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肌萎缩侧索硬化症血浆通过改变血管内皮生长因子的mRNA表达降低NSC34细胞的活力:一篇简短报告。

ALS plasma reduces the viability of NSC34 cells via altering mRNA expression of VEGF: A short report.

作者信息

Khosla Radhika, Bhagat Hemant, Lal Parth, Anand Akshay

机构信息

Neuroscience Research Lab, PGIMER, Chandigarh, India.

Department of Anesthesia and Intensive Care, PGIMER, Chandigarh, India.

出版信息

Heliyon. 2023 Jul 14;9(7):e18287. doi: 10.1016/j.heliyon.2023.e18287. eCollection 2023 Jul.

Abstract

INTRODUCTION

Amyotrophic Lateral Sclerosis (ALS) is a devastating neurodegenerative disorder that progressively leads to motor neuron degeneration at the neuromuscular junctions, resulting in paralysis in the patients. The clinical diagnosis of ALS is time taking and further delays the therapeutics that can be helpful if the disease is diagnosed at an early stage. Changes in plasma composition can be reflected upon CSF composition and hence, can be used to study the diagnosis and prognosis markers for the disease.

AIM

To develop a simple model system using motor neuron like cell line after plasma induction.

METHOD

Neuroblastoma × Spinal Cord hybridoma cell line (NSC34) was cultured under appropriate conditions. 10% ALS patients' plasma was added to the media, and cells were conditioned for 12 h. Cell survival analysis and differential gene expression of a panel of molecules (published previously, VEGF, VEGFR2, ANG, OPTN, TDP43, and MCP-1) were done.

RESULTS

ALS patients' plasma impacted the life of the cells and reduced survival to nearly 50% after induction. VEGF was found to be significantly down-regulated in the cells, which can be explained as a reason for reduced cell survival.

CONCLUSION

ALS plasma altered the expression of an essential neuroprotective and growth factor VEGF in NSC34 cells leading to reduced viability.

摘要

引言

肌萎缩侧索硬化症(ALS)是一种毁灭性的神经退行性疾病,会逐渐导致神经肌肉接头处的运动神经元退化,致使患者瘫痪。ALS的临床诊断耗时较长,这进一步延误了在疾病早期进行诊断时可能有用的治疗方法。血浆成分的变化可以反映在脑脊液成分上,因此可用于研究该疾病的诊断和预后标志物。

目的

在血浆诱导后,利用运动神经元样细胞系开发一个简单的模型系统。

方法

在适当条件下培养神经母细胞瘤×脊髓杂交瘤细胞系(NSC34)。将10%的ALS患者血浆添加到培养基中,使细胞处理12小时。进行细胞存活分析以及一组分子(先前已发表,包括血管内皮生长因子(VEGF)、血管内皮生长因子受体2(VEGFR2)、血管生成素(ANG)、视黄醛结合蛋白(OPTN)、TAR DNA结合蛋白43(TDP43)和单核细胞趋化蛋白-1(MCP-1))的差异基因表达分析。

结果

ALS患者血浆影响细胞寿命,诱导后细胞存活率降至近50%。发现细胞中的VEGF显著下调,这可以解释为细胞存活率降低的原因。

结论

ALS血浆改变了NSC34细胞中一种重要的神经保护和生长因子VEGF的表达,导致细胞活力降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c7d/10372388/1c4e53da78cd/gr1.jpg

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