Evidence map›Paper›PMID 25593327›Full record

ArticleJournal of lipid research2015

Overexpression of full-length cholesteryl ester transfer protein in SW872 cells reduces lipid accumulation.

Lahoucine Izem, Diane J Greene, Katarzyna Bialkowska, Richard E Morton

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. HDL and Cholesterol Ester Transfer Protein (CETP).Advances in experimental medicine and biology · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Lower Expression ofFrontiers in physiology · 2017
    Article
  12. Impacts of Alternative Splicing Events on the Differentiation of Adipocytes.International journal of molecular sciences · 2015
    Review
  13. 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

4 authors at 1 institution in 1 country.

Lahoucine IzemDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195.
Diane J GreeneDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195.
Katarzyna BialkowskaDepartment of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195.
Richard E MortonDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195. Electronic address: mortonr@ccf.org.
Cleveland Clinic · US

Funding

Role of cholesteryl ester transfer protein in cellular lipid homeostasisR01HL060934 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI MORTON, RICHARD E · 2000 to 2014
$3.9M
NHLBI NIH HHS HL60934NHLBI NIH HHS R01 HL060934
6 · The paper itself

Abstract

Cells produce two cholesteryl ester transfer protein (CETP) isoforms, full-length and a shorter variant produced by alternative splicing. Blocking synthesis of both isoforms disrupts lipid metabolism and storage. To further define the role of CETP in cellular lipid metabolism, we stably overexpressed full-length CETP in SW872 cells. These CETP(+) cells had several-fold higher intracellular CETP and accumulated 50% less TG due to a 26% decrease in TG synthesis and 2.5-fold higher TG turnover rate. Reduced TG synthesis was due to decreased fatty acid uptake and impaired conversion of diglyceride to TG even though diacylglycerol acyltransferase activity was normal. Sterol-regulatory element binding protein 1 mRNA levels were normal, and although PPARγ expression was reduced, the expression of several of its target genes including adipocyte triglyceride lipase, FASN, and APOE was normal. CETP(+) cells contained smaller lipid droplets, consistent with their higher levels of perilipin protein family (PLIN) 3 compared with PLIN1 and PLIN2. Intracellular CETP was mostly associated with the endoplasmic reticulum, although CETP near lipid droplets poorly colocalized with this membrane. A small pool of CETP resided in the cytoplasm, and a subfraction coisolated with lipid droplets. These data show that overexpression of full-length CETP disrupts lipid homeostasis resulting in the formation of smaller, more metabolically active lipid droplets.

Indexed as

Apolipoproteins ECell Line, TumorCholesterol Ester Transfer ProteinsCytoplasmFatty Acid Synthase, Type IGene Expression RegulationHumansLipid MetabolismPPAR gammaRNA, MessengerSterol Regulatory Element Binding Protein 1TriglyceridesApolipoproteins ECETP protein, humanCholesterol Ester Transfer ProteinsFASN protein, humanFatty Acid Synthase, Type IPPAR gammaRNA, MessengerSREBF1 protein, humanSterol Regulatory Element Binding Protein 1Triglyceridescellular localizationgene expressionlipid dropletslipid metabolismlipid turnover

Identifiers

PMID25593327
PMCPMC4340300
OpenAlexW2148417474

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.