Rodríguez-Gallardo Lucía, Lineros-Domínguez María del Carmen, Francisco-Morcillo Javier, Martín-Partido Gervasio
Departamento de Biología Celular, Facultad de Ciencias, Universidad de Extremadura, Avda de Elvas s/n, 06071, Badajoz, Spain.
Anat Embryol (Berl). 2005 Nov;210(4):303-16. doi: 10.1007/s00429-005-0051-3. Epub 2005 Nov 12.
We compared the spatial and temporal patterns of distribution of macrophages, with patterns of naturally occurring cell death and optic fibre growth during early retina and optic nerve development, in the mouse. We used embryos between day 10 of embryogenesis (E10; before the first optic fibres are generated in the retina) and E13 (when the first optic fibres have crossed the chiasmatic anlage). The macrophages and optic axons were identified by immunocytochemistry, and the apoptotic cells were detected by the TUNEL technique, which specifically labels fragmented DNA. Cell death was observed in the retina and the optic stalk long before the first optic axons appeared in either region. Subsequently, specialized F4/80-positive phagocytes were detected in chronological and topographical coincidence with cell death, which disappeared progressively. As development proceeded, the pioneer ganglion cell axons reached the regions where the macrophages were located. As the number of optic fibres increased, the macrophages disappeared. Therefore, cell death, accompanied by macrophages, preceded the growth of fibres in the retina and the optic nerve. Moreover, these macrophages synthesized NGF and the optic axons were p75 neurotrophin receptor (p75(NTR))- and TrkA-positive. These findings suggest that macrophages may be involved in optic axon guidance and fasciculation.
我们比较了小鼠视网膜和视神经早期发育过程中巨噬细胞的空间和时间分布模式,以及自然发生的细胞死亡模式和视神经纤维生长模式。我们使用了胚胎发育第10天(E10;视网膜中尚未产生第一批视神经纤维)至E13(第一批视神经纤维已穿过视交叉原基)之间的胚胎。通过免疫细胞化学鉴定巨噬细胞和视神经轴突,通过TUNEL技术检测凋亡细胞,该技术可特异性标记断裂的DNA。在视网膜和视柄中,早在任何一个区域出现第一批视神经轴突之前就观察到了细胞死亡。随后,在与细胞死亡的时间和地形上的巧合中检测到了专门的F4/80阳性吞噬细胞,这些吞噬细胞逐渐消失。随着发育的进行,先驱神经节细胞轴突到达了巨噬细胞所在的区域。随着视神经纤维数量的增加,巨噬细胞消失。因此,伴有巨噬细胞的细胞死亡先于视网膜和视神经中纤维的生长。此外,这些巨噬细胞合成神经生长因子(NGF),并且视神经轴突是p75神经营养因子受体(p75(NTR))和TrkA阳性。这些发现表明巨噬细胞可能参与视神经轴突的导向和束化。