Evidence map›Paper›PMID 11150339›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2001

Developmental expression of retinal cone cGMP-gated channels: evidence for rapid turnover and trophic regulation.

G Y Ko, M L Ko, S E Dryer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 95% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Nitric oxide regulates angiogenesis through a functional switch involving thrombospondin-1.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

G Y KoDepartment of Biology and Biochemistry, University of Houston, Houston, Texas 77204-5513, USA.
M L Ko
S E Dryer
University of Houston · US

Funding

CIRCADIAN REGULATION OF VERTEBRATE PHOTORECEPTORSR01EY011973 · NEI · UNIVERSITY OF HOUSTON · PI DRYER, STUART E. · 1998 to 2005
$1.4M
NEI NIH HHS EY-11973NEI NIH HHS R01 EY011973
6 · The paper itself

Abstract

The cyclic GMP-gated cationic channels of vertebrate photoreceptors are essential for visual phototransduction. We have examined the developmental regulation of cGMP-gated channels in morphologically identified cones in the chick retina. Expression of cone-type cGMP-gated channel mRNA can be detected at embryonic day 6 (E6), but expression of functional channels, as accessed by patch-clamp recordings, cannot be detected until E8. Plasma membrane channels in embryonic cones have a high turnover rate because inhibition of protein synthesis or disruption of the Golgi apparatus causes an almost complete loss of functional cGMP-gated channels within 12 hr. Different subpopulations of cones begin to express functional channels at different developmental stages, but all cones express channels by E10. Expression of cGMP-gated channels in at least one cone subpopulation appears to require one or more soluble differentiation factors, which are presumably present in the normal microenvironment of the developing retina. Application of chick embryo extract (CEE), a rich source of trophic factors, causes marked stimulation of cGMP-gated channel expression in chick cones at E8, but not at E6. Inhibition of MAP kinase (Erk) signaling using PD98059, or inhibition of PI3 kinase signaling by LY294002, blocked the stimulatory effects of CEE on E8 cones. Several recombinant trophic factors were also tested, but none could mimic the stimulatory effects of CEE on channel expression. In summary, the developmental expression of cGMP-gated cationic channels in embryonic cones appears to be regulated by epigenetic factors. The ability of cones to respond to these epigenetic factors is also developmentally regulated.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationCell ExtractsCells, CulturedCell SurvivalChick EmbryoChromonesCyclic GMPCyclic Nucleotide-Gated Cation ChannelsDose-Response Relationship, DrugEnzyme InhibitorsFlavonoidsIon Channel GatingIon ChannelsMAP Kinase Signaling System2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneCell ExtractsChromonesCyclic GMPCyclic Nucleotide-Gated Cation ChannelsEnzyme InhibitorsFlavonoidsIon ChannelsMorpholinesPhosphoinositide-3 Kinase InhibitorsRNA, Messenger

Identifiers

PMID11150339
PMCPMC6762422
OpenAlexW1863019843

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.