Evidence map›Paper›PMID 29757956›Full record

ArticleInternational journal of molecular sciences2018

Osteogenic Differentiation Modulates the Cytokine, Chemokine, and Growth Factor Profile of ASCs and SHED.

Federico Mussano, Tullio Genova, Sara Petrillo, Ilaria Roato, Riccardo Ferracini, Luca Munaron

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

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  18. Fibroblast Interaction with Different Abutment Surfaces: In Vitro Study.International journal of molecular sciences · 2020
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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

6 authors.

Federico MussanoCIR Dental School, Department of Surgical Sciences UNITO, via Nizza 230, 10126 Turin, Italy. federico.mussano@unito.it.ORCID 0000-0001-5800-0749
Tullio GenovaCIR Dental School, Department of Surgical Sciences UNITO, via Nizza 230, 10126 Turin, Italy. tullio.genova@unito.it.ORCID 0000-0001-7824-8389
Sara PetrilloDepartment of Molecular Biotechnology and Health Sciences, UNITO, Via Nizza 52, 10126 Turin, Italy. sara.petrillo@unito.it.
Ilaria RoatoCenter for Research and Medical Studies, A.O.U. Città della Salute e della Scienza, 10126 Turin, Italy. roato78@libero.it.ORCID 0000-0003-3029-4743
Riccardo FerraciniDepartment of Surgical Sciences (DISC), Orthopaedic Clinic-IRCCS A.O.U. San Martino, 16132 Genoa, Italy. riccardoferraciniweb@gmail.com.
Luca MunaronDepartment of Life Sciences and Systems Biology, UNITO, via Accademia Albertina 13, 10123 Turin, Italy. luca.munaron@unito.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Great efforts have been made to improve bone regeneration techniques owing to a growing variety of sources of stem cells suitable for autologous transplants. Specifically, adipose-derived stem cells (ASCs) and stems cells from human exfoliated deciduous teeth (SHED) hold great potential for bone tissue engineering and cell therapy. After a preliminary characterization of the main biomolecules ASCs and SHED released in their conditioned media, cells were kept both in normal and osteo-inducing conditions. Conventional assays were performed to prove their osteogenic potential such as quantitative real-time polymerase chain reaction (qRT-PCR) (for RUNX-2, collagen type I, osteopontin and osteonectin), alkaline phosphatase activity, osteocalcin production, and von Kossa staining. Conditioned media were tested again after the osteogenic induction and compared to maintaining condition both at base line and after 14 days of culture. The osteogenic condition inhibited the release of all the biomolecules, with the exception, concerning SHED, of growth-regulated alpha protein precursor (GROα), and, to a lesser extent, interleukin (IL)-8. In conclusion, our data support that undifferentiated ASCs and SHED may be preferable to committed ones for general cell therapy approaches, due to their higher paracrine activity. Osteoinduction significantly affects the cytokine, chemokine, and growth factor profile in a differential way, as SHED kept a more pronounced pro-angiogenic signature than ASCs.

Indexed as

Cell DifferentiationOsteogenesisAdipocytesAdipose TissueBiomarkersCells, CulturedCell SurvivalCytokinesHumansImmunophenotypingMesenchymal Stem CellsPhenotypeStem CellsTooth, DeciduousBiomarkersCytokinesadipose-derived stem cells (ASCs)Bio-Plexmesenchymal stem cells (MSCs)stem cells from human exfoliated deciduous teeth (SHED)

Identifiers

PMID29757956
PMCPMC5983594

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Registered trials

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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.