Evidence map›Paper›PMID 11320223›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Growth factors regulate phototransduction in retinal rods by modulating cyclic nucleotide-gated channels through dephosphorylation of a specific tyrosine residue.

A Savchenko, T W Kraft, E Molokanova, R H Kramer

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Insulin receptor regulates photoreceptor CNG channel activity.American journal of physiology. Endocrinology and metabolism · 2012
    Article
  9. Article
  10. Article
  11. Insulin-like growth factor-1 inhibits adult supraoptic neurons via complementary modulation of mechanoreceptors and glycine receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
  12. Circadian regulation of cGMP-gated channels of vertebrate cone photoreceptors: role of cAMP and Ras.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  13. Tyrosine phosphorylation of rod cyclic nucleotide-gated channels switches off Ca2+/calmodulin inhibition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003
    Article
  14. Article
  15. Review
  16. Article
  17. Regulated cationic channel function in Xenopus oocytes expressing Drosophila big brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    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

4 authors at 2 institutions in 1 country.

A SavchenkoDepartment of Molecular and Cellular Pharmacology, University of Miami School of Medicine, Miami, FL 33101, USA.
T W Kraft
E Molokanova
R H Kramer
University of Alabama · USUniversity of Miami · US

Funding

MODULATION OF RETINAL FUNCTION BY IGF-1R01EY012608 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI KRAMER, RICHARD H · 1999 to 2001
$475k
PHYSIOLOGY AND PATHOPHYSIOLOGY OF PHOTORECEPTORSR01EY010573 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KRAFT, TIMOTHY W · 1994 to 2002
$437k
SYNAPTIC FUNCTION OF CNG CHANNELS IN THE RETINAR01EY011877 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI KRAMER, RICHARD H · 1998 to 2001
$374k
NEI NIH HHS EY10573NEI NIH HHS EY11877NEI NIH HHS EY12608NEI NIH HHS R01 EY010573
6 · The paper itself

Abstract

Illumination of vertebrate rod photoreceptors leads to a decrease in the cytoplasmic cGMP concentration and closure of cyclic nucleotide-gated (CNG) channels. Except for Ca(2+), which plays a negative feedback role in adaptation, and 11-cis-retinal, supplied by the retinal pigment epithelium, all of the biochemical machinery of phototransduction is thought to be contained within rod outer segments without involvement of extrinsic regulatory molecules. Here we show that insulin-like growth factor-I (IGF-I), a paracrine factor released from the retinal pigment epithelium, alters phototransduction by rapidly increasing the cGMP sensitivity of CNG channels. The IGF-I-signaling pathway ultimately involves a protein tyrosine phosphatase that catalyzes dephosphorylation of a specific residue in the alpha-subunit of the rod CNG channel protein. IGF-I conjointly accelerates the kinetics and increases the amplitude of the light response, distinct from events that accompany adaptation. These effects of IGF-I could result from the enhancement of the cGMP sensitivity of CNG channels. Hence, in addition to long-term control of development and survival of rods, growth factors regulate phototransduction in the short term by modulating CNG channels.

Indexed as

LightSignal TransductionAnimalsCaudataInsulin-Like Growth Factor IRetinal Rod Photoreceptor CellsXenopusInsulin-Like Growth Factor I

Identifiers

PMID11320223
PMCPMC33307
OpenAlexW2019879265

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.