Scaffold stiffness affects oligodendrocyte proliferation <i>via</i> cell traction forces

Drugs that promote the regeneration of the central nervous system (CNS) have motivated the development of a method to assess the functions of CNS cells, such as oligodendrocytes, which sustain the homeostasis of neuronal networks. In this study, we evaluated the effects of scaffold stiffness on the phenotypic and transcriptomic levels of MO3.13 cells, a human oligodendrocyte lineage cell line. Cells cultured on gels of varying stiffness exhibited different growth potentials. RNA sequencing detected differences in the expression of genes associated with cell proliferation and actin cytoskeleton polymerization. Treatment with actin polymerization inhibitor prevented changes in the growth potential, which were mediated by cell traction forces. These results suggest that scaffold stiffness-transduced biological signaling is an important factor to consider when assessing CNS cell function.

Authors

Institutions

Publication Details

Journal
Biomaterials Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5bm00689a
Citations
1
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
Field-Weighted Citation Impact
1.32
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Scaffold stiffness affects oligodendrocyte proliferation via cell traction forces

Haruki Watanabe, Lili Quan, Shinjiro Umezu, Akiko Uyeda et al.
1 citations
Biomaterials Science
Neurogenesis and neuroplasticity mechanisms
1.32
article

Scaffold stiffness affects oligodendrocyte proliferation via cell traction forces

Haruki Watanabe, Lili Quan, Shinjiro Umezu, Akiko Uyeda, Rieko Muramatsu, Sumio Iwai, Tatsunori Suzuki, Ze Zhang
article en
1 citations

Abstract

Drugs that promote the regeneration of the central nervous system (CNS) have motivated the development of a method to assess the functions of CNS cells, such as oligodendrocytes, which sustain the homeostasis of neuronal networks. In this study, we evaluated the effects of scaffold stiffness on the phenotypic and transcriptomic levels of MO3.13 cells, a human oligodendrocyte lineage cell line. Cells cultured on gels of varying stiffness exhibited different growth potentials. RNA sequencing detected differences in the expression of genes associated with cell proliferation and actin cytoskeleton polymerization. Treatment with actin polymerization inhibitor prevented changes in the growth potential, which were mediated by cell traction forces. These results suggest that scaffold stiffness-transduced biological signaling is an important factor to consider when assessing CNS cell function.

Biomaterials ScienceVol. 13(16)
Waseda University (JP), Tokyo University of Science (JP), National Center of Neurology and Psychiatry (JP)
Zero hunger
Openalex Percentile: Top 19%
Neurogenesis and neuroplasticity mechanisms
1.32
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.