Evidence map›Paper›PMID 27655916›Full record

ArticleThe Journal of biological chemistry2016

Endoplasmic Reticulum Lipid Flux Influences Enterocyte Nuclear Morphology and Lipid-dependent Transcriptional Responses.

Erin M Zeituni, Meredith H Wilson, Xiaobin Zheng, Pablo A Iglesias, Michael A Sepanski, Mahmud A Siddiqi, Jennifer L Anderson, Yixian Zheng, Steven A Farber

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  4. Role of Na/K-ATPase α1 caveolin-binding motif in adipogenesis.American journal of physiology. Cell physiology · 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

9 authors at 3 institutions in 1 country.

Erin M ZeituniFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Meredith H WilsonFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Xiaobin ZhengFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Pablo A Iglesiasthe Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, Maryland 21218.
Michael A SepanskiFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Mahmud A SiddiqiFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Jennifer L AndersonFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Yixian ZhengFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and.
Steven A FarberFrom the Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218 and farber@ciwemb.edu.
Department of Embryology · USCarnegie Institution for Science · USJohns Hopkins University · US

Funding

Systematic Vertebrate Functional GenomicsR01GM063904 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI EKKER, STEPHEN CARL · 2001 to 2025
$10.7M
Identifying genes required for digestive physiology and lipid metabolismR01DK093399 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI STEVEN A FARBER, John F Rawls · 2013 to 2026
$7.6M
Mechanisms of cytoplasmic lipid droplet regulation in the intestineF32DK109592 · NIDDK · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI WILSON, MEREDITH H · 2016 to 2018
$173k
NIDDK NIH HHS F32 DK109592NIDDK NIH HHS R01 DK093399NIGMS NIH HHS R01 GM063904
6 · The paper itself

Abstract

Responding to a high-fat meal requires an interplay between multiple digestive tissues, sympathetic response pathways, and the gut microbiome. The epithelial enterocytes of the intestine are responsible for absorbing dietary nutrients and preparing them for circulation to distal tissues, which requires significant changes in cellular activity, including both morphological and transcriptional responses. Following a high-fat meal, we observe morphological changes in the enterocytes of larval zebrafish, including elongation of mitochondria, formation and expansion of lipid droplets, and the rapid and transient ruffling of the nuclear periphery. Dietary and pharmacological manipulation of zebrafish larvae demonstrated that these subcellular changes are specific to triglyceride absorption. The transcriptional changes that occur simultaneously with these morphological changes were determined using RNA sequencing, revealing a cohort of up-regulated genes associated with lipid droplet formation and lipid transport via lipoprotein particles. Using a microsomal triglyceride transfer protein (MTP) inhibitor to block β-lipoprotein particle formation, we demonstrate that the transcriptional response to a high-fat meal is associated with the transfer of ER triglyceride to nascent β-lipoproteins, possibly through the activation of Creb3l3/cyclic AMP-responsive element-binding protein. These data suggest that a transient increase in ER lipids is the likely mediator of the initial physiological response of intestinal enterocytes to dietary lipid.

Indexed as

Diet, High-FatLipid MetabolismTranscriptional ActivationAnimalsCyclic AMP Response Element-Binding ProteinEndoplasmic ReticulumEnterocytesLipid DropletsMitochondriaTriglyceridesZebrafishZebrafish ProteinsCyclic AMP Response Element-Binding ProteinTriglyceridesZebrafish ProteinsapoA-IVcreb3l3enterocyteintestinelipid dropletlipoproteinmitochondrianucleusplin2

Identifiers

PMID27655916
PMCPMC5095432
OpenAlexW2523515391

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.