Evidence map›Paper›PMID 30815352›Full record

ArticleTissue engineering and regenerative medicine2019

Induction of Chondrogenic Differentiation in Human Mesenchymal Stem Cells Cultured on Human Demineralized Bone Matrix Scaffold under Hydrostatic Pressure.

Saeid Reza Shahmoradi, Maryam Kabir Salmani, Hamid Reza Soleimanpour, Amir Hossein Tavakoli, Kazem Hosaini, Nooshin Haghighipour, Shahin Bonakdar

Open access · bronzeAbstract read
In one paragraph

Article in Tissue engineering and regenerative medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Saeid Reza Shahmoradi1Biomaterials and Tissue Engineering Department, Stem Cell Division, National Institute of Genetic Engineering and Biotechnology, Shahrak-e Pajoohesh, km 15, Tehran - Karaj Highway, Tehran, 1497716316 Iran.
Maryam Kabir Salmani1Biomaterials and Tissue Engineering Department, Stem Cell Division, National Institute of Genetic Engineering and Biotechnology, Shahrak-e Pajoohesh, km 15, Tehran - Karaj Highway, Tehran, 1497716316 Iran.
Hamid Reza Soleimanpour1Biomaterials and Tissue Engineering Department, Stem Cell Division, National Institute of Genetic Engineering and Biotechnology, Shahrak-e Pajoohesh, km 15, Tehran - Karaj Highway, Tehran, 1497716316 Iran.
Amir Hossein Tavakoli2Iranian Tissue Bank, Imam khomani Hospital, University of Medical Sciences, Keshavarz Blvd, Tehran, 1419733141 Iran.
Kazem Hosaini2Iranian Tissue Bank, Imam khomani Hospital, University of Medical Sciences, Keshavarz Blvd, Tehran, 1419733141 Iran.
Nooshin Haghighipour3National Cell Bank Department, Pasteur Institute of Iran (IPI), No. 69, Pasteur Ave, Tehran, 1316943551 Iran.
Shahin Bonakdar3National Cell Bank Department, Pasteur Institute of Iran (IPI), No. 69, Pasteur Ave, Tehran, 1316943551 Iran.ORCID 0000-0001-8759-3790
National Institute of Genetic Engineering and Biotechnology · IRImam Khomeini Hospital · IRPasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundArticular cartilage damage is still a troublesome problem. Hence, several researches have been performed for cartilage repair. The aim of this study was to evaluate the chondrogenicity of demineralized bone matrix (DBM) scaffolds under cyclic hydrostatic pressure (CHP)

methodsIn this study, CHP was applied to human bone marrow mesenchymal stem cells (hBMSCs) seeded on DBM scaffolds at a pressure of 5 MPa with a frequency of 0.5 Hz and 4 h per day for 1 week. Changes in chondrogenic and osteogenic gene expressions were analyzed by quantifying mRNA signal level of Sox9, collagen type I, collagen type II, aggrecan (ACAN), Osteocalcin, and Runx2. Histological analysis was carried out by hematoxylin and eosin, and Alcian blue staining. Moreover, DMMB and immunofluorescence staining were used for glycosaminoglycan (GAG) and collagen type II detection, respectively.

resultsReal-time PCR demonstrated that applying CHP to hBMSCs in DBM scaffolds increased mRNA levels by 1.3-fold, 1.2-fold, and 1.7-fold (

conclusionThe osteo-inductive DBM scaffolds showed chondrogenic characteristics under hydrostatic pressure. Our study can be a fundamental study for the use of DBM in articular cartilage defects GRAPHICAL ABSTRACT:

Indexed as

Bone marrow mesenchymal stem cellsChondrogenic differentiationDemineralized bone matrix scaffoldHydrostatic pressure

Identifiers

PMID30815352
PMCPMC6361102
OpenAlexW2901782010

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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.