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低强度脉冲聚焦超声介导内皮祖细胞衍生外泌体递送在大脑中动脉闭塞性脑卒中中的作用

Effects of low-intensity pulsed focal ultrasound-mediated delivery of endothelial progenitor-derived exosomes in tMCAo stroke.

作者信息

Alptekin Ahmet, Khan Mohammad B, Parvin Mahrima, Chowdhury Hasanul, Kashif Sawaiz, Selina Fowzia A, Bushra Anika, Kelleher Justin, Ghosh Santu, Williams Dylan, Blumling Emily, Ara Roxan, Bosomtwi Asamoah, Frank Joseph A, Dhandapani Krishnan M, Arbab Ali S

机构信息

Tumor Angiogenesis Laboratory, GCC, Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University, Augusta, GA, United States.

Department of Neurology, Medical College of Georgia, Augusta University, Augusta, GA, United States.

出版信息

Front Neurol. 2025 Apr 9;16:1543133. doi: 10.3389/fneur.2025.1543133. eCollection 2025.

Abstract

INTRODUCTION

Exosomes from different sources have been used for therapeutic purposes to target stroke and other disorders. However, exosomes from endothelial progenitor cells (EPCs) have not been tested in any stroke model, and bio-distribution study is lacking. Targeted delivery of IV-administered exosomes has been a significant challenge. Delivery of exosomes to the brain is a daunting task, and a blood-brain barrier (BBB)-penetrable peptide is being considered. However, the next step in practical treatment will be delivering naïve (unmodified) exosomes to the stroke site without destroying host tissues or disrupting BBB, or the membranes of the delivery vehicles. Low-intensity-pulsed focused ultrasound (LIPFUS) is approved for clinical use in the musculoskeletal, transcranial brain, and physiotherapy clinics. The objectives of the proposed studies were to determine whether LIPFUS-mediated increased delivery of EPC-derived exosomes enhances stroke recovery and functional improvement in mice with transient middle cerebral artery occlusion (tMCAo) stroke.

METHODS

To enhance exosome delivery to the stroke area, we utilized LIPFUS. We evaluated stroke volume using MRI at different time points and conducted behavioral studies parallel to MRI to determine recovery. Ultimately, we studied brain tissue using immunohistochemistry to assess the extent of stroke and tissue regeneration.

RESULTS AND DISCUSSION

, imaging showed a higher accumulation of EPC exosomes following LIPFUS without any damage to the underlying brain tissues, increased leakage of albumin, or accumulation of CD45+ cells. Groups of mice (14-16 months old) were treated with Vehicle (PBS), LIPFUS only, EPC-exosomes only, and LIPFUS+EPC-exosomes. LIPFUS + EPC exosomes groups showed a significantly decreased stroke volume on day 7, decreased FluoroJade+ cells, and significantly higher numbers of neovascularization in and around the stroke areas compared to that of other groups.

摘要

引言

来自不同来源的外泌体已被用于治疗中风和其他疾病。然而,内皮祖细胞(EPC)来源的外泌体尚未在任何中风模型中进行测试,且缺乏生物分布研究。静脉注射外泌体的靶向递送一直是一项重大挑战。将外泌体递送至大脑是一项艰巨的任务,目前正在考虑使用一种可穿透血脑屏障(BBB)的肽。然而,实际治疗的下一步将是在不破坏宿主组织、不破坏血脑屏障或递送载体膜的情况下,将未修饰的外泌体递送至中风部位。低强度脉冲聚焦超声(LIPFUS)已被批准用于肌肉骨骼、经颅脑部和物理治疗诊所的临床应用。本研究的目的是确定LIPFUS介导的EPC衍生外泌体递送增加是否能促进短暂性大脑中动脉闭塞(tMCAo)中风小鼠的中风恢复和功能改善。

方法

为了增强外泌体向中风区域的递送,我们使用了LIPFUS。我们在不同时间点使用MRI评估脑梗死体积,并与MRI并行进行行为学研究以确定恢复情况。最终,我们使用免疫组织化学研究脑组织,以评估中风程度和组织再生情况。

结果与讨论

成像显示,LIPFUS后EPC外泌体的积累更高,且对下层脑组织没有任何损伤,白蛋白渗漏增加或CD45+细胞积累。将14 - 16个月大的小鼠分为四组,分别给予赋形剂(PBS)、仅LIPFUS治疗、仅EPC外泌体治疗以及LIPFUS + EPC外泌体治疗。与其他组相比,LIPFUS + EPC外泌体组在第7天显示脑梗死体积显著减小,FluoroJade+细胞减少,中风区域及其周围的新生血管数量显著增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e94f/12014438/3f5e42bc4428/fneur-16-1543133-g001.jpg

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