Evidence map›Paper›PMID 38818120›Full record

ReviewBioengineering & translational medicine2024

Advances in high throughput cell culture technologies for therapeutic screening and biological discovery applications.

Hyeon Ryoo, Hannah Kimmel, Evi Rondo, Gregory H Underhill

Abstract readReview
In one paragraph

Review in Bioengineering & translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Preclinical human models of primary ciliary dyskinesia.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
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  8. Review
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  10. Article
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  13. Article
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  17. Violacein-Loaded Outer Membrane Vesicles fromACS biomaterials science & engineering · 2025
    Article
  18. Article
  19. Review
  20. 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

4 authors.

Hyeon RyooBioengineering Department University of Illinois Urbana-Champaign Urbana Illinois USA.ORCID https://orcid.org/0000-0002-7091-4524
Hannah KimmelBioengineering Department University of Illinois Urbana-Champaign Urbana Illinois USA.ORCID https://orcid.org/0000-0003-4460-1847
Evi RondoBioengineering Department University of Illinois Urbana-Champaign Urbana Illinois USA.
Gregory H UnderhillBioengineering Department University of Illinois Urbana-Champaign Urbana Illinois USA.ORCID https://orcid.org/0000-0003-1002-5335

Funding

Synergistic effects of ECM and heterotypic crosstalk on cellular responses in non-alcoholic fatty liver diseaseR01DK115747 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Salman R Khetani, Gregory H Underhill · 2018 to 2026
$3.7M
Microenvironmental Control of Liver Progenitor Cell Differentiation and Spatial PatterningR01DK125471 · NIDDK · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI UNDERHILL, GREGORY H · 2021 to 2024
$1.9M
NIDDK NIH HHS R01 DK115747NIDDK NIH HHS R01 DK125471
6 · The paper itself

Abstract

Cellular phenotypes and functional responses are modulated by the signals present in their microenvironment, including extracellular matrix (ECM) proteins, tissue mechanical properties, soluble signals and nutrients, and cell-cell interactions. To better recapitulate and analyze these complex signals within the framework of more physiologically relevant culture models, high throughput culture platforms can be transformative. High throughput methodologies enable scientists to extract increasingly robust and broad datasets from individual experiments, screen large numbers of conditions for potential hits, better qualify and predict responses for preclinical applications, and reduce reliance on animal studies. High throughput cell culture systems require uniformity, assay miniaturization, specific target identification, and process simplification. In this review, we detail the various techniques that researchers have used to face these challenges and explore cellular responses in a high throughput manner. We highlight several common approaches including two-dimensional multiwell microplates, microarrays, and microfluidic cell culture systems as well as unencapsulated and encapsulated three-dimensional high throughput cell culture systems, featuring multiwell microplates, micromolds, microwells, microarrays, granular hydrogels, and cell-encapsulated microgels. We also discuss current applications of these high throughput technologies, namely stem cell sourcing, drug discovery and predictive toxicology, and personalized medicine, along with emerging opportunities and future impact areas.

Indexed as

high‐throughputmicrofabricationorganoidorgan‐on‐a‐chip

Identifiers

PMID38818120
PMCPMC11135158

What Socratic 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 Socratic graph.