Suppr超能文献

环状 RNA-AGTPBP1 通过 miR-140-3p/Pcdh17 轴促进脑白质损伤环状 RNA-AGTPBP1 在脑白质损伤中的作用。

Circ-AGTPBP1 promotes white matter injury through miR-140-3p/Pcdh17 axis role of Circ-AGTPBP1 in white matter injury.

机构信息

Department of Pediatrics, School of Medicine, Zhongda Hospital, Southeast University, No. 87 Dingjiaqiao, Hunan Road, Nanjing, 210009, Jiangsu, China.

School of Medicine, The Hospital of Yangzhou University, Yangzhou, 210033, Jiangsu, China.

出版信息

J Bioenerg Biomembr. 2024 Feb;56(1):1-14. doi: 10.1007/s10863-023-09984-5. Epub 2023 Nov 23.

Abstract

White matter injury (WMI) resulting from intracerebral hemorrhage (ICH) is closely associated with adverse prognoses in ICH patients. Although Circ-AGTPBP1 has been reported to exhibit high expression in the serum of premature infants with WMI, its effects and mechanisms in ICH-induced WMI remain unclear. This study aimed to investigate the role of circ-AGTPBP1 in white matter injury after intracerebral hemorrhage. An intracerebral hemorrhage rat model was established by injecting autologous blood into rat left ventricles and circ-AGTPBP1 was knocked down at the ICH site using recombinant adeno-associated virus, AAV2/9. Magnetic resonance imaging (MRI) and gait analysis were conducted to assess long-term neurobehavioral effects. Primary oligodendrocyte progenitor cells (OPCs) were isolated from rats and overexpressed with circ-AGTPBP1. Downstream targets of circ-AGTPBP1 in OPCs were investigated using CircInteractome, qPCR, FISH analysis, and miRDB network. Luciferase gene assay was utilized to explore the relationship between miR-140-3p and Pcdh17 in OPCs and HEK-293T cells. Finally, CCK-8 assay, EdU staining, and flow cytometry were employed to evaluate the effects of mi-RNA-140-3p inhibitor or silencing of sh-pcd17 on the viability, proliferation, and apoptosis of OPCs. Low expression of circ-AGTPBP1 alleviates white matter injury and improves neurological functions in rats after intracerebral hemorrhage. Conversely, overexpression of circ-AGTPBP1 reduces the proliferative and migrative potential of oligodendrocyte progenitor cells and promotes apoptosis. CircInteractome web tool and qPCR confirmed that circ-AGTPBP1 binds with miR-140-3p in OPCs. Additionally, miRDB network predicted Pcdh17 as a downstream target of miR-140-3p. Moreover, pcdh17 expression was increased in the brain tissue of rats with intracerebral-induced white matter injury. Furthermore, inhibiting miR-140-3p suppressed the proliferation and migration of OPCs and facilitated apoptosis through Pcdh17. Circ-AGTPBP1 promotes white matter injury through modulating the miR-140-3p/Pcdh17 axis. The study provides a new direction for developing therapeutic strategies for white matter injury.

摘要

脑内出血(ICH)引起的白质损伤(WMI)与 ICH 患者的不良预后密切相关。Circ-AGTPBP1 已被报道在患有 WMI 的早产儿血清中高表达,但其在 ICH 诱导的 WMI 中的作用和机制尚不清楚。本研究旨在探讨 circ-AGTPBP1 在脑出血后白质损伤中的作用。通过向大鼠左心室注射自体血建立脑出血大鼠模型,并使用重组腺相关病毒 AAV2/9 在 ICH 部位敲低 circ-AGTPBP1。通过磁共振成像(MRI)和步态分析评估长期神经行为效应。从大鼠中分离出原代少突胶质前体细胞(OPC),并用 circ-AGTPBP1 过表达。使用 CircInteractome、qPCR、FISH 分析和 miRDB 网络研究 OPC 中 circ-AGTPBP1 的下游靶标。荧光素酶基因检测用于探索 miR-140-3p 在 OPCs 和 HEK-293T 细胞中与 Pcdh17 的关系。最后,使用 CCK-8 测定、EdU 染色和流式细胞术评估 miR-NA-140-3p 抑制剂或 sh-pcd17 沉默对 OPCs 活力、增殖和凋亡的影响。低表达 circ-AGTPBP1 可减轻脑出血后大鼠的白质损伤并改善神经功能。相反,circ-AGTPBP1 的过表达降低了少突胶质前体细胞的增殖和迁移潜力,并促进了凋亡。CircInteractome 网络工具和 qPCR 证实 circ-AGTPBP1 在 OPCs 中与 miR-140-3p 结合。此外,miRDB 网络预测 Pcdh17 是 miR-140-3p 的下游靶标。此外,脑出血诱导的白质损伤大鼠脑组织中 pcdh17 表达增加。此外,抑制 miR-140-3p 通过 Pcdh17 抑制 OPCs 的增殖和迁移并促进凋亡。Circ-AGTPBP1 通过调节 miR-140-3p/Pcdh17 轴促进白质损伤。该研究为开发白质损伤治疗策略提供了新的方向。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验