Evidence map›Paper›PMID 7989586›Full record

ArticleThe Journal of clinical investigation1994

Interleukin-1 beta-modulated gene expression in immortalized human chondrocytes.

M B Goldring, J R Birkhead, L F Suen, R Yamin, S Mizuno, J Glowacki, J L Arbiser, J F Apperley

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 188 papers.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

188 citing papers in PubMed, 475 citations in OpenAlex.

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128 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

M B GoldringArthritis Research Laboratory, Massachusetts General Hospital, Charlestown 02129.
J R Birkhead
L F Suen
R Yamin
S Mizuno
J Glowacki
J L Arbiser
J F Apperley
Massachusetts General Hospital · USBrigham and Women's Hospital · USHarvard University · USHammersmith Hospital · GB

Funding

Research Training in Rheumatology at Massachusetts General HospitalT32AR007258 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI ANDREW D LUSTER · 1986 to 2026
$6.9M
STUDY OF MESENCHYMAL TISSUES &THEIR DISEASESP01AR003564 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI KRANE, STEPHEN M · 1986 to 1997
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COLLAGEN GENE EXPRESSION IN CHONDROCYTES IN INFLAMMATIONR01AR034390 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI GOLDRING, MARY B. · 1988 to 1990
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ACTIVATION OF HUMAN CHONDROCYTESR23AR034390 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI GOLDRING, MARY B. · 1986 to 1986
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NIAMS NIH HHS AR-03564NIAMS NIH HHS AR-07258NIAMS NIH HHS AR-34390Wellcome Trust
6 · The paper itself

Abstract

Immortalized human chondrocytes were established by transfection of primary cultures of juvenile costal chondrocytes with vectors encoding simian virus 40 large T antigen and selection in suspension culture over agarose. Stable cell lines were generated that exhibited chondrocyte morphology, continuous proliferative capacity (> 80 passages) in monolayer culture in serum-containing medium, and expression of mRNAs encoding chondrocyte-specific collagens II, IX, and XI and proteoglycans in an insulin-containing serum substitute. They did not express type X collagen or versican mRNA. These cells synthesized and secreted extracellular matrix molecules that were reactive with monoclonal antibodies against type II collagen, large proteoglycan (PG-H, aggrecan), and chondroitin-4- and chondroitin-6-sulfate. Interleukin-1 beta (IL-1 beta) decreased the levels of type II collagen mRNA and increased the levels of mRNAs for collagenase, stromelysin, and immediate early genes (egr-1, c-fos, c-jun, and jun-B). These cell lines also expressed reporter gene constructs containing regulatory sequences (-577/+3,428 bp) of the type II collagen gene (COL2A1) in transient transfection experiments, and IL-1 beta suppressed this expression by 50-80%. These results show that immortalized human chondrocytes displaying cartilage-specific modulation by IL-1 beta can be used as a model for studying normal and pathological repair mechanisms.

Indexed as

Antigens, Viral, TumorCartilageCell LineCell Transformation, ViralChondroitin SulfatesCollagenCycloheximideFluorescent Antibody TechniqueGene ExpressionHumansImmunohistochemistryInterleukin-1PhenotypeProteoglycansRibsRNA, MessengerAntigens, Viral, TumorChondroitin SulfatesCollagenCycloheximideInterleukin-1ProteoglycansRNA, Messenger

Identifiers

PMID7989586
PMCPMC330059
OpenAlexW2167461417

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.