Circ-AGTPBP1通过miR-140-3p/Pcdh17轴在白质损伤中的作用促进白质损伤。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-02-01 Epub Date: 2023-11-23 DOI:10.1007/s10863-023-09984-5
Zhaokui Zhu, Sisi Mo, Xinyu Wang, Meng Meng, Lixing Qiao
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引用次数: 0

摘要

脑出血后脑白质损伤(WMI)与脑出血患者的不良预后密切相关。尽管Circ-AGTPBP1在WMI早产儿的血清中高表达,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。采用自体血注入大鼠左心室建立脑出血大鼠模型,利用重组腺相关病毒AAV2/9敲除ICH位点的circ-AGTPBP1。通过磁共振成像(MRI)和步态分析来评估长期的神经行为影响。从大鼠中分离出原代少突胶质细胞祖细胞(OPCs),并过表达circ-AGTPBP1。使用CircInteractome、qPCR、FISH分析和miRDB网络研究circ-AGTPBP1在OPCs中的下游靶点。利用荧光素酶基因检测,探讨OPCs和HEK-293T细胞中miR-140-3p与Pcdh17的关系。最后,采用CCK-8法、EdU染色法和流式细胞术评价mi-RNA-140-3p抑制剂或沉默sh-pcd17对OPCs存活、增殖和凋亡的影响。circ-AGTPBP1低表达可减轻脑出血后大鼠脑白质损伤,改善神经功能。相反,circ-AGTPBP1的过表达会降低少突胶质细胞祖细胞的增殖和迁移潜能,促进细胞凋亡。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。脑内白质损伤大鼠脑组织中pcdh17表达升高。此外,抑制miR-140-3p可通过Pcdh17抑制OPCs的增殖和迁移,促进凋亡。Circ-AGTPBP1通过调节miR-140-3p/Pcdh17轴促进白质损伤。本研究为制定脑白质损伤的治疗策略提供了新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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