Shape
changes
of
epithelia
during
animal
development,
such
as
convergent
extension,
are
achieved
through
concerted
mechanical
activity
individual
cells.
While
much
is
known
about
the
corresponding
large
scale
tissue
flow
and
its
genetic
drivers,
fundamental
questions
regarding
local
control
contractile
on
cellular
embryo-scale
coordination
remain
open.
To
address
these
questions,
we
develop
a
quantitative,
model-based
analysis
framework
to
relate
cell
geometry
tension
in
recently
obtained
timelapse
imaging
data
gastrulating
Drosophila
embryos.
This
provides
systematic
decomposition
shape
T1-rearrangements
into
internally
driven,
active,
externally
passive,
contributions.
Our
evidence
that
germ
band
extension
driven
by
active
T1
processes
self-organize
positive
feedback
acting
tensions.
More
generally,
our
findings
suggest
epithelial
results
from
controlled
transformation
internal
force
balance
which
combines
effects
bottom-up
self-organization
with
top-down,
regulation
gene
expression.
Convergence–extension
in
embryos
is
controlled
by
chemical
and
mechanical
signalling.
A
key
cellular
process
the
exchange
of
neighbours
via
T1
transitions.
We
propose
analyse
a
model
with
positive
feedback
between
recruitment
myosin
motors
tension
cell
junctions.
The
produces
active
events,
which
act
to
elongate
tissue
perpendicular
main
direction
stress.
Using
an
idealised
patch
comprising
several
cells
embedded
matrix
passive
hexagonal
cells,
we
identified
optimal
range
stresses
trigger
event.
show
that
directed
also
generate
chains
realistic
made
entirely
random
shapes
leads
convergence–extension
over
parameters.
Our
findings
intercalations
can
stress
activates
events
neighbouring
resulting
tension-dependent
reorganisation,
qualitative
agreement
experiments
on
gastrulation
chick
embryos.
ABSTRACT
During
embryonic
development,
a
simple
ball
of
cells
re-shapes
itself
into
the
elaborate
body
plan
an
animal.
This
requires
dramatic
cell
shape
changes
and
movements,
powered
by
contractile
force
generated
actin
myosin
linked
to
plasma
membrane
at
cell-cell
cell-matrix
junctions.
Here,
we
review
three
morphogenetic
events
common
most
animals:
apical
constriction,
convergent
extension
collective
migration.
Using
fruit
fly
Drosophila
as
example,
discuss
recent
work
that
has
revealed
exciting
new
insights
molecular
mechanisms
allow
change
move
without
tearing
tissues
apart.
We
also
point
out
parallel
in
other
animals,
which
suggest
underlying
these
processes
are
conserved.
The
actomyosin
cytoskeleton
is
a
crucial
driver
of
morphogenesis.
Yet
how
the
behavior
large-scale
cytoskeletal
patterns
in
deforming
tissues
emerges
from
interplay
geometry,
genetics,
and
mechanics
remains
incompletely
understood.
Convergent
extension
Drosophila
melanogaster
embryos
provides
opportunity
to
establish
quantitative
understanding
dynamics
anisotropic
non-muscle
myosin
II.
Cell-scale
analysis
protein
localization
fixed
suggests
that
gene
expression
govern
anisotropy
via
complex
rules.
However,
technical
limitations
have
impeded
dynamic
studies
this
process
at
whole
embryo
level,
leaving
role
geometry
open.
Here,
we
combine
toto
live
imaging
with
molecular
characterize
distribution
corresponding
genetic
patterning.
We
found
pair
rule
continuously
deformed,
flowing
tissue
frame.
In
contrast,
orientation
remained
approximately
static
was
only
weakly
deflected
stationary
dorsal-ventral
axis
embryo.
propose
recruited
by
geometrically
defined
source,
potentially
related
embryo-scale
epithelial
tension,
account
for
transient
deflections
turnover
junction
reorientation
flow.
With
one
parameter,
model
quantitatively
accounts
time
course
wild-type,
twist
,
even-skipped
embryos,
as
well
perturbed
egg
geometry.
Geometric
patterning
simple
physical
strategy
ensure
robust
flow
formation
shape.
During
vertebrate
gastrulation,
an
embryo
transforms
from
a
layer
of
epithelial
cells
into
multilayered
gastrula.
This
process
requires
the
coordinated
movements
hundreds
to
tens
thousands
cells,
depending
on
organism.
In
chick
embryo,
patterns
actomyosin
cables
spanning
several
drive
tissue
flows.
Here,
we
derive
minimal
theoretical
framework
that
couples
activity
global
Our
model
predicts
onset
and
development
gastrulation
flows
in
normal
experimentally
perturbed
embryos,
mimicking
different
modes
as
active
stress
instability.
Varying
initial
conditions
parameter
associated
with
cell
ingression,
our
recapitulates
distinct
morphologies,
consistent
recently
published
experiments
embryo.
Altogether,
results
show
how
changes
patterning
critical
behaviors
force-generating
mechanisms
contribute
via
self-organizing
mechanochemical
process.
ABSTRACT
Actomyosin
networks
are
some
of
the
most
crucial
force-generating
components
present
in
developing
tissues.
The
contractile
forces
generated
by
these
harnessed
during
morphogenesis
to
drive
various
cell
and
tissue
reshaping
events.
Recent
studies
processes
have
advanced
rapidly,
providing
us
with
insights
into
how
initiated,
positioned
regulated,
they
act
via
individual
pulses
and/or
formation
supracellular
cables.
Here,
we
review
discuss
mechanisms
that
underlie
construction
turnover
such
structures.
Furthermore,
provide
an
overview
ratcheted
processivity
emerges
from
pulsed
events,
tissue-level
mechanics
coordinated
output
many
cellular
behaviors.
Nature Communications,
Год журнала:
2022,
Номер
13(1)
Опубликована: Ноя. 17, 2022
Abstract
Morphogenesis,
the
coordinated
execution
of
developmental
programs
that
shape
embryos,
raises
many
fundamental
questions
at
interface
between
physics
and
biology.
In
particular,
how
dynamics
active
cytoskeletal
processes
are
across
surface
entire
embryos
to
generate
global
cell
flows
is
poorly
understood.
Two
distinct
regulatory
principles
have
been
identified:
genetic
dynamic
response
mechanical
stimuli.
Despite
progress,
disentangling
these
two
contributions
remains
challenging.
Here,
we
combine
in
toto
light
sheet
microscopy
with
optogenetic
perturbations
tissue
mechanics
examine
theoretically
predicted
recruitment
non-muscle
myosin
II
junctions
during
Drosophila
embryogenesis.
We
find
has
a
long-range
impact
on
configuration,
rate
junction
deformation
sets
recruitment.
Mathematical
modeling
high
frequency
analysis
reveal
fluctuations
around
mean
value
set
by
feedback.
Our
model
accounts
for
early
establishment
pattern
80%
fidelity.
Taken
together
our
results
indicate
spatially
modulated
feedback
as
key
input
gradients
configurations
flow
patterns.
Cell Reports,
Год журнала:
2024,
Номер
43(2), С. 113677 - 113677
Опубликована: Янв. 17, 2024
Toll
signaling
is
well
known
for
its
pivotal
role
in
the
host
response
against
invasion
of
external
pathogens.
Here,
we
investigate
potential
involvement
intersection
between
and
oncogenic
cells.
We
show
that
loss
myeloid
differentiation
factor
88
(Myd88)
leads
to
drastic
fly
death
after
injection
RasV12-GFP
Transcriptomic
analyses
challenging
flies
with
cells
or
bacteria
distinct
inductions
Myd88-dependent
genes.
note
downregulation
Myd88
tracheal
system
accounts
mortality,
ectopic
complementation
rescues
survival
defect
loss-of-function
mutants
following
injection.
Further,
molecular
genetic
evidence
indicate
modulates
resistance
through
mediating
airway
function
a
rolled-dependent
manner.
Collectively,
our
data
critical
homeostasis
Shape
changes
of
epithelia
during
animal
development,
such
as
convergent
extension,
are
achieved
through
the
concerted
mechanical
activity
individual
cells.
While
much
is
known
about
corresponding
large-scale
tissue
flow
and
its
genetic
drivers,
fundamental
questions
regarding
local
control
contractile
on
cellular
scale
embryo-scale
coordination
remain
open.
To
address
these
questions,
we
develop
a
quantitative,
model-based
analysis
framework
to
relate
cell
geometry
tension
in
recently
obtained
time-lapse
imaging
data
gastrulating
Drosophila
embryos.
This
systematically
decomposes
shape
T1
rearrangements
into
internally
driven,
active,
externally
passive,
contributions.
Our
provides
evidence
that
germ
band
extension
driven
by
active
processes
self-organize
positive
feedback
acting
tensions.
More
generally,
our
findings
suggest
epithelial
results
from
controlled
transformation
internal
force
balance
which
combines
effects
bottom-up
self-organization
with
top-down,
regulation
gene
expression.
PLoS Computational Biology,
Год журнала:
2022,
Номер
18(1), С. e1009812 - e1009812
Опубликована: Янв. 28, 2022
Cell
intercalation
is
a
key
cell
behaviour
of
morphogenesis
and
wound
healing,
where
local
neighbour
exchanges
can
cause
dramatic
tissue
deformations
such
as
body
axis
extension.
Substantial
experimental
work
has
identified
the
molecular
players
facilitating
intercalation,
but
there
remains
lack
consensus
understanding
their
physical
roles.
Existing
biophysical
models
that
represent
cell-cell
contacts
with
single
edges
cannot
study
exchange
continuous
process,
neighbouring
cortices
must
uncouple.
Here,
we
develop
an
Apposed-Cortex
Adhesion
Model
(ACAM)
to
understand
active
behaviours
in
context
2D
epithelial
tissue.
The
junctional
actomyosin
cortex
every
modelled
viscoelastic
rope-loop,
explicitly
representing
facing
each
other
at
bicellular
junctions
adhesion
molecules
couple
them.
model
parameters
relate
directly
properties
subcellular
drive
dynamics,
providing
multi-scale
behaviours.
We
show
be
driven
by
purely
mechanisms.
Active
contractility
cortical
turnover
junction
are
sufficient
shrink
remove
junction.
Next,
new,
orthogonal
extends
passively.
ACAM
reveals
how
regulates
tension
transmission
deformation
rates
controlling
slippage
between
apposed
cortices.
additionally
predicts
rosettes,
which
form
when
vertex
becomes
common
many
cells,
more
likely
occur
actively
intercalating
tissues
strong
friction
from
molecules.