Evidence map›Paper›PMID 25465389›Full record

ArticleJournal of lipid research2015

Alginic acid cell entrapment: a novel method for measuring in vivo macrophage cholesterol homeostasis.

Timothy J Sontag, Bijoy Chellan, Clarissa V Bhanvadia, Godfrey S Getz, Catherine A Reardon

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Apoprotein E and Reverse Cholesterol Transport.International journal of molecular sciences · 2018
    Review
  2. Do the Apoe-/- and Ldlr-/- Mice Yield the Same Insight on Atherogenesis?Arteriosclerosis, thrombosis, and vascular biology · 2016
    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 1 institution in 1 country.

Timothy J SontagDepartment of Pathology, University of Chicago, Chicago, IL.
Bijoy ChellanDepartment of Pathology, University of Chicago, Chicago, IL.
Clarissa V BhanvadiaDepartment of Pathology, University of Chicago, Chicago, IL.
Godfrey S GetzDepartment of Pathology, University of Chicago, Chicago, IL.
Catherine A ReardonDepartment of Pathology, University of Chicago, Chicago, IL.
University of Chicago · US

Funding

Role of Serum Amyloid A in Diabetic Vascular DiseaseP01HL092969 · NHLBI · UNIVERSITY OF WASHINGTON · PI BORNFELDT, KARIN E. · 2008 to 2019
$23.5M
NHLBI NIH HHS P01 HL092969
6 · The paper itself

Abstract

Macrophage conversion to atherosclerotic foam cells is partly due to the balance of uptake and efflux of cholesterol. Cholesterol efflux from cells by HDL and its apoproteins for subsequent hepatic elimination is known as reverse cholesterol transport. Numerous methods have been developed to measure in vivo macrophage cholesterol efflux. Most methods do not allow for macrophage recovery for analysis of changes in cellular cholesterol status. We describe a novel method for measuring cellular cholesterol balance using the in vivo entrapment of macrophages in alginate, which retains incorporated cells while being permeable to lipoproteins. Recipient mice were injected subcutaneously with CaCl2 forming a bubble into which a macrophage/alginate suspension was injected, entrapping the macrophages. Cells were recovered after 24 h. Cellular free and esterified cholesterol mass were determined enzymatically and normalized to cellular protein. Both normal and cholesterol loaded macrophages undergo measureable changes in cell cholesterol when injected into WT and apoA-I-, LDL-receptor-, or apoE-deficient mice. Cellular cholesterol balance is dependent on initial cellular cholesterol status, macrophage cholesterol transporter expression, and apolipoprotein deficiency. Alginate entrapment allows for the in vivo measurement of macrophage cholesterol homeostasis and is a novel platform for investigating the role of genetics and therapeutic interventions in atherogenesis.

Indexed as

AlginatesAnimalsApolipoprotein A-IApolipoproteins EBiological TransportCholesterolGlucuronic AcidHexuronic AcidsMacrophagesMiceMice, Inbred C57BLMice, KnockoutAlginatesApolipoprotein A-IApolipoproteins ECholesterolGlucuronic AcidHexuronic Acidsalginateapolipoproteinsatherosclerosischolesterol/traffickinghigh density lipoproteinlow density lipoprotein

Identifiers

PMID25465389
PMCPMC4306700
OpenAlexW2316082658

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.