Liu Yang, Hammel Grace, Shi Minjun, Cheng Zhijian, Zivkovic Sandra, Wang Xiaoqi, Xu Pingyi, He Xijing, Guo Bing, Ren Yi, Zuo Li
Department of Immunology, Guizhou Medical University, Guiyang, China.
Department of Biomedical Sciences, Florida State University College of Medicine, Tallahassee, FL, United States.
Front Cell Neurosci. 2021 Mar 19;15:651827. doi: 10.3389/fncel.2021.651827. eCollection 2021.
Although the increased expression of members of the chondroitin sulfate proteoglycan family, such as neuron-glial antigen 2 (NG2), have been well documented after an injury to the spinal cord, a complete picture as to the cellular origins and function of this NG2 expression has yet to be made. Using a spinal cord injury (SCI) mouse model, we describe that some infiltrated bone marrow-derived macrophages (BMDMΦ) are early contributors to NG2/CSPG4 expression and secretion after SCI. We demonstrate for the first time that a lesion-related form of cellular debris generated from damaged myelin sheaths can increase NG2/CSPG4 expression in BMDMΦ, which then exhibit enhanced proliferation and decreased phagocytic capacity. These results suggest that BMDMΦ may play a much more nuanced role in secondary spinal cord injury than previously thought, including acting as early contributors to the NG2 component of the glial scar.
尽管硫酸软骨素蛋白聚糖家族成员(如神经胶质抗原2,即NG2)的表达在脊髓损伤后增加已得到充分记录,但关于这种NG2表达的细胞起源和功能的全貌尚未明晰。利用脊髓损伤(SCI)小鼠模型,我们描述了一些浸润的骨髓源性巨噬细胞(BMDMΦ)是SCI后NG2/CSPG4表达和分泌的早期贡献者。我们首次证明,受损髓鞘产生的与损伤相关的细胞碎片形式可增加BMDMΦ中NG2/CSPG4的表达,随后这些细胞表现出增殖增强和吞噬能力下降。这些结果表明,BMDMΦ在继发性脊髓损伤中可能发挥比以前认为的更为微妙的作用,包括作为胶质瘢痕中NG2成分的早期贡献者。