Evidence map›Paper›PMID 11292747›Full record

ArticleInfection and immunity2001

Calprotectin expression by gingival epithelial cells.

K F Ross, M C Herzberg

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

40 citing papers in PubMed, 86 citations in OpenAlex.

  1. Trial
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  4. Role of Antimicrobial Peptides in Treatment and Prevention of Mycobacterium Tuberculosis: A Review.International journal of peptide research and therapeutics · 2022
    Review
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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

2 authors at 1 institution in 1 country.

K F RossDepartment of Preventive Science, School of Dentistry, University of Minnesota, Minneapolis, Minnesota 55455, USA.
M C Herzberg
University of Minnesota · US

Funding

INNATE INTRAEPITHELIAL DEFENSE AGAINST ORAL INFECTIONR01DE011831 · NIDCR · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HERZBERG, MARK C · 1997 to 2006
$2.0M
VALIDATION OF STIMULATED OCCLUSAL CONTACT PATTERNSP30DE009737 · NIDCR · UNIVERSITY OF MINNESOTA TWIN CITIES · PI FLORES, CHRISTOPHER · 1990 to 2000
$512k
NIDCR NIH HHS P30DE09737NIDCR NIH HHS R01 DE011831NIDCR NIH HHS R01DE11831
6 · The paper itself

Abstract

Calprotectin, a heterodimer of MRP8 and MRP14 with antimicrobial properties, is found in the cytosol of neutrophils, monocytes, and human gingival keratinocytes. During inflammation of the oral mucosa, the expression of immunoreactive calprotectin appears upregulated. Given the possible cell sources, we sought to learn if epithelial cells upregulate calprotectin in response to proinflammmatory agents. First, human gingival keratinocytes were maintained in primary culture until senescence. At each passage, cells were harvested and analyzed for quantitative expression of MRP8 and MRP14 subunit mRNA by RNase protection assays and calprotectin complex by enzyme-linked immunosorbent assay. Calprotectin expression was constitutive in the primary gingival keratinocytes, but calprotectin-specific mRNA and protein tended to increase as the cells neared senescence. To test whether calprotectin expression was inducible, immortalized gingival keratinocyte cultures were treated for 2 to 4 h with lipopolysaccharide (LPS) or interleukin-1 beta (IL-1 beta). As a positive control for inducible expression, immortalized keratinocytes were incubated with phorbol myristate acetate (PMA) (50 ng/ml) for 24 h. Incubation with PMA stimulated increased expression of MRP8 and MRP14 mRNA within 2 h, peaking within 5 h. MRP8- and MRP14-specific mRNA expression by immortalized keratinocytes appeared to be unaffected by LPS or IL-1 beta. In contrast, LPS, IL-1 beta, and PMA each upregulated IL-8. These data show that calprotectin mRNA is expressed constitutively in cultured keratinocytes, while expression by immortalized cells appears to be independent of the exogenous proinflammatory agents LPS and IL-1 beta.

Indexed as

Antigens, DifferentiationCalcium-Binding ProteinsCalgranulin ACalgranulin BCells, CulturedEpithelial CellsGingivaHistocompatibility Antigens Class IIHumansImmunohistochemistryInterleukin-8KeratinocytesLeukocyte L1 Antigen ComplexLipopolysaccharidesMembrane GlycoproteinsNeural Cell Adhesion MoleculesAntigens, DifferentiationCalcium-Binding ProteinsCalgranulin ACalgranulin BHistocompatibility Antigens Class IIInterleukin-8Leukocyte L1 Antigen ComplexLipopolysaccharidesMembrane GlycoproteinsNeural Cell Adhesion MoleculesRNA, MessengerS100 Proteins

Identifiers

PMID11292747
PMCPMC98283
OpenAlexW2137323762

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.