Evidence map›Paper›PMID 39209927›Full record

ArticleScientific reports2024

Polypeptide N-acetylgalactosaminyltransferase-15 regulates adipogenesis in human SGBS cells.

Asuka Takahashi, Ryo Koike, Shota Watanabe, Kyoko Kuribayashi, Martin Wabitsch, Masahiko Miyamoto, Akihiko Komuro, Mineaki Seki, Masayuki Nashimoto, Akiko Shimizu-Ibuka and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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.

Asuka TakahashiDepartment of Functional Morphology, Graduate School of Pharmaceutical Sciences, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan.
Ryo KoikeDepartment of Functional Morphology, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Medical and Life Sciences, 265-1 Higashijima, Akiha-ku, Niigata, 956-8603, Japan.
Shota WatanabeDepartment of Functional Morphology, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Medical and Life Sciences, 265-1 Higashijima, Akiha-ku, Niigata, 956-8603, Japan.
Kyoko KuribayashiDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Tōon, 791-0295, Japan.
Martin WabitschDivision of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, 89075, Ulm, Germany.
Masahiko MiyamotoDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan.
Akihiko KomuroDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan.
Mineaki SekiDivision of DNA Repair and Genome Integrity, Faculty of Medical Technology, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan.
Masayuki NashimotoRNA Therapeutics Division, Faculty of Medical Technology, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan.
Akiko Shimizu-IbukaGraduate School of Science, Kanagawa University, Yokohama, 221-8686, Japan.
Kikuji YamashitaDivision of Anatomy and Histology, Faculty of Medical Technology, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan.
Takeo IwataDepartment of Functional Morphology, Graduate School of Pharmaceutical Sciences, Niigata University of Pharmacy and Medical and Life Sciences, Niigata, 956-8603, Japan. iwata@nupals.ac.jp.

Funding

Japan Society for the Promotion of Science 22K06589
6 · The paper itself

Abstract

Adipogenesis involves intricate molecular mechanisms regulated by various transcription factors and signaling pathways. In this study, we aimed to identify factors specifically induced during adipogenesis in the human preadipocyte cell line, SGBS, but not in the mouse preadipocyte cell line, 3T3-L1. Microarray analysis revealed distinct gene expression profiles, with 1460 genes induced in SGBS cells and 1297 genes induced in 3T3-L1 cells during adipogenesis, with only 297 genes commonly induced. Among the genes uniquely induced in SGBS cells, we focused on GALNT15, which encodes polypeptide N-acetylgalactosaminyltransferase-15. Its expression increased transiently during adipogenesis in SGBS cells but remained low in 3T3-L1 cells. Overexpression of GALNT15 increased mRNA levels of CCAAT-enhancer binding protein (C/EBPα) and leptin but had no significant impact on adipogenesis in SGBS cells. Conversely, knockdown of GALNT15 suppressed mRNA expression of adipocyte marker genes, reduced lipid accumulation, and decreased the percentage of cells with oil droplets. The induction of C/EBPα and peroxisome proliferator-activated receptor γ during adipogenesis was promoted or suppressed in SGBS cells subjected to overexpression or knockdown of GALNT15, respectively. These data suggest that polypeptide N-acetylgalactosaminyltransferase-15 is a novel regulatory molecule that enhances adipogenesis in SGBS cells.

Indexed as

3T3-L1 CellsAdipogenesisN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferaseAdipocytesAnimalsCCAAT-Enhancer-Binding ProteinsCell LineHumansLeptinMicePPAR gammaCCAAT-Enhancer-Binding ProteinsLeptinN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferasePPAR gammaAdipocytesAdipogenesisGALNT15Polypeptide N-acetylgalactosaminyltransferasePreadipocytes

Identifiers

PMID39209927
PMCPMC11362553

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.