Evidence map›Paper›PMID 32948587›Full record

ArticleScience advances2020

Artificial cells drive neural differentiation.

Ö Duhan Toparlak, Jacopo Zasso, Simone Bridi, Mauro Dalla Serra, Paolo Macchi, Luciano Conti, Marie-Laure Baudet, Sheref S Mansy

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

68 citing papers in PubMed, 140 citations in OpenAlex.

  1. Membrane-Associated Biomolecules for Synthetic Cell Signalling.Chembiochem : a European journal of chemical biology · 2026
    Review
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  8. ATP-Powered Signaling Between Artificial and Living Cells.Angewandte Chemie (International ed. in English) · 2025
    Article
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  11. Review
  12. Article
  13. Article
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  15. Article
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  18. Article
  19. Article
  20. Article

8 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 2 countries.

Ö Duhan ToparlakDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy.ORCID 0000-0002-0859-1373
Jacopo ZassoDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy.ORCID 0000-0002-3151-6443
Simone BridiDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy.ORCID 0000-0002-7778-2261
Mauro Dalla SerraNational Research Council-Institute of Biophysics & Bruno Kessler Foundation, via alla Cascata 56/C, 38123 Trento, Italy.
Paolo MacchiDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy.ORCID 0000-0002-7245-9019
Luciano ContiDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy.ORCID 0000-0002-2050-9846
Marie-Laure BaudetDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy.ORCID 0000-0001-8957-5545
Sheref S MansyDepartment CIBIO, University of Trento, via Sommarive 9, 38123 Povo, Italy. sheref.mansy@ualberta.ca.ORCID 0000-0003-2382-198X
University of Trento · ITFondazione Bruno Kessler · ITUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the construction of artificial cells that chemically communicate with mammalian cells under physiological conditions. The artificial cells respond to the presence of a small molecule in the environment by synthesizing and releasing a potent protein signal, brain-derived neurotrophic factor. Genetically controlled artificial cells communicate with engineered human embryonic kidney cells and murine neural stem cells. The data suggest that artificial cells are a versatile chassis for the in situ synthesis and on-demand release of chemical signals that elicit desired phenotypic changes of eukaryotic cells, including neuronal differentiation. In the future, artificial cells could be engineered to go beyond the capabilities of typical smart drug delivery vehicles by synthesizing and delivering specific therapeutic molecules tailored to distinct physiological conditions.

Identifiers

PMID32948587
PMCPMC7500934
OpenAlexW3087100678

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.