Evidence map›Paper›PMID 24876859›Full record

ArticleKorean circulation journal2014

Angiopoietin-like 4 is involved in the poor angiogenic potential of high glucose-insulted bone marrow stem cells.

Yong Sook Kim, Hea Jin Kang, Moon Hwa Hong, Wan Seok Kang, Nakwon Choe, Hyun Kook, Myung Ho Jeong, Youngkeun Ahn

Open access · hybridAbstract read
In one paragraph

Article in Korean circulation journal, 2014. 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
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

6 citing papers in PubMed, 14 citations in OpenAlex.

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  6. Cellular & molecular biology letters · 2016
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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

8 authors at 2 institutions in 1 country.

Yong Sook KimResearch Laboratory of Cardiovascular Regeneration, Chonnam National University Hospital, Gwangju, Korea. ; Cardiovascular Convergence Research Center, Chonnam National University Hospital, Gwangju, Korea.
Hea Jin KangResearch Laboratory of Cardiovascular Regeneration, Chonnam National University Hospital, Gwangju, Korea. ; Center for Molecular Medicine, Graduate School, Chonnam National University, Gwangju, Korea.
Moon Hwa HongResearch Laboratory of Cardiovascular Regeneration, Chonnam National University Hospital, Gwangju, Korea.
Wan Seok KangResearch Laboratory of Cardiovascular Regeneration, Chonnam National University Hospital, Gwangju, Korea. ; Center for Molecular Medicine, Graduate School, Chonnam National University, Gwangju, Korea.
Nakwon ChoeDepartment of Pharmacology and Medical Research Center for Gene Regulation, Chonnam National University Medical School, Gwangju, Korea.
Hyun KookDepartment of Pharmacology and Medical Research Center for Gene Regulation, Chonnam National University Medical School, Gwangju, Korea.
Myung Ho JeongCardiovascular Convergence Research Center, Chonnam National University Hospital, Gwangju, Korea. ; Department of Cardiology, Chonnam National University Hospital, Gwangju, Korea.
Youngkeun AhnResearch Laboratory of Cardiovascular Regeneration, Chonnam National University Hospital, Gwangju, Korea. ; Cardiovascular Convergence Research Center, Chonnam National University Hospital, Gwangju, Korea. ; Department of Cardiology, Chonnam National University Hospital, Gwangju, Korea.
Chonnam National University Hospital · KRChonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesDiabetes is reported to reduce the function or number of progenitor cells. We compared the gene expression patterns of bone marrow-derived mesenchymal stem cells from diabetic (DM-BMCs) and healthy (non-DM-BMCs) rats and suggested Angiopoietin-like 4 (Angptl4) could be a responsible factor for impaired angiogenesis of DM-BMCs. SUBJECTS AND

methodsBMCs were isolated from DM or non-DM rat, and in vitro angiogenesis activity was compared by tube formation assay on Matrigel and complementary deoxyribonucleic acid expression was analyzed by microarray with or without oxytocin treatment. Human BMCs (hBMCs) were treated with high glucose, and were performed polymerase chain reaction, Western blot, and enzyme-linked immunosorbent assay. Angptl4 plasmid DNA and micro ribonucleic acid-132 (miR-132) were transfected to immortalized hBMCs.

resultsIn vitro angiogenesis assay showed the impaired tube formation in DM-BMCs, and slightly recovery by oxytocin treatment. Angptl4, an adipokine, was upregulated in DM-BMCs compared to non-DM-BMCs. Oxytocin treatment reduced Angptl4 in DM-BMCs. In hBMCs, overexpression of Angptl4 attenuated the tube formation. In addition to Angptl4, miR-132 was increased by high glucose treatment. Collectively, high glucose resulted in impaired tube formation through miR-132 induction and Angptl4 upregulation in BMCs.

conclusionOur results show that the angiogenic activity of BMCs is impaired by high glucose stress, which would be mediated by Angptl4 and miR-132.

Indexed as

ANGPTL4 protein, ratDiabetes mellitusMicroRNAsStem cells

Identifiers

PMID24876859
PMCPMC4037640
OpenAlexW2035888386

What OpenQuestion holds

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LicenceCC BY-NC
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.