Molecular Cell,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 1, 2024
Changing
environmental
conditions
necessitate
rapid
adaptation
of
cytoplasmic
and
nuclear
volumes.
We
use
the
slime
mold
Dictyostelium
discoideum,
known
for
its
ability
to
tolerate
extreme
changes
in
osmolarity,
assess
which
role
pore
complexes
(NPCs)
play
achieving
volume
relieving
mechanical
stress.
capitalize
on
unique
properties
D.
discoideum
quantify
fluid
flow
across
NPCs.
has
an
elaborate
NPC
structure
situ.
Its
dilation
state
affects
permeability
nucleocytosolic
flow.
Based
mathematical
concepts
adapted
from
hydrodynamics,
we
conceptualize
this
phenomenon
as
porous
NPCs,
is
distinct
canonically
characterized
modes
nucleocytoplasmic
transport
because
dependence
pressure.
Viral
blockage
decreased
Our
results
may
be
relevant
any
biological
that
entail
size
adaptation,
including
metastasizing
cancer
cells,
migrating
or
differentiating
tissues.
Oxford University Press eBooks,
Journal Year:
2024,
Volume and Issue:
unknown, P. 191 - 224
Published: Feb. 29, 2024
Abstract
Numerous
correlates
of
cell
growth
are
thought
to
be
general
enough
christened
as
laws,
although
few
have
been
examined
thoroughly
in
multiple
organisms.
One
well-established
relationship
is
the
linear
increase
ribosome
number
with
cell-division
rate,
which
reflects
necessity
ribosomes
for
construction
cellular
material.
Cell
division
rates
a
hyperbolic
concentrations
limiting
nutrients.
The
individual
cells
generally
exponential,
cytosolic
compositions
remaining
constant
throughout
growth.
Cells
often
determine
their
times
by
waiting
critical
increments
growth,
naturally
results
cell-size
homeostasis.
Although
detailed
molecular
mechanisms
governing
these
kinds
behavior
unknown,
modifications
small
genes
implicated
potential
routes
evolution.
In
all
observed
species,
whereas
size
increases
nutrient
availability,
it
decreases
increasing
temperature,
driving
universal
responses
remain
unknown.
Despite
features
stochastic
sources
internal
variation
translate
into
considerable
phenotypic
among
genetically
identical
cells.
Such
can
obscure
visibility
genetic
differences
natural
selection,
while
also
leading
parent–offspring
similarity
associated
non-genetic
effects.
These
aspects
inheritance
inevitable
consequences
structure
cells,
and
there
no
evidence
that
high
levels
advanced
selection
means
coping
variable
environments.
The
size
of
the
nucleus
scales
robustly
with
cell
so
that
nuclear-to-cell
volume
ratio
(N/C
ratio)
is
maintained
during
growth
in
many
types.
mechanism
responsible
for
this
scaling
remains
mysterious.
Previous
studies
have
established
N/C
not
determined
by
DNA
amount
but
instead
influenced
factors
such
as
nuclear
envelope
mechanics
and
transport.
Here,
we
developed
a
quantitative
model
control
based
upon
colloid
osmotic
pressure
tested
key
predictions
fission
yeast
Schizosaccharomyces
pombe
.
This
posits
numbers
macromolecules
nucleoplasm
cytoplasm.
Osmotic
shift
experiments
showed
behaves
an
ideal
osmometer
whose
primarily
dictated
forces.
Inhibition
export
caused
accumulation
nucleoplasm,
leading
to
swelling.
We
further
demonstrated
homeostasis
synthesis
growth.
These
demonstrate
functions
intracellular
organization
control.
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.
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.
We
show
evidence
of
the
association
RNA
polymerase
II
(RNAP)
with
chromatin
in
a
core-shell
organization,
reminiscent
microphase
separation
where
cores
comprise
dense
and
shell,
RNAP
low
density.
These
observations
motivate
our
physical
model
for
regulation
organization.
Here,
we
as
multiblock
copolymer,
comprising
active
inactive
regions
(blocks)
that
are
both
poor
solvent
tend
to
be
condensed
absence
binding
proteins.
However,
quality
can
regulated
by
protein
complexes
(e.g.,
transcription
factors).
Using
theory
polymer
brushes,
find
such
leads
swelling
which
turn
modifies
spatial
organization
regions.
In
addition,
use
simulations
study
spherical
micelles,
whose
shells
bound
complexes.
micelles
increases
number
controls
their
size.
Thus,
genetic
modifications
affecting
strength
chromatin-binding
may
modulate
experienced
regulate
genome.
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.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Nov. 23, 2023
Abstract
Microsporidia
are
an
early-diverging
group
of
fungal
pathogens
with
a
wide
host
range.
Several
microsporidian
species
cause
opportunistic
infections
in
humans
that
can
be
fatal.
As
obligate
intracellular
parasites
highly
reduced
genomes,
microsporidia
dependent
on
metabolites
for
successful
replication
and
development.
Our
knowledge
development
remains
rudimentary,
our
understanding
the
niche
occupied
by
has
relied
2D
TEM
images
light
microscopy.
Here,
we
use
serial
block-face
scanning
electron
microscopy
(SBF-SEM)
to
capture
3D
snapshots
human-infecting
species,
Encephalitozoon
intestinalis
,
within
cells.
We
track
E.
through
its
life
cycle,
which
allows
us
propose
model
how
infection
organelle,
polar
tube,
is
assembled
de
novo
developing
spores.
reconstructions
parasite-infected
cells
provide
insights
into
physical
interactions
between
cell
organelles
parasitophorous
vacuoles,
contain
parasites.
The
mitochondrial
network
substantially
remodeled
during
infection,
leading
fragmentation.
SBF-SEM
analysis
shows
changes
morphology
infected
cells,
live-cell
imaging
provides
dynamics
infection.
data
parasite
development,
tube
assembly,
microsporidia-induced
mitochondria
remodeling.