Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Nov. 22, 2024
Extracellular
matrix
(ECM)
stiffness
influences
cancer
cell
fate
by
altering
gene
expression.
Previous
studies
suggest
that
stiffness-induced
nuclear
deformation
may
regulate
expression
through
YAP
localization.
We
investigated
the
role
of
lamina
in
this
process.
show
exhibits
mechanical
threshold
behavior:
once
unwrinkled,
is
inextensible.
A
computational
model
predicts
unwrinkled
under
tension,
which
confirmed
using
a
lamin
tension
sensor.
Laminar
unwrinkling
caused
flattening
during
spreading
on
stiff
ECM.
Knockdown
A/C
eliminates
surface
and
decreases
These
findings
cells
conforms
to
drop
reveal
for
controlling
localization
cells.
Matrix
induced
regulates
This
study
finds
induces
promotes
yes
associated
protein
(YAP),
transcriptional
co-activator.
Developmental Cell,
Journal Year:
2022,
Volume and Issue:
57(4), P. 466 - 479.e6
Published: Feb. 1, 2022
The
cytoplasm
is
a
crowded,
visco-elastic
environment
whose
physical
properties
change
according
to
physiological
or
developmental
states.
How
the
of
impact
cellular
functions
in
vivo
remains
poorly
understood.
Here,
we
probe
effects
cytoplasmic
concentration
on
microtubules
by
applying
osmotic
shifts
fission
yeast,
moss,
and
mammalian
cells.
We
show
that
rates
both
microtubule
polymerization
depolymerization
scale
linearly
inversely
with
concentration;
an
increase
decreases
proportionally,
whereas
decrease
leads
opposite.
Numerous
lines
evidence
indicate
these
are
due
changes
viscosity
rather
than
stress
responses
macromolecular
crowding
per
se.
reconstituted
vitro
tuning
viscosity.
Our
findings
that,
even
normal
conditions,
modulates
reactions
underlie
dynamic
behaviors.
Proceedings of the National Academy of Sciences,
Journal Year:
2022,
Volume and Issue:
119(21)
Published: May 17, 2022
The
volume
of
the
cell
nucleus
varies
across
types
and
species
is
commonly
thought
to
be
determined
by
size
genome
degree
chromatin
compaction.
However,
this
notion
has
been
challenged
over
years
much
experimental
evidence.
Here,
we
consider
physical
condition
mechanical
force
balance
as
a
determining
nuclear
use
quantitative,
order-of-magnitude
analysis
estimate
forces
from
different
sources
cytoplasmic
pressure.
Our
estimates
suggest
that
dominant
pressure
within
cytoplasm
nonstriated
muscle
cells
originates
osmotic
proteins
RNA
molecules
are
localized
or
out-of-equilibrium,
active
nucleocytoplasmic
transport
rather
than
its
associated
ions.
This
motivates
us
formulate
model
for
ratio
volumes
in
which
pressures
determine
relative
volumes.
In
accordance
with
unexplained
observations
century
old,
our
predicts
constant,
robust
wide
variety
biochemical
biophysical
manipulations,
changed
only
if
gene
expression
modulated.
Cellular
growth
is
the
result
of
passive
physical
constraints
and
active
biological
processes.
Their
interplay
leads
to
appearance
robust
ubiquitous
scaling
laws
relating
linearly
cell
size,
dry
mass,
nuclear
size.
Despite
accumulating
experimental
evidence,
their
origin
still
unclear.
Here,
we
show
that
these
can
be
explained
quantitatively
by
a
single
model
size
regulation
based
on
three
simple,
yet
generic,
defining
altogether
Pump-Leak
model.
Based
quantitative
estimates,
clearly
map
coarse-grained
parameters
with
dominant
cellular
components.
We
propose
mass
density
homeostasis
arises
from
between
proteins
small
osmolytes,
mainly
amino
acids
ions.
Our
predicts
this
naturally
fail,
both
at
senescence
when
DNA
RNAs
are
saturated
RNA
polymerases
ribosomes,
respectively,
mitotic
entry
due
counterion
release
following
histone
tail
modifications.
same
laws,
further
results
osmotic
balance
envelope
large
pool
metabolites,
which
dilutes
chromatin
counterions
do
not
scale
during
growth.
Biophysical Journal,
Journal Year:
2023,
Volume and Issue:
122(5), P. 767 - 783
Published: Feb. 3, 2023
The
cytoplasm
is
a
complex,
crowded,
actively
driven
environment
whose
biophysical
characteristics
modulate
critical
cellular
processes
such
as
cytoskeletal
dynamics,
phase
separation,
and
stem
cell
fate.
Little
known
about
the
variance
in
these
cytoplasmic
properties.
Here,
we
employed
particle-tracking
nanorheology
on
genetically
encoded
multimeric
40
nm
nanoparticles
(GEMs)
to
measure
diffusion
within
of
individual
fission
yeast
(Schizosaccharomyces
pombe)
cellscells.
We
found
that
apparent
coefficients
GEM
particles
varied
over
400-fold
range,
while
differences
average
particle
diffusivity
among
cells
spanned
10-fold
range.
To
determine
origin
this
heterogeneity,
developed
Doppelgänger
simulation
approach
uses
stochastic
simulations
replicate
experimental
statistics
particle-by-particle
basis,
each
track
had
one-to-one
correspondence
with
their
simulated
counterpart.
These
showed
large
intra-
inter-cellular
variations
could
not
be
explained
by
variability
but
only
reproduced
models
assume
wide
variation
viscosity.
combining
viscosity
also
predicted
weak
nonergodicity
diffusion,
consistent
data.
probe
variation,
was
largely
independent
factors
temperature,
actin
microtubule
cytoskeletons,
cell-cyle
stage,
spatial
locations,
magnified
hyperosmotic
shocks.
Taken
together,
our
results
provide
striking
demonstration
"well-mixed"
represents
highly
heterogeneous
which
subcellular
components
at
size
scale
experience
dramatically
different
effective
viscosities
an
cell,
well
identical
population.
findings
carry
significant
implications
for
origins
regulation
biological
noise
levels.
Developmental Cell,
Journal Year:
2023,
Volume and Issue:
58(16), P. 1462 - 1476.e8
Published: June 19, 2023
Cell
proliferation
is
a
central
process
in
tissue
development,
homeostasis,
and
disease,
yet
how
regulated
the
context
remains
poorly
understood.
Here,
we
introduce
quantitative
framework
to
elucidate
growth
dynamics
regulate
cell
proliferation.
Using
MDCK
epithelial
monolayers,
show
that
limiting
rate
of
expansion
creates
confinement
suppresses
growth;
however,
this
does
not
directly
affect
cycle.
This
leads
uncoupling
between
rates
division
epithelia
and,
thereby,
reduces
volume.
Division
becomes
arrested
at
minimal
volume,
which
consistent
across
diverse
vivo.
nucleus
approaches
minimum
volume
capable
packaging
genome.
Loss
cyclin
D1-dependent
cell-volume
regulation
results
an
abnormally
high
nuclear-to-cytoplasmic
ratio
DNA
damage.
Overall,
demonstrate
by
interplay
regulation.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 17, 2024
Abstract
Changing
environmental
conditions
necessitate
an
immediate
cellular
adaptation
to
ensure
survival.
Dictyostelium
discoideum
,
a
bacteriovore
slime
mold
present
in
the
soil
of
most
terrestrial
ecosystems,
is
known
for
its
ability
tolerate
drastic
changes
osmolarity.
How
cells
cope
with
resulting
mechanical
stress
remains
understudied.
Here
we
show
that
D.
has
extraordinarily
elaborate
and
resilient
nuclear
pores
serve
as
conduits
massive
fluid
exchange
between
cytosol
nucleus.
We
capitalize
on
unique
properties
quantify
flow
across
envelope
necessitated
by
changing
size
response
osmotic
stress.
Based
mathematical
concepts
adapted
from
hydrodynamics,
conceptualize
this
phenomenon
porous
pores.
This
type
distinct
canonically
characterized
modes
nucleocytoplasmic
transport,
i.e.
passive
diffusion
active
because
dependence
pressure.
Our
insights
are
relevant
any
biological
condition
necessitates
rapid
changes,
which
includes
metastasizing
cancer
squeezing
through
constrictions,
migrating
differentiating
tissues.
Annual Review of Genetics,
Journal Year:
2022,
Volume and Issue:
56(1), P. 165 - 185
Published: Aug. 17, 2022
Though
cell
size
varies
between
different
cells
and
across
species,
the
nuclear-to-cytoplasmic
(N/C)
ratio
is
largely
maintained
species
within
types.
A
maintains
a
relatively
constant
N/C
by
coupling
DNA
content,
nuclear
size,
size.
We
explore
how
couple
division
growth
to
content.
In
some
cases,
use
as
molecular
yardstick
control
availability
of
cycle
regulators.
other
sets
limit
for
biosynthetic
capacity.
Developmentally
programmed
variations
in
given
type
suggest
that
specific
required
respond
physiological
demands.
Recent
observations
connecting
decreased
ratios
with
cellular
senescence
indicate
maintaining
proper
essential
functioning.
Together,
these
findings
causative,
not
simply
correlative,
role
regulating
progression.
Frontiers in Cell and Developmental Biology,
Journal Year:
2022,
Volume and Issue:
10
Published: Oct. 12, 2022
Cell
dry
mass
is
principally
determined
by
the
sum
of
biosynthesis
and
degradation.
Measurable
change
in
occurs
on
a
time
scale
hours.
By
contrast,
cell
volume
can
minutes
altering
osmotic
conditions.
How
changes
are
coupled
fundamental
question
size
control.
If
were
proportional
to
during
growth,
would
always
maintain
same
cellular
density,
defined
as
dividing
volume.
The
accuracy
stability
against
perturbation
this
proportionality
has
never
been
stringently
tested.
Normalized
Raman
Imaging
(NoRI),
measure
both
protein
lipid
density
directly
.
Using
new
technique
,
we
have
able
investigate
response
pharmaceutical
physiological
perturbations
three
cultured
mammalian
lines.
We
find
remarkably
narrow
distribution
within
cells,
that
is,
significantly
tighter
than
variability
or
distribution.
measured
independent
cycle.
be
modulated
extracellular
osmolytes
disruptions
cytoskeleton.
Yet,
surprisingly
resistant
pharmacological
synthesis
degradation,
suggesting
there
must
some
form
feedback
control
homeostasis
when
altered.
such
starvation
senescence
induce
significant
shifts
density.
begun
shed
light
how
why
remains
fixed
yet
sensitive
transitions
state.
Proceedings of the National Academy of Sciences,
Journal Year:
2023,
Volume and Issue:
120(9)
Published: Feb. 21, 2023
Many
studies
of
cytoplasm
rheology
have
focused
on
small
components
in
the
submicrometer
scale.
However,
also
baths
large
organelles
like
nuclei,
microtubule
asters,
or
spindles
that
often
take
significant
portions
cells
and
move
across
to
regulate
cell
division
polarization.
Here,
we
translated
passive
sizes
ranging
from
few
up
~50
percents
diameter,
through
vast
live
sea
urchin
eggs,
with
calibrated
magnetic
forces.
Creep
relaxation
responses
indicate
for
objects
larger
than
micron
size,
behaves
as
a
Jeffreys
material,
viscoelastic
at
short
timescales,
fluidizing
longer
times.
component
size
approached
cells,
resistance
increased
nonmonotonic
manner.
Flow
analysis
simulations
suggest
this
size-dependent
viscoelasticity
emerges
hydrodynamic
interactions
between
moving
object
static
surface.
This
effect
yields
position-dependent
initially
closer
surface
being
harder
displace.
These
findings
hydrodynamically
couples
restrain
their
motion,
important
implications
shape
sensing
cellular
organization.