Mechanical
forces
are
well
known
for
modulating
heart
valve
developmental
programs.
Yet,
it
is
still
unclear
how
genetic
programs
and
mechanosensation
interact
during
development.
Here,
we
assessed
the
mechanosensitive
pathways
involved
zebrafish
outflow
tract
(OFT)
development
in
vivo.
Our
results
show
that
hippo
effector
Yap1,
Klf2,
Notch
signaling
pathway
all
essential
OFT
morphogenesis
response
to
mechanical
forces,
albeit
active
different
cell
layers.
Furthermore,
Piezo
TRP
channels
important
factors
these
pathways.
In
addition,
live
reporters
reveal
controls
Klf2
activity
endothelium
Yap1
localization
smooth
muscle
progenitors
coordinate
morphogenesis.
Together,
this
work
identifies
a
unique
morphogenetic
program
formation
places
as
central
modulator
of
process.
Annual Review of Cell and Developmental Biology,
Journal Year:
2021,
Volume and Issue:
37(1), P. 311 - 340
Published: Aug. 10, 2021
Calcium
(Ca
2+
)
is
a
unique
mineral
that
serves
as
both
nutrient
and
signal
in
all
eukaryotes.
To
maintain
Ca
homeostasis
for
nutrition
signaling
purposes,
the
tool
kit
transport
has
expanded
across
kingdoms
of
eukaryotes
to
encode
specific
signals
referred
signatures.
In
parallel,
large
array
-binding
proteins
evolved
sensors
decode
By
comparing
these
coding
decoding
mechanisms
fungi,
animals,
plants,
unified
divergent
themes
have
emerged,
underlying
complexity
will
challenge
researchers
years
come.
Considering
scale
breadth
subject,
instead
literature
survey,
this
review
we
focus
on
conceptual
framework
aims
introduce
readers
principles
signaling.
We
finish
with
several
examples
-signaling
pathways,
including
polarized
cell
growth,
immunity
symbiosis,
systemic
signaling,
piece
together
plants
versus
animals.
Cell Reports,
Journal Year:
2022,
Volume and Issue:
38(6), P. 110342 - 110342
Published: Feb. 1, 2022
The
mechanically
activated
Piezo
channel
plays
a
versatile
role
in
conferring
mechanosensitivity
to
various
cell
types.
However,
how
it
incorporates
its
intrinsic
and
cellular
components
effectively
sense
long-range
mechanical
perturbation
across
remains
elusive.
Here
we
show
that
channels
are
biochemically
functionally
tethered
the
actin
cytoskeleton
via
cadherin-β-catenin
mechanotransduction
complex,
whose
significantly
impairs
Piezo-mediated
responses.
Mechanistically,
adhesive
extracellular
domain
of
E-cadherin
interacts
with
cap
Piezo1,
which
controls
transmembrane
gate,
while
cytosolic
tail
might
interact
domains
close
proximity
intracellular
gates,
allowing
direct
focus
adhesion-cytoskeleton-transmitted
force
for
gating.
Specific
disruption
intermolecular
interactions
prevents
cytoskeleton-dependent
gating
Piezo1.
Thus,
propose
force-from-filament
model
complement
previously
suggested
force-from-lipids
mechanogating
channels,
enabling
them
serve
as
tunable
mechanotransducers.
Frontiers in Bioengineering and Biotechnology,
Journal Year:
2019,
Volume and Issue:
7
Published: July 16, 2019
Cells
and
tissues
can
sense
react
to
the
modifications
of
physico-chemical
properties
extracellular
environment
(ECM)
through
integrin-based
adhesion
sites
adapt
their
physiological
response
in
a
process
called
mechanotransduction.
Due
critical
localization
at
cell-ECM
interface,
transmembrane
integrins
are
mediators
bidirectional
signaling,
playing
key
role
«
outside-in
»
inside-out
signal
transduction.
After
presenting
basic
conceptual
fundamentals
related
field
mechanobiology,
we
review
current
state-of-the-art
technologies
that
facilitate
understanding
mechanotransduction
signaling
pathways.
Finally,
highlight
innovative
technological
developments
help
advance
our
molecular
mechanisms
involved
nuclear
Frontiers in Physiology,
Journal Year:
2019,
Volume and Issue:
10
Published: July 31, 2019
Human
red
blood
cells
(RBC)
are
highly
differentiated
that
have
lost
all
organelles
and
most
intracellular
machineries
during
their
maturation
process.
RBC
fundamental
for
the
nearly
basic
physiologic
dynamics
they
key
in
body's
respiratory
system
by
being
responsible
oxygen
transport
to
tissues,
delivery
of
carbon
dioxide
lungs.
With
flexible
structure
capable
deform
order
travel
through
vessels
including
very
small
capillaries.
Throughout
average
120
days
lifespan,
human
bloodstream
come
contact
with
a
broad
range
different
cell
types.
In
fact,
able
interact
communicate
endothelial
(ECs),
platelets,
macrophages
bacteria.
Additionally,
involved
maintenance
thrombosis
hemostasis
play
an
important
role
immune
response
against
pathogens.
To
clarify
mechanisms
interaction
these
other
both
health
disease
as
well
highlight
players,
we
focused
our
interest
on
membrane
components
such
ion
channels,
proteins,
phospholipids.
Mechanical
forces
are
well
known
for
modulating
heart
valve
developmental
programs.
Yet,
it
is
still
unclear
how
genetic
programs
and
mechanosensation
interact
during
development.
Here,
we
assessed
the
mechanosensitive
pathways
involved
zebrafish
outflow
tract
(OFT)
development
in
vivo.
Our
results
show
that
hippo
effector
Yap1,
Klf2,
Notch
signaling
pathway
all
essential
OFT
morphogenesis
response
to
mechanical
forces,
albeit
active
different
cell
layers.
Furthermore,
Piezo
TRP
channels
important
factors
these
pathways.
In
addition,
live
reporters
reveal
controls
Klf2
activity
endothelium
Yap1
localization
smooth
muscle
progenitors
coordinate
morphogenesis.
Together,
this
work
identifies
a
unique
morphogenetic
program
formation
places
as
central
modulator
of
process.