Evidence map›Paper›PMID 27322256›Full record

ArticleInternational journal of molecular sciences2016

Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells.

Yoshie Arai, Sunghyun Park, Bogyu Choi, Kyoung-Won Ko, Won Chul Choi, Joong-Myung Lee, Dong-Wook Han, Hun-Kuk Park, Inbo Han, Jong Hun Lee and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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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

11 authors.

Yoshie AraiDepartment of Biomedical Science, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. ruddov@gmail.com.
Sunghyun ParkDepartment of Biomedical Science, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. nightsky9836@naver.com.
Bogyu ChoiDepartment of Biomedical Science, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. bgchoi725@gmail.com.
Kyoung-Won KoDepartment of Biomedical Science, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. glintk@naver.com.
Won Chul ChoiDepartment of Orthopedic Surgery, Bundang Medical Center, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. wcosdoc@gmail.com.
Joong-Myung LeeDepartment of Orthopedic Surgery, Bundang Medical Center, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. drjmlee@naver.com.
Dong-Wook HanDepartment of Optics and Mechatronics Engineering, BK21+ Nano-Integrated Cogno-Mechatronics Engineering, College of Nanoscience & Nanotechnology, Pusan National University, Busan 619-961, Korea. nanohan@pusan.ac.kr.
Hun-Kuk ParkDepartment of Biomedical Engineering, Collage of Medicine, Kyung Hee University, Seoul 151-742, Korea. sigmoidus@khu.ac.kr.
Inbo HanDepartment of Neurosurgery, Bundang Medical Center, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. hanib@cha.ac.kr.
Jong Hun LeeDepartment of Food Science and Biotechnology, College of Life Science, CHA University, Gyeonggi-do 443-742, Korea. mushroom14@gmail.com.
Soo-Hong LeeDepartment of Biomedical Science, CHA University, Seongnam-si, Gyeonggi-do 443-742, Korea. soohong@cha.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human adipose-derived stem cells (hASCs) have a capacity to undergo adipogenic, chondrogenic, and osteogenic differentiation. Recently, hASCs were applied to various fields including cell therapy for tissue regeneration. However, it is hard to predict the direction of differentiation of hASCs in real-time. Matrix metalloproteinases (MMPs) are one family of proteolytic enzymes that plays a pivotal role in regulating the biology of stem cells. MMPs secreted by hASCs are expected to show different expression patterns depending on the differentiation state of hASCs because biological functions exhibit different patterns during the differentiation of stem cells. Here, we investigated proteolytic enzyme activity, especially MMP-2 activity, in hASCs during their differentiation. The activities of proteolytic enzymes and MMP-2 were higher during chondrogenic differentiation than during adipogenic and osteogenic differentiation. During chondrogenic differentiation, mRNA expression of MMP-2 and the level of the active form of MMP-2 were increased, which also correlated with Col II. It is concluded that proteolytic enzyme activity and the level of the active form of MMP-2 were increased during chondrogenic differentiation, which was accelerated in the presence of Col II protein. According to our findings, MMP-2 could be a candidate maker for real-time detection of chondrogenic differentiation of hASCs.

Indexed as

Cell DifferentiationAdipose TissueBiomarkersCells, CulturedChondrocytesHumansMatrix Metalloproteinase 2Mesenchymal Stem CellsBiomarkersMatrix Metalloproteinase 2MMP2 protein, humanchondrogenic differentiationextracellular matrixhuman adipose-derived stem cellsmatrix metalloproteinase-2

Identifiers

PMID27322256
PMCPMC4926495

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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.