Analysis of Programmed Cell Death and Senescence Markers in the Developing Retina of an Altricial Bird Species

• Main Authors: Guadalupe Álvarez-Hernán, José Antonio de Mera-Rodríguez, Ismael Hernández-Núñez, Alfonso Marzal, Yolanda Gañán, Gervasio Martín-Partido, Joaquín Rodríguez-León, Javier Francisco-Morcillo
• Format: Article
• Language: English
• Published: MDPI AG 2021-02-01
• Series: Cells
• Subjects: programmed cell death; cellular senescence; retinogenesis; altricial bird species; precocial bird species; senescence-associated galactosidase activity
• Online Access: https://www.mdpi.com/2073-4409/10/3/504

This study shows the distribution patterns of apoptotic cells and biomarkers of cellular senescence during the ontogeny of the retina in the zebra finch (<i>T. guttata</i>). 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 <i>T. guttata </i>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-<i>β</i>-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-<i>β</i>-GAL activity and the distribution of TUNEL-positive cells in the developing tissue.