Evidence map›Paper›PMID 18936250›Full record

ArticleThe Journal of cell biology2008

Selective coupling of type 6 adenylyl cyclase with type 2 IP3 receptors mediates direct sensitization of IP3 receptors by cAMP.

Stephen C Tovey, Skarlatos G Dedos, Emily J A Taylor, Jarrod E Church, Colin W Taylor

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

55 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. Article
  3. Activation of IPAmerican journal of physiology. Heart and circulatory physiology · 2024
    Article
  4. A molecular mechanism to diversify CaNature communications · 2024
    Article
  5. Article
  6. 14-3-3Journal of neuroinflammation · 2023
    Article
  7. Article
  8. Resolvin D2 uses multiple CaJournal of cellular physiology · 2022
    Article
  9. Article
  10. IPAmerican journal of physiology. Heart and circulatory physiology · 2021
    Article
  11. Article
  12. Review
  13. Spatial-temporal patterning of CaSeminars in cell & developmental biology · 2019
    Review
  14. Resolvin D2 elevates cAMP to increase intracellular [CaFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  15. Structure and Function of IPCold Spring Harbor perspectives in biology · 2019
    Review
  16. IPCell reports · 2018
    Article
  17. Article
  18. All three IPJournal of cell science · 2018
    Article
  19. Article
  20. Prostaglandin EMolecular pharmacology · 2017
    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

5 authors at 1 institution in 1 country.

Stephen C ToveyDepartment of Pharmacology, Univesrsity of Cambridge, Cambridge, England, UK.
Skarlatos G Dedos
Emily J A Taylor
Jarrod E Church
Colin W Taylor
University of Cambridge · GB

Funding

Wellcome TrustWellcome Trust 072084
6 · The paper itself

Abstract

Interactions between cyclic adenosine monophosphate (cAMP) and Ca(2+) are widespread, and for both intracellular messengers, their spatial organization is important. Parathyroid hormone (PTH) stimulates formation of cAMP and sensitizes inositol 1,4,5-trisphosphate receptors (IP(3)R) to IP(3). We show that PTH communicates with IP(3)R via "cAMP junctions" that allow local delivery of a supramaximal concentration of cAMP to IP(3)R, directly increasing their sensitivity to IP(3). These junctions are robust binary switches that are digitally recruited by increasing concentrations of PTH. Human embryonic kidney cells express several isoforms of adenylyl cyclase (AC) and IP(3)R, but IP(3)R2 and AC6 are specifically associated, and inhibition of AC6 or IP(3)R2 expression by small interfering RNA selectively attenuates potentiation of Ca(2+) signals by PTH. We define two modes of cAMP signaling: binary, where cAMP passes directly from AC6 to IP(3)R2; and analogue, where local gradients of cAMP concentration regulate cAMP effectors more remote from AC. Binary signaling requires localized delivery of cAMP, whereas analogue signaling is more dependent on localized cAMP degradation.

Indexed as

Adenylyl Cyclase InhibitorsAdenylyl CyclasesCalcium SignalingCarbacholCell LineCell Membrane PermeabilityColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesGTP-Binding Protein alpha Subunits, GsGuanine Nucleotide Exchange FactorsHumansInositol 1,4,5-Trisphosphate ReceptorsIntercellular JunctionsIsoproterenolParathyroid Hormoneadenylyl cyclase 6Adenylyl Cyclase InhibitorsAdenylyl CyclasesCarbacholColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesGTP-Binding Protein alpha Subunits, GsGuanine Nucleotide Exchange FactorsInositol 1,4,5-Trisphosphate ReceptorsIsoproterenolParathyroid HormonePhosphoric Diester HydrolasesProtein IsoformsPTH protein, human

Identifiers

PMID18936250
PMCPMC2568025
OpenAlexW2127497045

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.