Evidence map›Paper›PMID 39121154›Full record

ArticlePloS one2024

Sample preparation and data collection for serial block face scanning electron microscopy of mammalian cell monolayers.

Noelle V Antao, Joseph Sall, Christopher Petzold, Damian C Ekiert, Gira Bhabha, Feng-Xia Liang

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Noelle V AntaoDepartment of Cell Biology, New York University School of Medicine, New York, NY, United States of America.ORCID 0000-0001-7845-8511
Joseph SallOffice of Science and Research Microscopy Laboratory, New York University School of Medicine, New York, NY, United States of America.
Christopher PetzoldOffice of Science and Research Microscopy Laboratory, New York University School of Medicine, New York, NY, United States of America.
Damian C EkiertDepartment of Cell Biology, New York University School of Medicine, New York, NY, United States of America.
Gira BhabhaDepartment of Cell Biology, New York University School of Medicine, New York, NY, United States of America.ORCID 0000-0003-0624-6178
Feng-Xia LiangDepartment of Cell Biology, New York University School of Medicine, New York, NY, United States of America.

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Structural basis of the polar tube invasion machinery from microsporidia parasitesR01AI147131 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHABHA, GIRA · 2020 to 2024
$3.4M
Scanning Electron Microscope with 3ViewS10OD019974 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LIANG, FENGXIA · 2016 to 2016
$1.1M
NCI NIH HHS P30 CA016087NIAID NIH HHS R01 AI147131NIH HHS S10 OD019974
6 · The paper itself

Abstract

Volume electron microscopy encompasses a set of electron microscopy techniques that can be used to examine the ultrastructure of biological tissues and cells in three dimensions. Two block face techniques, focused ion beam scanning electron microscopy (FIB-SEM) and serial block face scanning electron microscopy (SBF-SEM) have often been used to study biological tissue samples. More recently, these techniques have been adapted to in vitro tissue culture samples. Here we describe step-by-step protocols for two sample embedding methods for in vitro tissue culture cells intended to be studied using SBF-SEM. The first focuses on cell pellet embedding and the second on en face embedding. En face embedding can be combined with light microscopy, and this CLEM workflow can be used to identify specific biological events by light microscopy, which can then be imaged using SBF-SEM. We systematically outline the steps necessary to fix, stain, embed and image adherent tissue culture cell monolayers by SBF-SEM. In addition to sample preparation, we discuss optimization of parameters for data collection. We highlight the challenges and key steps of sample preparation, and the consideration of imaging variables.

Indexed as

Microscopy, Electron, ScanningAnimalsHumansSpecimen HandlingTissue EmbeddingVolume Electron Microscopy

Identifiers

PMID39121154
PMCPMC11315281

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.