Evidence map›Paper›PMID 41807773›Full record

ArticleNature materials2026

Stress-relaxing granular bioprinting materials enable complex and uniform organoid self-organization.

Austin J Graham, Michelle W L Khoo, Vasudha Srivastava, Sara Viragova, Honesty Kim, Kavita Parekh, Kelsey M Hennick, Malia Bird, Nadine Goldhammer, Jie Zeng Yu and 14 more

Abstract read
In one paragraph

Article in Nature materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Austin J GrahamDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0001-8924-181X
Michelle W L KhooChan Zuckerberg Biohub SF, San Francisco, CA, USA.ORCID 0009-0005-0634-6904
Vasudha SrivastavaDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0001-8845-9518
Sara ViragovaDepartment of Orofacial Sciences, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0003-0598-1445
Honesty KimDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.
Kavita ParekhDepartment of Bioengineering, University of California Berkeley, Berkeley, CA, USA.ORCID 0000-0001-5486-8794
Kelsey M HennickWeill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-6127-2400
Malia BirdDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0001-8871-155X
Nadine GoldhammerDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0003-1644-3984
Jie Zeng YuDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0009-0009-6663-4405
Grace HuGraduate Program in Bioengineering, University of California San Francisco and University of California Berkeley, San Francisco, CA, USA.ORCID 0000-0003-2288-5156
Natasha T BrinkleyGraduate Program in Bioengineering, University of California San Francisco and University of California Berkeley, San Francisco, CA, USA.ORCID 0009-0006-1647-7489
Lucas PardoGraduate Program in Bioengineering, University of California San Francisco and University of California Berkeley, San Francisco, CA, USA.
Jasmine S AmayaDepartment of Bioengineering, University of California Berkeley, Berkeley, CA, USA.ORCID 0009-0003-0119-3262
Cameron D MorleyDepartment of Bioengineering, University of California Berkeley, Berkeley, CA, USA.
Nishant ChadhaWeill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.
Paul LebelChan Zuckerberg Biohub SF, San Francisco, CA, USA.ORCID 0000-0003-4569-1493
Sanjay KumarDepartment of Bioengineering, University of California Berkeley, Berkeley, CA, USA.ORCID 0000-0002-9996-4883
Jennifer M RosenbluthChan Zuckerberg Biohub SF, San Francisco, CA, USA.
Tomasz J NowakowskiWeill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.
Ovijit ChaudhuriDepartment of Mechanical Engineering, Stanford University, Stanford, CA, USA.ORCID 0000-0002-9287-3401
Ophir KleinDepartment of Orofacial Sciences, University of California San Francisco, San Francisco, CA, USA.
Rafael Gómez-SjöbergChan Zuckerberg Biohub SF, San Francisco, CA, USA. rafael.gomez@czbiohub.org.ORCID 0000-0001-8017-9669
Zev J GartnerDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA. zev.gartner@ucsf.edu.ORCID 0000-0001-7803-1219

Funding

TRAINING PROGRAM IN PEDIATRIC GASTROENTEROLOGY/NUTRITIONT32DK007762 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI James Bayrer · 1998 to 2026
$7.3M
The physical and molecular mechanisms of intestinal villus morphogenesis and repairR01DK126376 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Zev Jordan Gartner · 2020 to 2026
$4.2M
A Team Science Approach to the Co Development of Oral Mucosa for Therapeutic PurposesRM1DE035338 · NIDCR · CEDARS-SINAI MEDICAL CENTER · PI Kevin Matthew Byrd, Zev Jordan Gartner · 2025 to 2026
$2.4M
Increasing organoid reproducibility and complexity for drug testing and disease modelingR33CA297969 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Zev Jordan Gartner · 2025 to 2026
$784k
Dynamically reconfigurable materials for 4D bioprinting of a human gut-brain axisK99EB037059 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Austin Joseph Graham · 2025 to 2026
$249k
NCI NIH HHS R33 CA297969NIBIB NIH HHS K99 EB037059NIDCR NIH HHS RM1 DE035338NIDDK NIH HHS R01 DK126376NIDDK NIH HHS T32 DK007762NSF | BIO | Division of Biological Infrastructure (DBI) DBI-1548297
6 · The paper itself

Abstract

Complex and robust tissue self-organization requires defined initial conditions and dynamic boundaries-neighbouring tissues and extracellular matrix that actively evolve to guide morphogenesis. A major challenge in tissue engineering is identifying material properties that are compatible with controlling initial culture conditions while mimicking dynamic tissue boundaries. Here we describe a highly tunable granular biomaterial, MAGIC matrix, that supports both long-term bioprinting and gold-standard tissue self-organization. We identify that significant stress relaxation at the long timescales and large deformation magnitudes relevant to self-organization is required for optimal morphogenesis. We apply optimized MAGIC matrices toward precise extrusion bioprinting of saturated cell suspensions directly into three-dimensional culture. Carefully controlling initial conditions for tissue growth yields dramatic increases in organoid reproducibility and complexity across multiple tissue types, enabling high-throughput generation of organoid arrays and perfusable three-dimensional microphysiological systems. Our results identify key biomaterial parameters for optimal organoid morphogenesis and lay the foundation for fabricating more complex and reproducible self-organized tissues.

Indexed as

Biocompatible MaterialsBioprintingOrganoidsTissue EngineeringAnimalsExtracellular MatrixHumansStress, MechanicalBiocompatible Materials

Identifiers

PMID41807773
PMCPMC13178435

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.