Evidence map›Paper›PMID 36998105›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Programming of Multicellular Patterning with Mechano-Chemically Microstructured Cell Niches.

Peter L H Newman, Queenie Yip, Pierre Osteil, Tim A Anderson, Jane Q J Sun, Daryan Kempe, Maté Biro, Jae-Won Shin, Patrick P L Tam, Hala Zreiqat

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. 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. 3D Printed Materials with Nanovoxelated Elastic Moduli.Advanced materials (Deerfield Beach, Fla.) · 2025
    Article
  2. Review
  3. Programming of Multicellular Patterning with Mechano-Chemically Microstructured Cell Niches.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
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

10 authors.

Peter L H NewmanARC Training Centre for Innovative Bioengineering, The University of Sydney, Sydney, 2006, Australia.ORCID 0000-0002-5202-4819
Queenie YipARC Training Centre for Innovative Bioengineering, The University of Sydney, Sydney, 2006, Australia.
Pierre OsteilEmbryology Research Unit, Children's Medical Research Institute, Sydney, 2145, Australia.
Tim A AndersonARC Training Centre for Innovative Bioengineering, The University of Sydney, Sydney, 2006, Australia.
Jane Q J SunEmbryology Research Unit, Children's Medical Research Institute, Sydney, 2145, Australia.
Daryan KempeEMBL Australia, Single Molecule Science Node, School of Medical Sciences, UNSW, Sydney, 2052, Australia.
Maté BiroEMBL Australia, Single Molecule Science Node, School of Medical Sciences, UNSW, Sydney, 2052, Australia.
Jae-Won ShinDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, 60607, USA.
Patrick P L TamEmbryology Research Unit, Children's Medical Research Institute, Sydney, 2145, Australia.
Hala ZreiqatARC Training Centre for Innovative Bioengineering, The University of Sydney, Sydney, 2006, Australia.

Funding

Encapsulation of mesenchymal stromal cells in engineered microgels for resolution of lung fibrosisR01HL141255 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2019 to 2023
$2.0M
Engineering microscale hydrogel deposition to direct single stem cell differentiationR01GM141147 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2021 to 2024
$1.9M
Mechanically controlled release of hematopoietic factors from mesenchymal stromal cells for blood regenerationR00HL125884 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2016 to 2018
$747k
Mechanically controlled release of hematopoietic factors from mesenchymal stromal cells for blood regenerationK99HL125884 · NHLBI · HARVARD UNIVERSITY · PI SHIN, JAE-WON · 2015 to 2016
$176k
NHLBI NIH HHS K99 HL125884NHLBI NIH HHS R00 HL125884NHLBI NIH HHS R01 HL141255NIGMS NIH HHS R01 GM141147NIH HHS R00-HL125884
6 · The paper itself

Abstract

Multicellular patterning of stem-cell-derived tissue models is commonly achieved via self-organizing activities triggered by exogenous morphogenetic stimuli. However, such tissue models are prone to stochastic behavior, limiting the reproducibility of cellular composition and forming non-physiological architectures. To enhance multicellular patterning in stem cell-derived tissues, a method for creating complex tissue microenvironments endowed with programmable multimodal mechano-chemical cues, including conjugated peptides, proteins, morphogens, and Young's moduli defined over a range of stiffnesses is developed. The ability of these cues to spatially guide tissue patterning processes, including mechanosensing and the biochemically driven differentiation of selected cell types, is demonstrated. By rationally designing niches, the authors engineered a bone-fat assembly from stromal mesenchyme cells and regionalized germ layer tissues from pluripotent stem cells. Through defined niche-material interactions, mechano-chemically microstructured niches enable the spatial programming of tissue patterning processes. Mechano-chemically microstructured cell niches thereby offer an entry point for enhancing the organization and composition of engineered tissues, potentiating structures that better recapitulate their native counterparts.

Indexed as

Pluripotent Stem CellsTissue EngineeringBone and BonesMorphogenesisReproducibility of Resultsmicropatterningmulticellularitypluripotent stem cellstissue modelstissue patterning

Identifiers

PMID36998105
PMCPMC10214222

What OpenQuestion holds

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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.