Institute of Neurobiology, University of Puerto Rico Medical Sciences Campus, Old San Juan, Puerto Rico.
Department of Anatomy and Neurobiology, University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
PLoS One. 2019 May 2;14(5):e0209733. doi: 10.1371/journal.pone.0209733. eCollection 2019.
We have previously shown that a single application of the growth factors ciliary neurotrophic factor (CNTF) or fibroblast growth factor 2 (FGF-2) to the crushed optic nerve of the frog, Rana pipiens, increases the numbers and elongation rate of regenerating retinal ganglion cell axons. Here we investigate the effects of these factors on the numbers and types of macrophages that invade the regeneration zone. In control PBS-treated nerves, many macrophages are present 100 μm distal to the crush site at 1 week after injury; their numbers halve by 2 weeks. A single application of CNTF at the time of injury triples the numbers of macrophages at 1 week, with this increase compared to control being maintained at 2 weeks. Application of FGF-2 is equally effective at 1 week, but the macrophage numbers have fallen to control levels at 2 weeks. Immunostaining with a pan-macrophage marker, ED1, and a marker for M2-like macrophages, Arg-1, showed that the proportion of the putative M2 phenotype remained at approximately 80% with all treatments. Electron microscopy of the macrophages at 1 week shows strong phagocytic activity with all treatments, with many vacuoles containing axon fragments and membrane debris. At 2 weeks with PBS or FGF-2 treatment the remaining macrophages are less phagocytically active, containing mainly lipid inclusions. With CNTF treatment, at 2 weeks many of the more numerous macrophages are still phagocytosing axonal debris, although they also contain lipid inclusions. We conclude that the increase in macrophage influx seen after growth factor application is beneficial for the regenerating axons, probably due to more extensive removal of degenerating distal axons, but also perhaps to secretion of growth-promoting substances.
我们之前已经表明,单次应用睫状神经营养因子(CNTF)或成纤维细胞生长因子 2(FGF-2)到青蛙(Rana pipiens)被压碎的视神经,可以增加再生视网膜神经节细胞轴突的数量和伸长率。在这里,我们研究了这些因子对入侵再生区的巨噬细胞数量和类型的影响。在对照 PBS 处理的神经中,许多巨噬细胞在损伤后 1 周时位于压碎部位的 100 μm 远处;到第 2 周时,其数量减半。在损伤时单次应用 CNTF 可使巨噬细胞数量在第 1 周增加两倍,与对照组相比,这种增加在第 2 周时保持不变。FGF-2 的应用在第 1 周时同样有效,但在第 2 周时巨噬细胞数量已降至对照水平。用泛巨噬细胞标志物 ED1 和 M2 样巨噬细胞标志物 Arg-1 进行免疫染色显示,在用所有处理方法处理后,假定的 M2 表型的比例仍保持在约 80%。在第 1 周用电子显微镜观察巨噬细胞,用所有处理方法都显示出强烈的吞噬活性,许多空泡中含有轴突片段和膜碎片。在第 2 周用 PBS 或 FGF-2 处理时,残留的巨噬细胞吞噬活性较弱,主要含有脂质内含物。用 CNTF 处理时,在第 2 周,许多数量较多的巨噬细胞仍在吞噬轴突碎片,尽管它们也含有脂质内含物。我们得出结论,生长因子应用后观察到的巨噬细胞涌入增加对再生轴突有益,可能是由于更广泛地清除了变性的远端轴突,但也可能是由于分泌了促进生长的物质。