Evidence map›Paper›PMID 10579714›Full record

ArticleThe Journal of cell biology1999

Morphological control of inositol-1,4,5-trisphosphate-dependent signals.

C C Fink, B Slepchenko, I I Moraru, J Schaff, J Watras, L M Loew

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Use of virtual cell in studies of cellular dynamics.International review of cell and molecular biology · 2010
    Review
  4. Ceramide activates JNK to inhibit a cAMP-gated K+ conductance and Cl- secretion in intestinal epithelia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009
    Article
  5. Article
  6. Where does all the PIP2 come from?The Journal of physiology · 2007
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Relationship between membrane phosphatidylinositol-4,5-bisphosphate and receptor-mediated inhibition of native neuronal M channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
  12. Review
  13. Modeling cell signaling networks.Biology of the cell · 2004
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

C C FinkDepartment of Physiology, University of Connecticut Health Center, Farmington, Connecticut 06030, USA.
B Slepchenko
I I Moraru
J Schaff
J Watras
L M Loew
UConn Health · US

Funding

VIRTUAL FCSP41RR013186 · NCRR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LOEW, LESLIE M · 1998 to 2011
$14.2M
POTENTIOMETRIC DYES AND MEMBRANE PERMEABILITYR01GM035063 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LOEW, LESLIE M · 1985 to 2002
$795k
NCRR NIH HHS P41 RR013186NCRR NIH HHS RR13186NIGMS NIH HHS GM35063
6 · The paper itself

Abstract

Inositol-1,4,5-trisphosphate (InsP(3))-mediated calcium signals represent an important mechanism for transmitting external stimuli to the cell. However, information about intracellular spatial patterns of InsP(3) itself is not generally available. In particular, it has not been determined how the interplay of InsP(3) generation, diffusion, and degradation within complex cellular geometries can control the patterns of InsP(3) signaling. Here, we explore the spatial and temporal characteristics of [InsP(3)](cyt) during a bradykinin-induced calcium wave in a neuroblastoma cell. This is achieved by using a unique image-based computer modeling system, Virtual Cell, to integrate experimental data on the rates and spatial distributions of the key molecular components of the process. We conclude that the characteristic calcium dynamics requires rapid, high-amplitude production of [InsP(3)](cyt) in the neurite. This requisite InsP(3) spatiotemporal profile is provided, in turn, as an intrinsic consequence of the cell's morphology, demonstrating how geometry can locally and dramatically intensify cytosolic signals that originate at the plasma membrane. In addition, the model predicts, and experiments confirm, that stimulation of just the neurite, but not the soma or growth cone, is sufficient to generate a calcium response throughout the cell.

Indexed as

AnimalsBradykininCalcium SignalingComputer SimulationDogsImage Processing, Computer-AssistedInositol 1,4,5-TrisphosphateMiceMicroscopy, FluorescenceModels, BiologicalNeuritesNeuroblastomaSignal TransductionTumor Cells, CulturedBradykininInositol 1,4,5-Trisphosphate

Identifiers

PMID10579714
PMCPMC2169350
OpenAlexW2152082557

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.