癫痫患者和大鼠模型中SLITRK5的上调。

IF 1.6 4区 医学 Q4 NEUROSCIENCES Synapse Pub Date : 2023-07-01 Epub Date: 2023-03-04 DOI:10.1002/syn.22266
Yan Liu, Linming Zhang, Mingda Ai, Di Xia, Hongyu Chen, Ruijing Pang, Rong Mei, Lianmei Zhong, Ling Chen
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引用次数: 0

摘要

SLIT和NTRK样蛋白-5(SLITRK5)是SLITRK蛋白家族的六个成员之一,在中枢神经系统中广泛表达。在大脑中,SLITRK5在神经元的轴突生长、树突分支、神经元分化、突触发生和信号传递中起着重要作用。癫痫是一种常见的慢性神经系统疾病,其特征是反复自发发作。癫痫的病理生理机制尚不清楚。神经元凋亡、异常神经兴奋性传递和突触重塑被认为与癫痫的发展有关。为了探讨SLITR55与癫痫之间是否存在潜在关系,我们研究了SLITR5在颞叶癫痫(TLE)患者和癫痫大鼠模型中的表达和分布。我们收集了药物难治性颞叶癫痫患者的大脑皮层样本,并建立了氯化锂/匹罗卡品诱导的癫痫大鼠模型。本研究采用免疫组织化学、双免疫荧光标记和蛋白质印迹等方法研究了SLITRK5在颞叶癫痫患者和癫痫动物模型中的表达和分布。所有结果表明,无论是在TLE患者还是在癫痫模型中,SLITRK5都主要定位于神经元的细胞质中。此外,与非癫痫对照组相比,TLE患者颞叶新皮层中SLITRK5的表达上调。在毛果芸香碱诱导的癫痫大鼠颞叶新皮层和海马中,SLITRK5的表达在癫痫持续状态(SE)后24小时增加,在30天内达到相对较高的水平,并在SE后第7天达到峰值,这可能为进一步研究SLITRK5与癫痫的潜在机制和抗癫痫药物的治疗靶点奠定基础。
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Upregulation of SLITRK5 in patients with epilepsy and in a rat model.

SLIT and NTRK-like protein-5 (SLITRK5) is one of the six members of SLITRK protein family, which is widely expressed in central nervous system (CNS). In brain, SLITRK5 plays important roles in neurite outgrowth, dendritic branching, neuron differentiation, synaptogenesis, and signal transmission of neurons. Epilepsy is a common, chronic neurological disorder characterized by recurrent spontaneous seizures. The pathophysiological mechanism of epilepsy remains unclear. Neuronal apoptosis, abnormal nerve excitatory transmission, and synaptic remodeling are thought to be involved in the development of epilepsy. To explore whether there is a potential relationship between SLITRK5 and epilepsy, we investigated the expression and distribution of SLITRK5 in patients with temporal lobe epilepsy (TLE) and a rat model of epilepsy. We collected cerebral cortex samples from patients with drug-refractory temporal lobe epilepsy, and a rat model of epilepsy induced by lithium chloride/pilocarpine was established. The ways of immunohistochemistry, double-immunofluorescence labeling and western blot have been used in our study to research the expression and distribution of SLITRK5 in the temporal lobe epilepsy patients and epilepsy animal model. All of the results have shown that SLITRK5 is mainly localized in the cell cytoplasm of neurons both in patients with TLE and in epilepsy model. In addition, compared with nonepileptic controls, the expression of SLITRK5 was upregulated in the temporal neocortex of TLE patients. And both in the temporal neocortex and hippocampus of pilocarpine-induced epilepsy rats, the expression of SLITRK5 was increased at 24 h after status epilepticus (SE), with a relatively high level within 30 days, and reached the peak on the 7th day after SE. Our preliminary results revealed that SLITRK5 may have a potential relationship with epilepsy, which may be a foundation for the further study of the underlying mechanism between SLITRK5 and epilepsy and the therapeutic targets of antiepileptic drugs.

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来源期刊
Synapse
Synapse 医学-神经科学
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
4-8 weeks
期刊介绍: SYNAPSE publishes articles concerned with all aspects of synaptic structure and function. This includes neurotransmitters, neuropeptides, neuromodulators, receptors, gap junctions, metabolism, plasticity, circuitry, mathematical modeling, ion channels, patch recording, single unit recording, development, behavior, pathology, toxicology, etc.
期刊最新文献
Correction to "Role of M4-receptor cholinergic signaling in direct pathway striatal projection neurons during dopamine depletion". Harnessing Miniscope Imaging in Freely Moving Animals to Unveil Migraine Pathophysiology and Validate Novel Therapeutic Strategies. ERK1/2 Regulates Epileptic Seizures by Modulating the DRP1‐Mediated Mitochondrial Dynamic microRNA-125b-5p alleviated CCI-induced neuropathic pain and modulated neuroinflammation via targeting SOX11. Calsyntenin-1 expression and function in brain tissue of lithium-pilocarpine rat seizure models.
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