Evidence map›Paper›PMID 39589396›Full record

ArticleeLife2024

High-throughput expansion microscopy enables scalable super-resolution imaging.

John H Day, Catherine M Della Santina, Pema Maretich, Alexander L Auld, Kirsten K Schnieder, Tay Shin, Edward S Boyden, Laurie A Boyer

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Combining ultrastructure expansion microscopy with immunofluorescence and Oligopaint DNA FISH.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
    Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

John H DayDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States.ORCID https://orcid.org/0000-0002-5515-6606
Catherine M Della Santina *Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States.
Pema Maretich *Department of Biology, Massachusetts Institute of Technology, Cambridge, United States.
Alexander L Auld *Department of Biology, Massachusetts Institute of Technology, Cambridge, United States.
Kirsten K SchniederDepartment of Biology, Massachusetts Institute of Technology, Cambridge, United States.
Tay ShinDepartment of Media Arts and Sciences, Massachusetts Institute of Technology, Cambridge, United States.
Edward S BoydenDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States.
Laurie A BoyerDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States.ORCID https://orcid.org/0000-0003-3491-4962

Funding

Expansion MicroscopyR01EB024261 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S. · 2017 to 2025
$4.6M
High-throughput approaches to local and long-range synaptic connectivityRF1MH123403 · NIMH · COLD SPRING HARBOR LABORATORY · PI BOYDEN, EDWARD S., ZADOR, ANTHONY M · 2020 to 2020
$3.3M
Mechanisms of pathology and neuronal hyperactivity in a memory circuit in Alzheimer's diseaseR01AG070831 · NIA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., TSAI, LI-HUEI · 2021 to 2025
$3.2M
Multiplexed Nanoscale Protein Mapping Through Expansion Microscopy and Immuno-SABERRF1MH124606 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., YIN, PENG · 2020 to 2020
$2.7M
Investigating the role of H2A.Z dynamics in regulating cardiac lineage commitmentR01HL140471 · NHLBI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYER, LAURIE A · 2018 to 2021
$2.2M
The infectious etiology of Alzheimer's disease revealed at nanoscale precisionR56AG069192 · NIA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI AN, BOBAE · 2020 to 2020
$1.5M
Opera Phenix high-throughput microplate confocal imager for high-content screeningS10OD026839 · OD · BROAD INSTITUTE, INC. · PI WAGNER, BRIDGET K · 2019 to 2019
$1.0M
National Science Foundation Graduate Research Fellowship Program 1122374National Science Foundation Graduate Research Fellowship Program 2141064NHLBI NIH HHS R01 HL140471NIA NIH HHS R01 AG070831NIA NIH HHS R56 AG069192NIBIB NIH HHS R01 EB024261NIH HHS S10 OD026839NIH Office of the Director 1R01AG070831NIH Office of the Director 1R01MH123403NIH Office of the Director 1R56AG069192NIH Office of the Director EB024261NIH Office of the Director OD-026839-01NIH Office of the Director R01HL140471NIH Office of the Director R01MH124606NIMH NIH HHS RF1 MH123403NIMH NIH HHS RF1 MH124606
6 · The paper itself

Abstract

Expansion microscopy (ExM) enables nanoscale imaging using a standard confocal microscope through the physical, isotropic expansion of fixed immunolabeled specimens. ExM is widely employed to image proteins, nucleic acids, and lipid membranes in single cells; however, current methods limit the number of samples that can be processed simultaneously. We developed High-throughput Expansion Microscopy (HiExM), a robust platform that enables expansion microscopy of cells cultured in a standard 96-well plate. Our method enables ~4.2 x expansion of cells within individual wells, across multiple wells, and between plates. We also demonstrate that HiExM can be combined with high-throughput confocal imaging platforms to greatly improve the ease and scalability of image acquisition. As an example, we analyzed the effects of doxorubicin, a known cardiotoxic agent, on human cardiomyocytes (CMs) as measured by the Hoechst signal across the nucleus. We show a dose-dependent effect on nuclear DNA that is not observed in unexpanded CMs, suggesting that HiExM improves the detection of cellular phenotypes in response to drug treatment. Our method broadens the application of ExM as a tool for scalable super-resolution imaging in biological research applications.

Indexed as

Myocytes, CardiacCells, CulturedDoxorubicinHigh-Throughput Screening AssaysHumansMicroscopyMicroscopy, ConfocalDoxorubicinA549 cellscardiomyocytescell biologycell culturehuman

Identifiers

PMID39589396
PMCPMC11594540

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.