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外泌体:保护和再生损伤后视神经的新途径。

Exosomes: a new way of protecting and regenerating optic nerve after injury.

机构信息

Department of Ophthalmology, The Fourth Affiliated Hospital, Harbin Medical University, Harbin, 150001, China.

Department of Ophthalmology, The First Affiliated Hospital, Harbin Medical University, Harbin, 150001, China.

出版信息

Hum Cell. 2022 May;35(3):771-778. doi: 10.1007/s13577-022-00688-3. Epub 2022 Mar 8.

DOI:10.1007/s13577-022-00688-3
PMID:35258808
Abstract

As an important part of the central nervous system (CNS), the optic nerve usually cannot regenerate directly after injury. Therefore, treating the injury and restoring the function of the optic nerve are a historical problem in the medical field. Due to the special anatomical position of the optic nerve, the microenvironment needed for protection and regeneration after injury is lacking. Therefore, preventing the continued loss of neurons, protecting the functional nerves, and promoting the effective protection of nerves are the main ways to solve the problem. Exosomes are nano-sized vesicles with a diameter of 30-150 nm, composed of lipid bilayers, proteins, and genetic material. They have key functions in cell-to-cell communication, immune regulation, inflammation, and regeneration. More and more shreds of evidence show that exosomes not only play an important role in systemic diseases such as cancer, cardiovascular diseases, and brain diseases; they also play a key role in ophthalmological diseases. This article reviews the role of exosomes in the protection and regeneration of the optic nerve after optic nerve injury in related experimental studies and clinical treatment methods. GRAPHICAL ABSTARCT: .

摘要

作为中枢神经系统(CNS)的重要组成部分,视神经通常在损伤后不能直接再生。因此,治疗损伤和恢复视神经功能是医学领域的一个历史问题。由于视神经的特殊解剖位置,损伤后缺乏所需的保护和再生的微环境。因此,防止神经元的持续丢失、保护功能神经、促进有效的神经保护是解决问题的主要途径。外泌体是直径为 30-150nm 的纳米大小囊泡,由脂双层、蛋白质和遗传物质组成。它们在细胞间通讯、免疫调节、炎症和再生中具有关键功能。越来越多的证据表明,外泌体不仅在癌症、心血管疾病和脑部疾病等全身性疾病中发挥着重要作用;它们在眼科疾病中也起着关键作用。本文综述了外泌体在视神经损伤后视神经保护和再生相关实验研究及临床治疗方法中的作用。

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本文引用的文献

1
Exosome-Mediated Delivery of the Neuroprotective Peptide PACAP38 Promotes Retinal Ganglion Cell Survival and Axon Regeneration in Rats With Traumatic Optic Neuropathy.外泌体介导的神经保护肽垂体腺苷酸环化酶激活肽38(PACAP38)递送促进创伤性视神经病变大鼠视网膜神经节细胞存活和轴突再生。
Front Cell Dev Biol. 2021 Apr 6;9:659783. doi: 10.3389/fcell.2021.659783. eCollection 2021.
2
Exosome-mediated delivery of an anti-angiogenic peptide inhibits pathological retinal angiogenesis.外泌体介导的抗血管生成肽递送可抑制病理性视网膜血管生成。
Theranostics. 2021 Mar 5;11(11):5107-5126. doi: 10.7150/thno.54755. eCollection 2021.
3
Improvement of sensory neuron growth and survival via negatively regulating PTEN by miR-21-5p-contained small extracellular vesicles from skin precursor-derived Schwann cells.
Extracellular vesicles as a new horizon in the diagnosis and treatment of inflammatory eye diseases: A narrative review of the literature.
细胞外囊泡作为炎症性眼病诊治的新领域:文献综述。
Front Immunol. 2023 Mar 9;14:1097456. doi: 10.3389/fimmu.2023.1097456. eCollection 2023.
4
Therapeutic Strategy of Mesenchymal-Stem-Cell-Derived Extracellular Vesicles as Regenerative Medicine.间充质干细胞衍生细胞外囊泡的治疗策略作为再生医学。
Int J Mol Sci. 2022 Jun 9;23(12):6480. doi: 10.3390/ijms23126480.
通过由皮肤前体细胞衍生的雪旺细胞来源的含有 miR-21-5p 的小细胞外囊泡负调控 PTEN,改善感觉神经元的生长和存活。
Stem Cell Res Ther. 2021 Jan 25;12(1):80. doi: 10.1186/s13287-020-02125-4.
4
Human mesenchymal stem cell therapy promotes retinal ganglion cell survival and target reconnection after optic nerve crush in adult rats.人骨髓间充质干细胞治疗促进成年大鼠视神经挤压后视网膜神经节细胞存活和靶重新连接。
Stem Cell Res Ther. 2021 Jan 19;12(1):69. doi: 10.1186/s13287-020-02130-7.
5
Photoreceptor protection by mesenchymal stem cell transplantation identifies exosomal MiR-21 as a therapeutic for retinal degeneration.间充质干细胞移植对光感受器的保护作用确定了外泌体 miR-21 可作为治疗视网膜变性的一种方法。
Cell Death Differ. 2021 Mar;28(3):1041-1061. doi: 10.1038/s41418-020-00636-4. Epub 2020 Oct 20.
6
UBA2 activates Wnt/β-catenin signaling pathway during protection of R28 retinal precursor cells from hypoxia by extracellular vesicles derived from placental mesenchymal stem cells.UBA2 通过胎盘间充质干细胞来源的细胞外囊泡在保护 R28 视网膜前体细胞免于缺氧中激活 Wnt/β-连环蛋白信号通路。
Stem Cell Res Ther. 2020 Oct 2;11(1):428. doi: 10.1186/s13287-020-01943-w.
7
Cellular Mechanisms of Rejection of Optic and Sciatic Nerve Transplants: An Observational Study.视神经和坐骨神经移植排斥反应的细胞机制:一项观察性研究。
Transplant Direct. 2020 Jul 24;6(8):e589. doi: 10.1097/TXD.0000000000001012. eCollection 2020 Aug.
8
Bone marrow stromal cells-derived exosomes target DAB2IP to induce microglial cell autophagy, a new strategy for neural stem cell transplantation in brain injury.骨髓基质细胞衍生的外泌体靶向DAB2IP以诱导小胶质细胞自噬,这是脑损伤中神经干细胞移植的一种新策略。
Exp Ther Med. 2020 Sep;20(3):2752-2764. doi: 10.3892/etm.2020.9008. Epub 2020 Jul 13.
9
miR-708 and miR-335-3p Inhibit the Apoptosis of Retinal Ganglion Cells Through Suppressing Autophagy.miR-708 和 miR-335-3p 通过抑制自噬抑制视网膜神经节细胞凋亡。
J Mol Neurosci. 2021 Feb;71(2):284-292. doi: 10.1007/s12031-020-01648-y. Epub 2020 Jul 19.
10
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Front Cell Neurosci. 2020 Jun 25;14:160. doi: 10.3389/fncel.2020.00160. eCollection 2020.