Evidence map›Paper›PMID 27279328›Full record

ArticleScientific reports2016

Effects of LDL Receptor Modulation on Lymphatic Function.

Andreea Milasan, François Dallaire, Gaétan Mayer, Catherine Martel

Open access · goldFull text read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Utility of anLab on a chip · 2025
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  7. Review
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  9. Promising Adventitia in Atherosclerosis.Current vascular pharmacology · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Lymphatics in Cardiovascular Physiology.Cold Spring Harbor perspectives in medicine · 2022
    Review
  17. Article
  18. Review
  19. High-Density Lipoproteins in Kidney Disease.International journal of molecular sciences · 2021
    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

4 authors at 2 institutions in 1 country.

Andreea MilasanDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
François DallaireMontreal Heart Institute, Montreal, Quebec, Canada.
Gaétan MayerLaboratory of Molecular Cell Biology, Montreal Heart Institute Research Center, Quebec, Canada.
Catherine MartelDepartment of Medicine, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Montreal Heart Institute · CAUniversité de Montréal · CA

Funding

CIHR MOP133598
6 · The paper itself

Abstract

Atherosclerosis is driven by the accumulation of immune cells and cholesterol in the arterial wall. Although recent studies have shown that lymphatic vessels play an important role in macrophage reverse cholesterol transport, the specific underlying mechanisms of this physiological feature remain unknown. In the current report, we sought to better characterize the lymphatic dysfunction that is associated with atherosclerosis by studying the physiological and temporal origins of this impairment. First, we assessed that athero-protected Pcsk9(-/-) mice exhibited improved collecting lymphatic vessel function throughout age when compared to WT mice for up to six months, while displaying enhanced expression of LDLR on lymphatic endothelial cells. Lymphatic dysfunction was present before the atherosclerotic lesion formation in a mouse model that is predisposed to develop atherosclerosis (Ldlr(-/-); hApoB100(+/+)). This dysfunction was presumably associated with a defect in the collecting lymphatic vessels in a non-specific cholesterol- but LDLR-dependent manner. Treatment with a selective VEGFR-3 agonist rescued this impairment observed early in the onset of this arterial disease. We suggest that LDLR modulation is associated with early atherosclerosis-related lymphatic dysfunction, and bring forth a pleiotropic role for PCSK9 in lymphatic function. Our study unveils new potential therapeutic targets for the prevention and treatment of atherosclerosis.

Indexed as

AnimalsAtherosclerosisDisease Models, AnimalEndothelial CellsFemaleLymphatic VesselsMaleMiceMice, KnockoutProprotein Convertase 9Receptors, LDLPcsk9 protein, mouseProprotein Convertase 9Receptors, LDL

Identifiers

PMID27279328
PMCPMC4899717
OpenAlexW2410100735

What OpenQuestion holds

Textfull text, public
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.