Evidence map›Paper›PMID 24957638›Full record

ArticleTissue engineering. Part C, Methods2015

BMP-2, hypoxia, and COL1A1/HtrA1 siRNAs favor neo-cartilage hyaline matrix formation in chondrocytes.

David Ollitrault, Florence Legendre, Carole Drougard, Mélanie Briand, Hervé Benateau, Didier Goux, Hanane Chajra, Laurent Poulain, Daniel Hartmann, Denis Vivien and 6 more

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

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  12. Strategies to Modulate the Redifferentiation of Chondrocytes.Frontiers in bioengineering and biotechnology · 2021
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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

16 authors at 6 institutions in 3 countries.

David Ollitrault1 Microenvironnement Cellulaire et Pathologies Laboratory (MILPAT) EA 4652, Federative Research Structure (FRS) 146 ICORE, Faculty of Medicine, IBFA, University of Caen/Lower-Normandy (UCLN) , Caen, France .
Florence Legendre
Carole Drougard
Mélanie Briand
Hervé Benateau
Didier Goux
Hanane Chajra
Laurent Poulain
Daniel Hartmann
Denis Vivien
Vijayalakshmi Shridhar
Alfonso Baldi
Frédéric Mallein-Gerin
Karim Boumediene
Magali Demoor
Philippe Galera
Université de Caen Normandie · FRUniversité Claude Bernard Lyon 1 · FRInserm · FRMayo Clinic · USNaples Anesthesia & Physician Associates · USSymatese (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is an irreversible pathology that causes a decrease in articular cartilage thickness, leading finally to the complete degradation of the affected joint. The low spontaneous repair capacity of cartilage prevents any restoration of the joint surface, making OA a major public health issue. Here, we developed an innovative combination of treatment conditions to improve the human chondrocyte phenotype before autologous chondrocyte implantation. First, we seeded human dedifferentiated chondrocytes into a collagen sponge as a scaffold, cultured them in hypoxia in the presence of a bone morphogenetic protein (BMP), BMP-2, and transfected them with small interfering RNAs targeting two markers overexpressed in OA dedifferentiated chondrocytes, that is, type I collagen and/or HtrA1 serine protease. This strategy significantly decreased mRNA and protein expression of type I collagen and HtrA1, and led to an improvement in the chondrocyte phenotype index of differentiation. The effectiveness of our in vitro culture process was also demonstrated in the nude mouse model in vivo after subcutaneous implantation. We, thus, provide here a new protocol able to favor human hyaline chondrocyte phenotype in primarily dedifferentiated cells, both in vitro and in vivo. Our study also offers an innovative strategy for chondrocyte redifferentiation and opens new opportunities for developing therapeutic targets.

Indexed as

AgedAged, 80 and overAnimalsBone Morphogenetic Protein 2Cartilage, ArticularCattleCell HypoxiaCells, CulturedChondrocytesChondrogenesisCollagen Type ICollagen Type I, alpha 1 ChainExtracellular MatrixHigh-Temperature Requirement A Serine Peptidase 1HumansHyalinBone Morphogenetic Protein 2Collagen Type ICollagen Type I, alpha 1 ChainHigh-Temperature Requirement A Serine Peptidase 1HTRA1 protein, humanRNA, MessengerRNA, Small InterferingSerine Endopeptidases

Identifiers

PMID24957638
PMCPMC4313417
OpenAlexW2331733892

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.