Evidence map›Paper›PMID 35235768›Full record

ArticleCell2022

Synthetic mammalian signaling circuits for robust cell population control.

Yitong Ma, Mark W Budde, Michaëlle N Mayalu, Junqin Zhu, Andrew C Lu, Richard M Murray, Michael B Elowitz

Open access · greenAbstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Human Synthetic Biology and Programmable Gene Regulation Control.Annual review of genomics and human genetics · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Open problems in synthetic multicellularity.NPJ systems biology and applications · 2024
    Article
  15. Engineering signalling pathways in mammalian cells.Nature biomedical engineering · 2024
    Review
  16. Post-Transcriptional Modular Synthetic Receptors.bioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Article
  19. Accelerating Diverse Cell-Based Therapies Through Scalable Design.Annual review of chemical and biomolecular engineering · 2024
    Review
  20. Designer cell therapy for tissue regeneration.Inflammation and regeneration · 2024
    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

7 authors at 2 institutions in 1 country.

Yitong MaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Mark W BuddeDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Primordium Labs, Arcadia, CA 91006, USA.
Michaëlle N MayaluDivision of Engineering and Applied Science, California Institute of Technology, Pasadena, CA 91125, USA.
Junqin ZhuDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Andrew C LuDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Richard M MurrayDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Division of Engineering and Applied Science, California Institute of Technology, Pasadena, CA 91125, USA.
Michael B ElowitzDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Division of Engineering and Applied Science, California Institute of Technology, Pasadena, CA 91125, USA; Howard Hughes Medical Institute, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: melowitz@caltech.edu.
California Institute of Technology · USStanford University · US

Funding

MEMOIR: Recording, and in situ readout of cell lineage and transcriptional historyR01MH116508 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAI, LONG, ELOWITZ, MICHAEL B · 2017 to 2021
$6.9M
NIMH NIH HHS R01 MH116508
6 · The paper itself

Abstract

In multicellular organisms, cells actively sense and control their own population density. Synthetic mammalian quorum-sensing circuits could provide insight into principles of population control and extend cell therapies. However, a key challenge is reducing their inherent sensitivity to "cheater" mutations that evade control. Here, we repurposed the plant hormone auxin to enable orthogonal mammalian cell-cell communication and quorum sensing. We designed a paradoxical population control circuit, termed "Paradaux," in which auxin stimulates and inhibits net cell growth at different concentrations. This circuit limited population size over extended timescales of up to 42 days of continuous culture. By contrast, when operating in a non-paradoxical regime, population control became more susceptible to mutational escape. These results establish auxin as a versatile "private" communication system and demonstrate that paradoxical circuit architectures can provide robust population control.

Indexed as

Cell CommunicationSignal TransductionAnimalsCell CountCell EngineeringIndoleacetic AcidsMammalsQuorum SensingSynthetic BiologyIndoleacetic Acidsauxincell population controlmammalian synthetic biologyparadoxical controlquorum sensingsynthetic circuitssynthetic signaling

Identifiers

PMID35235768
PMCPMC8995209
OpenAlexW4220969470

What OpenQuestion holds

Textmetadata
LicenceTDM
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.