Evidence map›Paper›PMID 25670801›Full record

ArticleJournal of lipid research2015

Sphingomyelin metabolism is involved in the differentiation of MDCK cells induced by environmental hypertonicity.

Nicolás Octavio Favale, Bruno Jaime Santacreu, Lucila Gisele Pescio, Maria Gabriela Marquez, Norma Beatriz Sterin-Speziale

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. The IRE1Cell stress · 2026
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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

5 authors at 3 institutions in 1 country.

Nicolás Octavio FavaleFacultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina IQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Bruno Jaime SantacreuFacultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina IQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Lucila Gisele PescioFacultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina IQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Maria Gabriela MarquezIQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina Instituto de Investigaciones en Ciencias de la Salud Humana (IICSHUM), Universidad Nacional de La Rioja , La Rioja, Argentina.
Norma Beatriz Sterin-SpezialeIQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversity of Buenos Aires · ARInstituto de Química y Fisicoquímica Biológicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingolipids (SLs) are relevant lipid components of eukaryotic cells. Besides regulating various cellular processes, SLs provide the structural framework for plasma membrane organization. Particularly, SM is associated with detergent-resistant microdomains. We have previously shown that the adherens junction (AJ) complex, the relevant cell-cell adhesion structure involved in cell differentiation and tissue organization, is located in an SM-rich membrane lipid domain. We have also demonstrated that under hypertonic conditions, Madin-Darby canine kidney (MDCK) cells acquire a differentiated phenotype with changes in SL metabolism. For these reasons, we decided to evaluate whether SM metabolism is involved in the acquisition of the differentiated phenotype of MDCK cells. We found that SM synthesis mediated by SM synthase 1 is involved in hypertonicity-induced formation of mature AJs, necessary for correct epithelial cell differentiation. Inhibition of SM synthesis impaired the acquisition of mature AJs, evoking a disintegration-like process reflected by the dissipation of E-cadherin and β- and α-catenins from the AJ complex. As a consequence, MDCK cells did not develop the hypertonicity-induced differentiated epithelial cell phenotype.

Indexed as

Cell DifferentiationOsmotic PressureAdherens Junctionsalpha CateninAnimalsbeta CateninCadherinsCell NucleusDogsDose-Response Relationship, DrugEnzyme InhibitorsGene Expression Regulation, EnzymologicGene Knockdown TechniquesMadin Darby Canine Kidney CellsPhenotypeSphingomyelinsalpha Cateninbeta CateninCadherinsEnzyme Inhibitorsphosphatidylcholine-ceramide phosphocholine transferaseSphingomyelinsTransferases (Other Substituted Phosphate Groups)Madin-Darby canine kidney cellsrenal epithelial cellssphingomyelin synthase

Identifiers

PMID25670801
PMCPMC4373737
OpenAlexW2087617952

What Socratic 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 Socratic graph.