Evidence map›Paper›PMID 8389770›Full record

ArticleThe Journal of cell biology1993

Signaling pathways for sphingosylphosphorylcholine-mediated mitogenesis in Swiss 3T3 fibroblasts.

N N Desai, R O Carlson, M E Mattie, A Olivera, N E Buckley, T Seki, G Brooker, S Spiegel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 116 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

N N DesaiDepartment of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, DC 20007.
R O Carlson
M E Mattie
A Olivera
N E Buckley
T Seki
G Brooker
S Spiegel
Georgetown University Medical Center · USGeorgetown University · US

Funding

SPHINGOSINE AS A MODULATOR OF CELLULAR PROLIFERATIONR01GM043880 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI SPIEGEL, SARAH · 1990 to 2023
$3.8M
METABOLIC AND HORMONAL CONTROL OF CARDIAC CONTRACTIONR01HL028940 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BROOKER, GARY · 1985 to 1998
–
GANGLIOSIDES AS MODULATORS OF CELL GROWTHR29GM039718 · NIGMS · GEORGETOWN UNIVERSITY · PI SPIEGEL, SARAH · 1988 to 1992
–
NHLBI NIH HHS HL28940NIGMS NIH HHS 1R29 GM 39718NIGMS NIH HHS 1RO1 GM43880
6 · The paper itself

Abstract

Sphingosylphosphorylcholine (SPC), or lysophingomyelin, a wide-spectrum growth promoting agent for a variety of cell types (Desai, N. N., and S. Spiegel. 1991. Biochem. Biophys. Res. Comm. 181: 361-366), stimulates cellular proliferation of quiescent Swiss 3T3 fibroblasts to a greater extent than other known growth factors or than the structurally related molecules, sphingosine and sphingosine-1-phosphate. SPC potentiated the mitogenic effect of an activator of protein kinase C, 12-O-tetradecanoylphorbol 13-acetate, and did not compete with phorbol esters for binding to protein kinase C in intact Swiss 3T3 fibroblasts. However, downregulation of protein kinase C, by prolonged treatment with phorbol ester, reduced, but did not eliminate, the ability of SPC to stimulate DNA synthesis, indicating that SPC may act via both protein kinase C-dependent and -independent signaling pathways. SPC induced a rapid rise in intracellular free calcium ([Ca2+]i) in viable 3T3 fibroblasts determined with a digital imaging system. Although the increases in [Ca2+]i were observed even in the absence of calcium in the external medium, no increase in the levels of inositol phosphates could be detected in response to mitogenic concentrations of SPC. Furthermore, in contrast to sphingosine or sphingosine-1-phosphate, the mitogenic effect of SPC was not accompanied by increases in phosphatidic acid levels or changes in cAMP levels. SPC, but not sphingosine or sphingosine-1-phosphate, stimulates the release of arachidonic acid. Therefore, the ability of SPC to act an extremely potent mitogen may be due to activation of signaling pathway(s) distinct from those used by sphingosine or sphingosine-1-phosphate.

Indexed as

Lysophospholipids3T3 CellsAnimalsArachidonic AcidCalciumCell DivisionCyclic AMPGrowth SubstancesMicePhosphatidylinositolsPhosphorylcholineProtein Kinase CSignal TransductionSphingosineArachidonic AcidCalciumCyclic AMPGrowth SubstancesLysophospholipidsPhosphatidylinositolsPhosphorylcholineProtein Kinase CSphingosinesphingosine 1-phosphatesphingosine phosphorylcholine

Identifiers

PMID8389770
PMCPMC2119705
OpenAlexW2116716030

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.