Evidence map›Paper›PMID 30384862›Full record

ArticleBiological research2018

Priming stem cells with protein kinase C activator enhances early stem cell-chondrocyte interaction by increasing adhesion molecules.

Dong-Sik Chae, Chang Youn Lee, Jiyun Lee, Hyang-Hee Seo, Chong-Hyuk Choi, Seahyoung Lee, Ki-Chul Hwang

Abstract read
In one paragraph

Article in Biological research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Article
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  5. Low Molecular Weight Sericin Enhances theFrontiers in bioengineering and biotechnology · 2022
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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.

Dong-Sik ChaeDepartment of Medicine, The Graduate School, Yonsei University, Seoul, South Korea.
Chang Youn LeeDepartment of Integrated Omics for Biomedical Sciences, Yonsei University, Seoul, South Korea.
Jiyun LeeBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, South Korea.
Hyang-Hee SeoBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, South Korea.
Chong-Hyuk ChoiDepartment of Orthopedic Surgery, Yonsei University College of Medicine, 50, Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.
Seahyoung LeeInstitute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung-si, Gangwon-do, South Korea. sam1017@ish.ac.kr.
Ki-Chul HwangInstitute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung-si, Gangwon-do, South Korea. kchwang@cku.ac.kr.

Funding

Catholic Kwandong University International St. Mary's Hospital CKURF-201406820001Korea Ministry of Science, ICT and Future Planning NFR-2015M3A9E6029407Korea Ministry of Science, ICT and Future Planning NRF-2015M3A9E6029519Ministry of Health and Welfare HI18C0661010018Ministry of Health and Welfare HI18C0661020018
6 · The paper itself

Abstract

backgroundOsteoarthritis (OA) can be defined as degradation of articular cartilage of the joint, and is the most common degenerative disease. To regenerate the damaged cartilage, different experimental approaches including stem cell therapy have been tried. One of the major limitations of stem cell therapy is the poor post-transplantation survival of the stem cells. Anoikis, where insufficient matrix support and adhesion to extracellular matrix causes apoptotic cell death, is one of the main causes of the low post-transplantation survival rate of stem cells. Therefore, enhancing the initial interaction of the transplanted stem cells with chondrocytes could improve the therapeutic efficacy of stem cell therapy for OA. Previously, protein kinase C activator phorbol 12-myristate 13-acetate (PMA)-induced increase of mesenchymal stem cell adhesion via activation of focal adhesion kinase (FAK) has been reported. In the present study, we examine the effect PMA on the adipose-derived stem cells (ADSCs) adhesion and spreading to culture substrates, and further on the initial interaction between ADSC and chondrocytes.

resultsPMA treatment increased the initial adhesion of ADSC to culture substrate and cellular spreading with increased expression of adhesion molecules, such as FAK, vinculin, talin, and paxillin, at both RNA and protein level. Priming of ADSC with PMA increased the number of ADSCs attached to confluent layer of cultured chondrocytes compared to that of untreated ADSCs at early time point (4 h after seeding).

conclusionTaken together, the results of this study suggest that priming ADSCs with PMA can increase the initial interaction with chondrocytes, and this proof of concept can be used to develop a non-invasive therapeutic approach for treating OA. It may also accelerate the regeneration process so that it can relieve the accompanied pain faster in OA patients. Further in vivo studies examining the therapeutic effect of PMA pretreatment of ADSCs for articular cartilage damage are required.

Indexed as

Blotting, WesternCartilage, ArticularCell AdhesionCell CommunicationCell Culture TechniquesCell DifferentiationCell SurvivalChondrocytesHumansProtein Kinase CReverse Transcriptase Polymerase Chain ReactionStem CellsProtein Kinase CADSCCellular adhesionChondrocyteOsteoarthritisPMA

Identifiers

PMID30384862
PMCPMC6211543

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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.