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研究脊髓损伤中胶质细胞限制前体细胞的特性和治疗潜力。

Examining the properties and therapeutic potential of glial restricted precursors in spinal cord injury.

作者信息

Hayakawa Kazuo, Haas Christopher, Fischer Itzhak

机构信息

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA; Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.

出版信息

Neural Regen Res. 2016 Apr;11(4):529-33. doi: 10.4103/1673-5374.180725.

Abstract

In the aftermath of spinal cord injury, glial restricted precursors (GRPs) and immature astrocytes offer the potential to modulate the inflammatory environment of the injured spinal cord and promote host axon regeneration. Nevertheless clinical application of cellular therapy for the repair of spinal cord injury requires strict quality-assured protocols for large-scale production and preservation that necessitates long-term in vitro expansion. Importantly, such processes have the potential to alter the phenotypic and functional properties and thus therapeutic potential of these cells. Furthermore, clinical use of cellular therapies may be limited by the inflammatory microenvironment of the injured spinal cord, altering the phenotypic and functional properties of grafted cells. This report simulates the process of large-scale GRP production and demonstrates the permissive properties of GRP following long-term in vitro culture. Furthermore, we defined the phenotypic and functional properties of GRP in the presence of inflammatory factors, and call attention to the importance of the microenvironment of grafted cells, underscoring the importance of modulating the environment of the injured spinal cord.

摘要

在脊髓损伤后,神经胶质限制前体细胞(GRPs)和未成熟星形胶质细胞具有调节损伤脊髓炎症环境并促进宿主轴突再生的潜力。然而,用于脊髓损伤修复的细胞疗法的临床应用需要严格的、质量有保证的大规模生产和保存方案,这就需要长期的体外扩增。重要的是,这样的过程有可能改变这些细胞的表型和功能特性,从而改变其治疗潜力。此外,细胞疗法的临床应用可能会受到损伤脊髓炎症微环境的限制,从而改变移植细胞的表型和功能特性。本报告模拟了GRPs大规模生产的过程,并展示了长期体外培养后GRPs的许可特性。此外,我们定义了炎症因子存在下GRPs的表型和功能特性,并提请注意移植细胞微环境的重要性,强调调节损伤脊髓环境的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad49/4870895/14bc4a595631/NRR-11-529-g001.jpg

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