Department of Neurosciences, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Department of Biomedical Engineering, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA; Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Exp Neurol. 2014 Apr;254:109-20. doi: 10.1016/j.expneurol.2014.01.013. Epub 2014 Jan 24.
After traumatic spinal cord injury, functional deficits increase as axons die back from the center of the lesion and the glial scar forms. Axonal dieback occurs in two phases: an initial axon intrinsic stage that occurs over the first several hours and a secondary phase which takes place over the first few weeks after injury. Here, we examine the secondary phase, which is marked by infiltration of macrophages. Using powerful time-lapse multi-photon imaging, we captured images of interactions between Cx3cr1(+/GFP) macrophages and microglia and Thy-1(YFP) axons in a mouse dorsal column crush spinal cord injury model. Over the first few weeks after injury, axonal retraction bulbs within the lesion are static except when axonal fragments are lost by a blebbing mechanism in response to physical contact followed by phagocytosis by mobile Cx3Cr1(+/GFP) cells. Utilizing a radiation chimera model to distinguish marrow-derived cells from radio-resistant CNS-resident microglia, we determined that the vast majority of accumulated cells in the lesion are derived from the blood and only these are associated with axonal damage. Interestingly, CNS-resident Cx3Cr1(+/GFP) microglia did not increasingly accumulate nor participate in neuronal destruction in the lesion during this time period. Additionally, we found that the blood-derived cells consisted mainly of singly labeled Ccr2(+/RFP) macrophages, singly labeled Cx3Cr1(+/GFP) macrophages and a small population of double-labeled cells. Since all axon destructive events were seen in contact with a Cx3Cr1(+/GFP) cell, we infer that the CCR2 single positive subset is likely not robustly involved in axonal dieback. Finally, in our model, deletion of CCR2, a chemokine receptor, did not alter the position of axons after dieback. Understanding the in vivo cellular interactions involved in secondary axonal injury may lead to clinical treatment candidates involving modulation of destructive infiltrating blood monocytes.
在创伤性脊髓损伤后,随着轴突从损伤中心回缩以及神经胶质瘢痕形成,功能缺陷会增加。轴突回缩分为两个阶段:最初的轴突内在阶段发生在最初的几个小时内,第二个阶段发生在损伤后的最初几周内。在这里,我们检查了第二个阶段,该阶段的特征是巨噬细胞的浸润。使用强大的时空调频多光子成像,我们捕获了 Cx3cr1(+/GFP) 巨噬细胞和 Thy-1(YFP) 轴突在小鼠背柱挤压脊髓损伤模型中的相互作用图像。在损伤后的最初几周内,损伤内的轴突回缩泡是静态的,除非轴突碎片通过出芽机制丢失,以响应物理接触,然后被移动的 Cx3Cr1(+/GFP) 细胞吞噬。利用辐射嵌合体模型来区分骨髓来源的细胞和对辐射有抗性的中枢神经系统常驻小胶质细胞,我们确定损伤中积累的绝大多数细胞来自血液,只有这些细胞与轴突损伤有关。有趣的是,中枢神经系统驻留的 Cx3Cr1(+/GFP) 小胶质细胞在此期间并没有增加积累,也没有参与损伤中的神经元破坏。此外,我们发现血液来源的细胞主要由单标记的 Ccr2(+/RFP) 巨噬细胞、单标记的 Cx3Cr1(+/GFP) 巨噬细胞和一小部分双标记细胞组成。由于所有的轴突破坏性事件都发生在与 Cx3Cr1(+/GFP) 细胞接触的情况下,我们推断 CCR2 单阳性亚群不太可能强烈参与轴突回缩。最后,在我们的模型中,趋化因子受体 CCR2 的缺失并没有改变轴突回缩后的位置。了解继发性轴突损伤中涉及的体内细胞相互作用可能会导致涉及调节破坏性浸润血液单核细胞的临床治疗候选物。