Myoblast Choreographic Alignment

The alignment of spindle-shaped cells is crucial for physiological processes, such as muscle regeneration and tissue engineering. Despite their importance, the underlying mechanisms that govern this alignment remain poorly understood. In this study, we explore the collective motion and alignment of C2C12 myoblasts, cells essential for muscle regeneration, across a range of cell densities and substrate stiffness. Contrary to the conventional view that C2C12 cells exhibit weak cell-cell adhesion, leading to uncoordinated motion, our study shows that these cells demonstrate anisotropic adhesion properties. Specifically, cells connected longitudinally by nanoscale focal adherens junctions (FAJs) exhibit strong adhesion, whereas those connected laterally by nanoscale linear adherens junctions (LAJs) display weak adhesion. The interplay between these molecular junctions facilitates spontaneous alignment, even beyond confluence, contributing to the formation of multinucleated myotubes. Moreover, we show that softer substrates reduce the level of C2C12 cell alignment, emphasizing the role of extracellular environments in regulating cell behavior. These insights into the alignment dynamics of C2C12 myoblasts advance our understanding of contractile cell behavior and offer valuable contributions to the fields of muscle regeneration, tissue engineering, and cellular biomechanics.

Authors

Institutions

Publication Details

Journal
ACS Nano
Published
2025-10-08
DOI
https://doi.org/10.1021/acsnano.5c08392
Citations
3
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
3.45
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Myoblast Choreographic Alignment

Endao Han, Marcus Lin, Yucheng Huo, Yukai Zhao et al.
3 citations
ACS Nano
Cellular Mechanics and Interactions
3.45
article

Myoblast Choreographic Alignment

Endao Han, Marcus Lin, Yucheng Huo, Yukai Zhao, K. Jimmy Hsia, Hongmei Xu
article en
3 citations

Abstract

The alignment of spindle-shaped cells is crucial for physiological processes, such as muscle regeneration and tissue engineering. Despite their importance, the underlying mechanisms that govern this alignment remain poorly understood. In this study, we explore the collective motion and alignment of C2C12 myoblasts, cells essential for muscle regeneration, across a range of cell densities and substrate stiffness. Contrary to the conventional view that C2C12 cells exhibit weak cell-cell adhesion, leading to uncoordinated motion, our study shows that these cells demonstrate anisotropic adhesion properties. Specifically, cells connected longitudinally by nanoscale focal adherens junctions (FAJs) exhibit strong adhesion, whereas those connected laterally by nanoscale linear adherens junctions (LAJs) display weak adhesion. The interplay between these molecular junctions facilitates spontaneous alignment, even beyond confluence, contributing to the formation of multinucleated myotubes. Moreover, we show that softer substrates reduce the level of C2C12 cell alignment, emphasizing the role of extracellular environments in regulating cell behavior. These insights into the alignment dynamics of C2C12 myoblasts advance our understanding of contractile cell behavior and offer valuable contributions to the fields of muscle regeneration, tissue engineering, and cellular biomechanics.

ACS NanoVol. 19(41)
Nanyang Technological University (SG), King Abdullah University of Science and Technology (SA)
Openalex Percentile: Top 7%
Cellular Mechanics and Interactions
3.45
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.