OSCR

Stress relaxation timescale and hydrogel network connectivity regulate neural progenitor cell stemness and differentiation.

Overview

Authors: Lauren E Brown1, Daphne Bakker2, Ping Zhou2, Christopher M Madl2,3
  1. Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA
  2. Department of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA
  3. Center for Precision Engineering for Health (CPE4H), University of Pennsylvania, Philadelphia, PA 19104, USA
Institutions: University of Pennsylvania (United States)
Journal: Journal of materials chemistry. B, volume 14, issue 15, pages 4740-4754
Dates: received 14 November 2025; accepted 30 March 2026; published online 1 April 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1039/d5tb02537k · PMID 41948829 · PMCID PMC13058797 · OpenAlex W7146996516
Open access: hybrid, a free copy (OpenAlex)
Status: data only
Categories: developmental (subfield)
Methods: Statistics, Preprocessing, Connectivity, Graphs, Machine learning
MeSH: Cell Differentiation*, Hydrogels*, Neural Stem Cells*, Animals, Cell Proliferation, Cells, Cultured (* major topic)
Topic: Hydrogels: synthesis, properties, applications (Molecular Medicine, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Funding: National Science Foundation (NNCI-2025608, DMR-2309043, CMMI-1548571); National Institute of General Medical Sciences (R35 GM154913); NIGMS NIH HHS (R35 GM154913)
Citations: cited by 1 paper (Europe PMC); 43 references in the paper

Abstract

Neural progenitor cells (NPCs) are promising candidates for cell replacement therapies, yet maintaining stemness while enabling expansion in chemically defined three-dimensional (3D) hydrogels remains a challenge. By tuning crosslink exchange kinetics, crosslinker functionality and stoichiometry, polymer phase separation behavior, and adhesive ligand presentation, a family of hydrogels was prepared to study the effects of stress relaxation timescale and network connectivity on NPC phenotype. Hydrogels with rapid relaxation and low connectivity promote expansion of NPCs as distributed single-cell networks that maintain stemness marker expression and differentiation capacity. NPCs embedded in slowly relaxing hydrogels maintained stemness marker expression through cell clustering but exhibited impaired proliferation and differentiation. Similarly, in the absence of integrin-binding cell adhesive ligands, NPCs also maintained stem cell marker expression but remained as clusters rather than distributed single-cell networks. Cadherin cell–cell contacts enable downstream β-catenin signaling and stemness maintenance, which are enhanced in rapidly relaxing, low connectivity networks. These findings identify a combination of network connectivity, stress relaxation timescale, and integrin-binding adhesive ligands as crucial design parameters for maintaining NPC stemness and differentiation capacity in 3D hydrogel networks.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data availability

All data supporting this study are contained in the main text, supplementary information (SI), or available as a publicly accessible database via Zenodo (https://doi.org/10.5281/zenodo.19005159). Supplementary information (theoretical prediction of extent of reaction and degradability, supporting figures and data tables, and detailed statistical analysis information). See DOI: https://doi.org/10.1039/d5tb02537k.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 29 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 4 authors, 6 MeSH terms, 3 funders, 43 references.

Cite

This paper

Brown, L. E., Bakker, D., Zhou, P., & Madl, C. M. (2026). Stress relaxation timescale and hydrogel network connectivity regulate neural progenitor cell stemness and differentiation. Journal of materials chemistry. B, 14(15), 4740-4754. https://doi.org/10.1039/d5tb02537k

BibTeX

@article{brown2026stress,
author = {Brown, Lauren E and Bakker, Daphne and Zhou, Ping and Madl, Christopher M},
title = {{Stress relaxation timescale and hydrogel network connectivity regulate neural progenitor cell stemness and differentiation}},
journal = {Journal of materials chemistry. B},
year = {2026},
month = apr,
volume = {14},
number = {15},
pages = {4740--4754},
publisher = {Royal Society of Chemistry},
issn = {2050-750X},
doi = {10.1039/d5tb02537k},
url = {https://doi.org/10.1039/d5tb02537k},
pmid = {41948829},
pmcid = {PMC13058797}
}

RIS

TY - JOUR
AU - Brown, Lauren E
AU - Bakker, Daphne
AU - Zhou, Ping
AU - Madl, Christopher M
TI - Stress relaxation timescale and hydrogel network connectivity regulate neural progenitor cell stemness and differentiation
T2 - Journal of materials chemistry. B
J2 - J Mater Chem B
PY - 2026
DA - 2026/04/22
VL - 14
IS - 15
SP - 4740
EP - 4754
SN - 2050-750X
PB - Royal Society of Chemistry
DO - 10.1039/d5tb02537k
UR - https://doi.org/10.1039/d5tb02537k
LA - en
ER -

CSL-JSON

{
"id": "10.1039/d5tb02537k",
"type": "article-journal",
"title": "Stress relaxation timescale and hydrogel network connectivity regulate neural progenitor cell stemness and differentiation",
"container-title": "Journal of materials chemistry. B",
"author": [
{
"family": "Brown",
"given": "Lauren E"
},
{
"family": "Bakker",
"given": "Daphne"
},
{
"family": "Zhou",
"given": "Ping"
},
{
"family": "Madl",
"given": "Christopher M"
}
],
"container-title-short": "J Mater Chem B",
"volume": "14",
"issue": "15",
"page": "4740-4754",
"DOI": "10.1039/d5tb02537k",
"PMID": "41948829",
"PMCID": "PMC13058797",
"ISSN": "2050-750X",
"publisher": "Royal Society of Chemistry",
"URL": "https://doi.org/10.1039/d5tb02537k",
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
22
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1016/j.isci.2026.115272
Physical crowding in 3D niche regulates neural stem cell differentiation via Cx43-mediated gap junction communication.
Journal: iScience
In common: 5 references
[2] doi:10.1039/d6tb01306f
Hyaluronic acid-alginate hydrazone crosslinked hydrogels support the generation and maturation of V2a interneurons.
Journal: Journal of materials chemistry. B
In common: developmental, 1 reference
[3] doi:10.1002/smll.74538
Stress-Adaptive Biomaterials With Tunable Yielding Architectures Regulate Organoid Morphogenesis.
Journal: Small (Weinheim an der Bergstrasse, Germany)
In common: developmental, 1 reference
[4] doi:10.1016/j.bbrep.2026.102655
Comprehensive characterization of the human neural stem cell line HNSC.100 as a versatile model for neurobiological research.
Journal: Biochemistry and biophysics reports
In common: 1 reference
[5] doi:10.1093/neuonc/noag059
Combined patch-clamp electrophysiology and single-cell genomic analysis reveal spiking tumor cells at the neocortical glioblastoma interface in humans.
Journal: Neuro-oncology
In common: 1 reference
[6] doi:10.1016/j.xcrm.2026.102787 [code]
A human iPSC-derived sensory neuron platform for high-throughput discovery of neuroprotectants against chemotherapy-induced peripheral neuropathy.
Journal: Cell reports. Medicine
In common: 1 reference
[7] doi:
Tutorial on using EEG microstates to study moment-to-moment large-scale functional brain network dynamics in neurodevelopment
Journal: Frontiers in neuroscience
In common: developmental
[8] doi:10.1038/s42003-026-10802-y
Transcriptome of fetal cortex of tree shrew underlying the emergence of outer subventricular zone.
Journal: Communications biology
In common: developmental
[9] doi:10.1016/j.isci.2026.117510
Single-cell transcriptomic atlas of the human fetal uveal tract reveals heterogeneity in melanocyte populations.
Journal: iScience
In common: developmental
[10] doi:10.1371/journal.pone.0358044 [code]
An exploratory fNIRS study on directional asymmetry in segmental discrimination: Lateral-rhotic (/la-ra/) and labial-dorsal (/ba-ga/) contrasts tested in 5- and 9-month-old Japanese infants.
Journal: PloS one
In common: developmental

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.