AJP Cell Physiology,
Journal Year:
2024,
Volume and Issue:
327(5), P. C1263 - C1273
Published: Oct. 7, 2024
The
structural
organization
of
cardiomyocyte
proteins
is
critical
for
their
efficient
functioning
as
a
contractile
unit
in
the
heart.
This
work
shows
that
diabetes
mellitus
induces
significant
changes
spatial
costamere
proteins,
t
tubules,
and
intercalated
discs.
We
obtained
first
elasticity
map
sections
living
diabetic
cardiomyocytes.
results
show
statistical
differences
control
cardiomyocytes,
with
cardiomyocytes
being
stiffer
than
normal
ones.
Cardiovascular Diabetology,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Feb. 20, 2023
Abstract
Diabetes
mellitus
is
one
of
the
prime
risk
factors
for
cardiovascular
complications
and
linked
with
high
morbidity
mortality.
Diabetic
cardiomyopathy
(DCM)
often
manifests
as
reduced
cardiac
contractility,
myocardial
fibrosis,
diastolic
dysfunction,
chronic
heart
failure.
Inflammation,
changes
in
calcium
(Ca
2+
)
handling
cardiomyocyte
loss
are
implicated
development
progression
DCM.
Although
existence
DCM
was
established
nearly
four
decades
ago,
exact
mechanisms
underlying
this
disease
pathophysiology
constantly
evolving.
Furthermore,
complex
exosomes,
which
has
recently
shown
to
facilitate
intercellular
(cell-to-cell)
communication
through
biomolecules
such
micro
RNA
(miRNA),
proteins,
enzymes,
cell
surface
receptors,
growth
factors,
cytokines,
lipids.
Inflammatory
response
Ca
signaling
interrelated
been
known
adversely
affect
many
these
molecules
either
qualitatively
and/or
quantitatively.
In
literature
review,
we
have
demonstrated
that
regulators
tightly
controlled
at
different
molecular
cellular
levels
during
various
biological
processes
heart.
mediators,
miRNA
exosomes
interact
regulators,
however
how
mediators
pathogenesis
remains
elusive.
Thus,
further
investigations
needed
understand
restore
homeostasis
function,
serve
potential
therapeutic
targets
treatment
Frontiers in Physiology,
Journal Year:
2021,
Volume and Issue:
12
Published: Oct. 27, 2021
Computational
modeling
has
contributed
significantly
to
present
understanding
of
cardiac
electrophysiology
including
conduction,
excitation-contraction
coupling,
and
the
effects
side-effects
drugs.
However,
accuracy
in
silico
analysis
electrochemical
wave
dynamics
tissue
is
limited
by
homogenization
procedure
(spatial
averaging)
intrinsic
standard
continuum
models
conduction.
Averaged
cannot
resolve
intricate
vicinity
individual
cardiomyocytes
simply
because
myocytes
are
not
these
models.
Here
we
demonstrate
how
recently
developed
mathematical
based
on
representing
every
myocyte
can
increase
accuracy,
thus
utility
electrophysiological
function
dysfunction
collections
coupled
cardiomyocytes.
The
gold
numerical
simulation
for
bidomain
model.
In
model,
extracellular
(E)
space,
cell
membrane
(M)
intracellular
(I)
space
all
assumed
be
everywhere
tissue.
Consequently,
it
impossible
study
biophysical
processes
taking
place
close
myocytes.
model
represents
averaging
over
several
hundred
this
inherently
limits
our
alternative
approach
both
E,
M,
I
represented
which
therefore
referred
as
EMI
allows
detailed
going
functionally
important
spaces
very
myocytes,
although
at
cost
increased
CPU-requirements.
Circulation Arrhythmia and Electrophysiology,
Journal Year:
2022,
Volume and Issue:
15(11)
Published: Oct. 28, 2022
Irreversible
electroporation
is
an
energy
form
utilizing
high-voltage
pulsed
electric
field,
leading
to
cellular
homeostasis
disruption
and
cell
death.
Recently,
irreversible
has
shown
promising
results
for
the
treatment
of
cardiac
arrhythmias.
However,
reversible
effects
field
on
myocytes
remain
poorly
understood.
Here,
we
evaluated
influence
a
monophasic
single
pulse
(EP)
contractility,
Ca2+
recovery
myocytes.Isolated
rat
left
ventricular
were
electroporated
using
EP
different
durations
voltages.
Sarcomere
length
intracellular
simultaneously
monitored
up
20
minutes
after
application
in
Fura-2
loaded
myocytes.
Lethal
voltage
thresholds
determined
100
µs
10
ms
pulses
by
discriminating
orientation
with
respect
field.Electroporation
led
immediate
increase
which
was
dependent
upon
delivered
cell.
Intermediate-voltage
(140
V,
µs)
increased
sarcomere
shortening,
transient
amplitude,
diastolic
level
measured
1
minute
post-EP.
Although
shortening
returned
pre-EP
within
5
minutes,
amplitude
decreased
further
below
remained
elevated
Spontaneous
contractions
observed
sublethal
but
their
frequency
progressively
minutes.
threshold
lower
oriented
perpendicular
than
parallel
while
opposite
effect
found
pulses.Sublethal
affected
contractility
disrupted
as
function
voltage.
Moreover,
EP-induced
lethality
preceded
large
duration,
field.
These
findings
provide
new
insights
into
Frontiers in Physiology,
Journal Year:
2022,
Volume and Issue:
13
Published: March 9, 2022
Regulation
of
intracellular
calcium
is
a
critical
component
cardiac
electrophysiology
and
excitation-contraction
coupling.
The
spark,
the
fundamental
element
transient,
initiated
in
specialized
nanodomains
which
co-locate
ryanodine
receptors
L-type
channels.
However,
homeostasis
ultimately
regulated
at
cellular
scale,
by
interaction
spatially
separated
but
diffusively
coupled
with
other
sub-cellular
surface-membrane
transport
channels
strong
non-linear
interactions;
arrhythmia
mechanisms
are
tissue-scale
phenomena,
heterogeneous
population
myocytes.
Recent
advances
imaging
modalities
image-analysis
enabling
super-resolution
reconstruction
structures
responsible
for
regulating
homeostasis,
including
internal
structure
themselves.
Extrapolating
functional
data
from
nanodomain
to
whole-heart
non-trivial,
yet
essential
translational
insight
into
disease
mechanisms.
Computational
modeling
has
important
roles
play
relating
structural
scale
translating
across
scales.
This
review
covers
recent
methodological
that
enable
image-based
single
whole
cardiomyocyte,
as
well
development
multi-scale
simulation
approaches
integrate
nanometer
whole-heart.
Firstly,
methods
overcome
computational
challenges
simulating
spatial
dynamics
discussed,
this
scale.
Then,
whole-cell
models,
capable
capturing
range
different
(such
T-system
mitochondria)
heterogeneity/variability
discussed
two
levels
discretization.
Novel
models
scales
simulate
stochastic
then
elucidation
remodeling
underlies
contractile
dysfunction.
Perspectives
on
model
differences
future
directions
provided
throughout.
The Journal of Physiology,
Journal Year:
2024,
Volume and Issue:
602(18), P. 4487 - 4510
Published: April 30, 2024
Mechanical
load
is
a
potent
regulator
of
cardiac
structure
and
function.
Although
high
workload
during
heart
failure
associated
with
disruption
cardiomyocyte
t-tubules
Ca
Frontiers in Physiology,
Journal Year:
2022,
Volume and Issue:
12
Published: Jan. 5, 2022
The
architectural
specializations
and
targeted
delivery
pathways
of
cardiomyocytes
ensure
that
L-type
Ca2+
channels
(CaV1.2)
are
concentrated
on
the
t-tubule
sarcolemma
within
nanometers
their
intracellular
partners
type
2
ryanodine
receptors
(RyR2)
which
cluster
junctional
sarcoplasmic
reticulum
(jSR).
organization
distribution
these
two
groups
cardiac
calcium
channel
clusters
critically
underlies
uniform
contraction
myocardium.
signaling
between
sets
adjacent
produces
sparks
in
health,
cannot
escalate
into
waves
because
there
is
sufficient
separation
so
release
from
one
RyR2
or
supercluster,
activate
sustain
neighboring
clusters.
Instead,
thousands
units
(CRUs)
generate
near
simultaneous
across
every
cardiomyocyte
during
action
potential
when
induced
stimulated
by
depolarization
influx
through
voltage
dependent
CaV1.2
These
summate
to
a
global
transient
activates
myofilaments
thus
electrical
signal
transduced
functional
output,
myocardial
contraction.
To
more,
less
contractile
force
match
hemodynamic
metabolic
demands
body,
heart
responds
β-adrenergic
altering
activity
tune
excitation-contraction
coupling
accordingly.
Recent
accumulating
evidence
suggests
this
tuning
process
also
involves
altered
expression,
dynamic
reorganization
respective
membranes
control
amplitude
entry,
SR
function.
In
failure
aging,
key
proteins
occurs
alongside
remodeling
thought
contribute
impaired
present
review
we
discuss
latest
developments,
implications,
future
questions
be
addressed.
Circulation Research,
Journal Year:
2022,
Volume and Issue:
130(9), P. 1306 - 1317
Published: March 23, 2022
Transcriptional
remodeling
is
known
to
contribute
heart
failure
(HF).
Targeting
stress-dependent
gene
expression
mechanisms
may
represent
a
clinically
relevant
therapy
option.
We
recently
uncovered
salutary
mechanism
in
the
whereby
JP2
(junctophilin-2),
an
essential
component
of
excitation-contraction
coupling
apparatus,
site-specifically
cleaved
and
releases
N-terminal
fragment
(JP2NT
[N-terminal
JP2])
that
translocates
into
nucleus
functions
as
transcriptional
repressor
HF-related
genes.
This
study
aims
determine
whether
JP2NT
can
be
leveraged
by
techniques
for
attenuating
HF
progression
preclinical
pressure
overload
model.
Frontiers in Physiology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 18, 2025
Caveolins
interact
with
signaling
molecules
within
caveolae
and
subcellular
membranes.
Dysregulation
of
caveolin
function
protein
abundance
contributes
to
cardiac
pathophysiological
processes,
driving
the
development
progression
heart
disease.
Reactive
oxygen
species
(ROS)
play
a
critical
role
in
maintaining
cellular
homeostasis
are
key
contributors
mechanisms
cardiovascular
disorders.
have
been
shown
modulate
oxidative
stress
regulate
redox
homeostasis.
However,
specific
roles
caveolins,
particularly
caveolin-1
caveolin-3,
regulating
ROS
production
during
pathology
remain
unclear.
This
mini-review
article
highlights
correlation
between
caveolins
health
modulating
diseases,
specifically
myocardial
ischemia,
failure,
diabetes-induced
metabolic
cardiomyopathy,
septic
cardiomyopathy.
A
deeper
understanding
caveolin-mediated
may
pave
way
for
innovative
therapeutic
approaches
treat
diseases.