Evidence map›Paper›PMID 25382306›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2014

Prostacyclin suppresses twist expression in the presence of indomethacin in bone marrow-derived mesenchymal stromal cells.

Oliver Kemper, Monika Herten, Johannes Fischer, Marcel Haversath, Sascha Beck, Tim Classen, Sebastian Warwas, Tjark Tassemeier, Stefan Landgraeber, Sabine Lensing-Höhn and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 86% 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

0 citing papers in PubMed, 7 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 1 institution in 1 country.

Oliver KemperDepartment of Orthopedics, Medical Faculty, University of Düsseldorf, Düsseldorf, Germany.
Monika HertenDepartment of Orthopedics, Medical Faculty, University of Düsseldorf, Düsseldorf, Germany.
Johannes FischerInstitute for Transplantation Diagnostics and Cell Therapy, University Düsseldorf, Düsseldorf, Germany.
Marcel HaversathDepartment of Orthopaedics, University Duisburg-Essen, Essen, Germany.
Sascha BeckDepartment of Orthopedics, University Duisburg-Essen, Essen, Germany.
Tim ClassenDepartment of Orthopaedics, University Hospital of Duisburg-Essen, Essen, Germany.
Sebastian WarwasDepartment of Orthopaedics, University Hospital of Duisburg-Essen, Essen, Germany.
Tjark TassemeierDepartment of Orthopaedics, University Hospital of Duisburg-Essen, Essen, Germany.
Stefan LandgraeberDepartment of Orthopedics, University Duisburg-Essen, Essen, Germany.
Sabine Lensing-HöhnDepartment of Orthopedics, Medical Faculty, University Düsseldorf, Düsseldorf, Germany.
Rüdiger KrauspeDepartment of Orthopedics, Medical Faculty, University of Düsseldorf, Düsseldorf, Germany.
Marcus JägerDepartment of Orthopedics, University Duisburg-Essen, Essen, Germany.
Heinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIloprost, a stable prostacyclin I2 analogue, seems to have an osteoblast-protective potential, whereas indomethacin suppresses new bone formation. The aim of this study was to investigate human bone marrow stromal cell (BMSC) proliferation and differentiation towards the osteoblastic lineage by administration of indomethacin and/or iloprost. MATERIAL/

methodsHuman bone marrow cells were obtained from 3 different donors (A=26 yrs/m; B=25 yrs/f, C=35 yrs/m) via vacuum aspiration of the iliac crest followed by density gradient centrifugation and flow cytometry with defined antigens (CD105+/73+/45-/14-). The cells were seeded and incubated as follows: without additives (Group 0; donor A/B/C), with 10(-7) M iloprost only (Group 0+ilo; A/B), with indomethacin only in concentrations of 10(-6) M (Group 1, A), 10(-5) M (Group 2, B), 10(-4) M (Group 3, A/B), and together with 10(-7) M iloprost (Groups 4-6, A/B/C). On Day 10 and 28, UV/Vis spectrometric and immunocytochemical assays (4 samples per group and donor) were performed to investigate cell proliferation (cell count measurement) and differentiation towards the osteoblastic lineage (CD34-, CD45-, CD105+, type 1 collagen (Col1), osteocalcin (OC), alkaline phosphatase (ALP), Runx2, Twist, specific ALP-activity).

resultsIndomethacin alone suppressed BMSC differentiation towards the osteoblastic lineage by downregulation of Runx2, Col1, and ALP. In combination with indomethacin, iloprost increased cell proliferation and differentiation and it completely suppressed Twist expression at Day 10 and 28. Iloprost alone did not promote cell proliferation, but moderately enhanced Runx2 and Twist expression. However, the proliferative effects and the specific ALP-activity varied donor-dependently.

conclusionsIloprost partially antagonized the suppressing effects of indomethacin on BMSC differentiation towards the osteoblast lineage. It enhanced the expression of Runx2 and, only in the presence of indomethacin, it completely suppressed Twist. Thus, in the treatment of avascular osteonecrosis or painful bone marrow edema, the undesirable effects of indomethacin might be counterbalanced by iloprost.

Indexed as

AdultAlkaline PhosphataseAntigens, CDBone Marrow CellsCell CountCell DifferentiationCell ProliferationCollagen Type ICore Binding Factor Alpha 1 SubunitEpoprostenolFemaleHumansIloprostImmunohistochemistryIndomethacinL-Lactate DehydrogenaseAlkaline PhosphataseAntigens, CDCollagen Type ICore Binding Factor Alpha 1 SubunitEpoprostenolIloprostIndomethacinL-Lactate DehydrogenaseNuclear ProteinsOsteocalcinRUNX2 protein, humanTWIST1 protein, humanTwist-Related Protein 1

Identifiers

PMID25382306
PMCPMC4238757
OpenAlexW2123366057

What OpenQuestion holds

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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.