Evidence map›Paper›PMID 25075860›Full record

ArticlePloS one2014

Analysis of transcription factor network underlying 3T3-L1 adipocyte differentiation.

KyungOh Choi, Bassel Ghaddar, Colby Moya, Hai Shi, Gautham V Sridharan, Kyongbum Lee, Arul Jayaraman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Antioxidant and lipid-reducing effects ofFood science and biotechnology · 2022
    Article
  5. Torreya nucifera seed oil improves 3T3-L1 adipocyte differentiation.BMC complementary medicine and therapies · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Long-chain bases fromFood science and biotechnology · 2016
    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

7 authors at 2 institutions in 1 country.

KyungOh ChoiDepartment of Chemical Engineering, Texas A&M University, College Station, Texas, United States of America.
Bassel GhaddarDepartment of Chemical and Biological Engineering, Tufts University, Medford, Massachusetts, United States of America.
Colby MoyaDepartment of Chemical Engineering, Texas A&M University, College Station, Texas, United States of America.
Hai ShiDepartment of Chemical and Biological Engineering, Tufts University, Medford, Massachusetts, United States of America.
Gautham V SridharanDepartment of Chemical and Biological Engineering, Tufts University, Medford, Massachusetts, United States of America.
Kyongbum LeeDepartment of Chemical and Biological Engineering, Tufts University, Medford, Massachusetts, United States of America.
Arul JayaramanDepartment of Chemical Engineering, Texas A&M University, College Station, Texas, United States of America.
Tufts University · USTexas A&M University · US

Funding

Phenotype-Targeted Inference of Flux-Enzyme Correlations in Adipocyte MetabolismR56DK081768 · NIDDK · TUFTS UNIVERSITY MEDFORD · PI LEE, KYONGBUM · 2010 to 2011
$489k
NIDDK NIH HHS 1R56DK081768NIDDK NIH HHS R56 DK081768
6 · The paper itself

Abstract

Lipid accumulation in adipocytes reflects a balance between enzymatic pathways leading to the formation and breakdown of esterified lipids, primarily triglycerides. This balance is extremely important, as both high and low lipid levels in adipocytes can have deleterious consequences. The enzymes responsible for lipid synthesis and breakdown (lipogenesis and lipolysis, respectively) are regulated through the coordinated actions of several transcription factors (TFs). In this study, we examined the dynamics of several key transcription factors (TFs) - PPARγ, C/EBPβ, CREB, NFAT, FoxO1, and SREBP-1c - during adipogenic differentiation (week 1) and ensuing lipid accumulation. The activation profiles of these TFs at different times following induction of adipogenic differentiation were quantified using 3T3-L1 reporter cell lines constructed to secrete the Gaussia luciferase enzyme upon binding of a TF to its DNA binding element. The dynamics of the TFs was also modeled using a combination of logical gates and ordinary differential equations, where the logical gates were used to explore different combinations of activating inputs for PPARγ, C/EBPβ, and SREBP-1c. Comparisons of the experimental profiles and model simulations suggest that SREBP-1c could be independently activated by either insulin or PPARγ, whereas PPARγ activation required both C/EBPβ as well as a putative ligand. Parameter estimation and sensitivity analysis indicate that feedback activation of SREBP-1c by PPARγ is negligible in comparison to activation of SREBP-1c by insulin. On the other hand, the production of an activating ligand could quantitatively contribute to a sustained elevation in PPARγ activity.

Indexed as

Adipogenesis3T3 CellsAdipocytesAnimalsMiceTranscription FactorsTranscription Factors

Identifiers

PMID25075860
PMCPMC4116336
OpenAlexW1987355713

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.