scholarly journals Retinal Cone Photoreceptors of the Deer Mouse Peromyscus maniculatus: Development, Topography, Opsin Expression and Spectral Tuning

PLoS ONE ◽  
2013 ◽  
Vol 8 (11) ◽  
pp. e80910 ◽  
Author(s):  
Patrick Arbogast ◽  
Martin Glösmann ◽  
Leo Peichl
2011 ◽  
Vol 51 (4) ◽  
pp. 447-458 ◽  
Author(s):  
Lauren L. Daniele ◽  
Christine Insinna ◽  
Rebecca Chance ◽  
Jinhua Wang ◽  
Sergei S. Nikonov ◽  
...  

1997 ◽  
Vol 14 (4) ◽  
pp. 609-615 ◽  
Author(s):  
Shu-Ichi Watanabe ◽  
Jing Shen

AbstractEffects of ATP on the activity of cGMP-gated channels from carp cone photoreceptors were studied. In 29% of the patches examined (N = 45), ATP (1 mM) enhanced a current evoked by cGMP (20 μM, up to about 100%), in 33%, ATP suppressed it by up to about 90%, and in the remaining 38%, ATP had no effect. ATP showed similar effects on a current evoked by 8-bromoguanosine 3′,5′-cyclic monophosphate (2 μM, enhancing in 42% of the patches, suppressing in 25%, no effect in 33%, N = 12), suggesting that the effects were not through modulation of the phosphodiesterase. Both of the effects, enhancement and suppression, were produced by a change in apparent affinity for cGMP, since (1) the maximum current evoked by cGMP of the saturating concentration (≥1 mM) was not affected, and (2) the A1/2 value decreased by approximately 45% (N = 2) or increased by approximately 25% (N = 2). A lower pH (approximately 6) facilitated the enhancing effect. ATP-γ-S (1 mM) showed a suppressing effect in 80% of the patches and no effect in 20% of the patches (N = 10). However, ATP-γ-S did not show an enhancing effect. Thus, ATP had two opposite effects through different mechanisms on the apparent sensitivity of the channel to cGMP; increasing and decreasing.


2002 ◽  
Vol 83 (7) ◽  
pp. 1745-1751 ◽  
Author(s):  
Mausumi Bharadwaj ◽  
Katy Mirowsky ◽  
Chunyan Ye ◽  
Jason Botten ◽  
Barbara Masten ◽  
...  

2015 ◽  
Vol 218 (10) ◽  
pp. 1556-1563 ◽  
Author(s):  
M. S. Yewers ◽  
C. A. McLean ◽  
A. Moussalli ◽  
D. Stuart-Fox ◽  
A. T. D. Bennett ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (3) ◽  
pp. e0150598 ◽  
Author(s):  
Shannon W. Davis ◽  
Jessica L. Keisler

Viruses ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 183 ◽  
Author(s):  
Bryce Warner ◽  
Derek Stein ◽  
Bryan Griffin ◽  
Kevin Tierney ◽  
Anders Leung ◽  
...  

In North America, Sin Nombre virus (SNV) is the main cause of hantavirus cardiopulmonary syndrome (HCPS), a severe respiratory disease with a fatality rate of 35–40%. SNV is a zoonotic pathogen carried by deer mice (Peromyscus maniculatus), and few studies have been performed examining its transmission in deer mouse populations. Studying SNV and other hantaviruses can be difficult due to the need to propagate the virus in vivo for subsequent experiments. We show that when compared with standard intramuscular infection, the intraperitoneal infection of deer mice can be as effective in producing SNV stocks with a high viral RNA copy number, and this method of infection provides a more reproducible infection model. Furthermore, the age and sex of the infected deer mice have little effect on viral replication and shedding. We also describe a reliable model of direct experimental SNV transmission. We examined the transmission of SNV between deer mice and found that direct contact between deer mice is the main driver of SNV transmission rather than exposure to contaminated excreta/secreta, which is thought to be the main driver of transmission of the virus to humans. Furthermore, increases in heat shock responses or testosterone levels in SNV-infected deer mice do not increase the replication, shedding, or rate of transmission. Here, we have demonstrated a model for the transmission of SNV between deer mice, the natural rodent reservoir for the virus. The use of this model will have important implications for further examining SNV transmission and in developing strategies for the prevention of SNV infection in deer mouse populations.


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