The long-term objective of the proposed research is to understand in detail the phototransduction mechanism in retinal cones.
The specific aims are: 1) to measure the rate constant of spontaneous isomerization of human red cone pigment with 11-cis retinal as chromophore in a transgenic mouse line, in order to assess its importance in human cones. 2) to measure and analyze the response properties and background-adaptation behavior of goldfish red, green and blue cones and to correlate these parameters with the separately measured dark phosphodiesterase activity in each cone type (from which the spontaneous isomerization rate of each pigment type can also be obtained). Goldfish retina has the advantage that it has all three cone types like human retina, and the correlate of biochemical studies by others. 3) to examine the 50-year-old question of whether there is a strict quantitative relation for various pigments between the lambda-max of the action spectrum and the activation energy of photoisomerization, and to correlate this information with the energetics of the associated spontaneous isomerization activity in order to firmly establish photoisomerization and thermal isomerization as fundamentally the same process. 4) to examine the contributions of the pigment kinase (GRK1 and 7), arrestin, and the GAP protein RGS9 to the response properties of cones. We shall employ morpholinos to knockdown each transduction protein in turn in Xenopus and see how this affects the cone response to light. The proposed work will lead to a much greater understanding of the light response of cones, which are more important than rods for human vision. The gained knowledge will also help understand and treat human diseases affecting cone function.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY006837-24
Application #
8045424
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Neuhold, Lisa
Project Start
1987-02-21
Project End
2012-03-31
Budget Start
2011-04-01
Budget End
2012-03-31
Support Year
24
Fiscal Year
2011
Total Cost
$389,664
Indirect Cost
Name
Johns Hopkins University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Yue, Wendy Wing Sze; Frederiksen, Rikard; Ren, Xiaozhi et al. (2017) Spontaneous activation of visual pigments in relation to openness/closedness of chromophore-binding pocket. Elife 6:
Liao, Hsi-Wen; Ren, Xiaozhi; Peterson, Beth B et al. (2016) Melanopsin-expressing ganglion cells on macaque and human retinas form two morphologically distinct populations. J Comp Neurol 524:2845-72
Zhang, Tao; Cao, Li-Hui; Kumar, Sandeep et al. (2016) Dimerization of visual pigments in vivo. Proc Natl Acad Sci U S A 113:9093-8
Cao, Li-Hui; Luo, Dong-Gen; Yau, King-Wai (2014) Light responses of primate and other mammalian cones. Proc Natl Acad Sci U S A 111:2752-7
Zhong, Xiufeng; Gutierrez, Christian; Xue, Tian et al. (2014) Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs. Nat Commun 5:4047
Sun, Lu O; Jiang, Zheng; Rivlin-Etzion, Michal et al. (2013) On and off retinal circuit assembly by divergent molecular mechanisms. Science 342:1241974
Welsbie, Derek S; Yang, Zhiyong; Ge, Yan et al. (2013) Functional genomic screening identifies dual leucine zipper kinase as a key mediator of retinal ganglion cell death. Proc Natl Acad Sci U S A 110:4045-50
Pearson, R A; Barber, A C; Rizzi, M et al. (2012) Restoration of vision after transplantation of photoreceptors. Nature 485:99-103
Matsuoka, Ryota L; Jiang, Zheng; Samuels, Ivy S et al. (2012) Guidance-cue control of horizontal cell morphology, lamination, and synapse formation in the mammalian outer retina. J Neurosci 32:6859-68
Sakai, Kazumi; Imamoto, Yasushi; Su, Chih-Ying et al. (2012) Photochemical nature of parietopsin. Biochemistry 51:1933-41

Showing the most recent 10 out of 26 publications