Evidence map›Paper›PMID 35705590›Full record

ArticleScientific reports2022

Coplanar embedding of multiple 3D cell models in hydrogel towards high-throughput micro-histology.

Sarah Heub, Fatemeh Navaee, Daniel Migliozzi, Diane Ledroit, Stéphanie Boder-Pasche, Jonas Goldowsky, Emilie Vuille-Dit-Bille, Joëlle Hofer, Carine Gaiser, Vincent Revol and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

12 authors.

Sarah HeubCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland. sarah.heub@csem.ch.
Fatemeh NavaeeCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Daniel MigliozziCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Diane LedroitCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Stéphanie Boder-PascheCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Jonas GoldowskyCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Emilie Vuille-Dit-BilleCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Joëlle HoferSchool of Life Sciences, University of Applied Sciences and Arts Northwestern Switzerland, 4132, Muttenz, Switzerland.
Carine GaiserSchool of Life Sciences, University of Applied Sciences and Arts Northwestern Switzerland, 4132, Muttenz, Switzerland.
Vincent RevolCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.
Laura Suter-DickSchool of Life Sciences, University of Applied Sciences and Arts Northwestern Switzerland, 4132, Muttenz, Switzerland.
Gilles WederCSEM SA, Jaquet-Droz 1, 2002, Neuchâtel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Standardised and high-throughput methods have been developed for the production and experimental handling of some 3D in vitro models. However, adapted analytical tools are still missing for scientists and researchers to fully exploit the potential of complex cellular models in pre-clinical drug testing and precision medicine. Histology is the established, cost-effective and gold standard method for structural and functional tissue analysis. However, standard histological processes are challenging and costly to apply to 3D cell models, as their small size often leads to poor alignment of samples, which lowers analysis throughput. This body of work proposes a new approach: HistoBrick facilitates histological processing of spheroids and organoids by enabling gel embedding of 3D cell models with precise coplanar alignment, parallel to the sectioning plane, thus minimising the loss of sample material. HistoBrick's features are compatible with automation standards, potentially allowing automated sample transfer from a multi-well plate to the gel device. Moreover, HistoBrick's technology was validated by demonstrating the alignment of HepG2 cultured spheroids measuring 150-200 µm in diameter with a height precision of ± 80 µm. HistoBrick allows up to 96 samples to be studied across minimal sections, paving the way towards high-throughput micro-histology.

Indexed as

HydrogelsSpheroids, CellularCell Culture TechniquesHistological TechniquesHydrogels

Identifiers

PMID35705590
PMCPMC9200833

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Registered trials

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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.