Evidence map›Paper›PMID 36672268›Full record

ArticleCells2023

Synovial Fluid Derived from Human Knee Osteoarthritis Increases the Viability of Human Adipose-Derived Stem Cells through Upregulation of FOSL1.

Hironori Kitajima, Takuya Sakamoto, Tetsuhiro Horie, Ayane Kuwano, Atsushi Fuku, Yasuhiko Taki, Yuka Nakamura, Ikuhiro Tanida, Hiroshi Sunami, Hiroaki Hirata and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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

21 authors at 4 institutions in 1 country.

Hironori KitajimaDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0002-5285-9429
Takuya SakamotoMedical Research Institute, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0003-2519-4510
Tetsuhiro HorieMedical Research Institute, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0002-2095-9425
Ayane KuwanoGenome Biotechnology Laboratory, Kanazawa Institute of Technology, Hakusan 924-0838, Ishikawa, Japan.
Atsushi FukuDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0001-7229-4974
Yasuhiko TakiDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Yuka NakamuraMedical Research Institute, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Ikuhiro TanidaGenome Biotechnology Laboratory, Kanazawa Institute of Technology, Hakusan 924-0838, Ishikawa, Japan.
Hiroshi SunamiFaculty of Medicine, Advanced Medical Research Center, University of the Ryukyus, Nakagami 903-0215, Okinawa, Japan.
Hiroaki HirataDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Yoshiyuki TachiDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Naoki YamamotoSupport Office for Bioresource Research, Research Promotion Headquarters, Fujita Health University, Toyoake 470-1192, Aichi, Japan.ORCID 0000-0002-9659-3204
Yasuo IidaDepartment of Mathematics, Division of General Education, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Yasuhito IshigakiMedical Research Institute, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0003-1012-8430
Sohsuke YamadaCenter for Regenerative Medicine, Kanazawa Medical University Hospital, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0003-2662-0024
Shigetaka ShimodairaCenter for Regenerative Medicine, Kanazawa Medical University Hospital, Kahoku 920-0293, Ishikawa, Japan.ORCID 0000-0002-6612-6912
Yusuke ShimizuDepartment of Plastic and Reconstructive Surgery, Graduate School of Medicine, University of the Ryukyus, Nakagami 903-0215, Okinawa, Japan.ORCID 0000-0002-2528-2003
Toru IchisekiDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Ayumi KaneujiDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Satoshi OsawaGenome Biotechnology Laboratory, Kanazawa Institute of Technology, Hakusan 924-0838, Ishikawa, Japan.
Norio KawaharaDepartment of Orthopedic Surgery, Kanazawa Medical University, Kahoku 920-0293, Ishikawa, Japan.
Kanazawa Medical University · JPKanazawa Institute of Technology · JPUniversity of the Ryukyus · JPFujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knee osteoarthritis (Knee OA) is an irreversible condition that causes bone deformity and degeneration of the articular cartilage that comprises the joints, resulting in chronic pain and movement disorders. The administration of cultured adipose-derived stem cells (ADSCs) into the knee joint cavity improves the clinical symptoms of Knee OA; however, the effect of synovial fluid (SF) filling the joint cavity on the injected ADSCs remains unclear. In this study, we investigated the effect of adding SF from Knee OA patients to cultured ADSCs prepared for therapeutic use in an environment that mimics the joint cavity. An increase in the viability of ADSCs was observed following the addition of SF. Gene expression profiling of SF-treated ADSCs using DNA microarrays revealed changes in several genes involved in cell survival. Of these genes, we focused on FOSL1, which is involved in the therapeutic effect of ADSCs and the survival and proliferation of cancer stem cells. We confirmed the upregulation of FOSL1 mRNA and protein expression using RT-PCR and western blot analysis, respectively. Next, we knocked down FOSL1 in ADSCs using siRNA and observed a decrease in cell viability, indicating the involvement of FOSL1 in the survival of ADSCs. Interestingly, in the knockdown cells, ADSC viability was also decreased by SF exposure. These results suggest that SF enhances cell viability by upregulating FOSL1 expression in ADSCs. For therapy using cultured ADSCs, the therapeutic effect of ADSCs may be further enhanced if an environment more conducive to the upregulation of FOSL1 expression in ADSCs can be established.

Indexed as

Osteoarthritis, KneeFos-Related Antigen 1HumansKnee JointStem CellsSynovial FluidUp-RegulationFos-Related Antigen 1FOSL1human adipose-derived stem cellhuman knee osteoarthritissynovial fluid

Identifiers

PMID36672268
PMCPMC9856741
OpenAlexW4316466124

What OpenQuestion holds

Textmetadata
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.