Proper
muscle function requires specific orientation of myotubes.
Cell chirality, a mechanical behavior of cells, may participate in
myogenesis and give rise to left–right (LR) orientation of
muscle tissue. Thus, it is essential to understand the factors effecting
the cell chirality. Here, using C2C12 cells as a model system, we
report that prior culture condition with high/low density can create
remnant effects on cell chirality after reseeding. C2C12 myoblasts
were first conditioned by a series of subcultures with plating density
at 2200 cells/cm2 (low density) or 22 000 cells/cm2 (high density). After reseeding on micropatterned stripes
fabricated on glass or polydimethylsiloxane (PDMS) substrates, we
found that the cells after low-density cultures exhibited a reduced
cell aspect ratio and intercellular alignment, leading to an attenuated
chiral orientation only appearing on glass substrate. In contrast,
chiral orientation was observed in cells after high-density culture
on both substrates. By comparing it to the original cells without
being subcultured with high/low density, we found that the series
of low-density cultures disorganized the formation of actin rings
in single cells, which is an essential structure for cell chirality.
Moreover, by using high-density culture supplemented with inhibitors
of actin polymerization, the effect of low-density cultures was recaptured,
suggesting that the series of subcultures with high/low density may
be an in vitro aging process that modifies the actin cytoskeleton,
causing a remnant attenuation of cell chirality even after trypsin
digestion and reseeding. Together, our result suggests a mechanistic
insight of how cytoskeletal structures “memorize” the
previous experience through modification of the actin filament, opening
up new possibilities for morphogenesis and mechanobiology.