Evidence map›Paper›PMID 31845180›Full record

ArticleEndocrine2020

Exogenous FABP4 interferes with differentiation, promotes lipolysis and inflammation in adipocytes.

Hui-Xia Dou, Ting Wang, Hai-Xia Su, Ding-Ding Gao, Ye-Chun Xu, Ying-Xia Li, He-Yao Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 75 citations in OpenAlex.

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  11. Eugenol inhibits preadipocyte differentiation and lipid accumulation via upregulating ATF3.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
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  13. Effects of Prolactin Inhibition on Lipid Metabolism in Goats.Animals : an open access journal from MDPI · 2024
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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

7 authors at 4 institutions in 1 country.

Hui-Xia DouShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Ting WangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Hai-Xia SuShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Ding-Ding GaoSchool of Pharmacy, Fudan University, Shanghai, 201203, China.
Ye-Chun XuShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Ying-Xia LiSchool of Pharmacy, Fudan University, Shanghai, 201203, China.
He-Yao WangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. hywang@simm.ac.cn.
Chinese Academy of Sciences · CNFudan University · CNUniversity of Chinese Academy of Sciences · CNShanghai Institute of Materia Medica · CN

Funding

National Natural Science Foundation of China 81473262, 81773791National Science & Technology Major Project "Key New Drug Creation and Manufacturing Program", China 2018ZX09711002-002-007
6 · The paper itself

Abstract

purposeFatty acid binding protein 4 (FABP4) has been demonstrated to be secreted from adipocytes in an unconventional pathway associated with lipolysis. Circulating FABP4 is elevated in metabolic disorders and has been shown to affect various peripheral cells such as pancreatic β-cells, hepatocytes and macrophages, but its effects on adipocytes remains unclear. The aim of this study was to investigate the effects of exogenous FABP4 (eFABP4) on adipocyte differentiation and function.

methods3T3-L1 pre-adipocytes or mature adipocytes were treated with recombinant FABP4 in the absence or presence of FABP4 inhibitor I-9/p38 MAPK inhibitor SB203580; Meanwhile male C57BL/6J mice were subcutaneously injected twice a day with recombinant FABP4 (0.35 mg/kg) with or without I-9 (50 mg/kg) for 2 weeks. The effects of eFABP4 on differentiation, lipolysis and inflammation were determined by triglyceride measurement or lipolysis assay, western blotting, or RT-qPCR analysis.

resultseFABP4 treatment significantly reduced intracellular triglyceride content and decreased expression of adipogenic markers peroxisome proliferator-activated receptor gamma (PPARγ), CCAAT/enhancer binding protein alpha (C/EBPα), intracellular FABP4, and adiponectin in 3T3-L1 cells. Besides, eFABP4 promoted lipolysis and inflammation in differentiated 3T3-L1 adipocytes as well as in adipose tissue of eFABP4-treated C57BL/6J mice, with elevated gene expression of monocyte chemoattractant protein (MCP)-1, tumor necrosis factor (TNF)-α, and elevated protein expression of adipose triglyceride lipase (ATGL), phosphorylation of hormone-sensitive lipase (HSL) (Ser-660), p38, and nuclear factor-kappa B (NF-κB). The pro-inflammatory and pro-lipolytic effects of eFABP4 could be reversed by SB203580/I-9.

conclusionsThese findings indicate that eFABP4 interferes with adipocyte differentiation, induces p38/HSL mediated lipolysis and p38/NF-κB mediated inflammation in adipocytes in vitro and in vivo.

Indexed as

AdipocytesLipolysis3T3-L1 CellsAnimalsCell DifferentiationFatty Acid-Binding ProteinsInflammationMaleMiceMice, Inbred C57BLFabp4 protein, mouseFatty Acid-Binding ProteinseFABP4; Adipocyte; Differentiation; Lipolysis; Inflammation

Identifiers

PMID31845180
OpenAlexW2994744005

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.