Evidence map›Paper›PMID 35939716›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Examining atherosclerotic lesions in three dimensions at the nanometer scale with cryo-FIB-SEM.

Jenny Capua-Shenkar, Neta Varsano, Noya-Ruth Itzhak, Ifat Kaplan-Ashiri, Katya Rechav, Xueting Jin, Manabu Niimi, Jianglin Fan, Howard S Kruth, Lia Addadi

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

9 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Cholesterol-containing lipid crystals can directly stiffen the rat steatotic liver before fibrosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. 3D cryoimaging of cell-mediated cholesterol crystal clearance in human atherosclerotic lesions.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. 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

10 authors at 2 institutions in 2 countries.

Jenny Capua-ShenkarDepartment of Chemical and Structural Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Neta VarsanoDepartment of Chemical and Structural Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Noya-Ruth ItzhakDepartment of Chemical and Structural Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Ifat Kaplan-AshiriDepartment of Chemical Research Support, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Katya RechavDepartment of Chemical Research Support, Weizmann Institute of Science, 7610001 Rehovot, Israel.ORCID 0000-0003-4664-5704
Xueting JinExperimental Atherosclerosis Section, NIH, Bethesda, MD 20892.
Manabu NiimiDepartment of Molecular Pathology, University of Yamanashi, Yamanashi 409-3898, Japan.
Jianglin FanDepartment of Molecular Pathology, University of Yamanashi, Yamanashi 409-3898, Japan.
Howard S KruthExperimental Atherosclerosis Section, NIH, Bethesda, MD 20892.
Lia AddadiDepartment of Chemical and Structural Biology, Weizmann Institute of Science, 7610001 Rehovot, Israel.ORCID 0000-0003-1693-648X
Weizmann Institute of Science · ILUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We employed in a correlative manner an unconventional combination of methods, comprising cathodoluminescence, cryo-scanning electron microscopy (SEM), and cryo-focused ion beam (FIB)-SEM, to examine the volumes of thousands of cubed micrometers from rabbit atherosclerotic tissues, maintained in close-to-native conditions, with a resolution of tens of nanometers. Data from three different intralesional regions, at the media-lesion interface, in the core, and toward the lumen, were analyzed following segmentation and volume or surface representation. The media-lesion interface region is rich in cells and lipid droplets, whereas the core region is markedly richer in crystals and has lower cell density. In the three regions, thin crystals appear to be associated with intracellular or extracellular lipid droplets and multilamellar bodies. Large crystals are independently positioned in the tissue, not associated with specific cellular components. This extensive evidence strongly supports the idea that the lipid droplet surfaces and the outer membranes of multilamellar bodies play a role in cholesterol crystal nucleation and growth and that crystal formation occurs, in part, inside cells. The correlative combination of methods that allowed the direct examination of cholesterol crystals and lipid deposits in the atherosclerotic lesions may be similarly used for high-resolution examination of other tissues containing pathological or physiological cholesterol deposits.

Indexed as

AtherosclerosisCholesterolCryoelectron MicroscopyImaging, Three-DimensionalMicroscopy, Electron, ScanningAnimalsNanotechnologyRabbitsCholesterolatherosclerosis in rabbit modelscathodoluminescencecholesterol crystalscorrelative electron microscopylipid droplet

Identifiers

PMID35939716
PMCPMC9407640
OpenAlexW4290725087

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.