Evidence map›Paper›PMID 24627478›Full record

ArticleThe Journal of biological chemistry2014

Fat-specific protein 27 (FSP27) interacts with adipose triglyceride lipase (ATGL) to regulate lipolysis and insulin sensitivity in human adipocytes.

Tan Hooi Min Grahn, Rajween Kaur, Jun Yin, Martina Schweiger, Vishva Mitra Sharma, Mi-Jeong Lee, Yasuo Ido, Cynthia M Smas, Rudolf Zechner, Achim Lass and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 116 citations in OpenAlex.

  1. Trial
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  4. Review
  5. Mixtures ofToxics · 2025
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  8. Article
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  11. Mechanism of Obesity-Related Lipotoxicity and Clinical Perspective.Advances in experimental medicine and biology · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Fsp27 plays a crucial role in muscle performance.American journal of physiology. Endocrinology and metabolism · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Review

5 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 2 countries.

Tan Hooi Min GrahnSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118.
Rajween KaurSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118.
Jun YinSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118.
Martina SchweigerInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, A-8010 Graz.
Vishva Mitra SharmaSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118.
Mi-Jeong LeeSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118.
Yasuo IdoSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118.
Cynthia M SmasDepartment of Biochemistry and Cancer Biology, University of Toledo College of Medicine, Toledo, Ohio 43614.
Rudolf ZechnerInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, A-8010 Graz.
Achim LassInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, A-8010 Graz.
Vishwajeet PuriSection of Endocrinology, Diabetes, and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118. Electronic address: vpuri@bu.edu.
Boston University · USUniversity of Graz · ATUniversity of Toledo · US

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
Boston University Clinical and Translational Science Award (CTSA) Program UL1UL1TR000157 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2012 to 2013
$7.9M
Boston University Clinical and Translational Science Award (CTSA) Program KL2KL2TR000158 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2012 to 2013
$749k
Lipid droplet morphology and triglyceride storageR56DK094815 · NIDDK · BOSTON MEDICAL CENTER · PI PURI, VISHWAJEET · 2012 to 2012
$203k
Austrian Science Fund FWF F 3001Austrian Science Fund FWF F 3002Austrian Science Fund FWF P 25193Austrian Science Fund FWF Z 136NCATS NIH HHS 8KL2TR000158NCATS NIH HHS KL2 TR000158NCATS NIH HHS UL1 TR000157NCATS NIH HHS UL1-TR000157NIDDK NIH HHS P30 DK046200NIDDK NIH HHS P30DK046200NIDDK NIH HHS R56 DK094815NIDDK NIH HHS R56DK094815
6 · The paper itself

Abstract

In adipocytes, lipolysis is a highly regulated process involving hormonal signals, lipid droplet-associated proteins, and lipases. The discovery of new lipid droplet-associated proteins added complexity to the current model of lipolysis. In this study, we used cultured human adipocytes to demonstrate that fat-specific protein 27 (FSP27), an abundantly expressed protein in adipocytes, regulates both basal and stimulated lipolysis by interacting with adipose triglyceride lipase (ATGL, also called desnutrin or PNPLA2). We identified a core domain of FSP27, amino acids 120-220, that interacts with ATGL to inhibit its lipolytic function and promote triglyceride storage. We also defined the role of FSP27 in free fatty acid-induced insulin resistance in adipocytes. FSP27 depletion in human adipocytes increased lipolysis and inhibited insulin signaling by decreasing AKT phosphorylation. However, reducing lipolysis by either depletion of ATGL or expression of exogenous full-length FSP27 or amino acids 120-220 protected human adipocytes against the adverse effects of free fatty acids on insulin signaling. In embryonic fibroblasts derived from ATGL KO mice, exogenous free fatty acids did not affect insulin sensitivity. Our results demonstrate a crucial role for FSP27-ATGL interactions in regulating lipolysis, triglyceride accumulation, and insulin signaling in human adipocytes.

Indexed as

Insulin Resistance3T3-L1 CellsAdipocytesAnimalsApoptosis Regulatory ProteinsHumansInsulinLipaseLipolysisMiceMice, KnockoutPhosphorylationProtein BindingProteinsSignal TransductionTriglyceridesApoptosis Regulatory ProteinsCIDEC protein, humanInsulinLipaseProteinsTriglyceridesAdipocyteAdipose Tissue MetabolismAdipose Triglyceride LipaseDiabetesDiacylglycerolFatty AcidFatty Acid MetabolismInsulin ResistanceObesity

Identifiers

PMID24627478
PMCPMC4002109
OpenAlexW2030251861

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.