Evidence map›Paper›PMID 33255398›Full record

ArticleInternational journal of molecular sciences2020

Matrilin-3-Primed Adipose-Derived Mesenchymal Stromal Cell Spheroids Prevent Mesenchymal Stromal-Cell-Derived Chondrocyte Hypertrophy.

Manjunatha S Muttigi, Byoung Ju Kim, Bogyu Choi, Inbo Han, Hansoo Park, Soo-Hong Lee

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  7. Genetic Therapy for Intervertebral Disc Degeneration.International journal of molecular sciences · 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

6 authors at 4 institutions in 1 country.

Manjunatha S MuttigiSchool of Integrative Engineering, Chung-Ang University, Seoul 06911, Korea.
Byoung Ju KimDepartment of Medical Biotechnology, Dongguk University-Seoul, Seoul 04620, Korea.
Bogyu ChoiDepartment of Biomedical Science, CHA University, 335 Pangyo-ro, Bundang-gu, 13488 Seongnam, Korea.
Inbo HanDepartment of Neurosurgery, CHA Bundang Medical Center, CHA University, Seongnam-si 13496, Korea.ORCID 0000-0002-0834-9325
Hansoo ParkSchool of Integrative Engineering, Chung-Ang University, Seoul 06911, Korea.
Soo-Hong LeeDepartment of Medical Biotechnology, Dongguk University-Seoul, Seoul 04620, Korea.
Chung-Ang University · KRDongguk University · KRCHA University · KRCHA University Bundang Medical Center · KR

Funding

Dongguk University Research Fund 2018Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) HI16C0106National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) 2019R1C1C1008479Research of Korea Centers for Disease Control and Prevention 2018ER610300
6 · The paper itself

Abstract

Adipose-derived mesenchymal stromal cells (Ad-MSCs) are a promising tool for articular cartilage repair and regeneration. However, the terminal hypertrophic differentiation of Ad-MSC-derived cartilage is a critical barrier during hyaline cartilage regeneration. In this study, we investigated the role of matrilin-3 in preventing Ad-MSC-derived chondrocyte hypertrophy in vitro and in an osteoarthritis (OA) destabilization of the medial meniscus (DMM) model. Methacrylated hyaluron (MAHA) (1%) was used to encapsulate and make scaffolds containing Ad-MSCs and matrilin-3. Subsequently, the encapsulated cells in the scaffolds were differentiated in chondrogenic medium (TGF-β, 1-14 days) and thyroid hormone hypertrophic medium (T3, 15-28 days). The presence of matrilin-3 with Ad-MSCs in the MAHA scaffold significantly increased the chondrogenic marker and decreased the hypertrophy marker mRNA and protein expression. Furthermore, matrilin-3 significantly modified the expression of TGF-β2, BMP-2, and BMP-4. Next, we prepared the OA model and transplanted Ad-MSCs primed with matrilin-3, either as a single-cell suspension or in spheroid form. Safranin-O staining and the OA score suggested that the regenerated cartilage morphology in the matrilin-3-primed Ad-MSC spheroids was similar to the positive control. Furthermore, matrilin-3-primed Ad-MSC spheroids prevented subchondral bone sclerosis in the mouse model. Here, we show that matrilin-3 plays a major role in modulating Ad-MSCs' therapeutic effect on cartilage regeneration and hypertrophy suppression.

Indexed as

AnimalsBone Morphogenetic Protein 2Cell DifferentiationCell ProliferationChondrocytesChondrogenesisHumansHyaline CartilageHyaluronic AcidHypertrophyMatrilin ProteinsMesenchymal Stem CellsMiceOsteoarthritisRegenerationSpheroids, CellularBMP2 protein, humanBone Morphogenetic Protein 2Hyaluronic AcidMatrilin ProteinsTransforming Growth Factor betaadipose-derived mesenchymal stromal cellcell spheroidsdestabilization of the medial meniscus (DMM)hypertrophyosteoarthritis

Identifiers

PMID33255398
PMCPMC7727796
OpenAlexW3107958364

What OpenQuestion holds

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LicenceCC BY
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.