Evidence map›Paper›PMID 26147095›Full record

ArticlePloS one2015

Perilipin-2 Modulates Lipid Absorption and Microbiome Responses in the Mouse Intestine.

Daniel N Frank, Elise S Bales, Jenifer Monks, Matthew J Jackman, Paul S MacLean, Diana Ir, Charles E Robertson, David J Orlicky, James L McManaman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Cell lipid biology in infections: an overview.Frontiers in cellular and infection microbiology · 2023
    Review
  5. Review
  6. Review
  7. Perilipins at a glance.Journal of cell science · 2022
    Article
  8. A nexus of lipid andFrontiers in endocrinology · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. PasteurizedGut microbes · 2020
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Regulation of Chylomicron Secretion: Focus on Post-Assembly Mechanisms.Cellular and molecular gastroenterology and hepatology · 2019
    Review
  20. Article
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 1 institution in 1 country.

Daniel N FrankDivision of Infectious Disease, University of Colorado School of Medicine, Aurora, Colorado, United States of America; Microbiome Research Consortium, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Elise S BalesDivision of Basic Reproductive Sciences, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Jenifer MonksDivision of Basic Reproductive Sciences, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Matthew J JackmanDivision of Endocrinology and Metabolism, University of Colorado School of Medicine, Aurora, Colorado, United States of America; The Center for Human Nutrition, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Paul S MacLeanDivision of Endocrinology and Metabolism, University of Colorado School of Medicine, Aurora, Colorado, United States of America; The Center for Human Nutrition, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Diana IrDivision of Infectious Disease, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
Charles E RobertsonDivision of Infectious Disease, University of Colorado School of Medicine, Aurora, Colorado, United States of America; Microbiome Research Consortium, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
David J OrlickyDepartment of Pathology, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
James L McManamanDivision of Basic Reproductive Sciences, University of Colorado School of Medicine, Aurora, Colorado, United States of America; The Center for Human Nutrition, University of Colorado School of Medicine, Aurora, Colorado, United States of America.
University of Colorado Denver · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
North Carolina Collaborative PPRU NetworkU10HD045962 · NICHD · DUKE UNIVERSITY · PI BENJAMIN, DANIEL K. · 2004 to 2009
$2.1M
Postnatal Actions of Maternal Obesity on Neonatal Metabolic HealthR01HD075285 · NICHD · UNIVERSITY OF COLORADO DENVER · PI MACLEAN, PAUL S., MCMANAMAN, JAMES LEWIS · 2013 to 2017
$1.6M
NCATS NIH HHS UL1 TR001082NCI NIH HHS P30 CA046934NCI NIH HHS P30CA046934NICHD NIH HHS 2R01HD045962NICHD NIH HHS R01 HD075285NICHD NIH HHS U10 HD045962NIDDK NIH HHS DK48520NIDDK NIH HHS P30 DK048520
6 · The paper itself

Abstract

Obesity and its co-morbidities, such as fatty liver disease, are increasingly prevalent worldwide health problems. Intestinal microorganisms have emerged as critical factors linking diet to host physiology and metabolic function, particularly in the context of lipid homeostasis. We previously demonstrated that deletion of the cytoplasmic lipid drop (CLD) protein Perilipin-2 (Plin2) in mice largely abrogates long-term deleterious effects of a high fat (HF) diet. Here we test the hypotheses that Plin2 function impacts the earliest steps of HF diet-mediated pathogenesis as well as the dynamics of diet-associated changes in gut microbiome diversity and function. WT and perilipin-2 null mice raised on a standard chow diet were randomized to either low fat (LF) or HF diets. After four days, animals were assessed for changes in physiological (body weight, energy balance, and fecal triglyceride levels), histochemical (enterocyte CLD content), and fecal microbiome parameters. Plin2-null mice had significantly lower respiratory exchange ratios, diminished frequencies of enterocyte CLDs, and increased fecal triglyceride levels compared with WT mice. Microbiome analyses, employing both 16S rRNA profiling and metagenomic deep sequencing, indicated that dietary fat content and Plin2 genotype were significantly and independently associated with gut microbiome composition, diversity, and functional differences. These data demonstrate that Plin2 modulates rapid effects of diet on fecal lipid levels, enterocyte CLD contents, and fuel utilization properties of mice that correlate with structural and functional differences in their gut microbial communities. Collectively, the data provide evidence of Plin2 regulated intestinal lipid uptake, which contributes to rapid changes in the gut microbial communities implicated in diet-induced obesity.

Indexed as

AdiposityAnimalsBody WeightDiet, Fat-RestrictedDiet, High-FatFatty LiverFecesGastrointestinal MicrobiomeIntestinal MucosaIntestinesLipid MetabolismLiverMaleMembrane ProteinsMiceMice, Inbred C57BLMembrane ProteinsPerilipin-2PLIN2 protein, humanPlin2 protein, mouseRNA, Ribosomal, 16S

Identifiers

PMID26147095
PMCPMC4493139
OpenAlexW2282737989

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.