Evidence map›Paper›PMID 37023529›Full record

ArticleBiomaterials2023

Instructional materials that control cellular activity through synthetic Notch receptors.

Joanne C Lee, Hannah J Brien, Bonnie L Walton, Zachary M Eidman, Satoshi Toda, Wendell A Lim, Jonathan M Brunger

Open access · hybridAbstract read
In one paragraph

Article in Biomaterials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  4. bioRxiv : the preprint server for biology · 2026
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  14. Bioengineering vascularization.Development (Cambridge, England) · 2024
    Review
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  17. bioRxiv : the preprint server for biology · 2024
    Article
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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

7 authors at 3 institutions in 2 countries.

Joanne C LeeDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37212, USA.
Hannah J BrienDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37212, USA.
Bonnie L WaltonDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37212, USA.
Zachary M EidmanDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37212, USA.
Satoshi TodaWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Ishikawa, Japan.
Wendell A LimCell Design Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, 94158, USA. Electronic address: wendell.lim@ucsf.edu.
Jonathan M BrungerDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37212, USA; Center for Stem Cell Biology, Vanderbilt University, Nashville, TN, 37212, USA. Electronic address: jonathan.m.brunger@vanderbilt.edu.
Vanderbilt University · USKanazawa University · JPUniversity of California, San Francisco · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
Rewiring Therapeutic Cells: User-Controlled T Cells and Stem CellsP50GM081879 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIM, WENDELL A · 2010 to 2017
$19.0M
Engineered Sense and Response Circuits for Stem Cell-Based Tissue Regeneration and RepairF32EB024391 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BRUNGER, JONATHAN MATTHEW · 2017 to 2018
$116k
Howard Hughes Medical InstituteNCI NIH HHS P30 CA068485NIBIB NIH HHS F32 EB024391NIDDK NIH HHS P30 DK058404NIGMS NIH HHS P50 GM081879
6 · The paper itself

Abstract

The field of regenerative engineering relies primarily on the dual technical platforms of cell selection/conditioning and biomaterial fabrication to support directed cell differentiation. As the field has matured, an appreciation for the influence of biomaterials on cell behaviors has resulted in engineered matrices that meet biomechanical and biochemical demands of target pathologies. Yet, despite advances in methods to produce designer matrices, regenerative engineers remain unable to reliably orchestrate behaviors of therapeutic cells in situ. Here, we present a platform named MATRIX whereby cellular responses to biomaterials can be custom defined by combining engineered materials with cells expressing cognate synthetic biology control modules. Such privileged channels of material-to-cell communication can activate synthetic Notch receptors and govern activities as diverse as transcriptome engineering, inflammation attenuation, and pluripotent stem cell differentiation, all in response to materials decorated with otherwise bioinert ligands. Further, we show that engineered cellular behaviors are confined to programmed biomaterial surfaces, highlighting the potential to use this platform to spatially organize cellular responses to bulk, soluble factors. This integrated approach of co-engineering cells and biomaterials for orthogonal interactions opens new avenues for reproducible control of cell-based therapies and tissue replacements.

Indexed as

Pluripotent Stem CellsReceptors, ArtificialBiocompatible MaterialsCell DifferentiationReceptors, NotchTissue EngineeringBiocompatible MaterialsReceptors, ArtificialReceptors, NotchCell therapiesDesigner matricesRegenerative medicineStem cellssynNotchSynthetic biology

Identifiers

PMID37023529
PMCPMC10320837
OpenAlexW4361284858

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.