Purdue University, Weldon School of Biomedical Engineering, West Lafayette, Indiana 47907, USA.
J Biomed Opt. 2011 Oct;16(10):106012. doi: 10.1117/1.3641988.
In vivo imaging of white matter is important for the mechanistic understanding of demyelination and evaluation of remyelination therapies. Although white matter can be visualized by a strong coherent anti-Stokes Raman scattering (CARS) signal from axonal myelin, in vivo repetitive CARS imaging of the spinal cord remains a challenge due to complexities induced by the laminectomy surgery. We present a careful experimental design that enabled longitudinal CARS imaging of de- and remyelination at single axon level in live rats. In vivo CARS imaging of secretory phospholipase A(2) induced myelin vesiculation, macrophage uptake of myelin debris, and spontaneous remyelination by Schwann cells are sequentially monitored over a 3 week period. Longitudinal visualization of de- and remyelination at a single axon level provides a novel platform for rational design of therapies aimed at promoting myelin plasticity and repair.
在体白质成像对于脱髓鞘和评估髓鞘再生治疗的机制理解非常重要。尽管轴突髓鞘的强相干反斯托克斯拉曼散射(CARS)信号可使白质可视化,但由于椎板切除术引起的复杂性,脊髓的在体重复 CARS 成像仍然是一个挑战。我们提出了一个精心设计的实验方案,使我们能够在活鼠中对单个轴突水平的脱髓鞘和髓鞘再生进行纵向 CARS 成像。在 3 周的时间内,依次监测了分泌型磷脂酶 A(2)诱导的髓鞘空泡化、巨噬细胞摄取髓鞘碎片和施万细胞自发的髓鞘再生的 CARS 成像。在单个轴突水平上的脱髓鞘和髓鞘再生的纵向可视化,为旨在促进髓鞘可塑性和修复的治疗方法的合理设计提供了一个新的平台。