Sarah E. Hocevar, Brian C. Ross, Yinghao Wang, Cecelia R. Crowther, Samantha R. Schwartz, Brain J. Cummings, Aileen J. Anderson, Lonnie D. Shea
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The dynamics of immune cell infiltration and secondary tissue damage were studied following the injection of NPs intravenously every 24 h for 7 days following injury, with the first injection starting at 2, 4, or 24 hours post‐injury (hpi). At 7 days post‐injury (dpi), early NP intervention decreased the number of infiltrating macrophages and neutrophils, but delaying treatment until 24 hpi increased the number of neutrophils above control. All mice that received NPs had greater neuronal sparing contralateral to the injury, but mice that received NPs at early timepoints had greater neuromuscular junction innervation and motor endplate sparing. The increased sparing of neurons and neural circuits in the 2 hpi NP group corresponded with increased motor function, as measured by a ladder beam test. 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引用次数: 0
摘要
脊髓损伤(SCI)触发免疫细胞立即涌入,分泌促炎细胞因子和活性氧,导致继发于初始物理创伤的组织损伤。我们的目标是重新编程这些免疫细胞,以促进炎症减少和更有利于再生的环境。在此,我们研究了聚(丙交酯- co -乙醇内酯)纳米颗粒(NPs)给药能够成功调节免疫反应并促进功能保留的时间窗口。在损伤后7天内,每24小时静脉注射一次NPs,第一次注射开始于损伤后2、4或24小时(hpi),研究免疫细胞浸润和继发性组织损伤的动力学。在损伤后7天(dpi),早期NP干预降低了浸润的巨噬细胞和中性粒细胞的数量,但延迟治疗至24 hpi后中性粒细胞的数量高于对照组。所有接受NPs的小鼠在损伤的对侧都有更大的神经元保留,但在早期时间点接受NPs的小鼠有更大的神经肌肉连接神经支配和运动终板保留。通过梯梁测试,2 hpi NP组神经元和神经回路的增加与运动功能的增加相对应。综上所述,这些结果表明,早期干预NPs可以调节脊髓损伤后的炎症反应,保护运动功能和神经回路。
Early nanoparticle intervention preserves motor function following cervical spinal cord injury
Spinal cord injury (SCI) triggers an immediate influx of immune cells that secrete pro‐inflammatory cytokines and reactive oxygen species that cause tissue damage that is secondary to the initial physical trauma. We aim to reprogram these immune cells to promote a less inflammatory and more pro‐regenerative environment. Herein, we investigated the window in time during which poly(lactide‐co‐glycolide) nanoparticles (NPs) administration can successfully modulate the immune response and promote functional sparing. The dynamics of immune cell infiltration and secondary tissue damage were studied following the injection of NPs intravenously every 24 h for 7 days following injury, with the first injection starting at 2, 4, or 24 hours post‐injury (hpi). At 7 days post‐injury (dpi), early NP intervention decreased the number of infiltrating macrophages and neutrophils, but delaying treatment until 24 hpi increased the number of neutrophils above control. All mice that received NPs had greater neuronal sparing contralateral to the injury, but mice that received NPs at early timepoints had greater neuromuscular junction innervation and motor endplate sparing. The increased sparing of neurons and neural circuits in the 2 hpi NP group corresponded with increased motor function, as measured by a ladder beam test. Collectively, these results suggest that early intervention with NPs can modulate the inflammatory response and preserve motor function and circuits following SCI.
期刊介绍:
Bioengineering & Translational Medicine, an official, peer-reviewed online open-access journal of the American Institute of Chemical Engineers (AIChE) and the Society for Biological Engineering (SBE), focuses on how chemical and biological engineering approaches drive innovative technologies and solutions that impact clinical practice and commercial healthcare products.