Enigma of Pyramidal Neurons: Chirality-Centric View on Biological Evolution. Congruence to Molecular, Cellular, Physiological, Cognitive, and Psychological Functions
Victor V. Dyakin,
Nika Viktorovna Dyakina-Fagnano
Symmetry,
Год журнала:
2024,
Номер
16(3), С. 355 - 355
Опубликована: Март 15, 2024
The
mechanism
of
brain
information
processing
unfolds
within
spatial
and
temporal
domains
inherently
linked
to
the
concept
space–time
symmetry.
Biological
evolution,
beginning
with
prevalent
molecular
chirality,
results
in
handedness
human
cognitive
psychological
functions
(the
phenomena
known
as
biochirality).
key
element
chain
chirality
transfer
from
downstream
upstream
processes
is
pyramidal
neuron
(PyrN)
morphology–function
paradigm
(archetype).
most
apparent
landmark
PyrNs
geometry
cell
soma.
However,
“why/how
PyrN’s
soma
gains
shape
quasi-tetrahedral
symmetry”
has
never
been
explicitly
articulated.
Resolving
above
inquiry
only
possible
based
on
broad-view
assumption
that
encoding
3D
space
requires
specific
neuronal
detector
corresponding
network.
Accordingly,
our
hypothesis
states
if
primary
function
PyrNs,
at
organism
level,
sensory
symmetry
perception,
then
best
evolutionary-selected
support
sensory-motor
coupling.
biological
system’s
non-equilibrium
(NE)
state
fundamentally
an
asymmetric,
non-racemic,
steady
constituents.
chiral
theory
conceptually
agrees
living
systems
have
evolved
exchange
energy
environment.
involved
developing
studied
detail.
crucial
missing
element—the
reference
fundamental
link
between
navigation—is
main
obstacle
resolving
question
demand:
why
did
PyrNs’
gain
symmetry?
Язык: Английский
Drebrin Regulates Collateral Axon Branching in Cortical Layer II/III Somatosensory Neurons
Journal of Neuroscience,
Год журнала:
2023,
Номер
43(46), С. 7745 - 7765
Опубликована: Окт. 5, 2023
Proper
cortical
lamination
is
essential
for
cognition,
learning,
and
memory.
Within
the
somatosensory
cortex,
pyramidal
excitatory
neurons
elaborate
axon
collateral
branches
in
a
laminar-specific
manner
that
dictates
synaptic
partners
overall
circuit
organization.
Here,
we
leverage
both
male
female
mouse
models,
single-cell
labeling
imaging
approaches
to
identify
intrinsic
regulators
of
collateral,
also
termed
interstitial,
branching.
We
developed
new
robust,
sparse,
Layer
II/III
obtain
quantitative
assessment
branch
morphologies.
combined
these
with
cell-autonomous
loss-of-function
(LOF)
overexpression
(OE)
manipulations
an
Язык: Английский
Microtubule-associated septin complexes modulate kinesin and dynein motility with differential specificities
Journal of Biological Chemistry,
Год журнала:
2023,
Номер
299(9), С. 105084 - 105084
Опубликована: Июль 24, 2023
Long-range
membrane
traffic
is
guided
by
microtubule-associated
proteins
and
posttranslational
modifications,
which
collectively
comprise
a
code.
The
regulatory
principles
of
this
code
how
it
orchestrates
the
motility
kinesin
dynein
motors
are
largely
unknown.
Septins
large
family
GTP-binding
proteins,
assemble
into
complexes
that
associate
with
microtubules.
Using
single-molecule
in
vitro
assays,
we
tested
SEPT2/6/7,
SEPT2/6/7/9,
SEPT5/7/11
affect
motilities
constitutively
active
kinesins
KIF5C
KIF1A
dynein-dynactin-bicaudal
D
(DDB)
motor
complex.
We
found
SEPT2/6/7
potent
inhibitor
DDB
KIF5C,
preventing
mainly
their
association
also
inhibits
obstructing
stepping
along
On
SEPT2/6/7/9-coated
microtubules,
inhibition
dampened
SEPT9,
alone
enhances
KIF1A,
showing
individual
septin
subunits
determine
properties
complexes.
Strikingly,
differs
from
permitting
immobilizing
to
microtubule
lattice.
In
hippocampal
neurons,
filamentous
SEPT5
colocalizes
somatodendritic
microtubules
underlie
Golgi
membranes
lack
SEPT6.
Depletion
disrupts
morphology
polarization
ribbons
shaft
somato-proximal
dendrites,
consistent
tethering
SEPT5/7/11.
Collectively,
these
results
suggest
have
differential
specificities
regulation
positioning
motors.
posit
septins
an
integral
part
microtubule-based
spatially
controls
traffic.
Язык: Английский
Boosting neurite outgrowth and anti-oxidative stress for treatment of Parkinson's disease by biomimetic ultrasmall nanoparticles
Sustainable materials and technologies,
Год журнала:
2023,
Номер
39, С. e00807 - e00807
Опубликована: Дек. 27, 2023
Язык: Английский
Non-muscle myosin II and the plasticity of 3D cell migration
James M. Cowan,
Jacob J. Duggan,
Breanne R. Hewitt
и другие.
Frontiers in Cell and Developmental Biology,
Год журнала:
2022,
Номер
10
Опубликована: Ноя. 10, 2022
Confined
cells
migrating
through
3D
environments
are
also
constrained
by
the
laws
of
physics,
meaning
for
every
action
there
must
be
an
equal
and
opposite
reaction
to
achieve
motion.
Fascinatingly,
several
distinct
molecular
mechanisms
that
can
use
move,
this
is
reflected
in
diverse
ways
non-muscle
myosin
II
(NMII)
generate
mechanical
forces
necessary
sustain
cell
migration.
This
review
summarizes
unique
modes
migration,
as
well
how
NMII
activity
regulated
localized
within
each
these
different
modes.
In
addition,
we
highlight
tropomyosins
septins
two
protein
families
likely
have
more
secrets
reveal
about
governed
during
Together,
information
suggests
investigating
controlling
will
helpful
understanding
a
single
transitions
between
migration
response
physical
environment.
Язык: Английский
Cytoskeleton: Septin wreaths regulate actin in neuritogenesis
Current Biology,
Год журнала:
2023,
Номер
33(3), С. R98 - R100
Опубликована: Фев. 1, 2023
Язык: Английский
Drebrin Regulates Collateral Axon Branching in Cortical Layer II/III Somatosensory Neurons
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Июнь 21, 2023
Abstract
Proper
cortical
lamination
is
essential
for
cognition,
learning,
and
memory.
Within
the
somatosensory
cortex,
pyramidal
excitatory
neurons
elaborate
axon
collateral
branches
in
a
laminar-specific
manner
that
dictates
synaptic
partners
overall
circuit
organization.
Here,
we
leverage
mouse
models,
single-cell
labeling
imaging
approaches
to
identify
intrinsic
regulators
of
collateral,
also
termed
interstitial,
branching.
We
developed
new
robust,
sparse,
layer
II/III
obtain
quantitative
assessment
branch
morphologies.
combined
these
with
cell-autonomous
loss-of-function
(LOF)
over-expression
(OE)
manipulations
an
vivo
candidate
screen
neuron
lamination.
role
cytoskeletal
binding
protein
drebrin
(Dbn1)
regulating
projection
(CPN)
branching
vitro.
LOF
experiments
show
Dbn1
necessary
suppress
elongation
CPN
within
IV,
where
by
CPNs
normally
absent.
Conversely,
OE
produces
excess
short
axonal
protrusions
reminiscent
nascent
collaterals
fail
elongate.
Structure-function
analyses
implicate
S142
phosphorylation
domains
known
mediate
F-actin
bundling
microtubule
(MT)
coupling
as
initiation
upon
OE.
Taken
together,
results
contribute
our
understanding
molecular
mechanisms
regulate
CPNs,
key
process
elaboration
neocortical
formation.
Significance
Statement
Laminar-specific
targeting
regulates
branching,
lending
insight
into
underlie
innervation.
To
patterns
single
,
have
tools
allow
us
detailed
images
individual
morphologies
throughout
postnatal
development
manipulate
gene
expression
same
neurons.
Our
showing
interstitial
both
vitro
may
aid
how
aberrant
morphology
contributes
dysfunctions
observed
Autism
Spectrum
Disorder
(ASD)
epilepsy.
Язык: Английский
Thalamic Neuron Resilience during Osmotic Demyelination Syndrome (ODS) Is Revealed by Primary Cilium Outgrowth and ADP-ribosylation factor-like protein 13B Labeling in Axon Initial Segment
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(22), С. 16448 - 16448
Опубликована: Ноя. 17, 2023
A
murine
osmotic
demyelinating
syndrome
(ODS)
model
was
developed
through
chronic
hyponatremia,
induced
by
desmopressin
subcutaneous
implants,
followed
precipitous
sodium
restoration.
The
thalamic
ventral
posterolateral
(VPL)
and
posteromedial
(VPM)
relay
nuclei
were
the
most
demyelinated
regions
where
neuroglial
damage
could
be
evidenced
without
immune
response.
This
report
showed
that
following
12
h
48
time
lapses
after
rebalancing
osmolarity,
amid
ODS-degraded
outskirts,
some
resilient
neuronal
cell
bodies
built
up
primary
cilium
axon
hillock
extended
into
initial
segments
(AIS)
ADP-ribosylation
factor-like
protein
13B
(ARL13B)-immunolabeled
rod-like
shape
content
revealed.
These
AIS-labeled
shaft
lengths
appeared
proportional
with
distance
of
away
from
ODS
damaged
epicenter
correction
hyponatremia.
Fine
structure
examination
verified
these
neuron
abundant
transcriptions
translation
marked
ARL13B
labeling
associated
neurotubules
their
complex
cytoskeletal
macromolecular
architecture.
necessitated
energetic
transport
to
organize
restore
those
AIS
core
zone
in
model.
labeled
structures
substantiate
how
resilience
occurred
as
possible
steps
a
healing
course
out
ODS.
Язык: Английский
Quantitative Evaluation of Neurite Morphology Using Graph Structure
Electronics,
Год журнала:
2023,
Номер
12(23), С. 4750 - 4750
Опубликована: Ноя. 23, 2023
Recently,
the
analysis
of
cellular
images,
particularly
assessment
neurite
activity,
has
gained
increasing
significance
in
study
neurodegenerative
diseases,
including
Alzheimer’s
disease.
This
introduces
an
automated
approach
that
focuses
on
activity
through
application
segmentation
techniques
to
bright-field
images
neurons.
proposes
a
method
for
treating
individual
cell
instances
as
graphs
consisting
nodes
and
edges.
Furthermore,
this
suggests
quantitative
precisely
identified
neurites
definition
several
evaluation
metrics.
enables
fast
objective
focused
In
variety
experiments,
precision
our
proposed
was
verified
comparative
by
comparing
results
manual
data
using
ImageJ
measuring
length
rat
adrenal
pheochromocytoma
PC12
cells.
The
findings
revealed
average
discrepancy
is
only
4.387
μm,
highlighting
high
level
accuracy
method’s
ability
detect
neurites,
which
almost
par
with
analysis.
observation
holds
analytical
applications
pertinent
Язык: Английский