scholarly journals Characterization of Progenitor Cells during Canine Retinal Development

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Mallely Ávila-García ◽  
Gustavo García-Sánchez ◽  
Esmeralda Lira-Romero ◽  
Norma Moreno-Mendoza

We identify the presence of progenitor cells during retinal development in the dog, as this species represents a natural model for studying several breed-specific degenerative retinal disorders. Antibodies to detected progenitor cells (Pax6, C-kit, and nestin) and ganglion cells (BDNF, Brn3a, and Thy1) were used in combination with H3 for the purpose of identifying proliferating cells. Pax6, nestin, C-kit, and H3 were localized mainly in the neuroblastic layer of the retina during the embryonic stage. During the fetal stage, proteins were expressed in the inner neuroblastic layer (INL) as well as in the outer neuroblastic layer; BDNF, Thy1, and Brn3a were also expressed in the INL. During the neonatal stage only C-kit was not expressed. Proliferating cells were present in both undifferentiated and differentiated retina. These results suggest that, during canine retinogenesis, progenitor cells are distributed along the retina and some of these cells remain as progenitor cells of the ganglion cells during the first postnatal days.

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Shawn C. Maloney ◽  
Emilia Antecka ◽  
Alexandre N. Odashiro ◽  
Bruno F. Fernandes ◽  
Madeline Doyle ◽  
...  

Sirtuin 1 (SIRT1) is a deacetylase that can regulate various biological processes via repression of transcription. Its activity has been linked to the differentiation of neural progenitor cells, although little is known about its function during retinal development. The study described herein was undertaken to evaluate the expression of SIRT1 and its innate inhibitor, DBC1, in retinal tissues and progenitor cells. We found both SIRT1 and DBC1 to be widely expressed in mouse and human retinas, with subtle differences in subcellular distribution of each protein. We further demonstrate that nuclear-localized SIRT1 is only seen in human-derived retinal progenitor cells and not in adult retinas, suggesting that this nuclear localization may be important in retinal development. Moreover, we observed cytoplasmic DBC1 in a subset of progenitor cells as well as in mature ganglion cells, indicating that the progenitor cell subset, which was comprised predominantly of small cells, may represent a population of ganglion cell precursors. Collectively, the data presented in this study provide support for SIRT1 and DBC1 as regulators of retinal development and normal retinal physiology.


1990 ◽  
Author(s):  
N. Lugo-Garcia ◽  
R. E. Blanco ◽  
Ivonne Santiago

2007 ◽  
Vol 313 (5) ◽  
pp. 1008-1023 ◽  
Author(s):  
Mitsutaka Shiota ◽  
Toshio Heike ◽  
Munetada Haruyama ◽  
Shiro Baba ◽  
Atsunori Tsuchiya ◽  
...  

2015 ◽  
Vol 35 (8) ◽  
pp. 1203-1216 ◽  
Author(s):  
Alexandra Jaeger ◽  
Michael Fröhlich ◽  
Susanne Klum ◽  
Margareta Lantow ◽  
Torsten Viergutz ◽  
...  

2016 ◽  
Vol 68 (6) ◽  
pp. 2257-2269 ◽  
Author(s):  
Ahmad Abu-Khader ◽  
Roya Pasha ◽  
Gwendoline C. D. Ward ◽  
Gavin Boisjoli ◽  
Nicolas Pineault

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