MSC Promotes the Secretion of Exosomal lncRNA KLF3-AS1 to Regulate Sphk1 Through YY1-Musashi-1 Axis and Improve Cerebral Ischemia-Reperfusion Injury.

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2024-12-01 Epub Date: 2024-05-13 DOI:10.1007/s12035-024-04150-3
Yu Cao, Daodao Wang, Dingzhou Zhou
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引用次数: 0

Abstract

Stroke remains the 3rd leading cause of long-term disability globally. Over the past decade, mesenchymal stem cell (MSC) transplantation has been proven as an effective therapy for ischemic stroke. However, the mechanism of MSC-derived exosomal lncRNAs during cerebral ischemia/reperfusion (I/R) remains ambiguous. The oxygen-glucose deprivation/reoxygenation (OGD/R) and middle cerebral artery occlusion (MCAO) rat model were generated. MSCs were isolated and characterized by flow cytometry and histochemical staining, and MSC exosomes were purified and characterized by transmission electron microscopy, flow cytometry and Western blot. Western blot, RT-qPCR and ELISA assay were employed to examine the expression or secretion of key molecules. CCK-8 and TUNEL assays were used to assess cell viability and apoptosis. RNA immunoprecipitation and RNA pull-down were used to investigate the direct association between krüppel-like factor 3 antisense RNA 1 (KLF3-AS1) and musashi-1(MSI1). Yin Yang 1 (YY1)-mediated transcriptional regulation was assessed by chromatin immunoprecipitation and luciferase assays. The histological changes and immunoreactivity of key molecules in brain tissues were examined by H&E and immunohistochemistry. MSCs were successfully isolated and exhibited directionally differential potentials. MSC exosomal KLF3-AS1 alleviated OGD/R-induced inflammation in SK-N-SH and SH-SY5Y cells via modulating Sphk1. Mechanistical studies showed that MSI1 positively regulated KLF3-AS1 expression through its direct binding to KLF3-AS1. YY1 was identified as a transcription activator of MSI1 in MSCs. Functionally, YY1/MSI1 axis regulated the release of MSC exosomal KLF3-AS1 to modulate sphingosine kinase 1 (Sphk1)/NF-κB pathway, thereby ameliorating OGD/R- or cerebral I/R-induced injury. MSCs promote the release of exosomal KLF3-AS1 to regulate Sphk1 through YY1/MSI axis and improve cerebral I/R injury.

Abstract Image

间充质干细胞通过YY1-Musashi-1轴促进外泌体lncRNA KLF3-AS1的分泌以调控Sphk1并改善脑缺血再灌注损伤
中风仍是全球第三大长期致残原因。在过去十年中,间充质干细胞(MSC)移植已被证明是治疗缺血性中风的有效方法。然而,间充质干细胞衍生的外泌体lncRNA在脑缺血/再灌注(I/R)过程中的作用机制仍不明确。研究人员建立了氧-葡萄糖剥夺/再氧合(OGD/R)和大脑中动脉闭塞(MCAO)大鼠模型。通过流式细胞术和组织化学染色分离间充质干细胞并对其进行表征,通过透射电子显微镜、流式细胞术和 Western 印迹纯化间充质干细胞外泌体并对其进行表征。采用 Western 印迹、RT-qPCR 和 ELISA 检测关键分子的表达或分泌。CCK-8 和 TUNEL 检测法用于评估细胞活力和凋亡。采用 RNA 免疫沉淀和 RNA pull-down 方法研究克鲁佩尔样因子 3 反义 RNA 1(KLF3-AS1)与 musashi-1(MSI1) 之间的直接关联。染色质免疫沉淀和荧光素酶实验评估了阴阳1(YY1)介导的转录调控。通过H&E和免疫组化检查了脑组织的组织学变化和关键分子的免疫活性。间充质干细胞被成功分离,并表现出方向性差异潜能。间充质干细胞外泌体KLF3-AS1通过调节Sphk1缓解了OGD/R诱导的SK-N-SH和SH-SY5Y细胞炎症。机理研究表明,MSI1通过与KLF3-AS1直接结合来正向调节KLF3-AS1的表达。研究发现YY1是间充质干细胞中MSI1的转录激活因子。在功能上,YY1/MSI1轴调节间充质干细胞外泌体KLF3-AS1的释放,从而调节鞘磷脂激酶1(Sphk1)/NF-κB通路,从而改善OGD/R-或脑I/R-诱导的损伤。间充质干细胞促进外泌体KLF3-AS1的释放,通过YY1/MSI轴调节Sphk1,改善脑I/R损伤。
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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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