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Title: Analysis of programmed cell death and senescence markers in the developing retina of an altricial bird species
Authors: Álvarez Hernán, Guadalupe
Mera Rodríguez, José Antonio de
Hernández Núñez, Ismael
Marzal Reynolds, Alfonso
Gañán Presmanes, Yolanda
Martín Partido, Gervasio
Rodríguez León, Joaquín María
Francisco Morcillo, Javier de
Keywords: Muerte celular programada;Senescencia celular;Retinogénesis;Altricial;Precocial;Senescencia;Programmed cell death;Cellular senescence;Retinogenesis
Issue Date: 2021
Publisher: MDPI
Abstract: This study shows the distribution patterns of apoptotic cells and biomarkers of cellular senescence during the ontogeny of the retina in the zebra finch (T. guttata). 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 T. guttata 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–St20). 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-β-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-β-GAL activity and the distribution of TUNEL-positive cells in the developing tissue.
ISSN: 2073-4409
DOI: 10.3390/ cells10030504
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