurons, resulting in altered chloride homeostasis and increased seizure susceptibility. This study reveals unexpected functions of Smo signaling in the regulation of chloride homeostasis, through control of KCC2 cell-surface stability, and the timing of the GABA excitatory-to-inhibitory shift in brain maturation.

摘要

声波刺猬(Shh)及其 patched-smoothened 受体复合物在中枢神经系统的发育过程中控制着多种功能,如神经细胞的增殖和分化。最近,在出生后的大脑中发现 Shh 信号转导成分在突触水平上表达,这表明它在调节突触传递方面具有潜在作用。通过对 Shh 信号转导蛋白 smoothened(Smo)的组成激活和负表型形式进行电穿孔,我们研究了 Smo 信号在躯体感觉皮层 GABA 能传递的发育和成熟中的作用。我们的结果表明,在发育过程中增强 Smo 活性会加速 GABA 从去极化向超极化的转变,这种转变依赖于钾氯离子共转运蛋白 2(KCC2,也称为 SLC12A5)的功能表达。另一方面,阻断 Smo 活性会使成熟皮质神经元中的 GABA 反应保持在去极化状态,导致氯离子稳态改变和癫痫易感性增加。这项研究揭示了 Smo 信号在调节氯离子稳态方面的意外功能,通过控制 KCC2 细胞表面稳定性和脑成熟过程中 GABA 兴奋性向抑制性转变的时机来实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e9/7595691/8afdd17f3428/joces-133-247700-g1.jpg

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