首页> 美国卫生研究院文献>Micromachines >A Milled Microdevice to Advance Glia-Mediated Therapies in the Adult Nervous System
【2h】

A Milled Microdevice to Advance Glia-Mediated Therapies in the Adult Nervous System

机译:一种用于在成人神经系统中推进神经胶质介导疗法的微器械

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Neurodegenerative disorders affect millions of adults worldwide. Neuroglia have become recent therapeutic targets due to their reparative abilities in the recycling of exogenous neurotoxins and production of endogenous growth factors for proper functioning of the adult nervous system (NS). Since neuroglia respond effectively to stimuli within in vivo environments on the micron scale, adult glial physiology has remarkable synergy with microscale systems. While clinical studies have begun to explore the reparative action of Müller glia (MG) of the visual system and Schwann Cells (ShC) of the peripheral NS after neural injury, few platforms enable the study of intrinsic neuroglia responses to changes in the local microenvironment. This project developed a low-cost, benchtop-friendly microfluidic system called the glia line system, or gLL, to advance the cellular study needed for emerging glial-based therapies. The gLL was fabricated using elastomeric kits coupled with a metal mold milled via conventional computer numerical controlled (CNC) machines. Experiments used the gLL to measure the viability, adhesion, proliferation, and migration of MG and ShC within scales similar to their respective in vivo microenvironments. Results illustrate differences in neuroglia adhesion patterns and chemotactic behavior significant to advances in regenerative medicine using implants and biomaterials, as well as cell transplantation techniques. Data showed highest survival and proliferation of MG and ShC upon laminin and illustrated a four-fold and two-fold increase of MG migration to dosage-dependent signaling from vascular endothelial growth factor (VEGF) and epidermal growth factor (EGF), respectively, as well as a 20-fold increase of ShC migration toward exogenous brain-derived neurotrophic factor (BDNF), compared to media control. The ability to quantify these biological parameters within the gLL offers an effective and reliable alternative to photolithography study neuroglia in a local environment ranging from the tens to hundreds of microns, using a low-cost and easily fabricated system.
机译:神经退行性疾病影响全世界数百万成年人。由于神经胶质细胞在外源性神经毒素的循环利用中的修复能力以及成人神经系统(NS)正常功能的内生性生长因子的产生,它们已成为近期的治疗靶标。由于神经胶质细胞可以在微米级别对体内环境中的刺激做出有效反应,因此成人神经胶质生理学与微米级别系统具有显着的协同作用。虽然临床研究已经开始探索神经损伤后视觉系统的Müller胶质细胞(MG)和周围NS的雪旺细胞(ShC)的修复作用,但很少有平台能够研究内在神经胶质细胞对局部微环境变化的反应。该项目开发了一种低成本,台式友好的微流控系统,称为神经胶质细胞系或gLL,以促进新兴的基于神经胶质疗法的细胞研究。 gLL是使用弹性体套件与通过常规计算机数控(CNC)机器铣削的金属模具耦合制成的。实验使用gLL来测量MG和ShC在与其各自体内微环境相似的范围内的生存力,粘附力,增殖和迁移。结果表明,神经胶质粘附模式和趋化行为的差异对于使用植入物和生物材料以及细胞移植技术的再生医学的进步具有重大意义。数据显示,层粘连蛋白后MG和ShC的存活和增殖最高,说明MG从血管内皮生长因子(VEGF)和表皮生长因子(EGF)迁移至剂量依赖性信号传递分别增加了4倍和2倍,与媒体对照相比,ShC向外源性脑源性神经营养因子(BDNF)迁移的比例增加了20倍。量化gLL内这些生物学参数的能力提供了一种有效且可靠的替代方法,可以使用低成本且易于制造的系统在数十至数百微米的局部环境中进行光刻研究神经胶质细胞的研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号