scholarly journals Single residue AAV capsid mutation improves transduction of photoreceptors in the Abca4−/− mouse and bipolar cells in the rd1 mouse and human retina ex vivo

Gene Therapy ◽  
2016 ◽  
Vol 23 (11) ◽  
pp. 767-774 ◽  
Author(s):  
S R De Silva ◽  
P Charbel Issa ◽  
M S Singh ◽  
D M Lipinski ◽  
A O Barnea-Cramer ◽  
...  
Keyword(s):  
Ex Vivo ◽  
Gene Therapy ◽  
2017 ◽  
Vol 24 (12) ◽  
pp. 787-800 ◽  
Author(s):  
D G Hickey ◽  
T L Edwards ◽  
A R Barnard ◽  
M S Singh ◽  
S R de Silva ◽  
...  
Keyword(s):  
Ex Vivo ◽  

1991 ◽  
Vol 66 (2) ◽  
pp. 137-150 ◽  
Author(s):  
R. Siminoff
Keyword(s):  

1991 ◽  
Vol 64 (6) ◽  
pp. 505-510 ◽  
Author(s):  
R. Siminoff
Keyword(s):  

PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0246952
Author(s):  
Katja Reinhard ◽  
Thomas A. Münch

The retinal output is the sole source of visual information for the brain. Studies in non-primate mammals estimate that this information is carried by several dozens of retinal ganglion cell types, each informing the brain about different aspects of a visual scene. Even though morphological studies of primate retina suggest a similar diversity of ganglion cell types, research has focused on the function of only a few cell types. In human retina, recordings from individual cells are anecdotal or focus on a small subset of identified types. Here, we present the first systematic ex-vivo recording of light responses from 342 ganglion cells in human retinas obtained from donors. We find a great variety in the human retinal output in terms of preferences for positive or negative contrast, spatio-temporal frequency encoding, contrast sensitivity, and speed tuning. Some human ganglion cells showed similar response behavior as known cell types in other primate retinas, while we also recorded light responses that have not been described previously. This first extensive description of the human retinal output should facilitate interpretation of primate data and comparison to other mammalian species, and it lays the basis for the use of ex-vivo human retina for in-vitro analysis of novel treatment approaches.


2019 ◽  
Author(s):  
Katja Reinhard ◽  
Thomas A. Münch

The retinal output is the sole source of visual information for the brain. Studies in non-primate mammals estimate that this information is carried by several dozens of retinal ganglion cell types, each informing the brain about different aspects of a visual scene. Even though morphological studies of primate retina suggest a similar diversity of ganglion cell types, research has focused on the function of only a few cell types. In human retina, recordings from individual cells are anecdotal or focus on a small subset of identified types. Here, we present the first systematic ex-vivo recording of light responses from 342 ganglion cells in human retinas obtained from donors. We find a great variety in the human retinal output in terms of preferences for positive or negative contrast, spatio-temporal frequency encoding, contrast sensitivity, and speed tuning. Some human ganglion cells showed similar response behavior as known cell types in other primates, while we also recorded light responses that have not been described previously. This first extensive description of the human retinal output should facilitate interpretation of primate data and comparison to other mammalian species, and it lays the basis for the use of ex-vivo human retina for in-vitro analysis of novel treatment approaches.


2019 ◽  
Vol 36 ◽  
Author(s):  
Ashleigh J. Chandra ◽  
Sammy C.S. Lee ◽  
Ulrike Grünert

Abstract In primate retina, the calcium-binding protein calbindin is expressed by a variety of neurons including cones, bipolar cells, and amacrine cells but it is not known which type(s) of cell express calbindin in the ganglion cell layer. The present study aimed to identify calbindin-positive cell type(s) in the amacrine and ganglion cell layer of human and marmoset retina using immunohistochemical markers for ganglion cells (RBPMS and melanopsin) and cholinergic amacrine (ChAT) cells. Intracellular injections following immunolabeling was used to reveal the morphology of calbindin-positive cells. In human retina, calbindin-labeled cells in the ganglion cell layer were identified as inner and outer stratifying melanopsin-expressing ganglion cells, and ON ChAT (starburst amacrine) cells. In marmoset, calbindin immunoreactivity in the ganglion cell layer was absent from ganglion cells but present in ON ChAT cells. In the inner nuclear layer of human retina, calbindin was found in melanopsin-expressing displaced ganglion cells and in at least two populations of amacrine cells including about a quarter of the OFF ChAT cells. In marmoset, a very low proportion of OFF ChAT cells was calbindin-positive. These results suggest that in both species there may be two types of OFF ChAT cells. Consistent with previous studies, the ratio of ON to OFF ChAT cells was about 70 to 30 in human and 30 to 70 in marmoset. Our results show that there are species-related differences between different primates with respect to the expression of calbindin.


1991 ◽  
Vol 65 (5) ◽  
pp. 365-374 ◽  
Author(s):  
R. Siminoff
Keyword(s):  

1991 ◽  
Vol 64 (6) ◽  
pp. 497-504 ◽  
Author(s):  
R. Siminoff
Keyword(s):  

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