BMSCs条件培养基通过LDLR途径缓解h2o2诱导的PC12细胞氧化损伤

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-07-01 Epub Date: 2025-03-06 DOI:10.1007/s12035-025-04804-w
MingDong Li, Zhongquan Fu, Xing Gao, Yuchen Zhang, Zengxin Gao
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引用次数: 0

摘要

氧化损伤是关键的发病机制和进展的无数神经系统疾病。目前的研究旨在阐明骨髓间充质基质细胞(BMSC-CM)条件培养基的治疗潜力,并利用神经元氧化损伤模型描述其潜在机制。将大鼠嗜铬细胞瘤PC12细胞暴露于H2O2中建立氧化损伤模型,然后用骨髓间充质干细胞- cm处理或在transwell装置中与骨髓间充质干细胞共培养。通过PCR和western blot分析定量评估干预前后或共培养的氧化应激水平。此外,转录组学和生物信息学分析被用于鉴定与观察到的效应有关的关键基因和信号通路。BMSC- cm处理和BMSC共培养均能降低PC12细胞的氧化损伤,抑制细胞凋亡。转录组学数据和富集分析显示,BMSC-CM未处理和h2o2处理的PC12细胞之间存在106个差异表达基因,包括67个下调基因和39个上调基因。值得注意的是,显著差异表达的基因主要是参与脂质代谢途径的基因,低密度脂蛋白受体(LDLR)是一个统计学上显著上调的基因。蛋白转化酶subtilisin/kexin type 9是一种特异性的LDLR抑制剂,它减弱了BMSC-CM处理的积极作用,证实了LDLR激活在减轻神经元氧化损伤中起着至关重要的作用。本研究的结果强调了BMSC-CM的神经保护能力,我们发现这是通过其通过LDLR调节神经元细胞脂质代谢的能力来介导的。进一步研究骨髓间充质干细胞- cm的神经保护特性可能会导致以氧化应激为特征的神经系统疾病的治疗途径的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Conditioned Medium of BMSCs Alleviates H2O2-Induced Oxidative Damage in PC12 Cells Through the LDLR Pathway.

Oxidative damage is pivotal in the pathogenesis and progression of a myriad of neurological disorders. The current study was designed to elucidate the therapeutic potential of conditioned medium from bone marrow-derived mesenchymal stromal cells (BMSC-CM) and to delineate the underlying mechanisms, using a neuronal oxidative injury model for this purpose. Rat pheochromocytoma PC12 cells were exposed to H2O2 to establish an oxidative injury model, followed by treatment with BMSC-CM or co-cultivation with BMSCs in a transwell apparatus. The oxidative stress levels pre- and post-intervention or co-cultivation were quantitatively assessed by PCR and western blot analyses. Furthermore, transcriptomic and bioinformatic analyses were used to identify pivotal genes and signaling pathways implicated in the observed effects. Both BMSC-CM treatment and BMSC co-culture decreased oxidative damage and inhibited apoptosis in PC12 cells. Transcriptomic data and enrichment analysis revealed 106 differentially expressed genes between BMSC-CM untreated and treated H2O2-exposed PC12 cells, including 67 downregulated and 39 upregulated genes. Notably, the significantly differentially expressed genes were predominantly those involved in lipid metabolism pathways, and the low-density lipoprotein receptor (LDLR) emerged as one statistically significant upregulated gene. The proprotein convertase subtilisin/kexin type 9, a specific inhibitor of LDLR, attenuated the positive effects of BMSC-CM treatment, corroborating that LDLR activation plays a crucial role in mitigating neuronal oxidative damage. The results of this investigation underscore the neuroprotective capacity of BMSC-CM, which we show is mediated through its ability to module lipid metabolism in neuronal cells via the LDLR. Further research into the neuroprotective properties of BMSC-CM could lead to the development of promising therapeutic avenues for neurological diseases characterized by oxidative stress.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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