Área de Biología Celular Departamento de Anatomía Biología Celular y Zoología, Facultad de Ciencias, Universidad de Extremadura, Badajoz, 06006, Spain.
Área de Zoología, Departamento de Anatomía, Biología Celular y Zoología, Facultad de Ciencias, Universidad de Extremadura, 06006 Badajoz, Spain.
Cells. 2021 Feb 26;10(3):504. doi: 10.3390/cells10030504.
This study shows the distribution patterns of apoptotic cells and biomarkers of cellular senescence during the ontogeny of the retina in the zebra finch (). Neurogenesis in this altricial bird species is intense in the retina at perinatal and post-hatching stages, as opposed to precocial bird species in which retinogenesis occurs entirely during the embryonic period. Various phases of programmed cell death (PCD) were distinguishable in the visual system. These included areas of PCD in the central region of the neuroretina at the stages of optic cup morphogenesis, and in the sub-optic necrotic centers (St15-20). A small focus of early neural PCD was detected in the neuroblastic layer, dorsal to the optic nerve head, coinciding with the appearance of the first differentiated neuroblasts (St24-St25). There were sparse pyknotic bodies in the non-laminated retina between St26 and St37. An intense wave of neurotrophic PCD was detected in the laminated retina between St42 and P8, the last post-hatching stage included in the present study. PCD was absent from the photoreceptor layer. Phagocytic activity was also detected in Müller cells during the wave of neurotrophic PCD. With regard to the chronotopographical staining patterns of senescence biomarkers, there was strong parallelism between the SA--GAL signal and p21 immunoreactivity in both the undifferentiated and the laminated retina, coinciding in the cell body of differentiated neurons. In contrast, no correlation was found between SA--GAL activity and the distribution of TUNEL-positive cells in the developing tissue.
这项研究展示了在斑马雀()视网膜发生过程中细胞凋亡和细胞衰老生物标志物的分布模式。与在胚胎期发生视网膜形成的早成性鸟类相反,这种晚成性鸟类的视网膜在围产期和孵化后阶段具有强烈的神经发生。在视觉系统中可以区分各种程序性细胞死亡(PCD)阶段。这些阶段包括视杯形态发生阶段的神经视网膜中央区域和视下坏死中心(St15-20)的 PCD 区域。在视神经头部上方的神经母细胞层中检测到早期神经 PCD 的一小焦点,与第一个分化的神经母细胞(St24-St25)的出现相吻合。在 St26 和 St37 之间的非分层视网膜中有稀疏的固缩体。在包含在本研究中的最后一个孵化后阶段 St42 和 P8 之间,检测到强烈的神经营养性 PCD 波。在光感受器层中没有 PCD。在神经营养性 PCD 波期间,也在 Müller 细胞中检测到吞噬活性。就衰老生物标志物的chronotopographical 染色模式而言,在未分化和分层视网膜中,SA--GAL 信号和 p21 免疫反应性之间存在强烈的平行性,在分化神经元的细胞体中一致。相比之下,在发育组织中,SA--GAL 活性与 TUNEL 阳性细胞的分布之间没有相关性。