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脂肪组织来源的间充质干细胞浓缩条件培养基改变轻度创伤性脑损伤后视网膜中谷氨酸调节蛋白和水通道蛋白-4 的表达模式。

Adipose Tissue-Derived Mesenchymal Stem Cell Concentrated Conditioned Medium Alters the Expression Pattern of Glutamate Regulatory Proteins and Aquaporin-4 in the Retina after Mild Traumatic Brain Injury.

机构信息

Department of Ophthalmology, Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Cell Care Therapeutics, Inc., Monrovia, California, USA.

出版信息

J Neurotrauma. 2021 Jun 15;38(12):1702-1716. doi: 10.1089/neu.2020.7309. Epub 2021 Jan 12.

Abstract

Concentrated conditioned media from adipose tissue-derived mesenchymal stem cells (ASC-CCM) show promise for retinal degenerative diseases. In this study, we hypothesized that ASC-CCM could rescue retinal damage and thereby improve visual function by acting through Müller glia in mild traumatic brain injury (mTBI). Adult C57Bl/6 mice were subjected to a 50-psi air pulse on the left side of the head, resulting in an mTBI. After blast injury, 1 μL (∼100 ng total protein) of human ASC-CCM was delivered intravitreally and followed up after 4 weeks for visual function assessed by electroretinogram and histopathological markers for Müller cell-related markers. Blast mice that received ASC-CCM, compared with blast mice that received saline, demonstrated a significant improvement in a- and b-wave response correlated with a 1.3-fold decrease in extracellular glutamate levels and a concomitant increase in glutamine synthetase (GS), as well as the glutamate transporter (GLAST) in Müller cells. Additionally, an increase in aquaporin-4 (AQP4) in Müller cells in blast mice received saline restored to normal levels in blast mice that received ASC-CCM. studies on rMC-1 Müller glia exposed to 100 ng/mL glutamate or RNA interference knockdown of GLAST expression mimicked the increased Müller cell glial fibrillary acidic protein (a marker of gliosis) seen with mTBI, and suggested that an increase in glutamate and/or a decrease in GLAST might contribute to the Müller cell activation Taken together, our data suggest a novel neuroprotective role for ASC-CCM in the rescue of the visual deficits and pathologies of mTBI via restoration of Müller cell health.

摘要

脂肪组织来源的间充质干细胞(ASC-CCM)的浓缩条件培养基有望用于治疗视网膜退行性疾病。在这项研究中,我们假设 ASC-CCM 可以通过作用于轻度创伤性脑损伤(mTBI)中的 Müller 胶质细胞来挽救视网膜损伤,从而改善视觉功能。成年 C57Bl/6 小鼠头部左侧接受 50psi 空气脉冲,导致 mTBI。在爆炸伤后,将 1μL(约 100ng 总蛋白)人 ASC-CCM 玻璃体内给药,并在 4 周后进行电生理和组织病理学评估,以评估 Müller 细胞相关标志物的视觉功能。与接受盐水的爆炸伤小鼠相比,接受 ASC-CCM 的爆炸伤小鼠的 a-和 b-波反应显著改善,与细胞外谷氨酸水平降低 1.3 倍以及谷氨酸合成酶(GS)和谷氨酸转运蛋白(GLAST)在 Müller 细胞中的相应增加相关。此外,接受盐水的爆炸伤小鼠中 Müller 细胞中的水通道蛋白-4(AQP4)增加恢复至正常水平在接受 ASC-CCM 的爆炸伤小鼠中。研究表明,100ng/mL 谷氨酸或 GLAST 表达 RNA 干扰敲低暴露于 rMC-1 Müller 胶质细胞可模拟 mTBI 中观察到的 Müller 细胞胶质纤维酸性蛋白(星形胶质细胞增生的标志物)增加,并表明谷氨酸增加和/或 GLAST 减少可能有助于 Müller 细胞激活。总之,我们的数据表明 ASC-CCM 在通过恢复 Müller 细胞健康来挽救 mTBI 的视觉缺陷和病理学方面具有新的神经保护作用。

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