Evidence map›Paper›PMID 26191331›Full record

ArticleInternational journal of clinical and experimental pathology2015

CaMKII plays a part in the chondrogenesis of bone marrow-derived mesenchymal stem cells.

Feng Qu, Zhikun Zhao, Bangtuo Yuan, Wei Qi, Chunbao Li, Xuezhen Shen, Chang Liu, Hongliang Li, Gang Zhao, Jiangtao Wang and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 99% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. CaIn vivo (Athens, Greece)
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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

12 authors at 2 institutions in 1 country.

Feng QuDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Zhikun ZhaoDepartment of Orthopedics, The First Affiliated Hospital of Chinese PLA General Hospital 51 Fucheng Road, Haidian District, Beijing 100048, China.
Bangtuo YuanDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Wei QiDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Chunbao LiDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Xuezhen ShenDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Chang LiuDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Hongliang LiDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Gang ZhaoDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Jiangtao WangDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Qi GuoDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Yujie LiuDepartment of Orthopedics, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.
Chinese PLA General Hospital · CNFirst Affiliated Hospital of Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe purpose of the study is to observe the functions of calcium/calmodulin dependent protein kinase II (CaMKII) in the induced chondrogenic differentiation of bone marrow derived mesenchymal stem cells (BMSCs).

methodsBMSCs was in vitro isolated and cultured for induced chondrogenesis. Western blot was used to ascertain the expression of CaMKII and phosphorylated CaMKII (PCaMKII, activatory CaMKII) in chondrogenic induced BMSCs. MTT method was utilized to observe the impact of CaMKII on the proliferation of BMSCs. The generation of cartilage matrix in BMSCs cells was detected by toluidine blue staining. The levels of cartilage marker genes COL2A1, Aggrecan and SOX9 in BMSCs were gained by real-time fluorescence quantitative polymerase chain reaction (RT-QPCR). Finally, BMSCs proliferation, cartilage matrix generation and the changes of COL2A1, Aggrecan and SOX9 were surveyed after CaMKII being blocked by CaMKII inhibitor KN93.

resultsExpression of CaMKII and PCaMKII could be found in chondrogenic induced BMSCs. CaMKII had no significant influence on BMSCs proliferation, but the toluidine blue staining was obviously lighter, indicating a significant decline in the expression of COL2A1, Aggrecan and SOX9.

conclusionAs one of the factors influencing the chondrogenic capacity of BMSCs, CaMKII does not impact on BMSCs proliferation, but it can inhibit the chondrogenic ability of BMSCs by influencing its differentiation.

Indexed as

ChondrogenesisAggrecansAnimalsBone Marrow CellsCalcium-Calmodulin-Dependent Protein Kinase Type 2Cell DifferentiationCell ProliferationCells, CulturedChondrocytesCollagen Type IIGene Expression RegulationMesenchymal Stem CellsPhosphorylationProtein Kinase InhibitorsRatsSignal TransductionAggrecansCalcium-Calmodulin-Dependent Protein Kinase Type 2Col2a1 protein, mouseCollagen Type IIProtein Kinase InhibitorsSOX9 protein, humanSOX9 Transcription Factorbone marrow derived mesenchymal stem cells (BMSCs)CaMKIIchondrogenesis

Identifiers

PMID26191331
PMCPMC4503202
OpenAlexW1011576907

What OpenQuestion holds

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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.