Evidence map›Paper›PMID 24040321›Full record

ArticlePloS one2013

The rab11 effector protein FIP1 regulates adiponectin trafficking and secretion.

Brian P Carson, Josep Maria Del Bas, Jose Maria Moreno-Navarrete, Jose Manuel Fernandez-Real, Silvia Mora

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Rab11FIP1-deficient mice develop spontaneous inflammation and show increased susceptibility to colon damage.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
  5. Article
  6. Review
  7. Article
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  10. Article
  11. Article
  12. Article
  13. Relationship between adiponectin receptor 1 gene polymorphisms and ischemic stroke.International journal of clinical and experimental medicine · 2015
    Article
  14. Review
  15. 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 2 countries.

Brian P CarsonDepartment of Cellular and Molecular Physiology, Institute of Translational Medicine, the University of Liverpool, Liverpool, United Kingdom.
Josep Maria Del Bas
Jose Maria Moreno-Navarrete
Jose Manuel Fernandez-Real
Silvia Mora
University of Liverpool · GBHospital Universitari de Girona Doctor Josep Trueta · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adiponectin is an adipokine secreted by white adipocytes involved in regulating insulin sensitivity in peripheral tissues. Secretion of adiponectin in adipocytes relies on the endosomal system, however, the intracellular machinery involved in mediating adiponectin release is unknown. We have previously reported that intracellular adiponectin partially compartmentalizes with rab 5 and rab11, markers for the early/sorting and recycling compartments respectively. Here we have examined the role of several rab11 downstream effector proteins (rab11 FIPs) in regulating adiponectin trafficking and secretion. Overexpression of wild type rab11 FIP1, FIP3 and FIP5 decreased the amount of secreted adiponectin expressed in HEK293 cells, whereas overexpression of rab11 FIP2 or FIP4 had no effect. Furthermore shRNA-mediated depletion of FIP1 enhanced adiponectin release whereas knock down of FIP5 decreased adiponectin secretion. Knock down of FIP3 had no effect. In 3T3L1 adipocytes, endogenous FIP1 co-distributed intracellularly with endogenous adiponectin and FIP1 depletion enhanced adiponectin release without altering insulin-mediated trafficking of the glucose transporter Glut4. While adiponectin receptors internalized with transferrin receptors, there were no differences in transferrin receptor recycling between wild type and FIP1 depleted adipocytes. Consistent with its inhibitory role, FIP1 expression was decreased during adipocyte differentiation, by treatment with thiazolidinediones, and with increased BMI in humans. In contrast, FIP1 expression increased upon exposure of adipocytes to TNFα. In all, our findings identify FIP1 as a novel protein involved in the regulation of adiponectin trafficking and release.

Indexed as

Adaptor Proteins, Signal TransducingAdipocytesAdiponectinAnimalsBody Mass IndexEndosomesGene Expression RegulationGlucose Transporter Type 4HEK293 CellsHumansMembrane ProteinsMiceMonomeric GTP-Binding ProteinsmRNA Cleavage and Polyadenylation FactorsNIH 3T3 CellsObesityAdaptor Proteins, Signal TransducingAdiponectinFIP1L1 protein, humanFip1l1 protein, mouseGlucose Transporter Type 4Membrane ProteinsMonomeric GTP-Binding ProteinsmRNA Cleavage and Polyadenylation FactorsRAB11FIP1 protein, humanrab11 GTP-Binding Proteinsrab5 GTP-Binding Proteinsrab GTP-Binding ProteinsSLC2A4 protein, humanSlc2a4 protein, mouseTransferrin

Identifiers

PMID24040321
PMCPMC3770573
OpenAlexW2122502167

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.