Evidence map›Paper›PMID 39562554›Full record

ArticleNature communications2024

Control of spatio-temporal patterning via cell growth in a multicellular synthetic gene circuit.

Marco Santorelli, Pranav S Bhamidipati, Josquin Courte, Benjamin Swedlund, Naisargee Jain, Kyle Poon, Dominik Schildknecht, Andriu Kavanagh, Victoria A MacKrell, Trusha Sondkar and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

15 authors.

Marco Santorelli *Eli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0002-9633-7825
Pranav S Bhamidipati *Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Josquin Courte *Eli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Benjamin SwedlundEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Naisargee JainEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID 0009-0004-2505-2189
Kyle PoonEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Dominik SchildknechtDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Andriu KavanaghEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Victoria A MacKrellEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Trusha SondkarEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Mattias MalagutiCentre for Regenerative Medicine, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-4392-7183
Giorgia QuadratoEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0003-0717-4874
Sally LowellCentre for Regenerative Medicine, The University of Edinburgh, Edinburgh, UK.
Matt ThomsonDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA. mthomson@caltech.edu.ORCID 0000-0003-1021-1234
Leonardo MorsutEli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. leonardo.morsut@med.usc.edu.ORCID 0000-0001-7049-3478

Funding

Synthetic development: dissection of morphogenetic programs via reconstructive and perturbative approachesR35GM138256 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MORSUT, LEONARDO · 2020 to 2024
$2.1M
NIGMS NIH HHS R35 GM138256NSF | ENG/OAD | Division of Chemical, Bioengineering, Environmental, and Transport Systems (CBET) CBET-2034495 RECODENSF | ENG/OAD | Division of Chemical, Bioengineering, Environmental, and Transport Systems (CBET) CBET-2145528 CAREERU.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) GM138256Wellcome Trust 220298
6 · The paper itself

Abstract

A major goal in synthetic development is to build gene regulatory circuits that control patterning. In natural development, an interplay between mechanical and chemical communication shapes the dynamics of multicellular gene regulatory circuits. For synthetic circuits, how non-genetic properties of the growth environment impact circuit behavior remains poorly explored. Here, we first describe an occurrence of mechano-chemical coupling in synthetic Notch (synNotch) patterning circuits: high cell density decreases synNotch-gated gene expression in different cellular systems in vitro. We then construct, both in vitro and in silico, a synNotch-based signal propagation circuit whose outcome can be regulated by cell density. Spatial and temporal patterning outcomes of this circuit can be predicted and controlled via modulation of cell proliferation, initial cell density, and/or spatial distribution of cell density. Our work demonstrates that synthetic patterning circuit outcome can be controlled via cellular growth, providing a means for programming multicellular circuit patterning outcomes.

Indexed as

Cell ProliferationGene Regulatory NetworksReceptors, NotchAnimalsBody PatterningCell CountGenes, SyntheticHumansSignal TransductionSynthetic BiologyReceptors, Notch

Identifiers

PMID39562554
PMCPMC11577002

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.