bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 3, 2024
Abstract
Tissue
regeneration
requires
the
directed
activity
of
numerous
genes,
which
are
often
reused
from
development.
Although
identities
many
key
factors
have
been
established,
how
their
expression
is
activated
and
subsequently
coordinated
over
regenerative
time
remains
unclear.
One
highly
conserved
signal
central
to
diverse
examples
stress
MAP
kinase
JNK.
In
Drosophila
,
damage-induced
JNK
signaling
promotes
multiple
genes
that
direct
proliferation,
growth
changes
in
cellular
identity.
However,
these
targets
selectively
upregulated
context
injury,
expressed
specific
patterns
responsible
for
repair
unknown.
Our
work
previously
characterized
Damage-Responsive,
Maturity-Silenced
(DRMS)
enhancers;
regulatory
elements
directly
by
promote
gene
expression.
Here
we
investigated
damage-responsive
(DR)
module
enhancers
engaged,
finding
cell
death
entirely
dispensable
activation.
We
identify
JAK/STAT
as
an
additional
input
into
DR
downstream
JNK,
acts
broaden
enhancer
wound
periphery
where
levels
insufficient
alone.
Finally,
demonstrate
a
distinct
threshold
level
exists
must
be
achieved
activate
via
enhancers,
which,
alongside
JAK/STAT,
results
temporally
spatially
appropriate
necessary
regeneration.
Author
Summary
Wound
healing
require
activation
whose
carefully
division,
identity
organ
development
restoration
tissue
integrity
patterning.
The
imaginal
disc
well-established
model
used
better
understand
spatiotemporal
control
reparative
response
damage
discs
primarily
mediated
thorough
pathway,
but
leads
diversity
occurs
around
not
well
understood.
discrete
genomic
regions
called
Damage-Responsive
respond
program.
show
behavior
depends
on
they
integrate
both
its
immediate
target
establish
proper
regionality
expression,
promoting
spread
wound.
These
findings
improve
our
understanding
patterning
established
damage.
PLoS Genetics,
Год журнала:
2022,
Номер
18(12), С. e1010516 - e1010516
Опубликована: Дек. 15, 2022
Regeneration
relies
on
cell
proliferation
to
restore
damaged
tissues.
Multiple
signaling
pathways
activated
by
local
or
paracrine
cues
have
been
identified
promote
regenerative
proliferation.
How
different
types
of
tissue
damage
may
activate
distinct
and
how
these
differences
converge
is
less
well
defined.
To
better
understand
proliferative
signals
are
integrated
during
regeneration,
we
investigate
models
compensatory
in
Drosophila
imaginal
discs.
We
find
that
associated
with
a
unique
cycle
profile,
which
characterized
short
G1
G2
phases
and,
surprisingly,
acceleration
the
S-phase.
S-phase
can
be
induced
two
signatures,
aligning
inflammatory
non-inflammatory
damage.
Specifically,
non-autonomous
activation
JAK/STAT
Myc
response
damage,
Ras/ERK
Hippo/Yki
elevated
death,
accelerated
nucleotide
incorporation
This
previously
unappreciated
convergence
damaging
insults
same
program
reconciles
previous
conflicting
observations
regeneration
tumor
models.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 31, 2024
Summary
Injury
is
a
common
occurrence
in
the
life
of
organisms.
Because
extent
damage
cannot
be
predicted,
injured
organisms
must
determine
how
much
tissue
needs
to
restored.
It
known
that
amputation
position
determines
regeneration
speed
amputated
appendages
regeneration-competent
animals.
Yet,
it
not
clear
positional
information
conveyed
during
regeneration.
Here,
we
investigated
dynamics
regenerating
caudal
fins
African
killifish
(
Nothobranchius
furzeri
).
We
report
position-specific,
differential
modulation
spatial
distribution,
duration,
and
magnitude
proliferation.
Regenerating
profiled
by
single
cell
RNA
sequencing
identified
Transient
Regeneration-Activated
Cell
State
(TRACS)
amplified
match
given
position.
located
this
TRACS
basal
epidermis
found
them
express
components
modifiers
extracellular
matrix
(ECM).
propose
role
for
these
cells
transducing
blastema
remodeling
ECM.
Highlights
Amputation
changes
tissue-wide
proliferation
response
Transcriptional
compartmentalization
relative
injury
type
Regeneration
deploys
States
Prediction:
transduced
ECM
Tissue
necrosis
is
a
devastating
complication
for
many
human
diseases
and
injuries.
Unfortunately,
our
understanding
of
how
it
impacts
surrounding
healthy
tissue
-
an
essential
consideration
when
developing
effective
methods
to
treat
such
injuries
has
been
limited
by
lack
robust
genetically
tractable
models.
Our
lab
previously
established
method
study
necrosis-induced
regeneration
in
the
Drosophila
wing
imaginal
disc,
which
revealed
unique
phenomenon
whereby
cells
at
distance
from
injury
upregulate
caspase
activity
process
called
Necrosis-induced
Apoptosis
(NiA)
that
vital
regeneration.
Here,
we
have
further
investigated
this
phenomenon,
showing
NiA
predominantly
associated
with
highly
regenerative
pouch
region
shaped
genetic
factors
present
presumptive
hinge.
Furthermore,
find
proportion
fail
undergo
apoptosis,
instead
surviving
effector
activation
persist
within
stimulate
reparative
proliferation
late
This
relies
on
initiator
Dronc,
occurs
independent
JNK,
ROS
or
mitogens
characterized
Apoptosis-induced
Proliferation
(AiP)
mechanism.
These
data
reveal
new
means
non-apoptotic
Dronc
signaling
promotes
response
necrotic
damage.
Archives of Insect Biochemistry and Physiology,
Год журнала:
2023,
Номер
115(1)
Опубликована: Ноя. 28, 2023
Abstract
Suppressors
of
cytokine
signaling
(SOCS)
play
important
roles
in
the
regulation
growth,
development,
and
immunity
eukaryotic
organisms.
SOCS7
is
an
member
SOCS
family,
but
its
physiological
pathological
functions
remain
largely
unknown
invertebrates
including
insects.
Here,
we
first
report
cloning
a
gene
from
domesticated
silkworm
(
Bombyx
mori
),
named
BmSOCS7
.
We
have
characterized
expression
profiles
varieties
susceptible
or
resistant
to
infection
nucleopolyhedrovirus
(BmNPV)
using
real‐time
fluorescence
quantitative
PCR.
expresses
highly
embryogenesis
lowly
metamorphosis
silkworms
does
opposite
contrast
silkworms.
Its
at
very
low
level
fat
body
relatively
high
ones.
BmNPV
inoculation
induces
transient
downregulation
then
general
upregulation
BmN
cells,
while
it
midgut,
hemolymph
with
more
pronounced
effect
than
ones
prominent
midgut.
Together,
our
work
reveals
that
may
be
strategy
for
anti‐BmNPV
immune
response,
mainly
function
rather
midgut
participate
process.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Май 12, 2024
Abstract
Drosophila
models
for
tumorigenesis
and
metastasis
have
revealed
conserved
mechanisms
of
signaling
that
are
also
involved
in
mammalian
cancer.
Many
these
use
the
proliferating
tissues
larval
stages
development,
when
highly
mitotically
active,
or
stem
cells
abundant.
Fewer
adult
animals
to
initiate
tumor
formation
many
largely
terminally
differentiated
postmitotic.
The
accessory
glands
prostate-like
a
model
some
aspects
prostate
using
this
tissue
has
been
explored.
In
model,
oncogenic
was
induced
during
proliferative
stage
gland
raising
question
how
activity
would
impact
postmitotic
tissue.
Here,
we
show
leads
activation
pro-tumorigenic
program,
similar
observed
mitotic
tissues,
but
absence
proliferation.
Oncogenic
hyperplasia
with
nuclear
anaplasia
aneuploidy
through
endoreduplication,
which
increases
polyploidy
occasionally
results
non-mitotic
neoplastic-like
extrusions.
We
compare
gene
expression
changes
our
endocycling
cancer
by
chemotherapy,
potentially
mediate
recurrence
after
treatment.
Similar
pathways
activated
cells,
suggesting
provide
useful
progression
do
not
involve
cellular
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 26, 2024
Abstract
Tissue
necrosis
is
a
devastating
complication
for
many
human
diseases
and
injuries.
Unfortunately,
our
understanding
of
how
it
impacts
surrounding
healthy
tissue
–
an
essential
consideration
when
developing
methods
to
treat
such
injuries
has
been
limited
by
lack
robust
genetically
tractable
models.
Our
lab
previously
established
method
study
necrosis-induced
regeneration
in
the
Drosophila
wing
imaginal
disc,
which
revealed
unique
phenomenon
whereby
cells
at
distance
from
injury
upregulate
caspase
activity
process
called
Necrosis-induced
Apoptosis
(NiA)
that
vital
regeneration.
Here
we
have
further
investigated
this
phenomenon,
showing
NiA
predominantly
associated
with
highly
regenerative
pouch
region
shaped
genetic
factors
present
presumptive
hinge.
Furthermore,
find
proportion
fail
undergo
apoptosis,
instead
surviving
effector
activation
persist
within
stimulate
reparative
proliferation
late
This
relies
on
initiator
Dronc,
occurs
independent
JNK,
ROS
or
mitogens
characterized
Apoptosis-induced
Proliferation
(AiP)
mechanism.
These
data
reveal
new
means
non-apoptotic
Dronc
signaling
promotes
response
necrotic
damage.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Авг. 6, 2024
Abstract
Tissue
damage
and
inflammation
trigger
systemic
signals
that
induce
catabolic
breakdown
nutrient
release
in
distant
organs,
a
process
well-characterized
the
context
of
tumor
cachexia.
While
mechanisms
allowing
tumors
to
circumvent
these
growth
restrictions
are
known,
physiological
processes
overcome
inflammation-induced
support
tissue
repair
regeneration
remain
largely
unexplored.
In
our
study,
we
use
model
developing
Drosophila
imaginal
discs
dissect
key
metabolic
signaling
adaptations
help
restrictions.
Our
findings
reveal
unique
strategy
used
by
rapidly
proliferating
cells
regenerating
domain.
Instead
relying
on
conventional
Insulin-PI3K-Akt
pathway,
utilize
JAK/STAT-PDK1-S6K
axis.
This
adaptation
facilitates
sustained
protein
synthesis
cellular
despite
catabolism
associated
with
low
insulin
signaling.
Specifically,
find
fat
body
is
driven
insulin-binding
factor
Impl2,
which
expressed
at
site
inflammatory
damage.
Notably,
regenerative
proliferation
also
supported
mTORC1
activity
upregulation
amino
acid
transporters
These
align
specific
metabolite
signature
hemolymph,
revealing
specialized
program
meets
demands
fast-proliferating
cells.
work
provides
insight
into
how
tissues
rewire
pathways
adapt
their
coordinate
conserved
provision
response.
have
important
implications
for
understanding
human
diseases
such
as
chronic
wounds
cancer.
Research Square (Research Square),
Год журнала:
2024,
Номер
unknown
Опубликована: Авг. 9, 2024
Abstract
Background
Hemorrhagic
fever
with
renal
syndrome
(HFRS),
a
life-threatening
zoonosis
caused
by
hantavirus,
poses
significant
mortality
risks
and
lacks
specific
treatments.
This
study
aimed
to
delineate
the
transcriptomic
alterations
during
recovery
phases
of
HFRS.
Methods
RNA
sequencing
was
employed
analyze
in
peripheral
blood
mononuclear
cells
from
HFRS
patients
across
oliguric
phase
(OP),
diuretic
(DP),
convalescent
(CP).
Twelve
differentially
expressed
genes
(DEGs)
were
validated
using
quantitative
real-time
PCR
larger
sample
sets.
Results
Our
analysis
revealed
pronounced
differences
between
DP
OP,
38
DEGs
showing
consistent
expression
changes
all
three
phases.
Notably,
immune
checkpoint
like
CD83NR4A1
demonstrated
monotonic
increase,
contrast
decrease
observed
antiviral
immunomodulatory
genes,
including
IFI27RNASE2.
Furthermore,
this
research
elucidates
sustained
attenuation
responses
phases,
alongside
an
upregulation
pathways
related
tissue
repair
regeneration.
Conclusion
reveals
shifts
HFRS,
illuminating
key
that
may
serve
as
biomarkers
for
disease
progression
recovery.