Evidence map›Paper›PMID 9861004›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

A potential role for the nuclear factor of activated T cells family of transcriptional regulatory proteins in adipogenesis.

I C Ho, J H Kim, J W Rooney, B M Spiegelman, L H Glimcher

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 120 citations in OpenAlex.

  1. Article
  2. Article
  3. Unlocking the therapeutic potential of the NFAT pathway in kidney diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  4. STIM2β is a CaThe FEBS journal · 2025
    Article
  5. Article
  6. Article
  7. Aging and obesity prime the methylome and transcriptome of adipose stem cells for disease and dysfunction.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  8. Article
  9. Regulatory role of NFAT1 signaling in articular chondrocyte activities and osteoarthritis pathogenesis.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2023
    Article
  10. Article
  11. Article
  12. Lack of adipocyte purinergic P2YProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. p38β and Cancer: The Beginning of the Road.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Article
  16. Post-Liver Transplantation Diabetes Mellitus: A Review of Relevance and Approach to Treatment.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2018
    Review
  17. Article
  18. Review
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

I C HoDepartment of Immunology and Infectious Diseases, Harvard School of Public Health, 651 Huntington Avenue, Boston, MA 02115, USA.
J H Kim
J W Rooney
B M Spiegelman
L H Glimcher
Columbia University · USDana-Farber Cancer Institute · US

Funding

T CELL RECEPTOR COUPLED SIGNALING AND APOPTOSISP01AI037833 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 1995 to 1998
–
NIAID NIH HHS AI/AG37833
6 · The paper itself

Abstract

NFAT (nuclear factor of activated T cells) is a family of transcription factors implicated in the control of cytokine and early immune response gene expression. Recent studies have pointed to a role for NFAT proteins in gene regulation outside of the immune system. Herein we demonstrate that NFAT proteins are present in 3T3-L1 adipocytes and, upon fat cell differentiation, bind to and transactivate the promoter of the adipocyte-specific gene aP2. Further, fat cell differentiation is inhibited by cyclosporin A, a drug shown to prevent NFAT nuclear localization and hence function. Thus, these data suggest a role for NFAT transcription factors in the regulation of the aP2 gene and in the process of adipocyte differentiation.

Indexed as

Cell DifferentiationLymphocyte Activation3T3 CellsAdipocytesAnimalsChloramphenicol O-AcetyltransferaseCyclosporineDNA-Binding ProteinsMiceNFATC Transcription FactorsNuclear ProteinsPromoter Regions, GeneticRecombinant ProteinsT-LymphocytesTranscription FactorsTransfectionChloramphenicol O-AcetyltransferaseCyclosporineDNA-Binding ProteinsNFATC Transcription FactorsNuclear ProteinsRecombinant ProteinsTranscription Factors

Identifiers

PMID9861004
PMCPMC28078
OpenAlexW2121270780

What OpenQuestion holds

Textmetadata
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.