The Journals of Gerontology Series A,
Journal Year:
2024,
Volume and Issue:
79(11)
Published: Nov. 1, 2024
Abstract
The
Midwest
Aging
Consortium
(MAC)
has
emerged
as
a
critical
collaborative
initiative
aimed
at
advancing
our
understanding
of
aging
and
developing
strategies
to
combat
the
rising
prevalence
age-related
diseases.
Founded
in
2019,
MAC
brings
together
researchers
from
various
disciplines
institutions
across
Midwestern
United
States
foster
interdisciplinary
geroscience
research.
This
report
summarizes
highlights
Fourth
Annual
Symposium
MAC,
which
was
held
Iowa
State
University
May
2023.
symposium
featured
presentations
on
wide
array
topics,
including
studies
slow-aging
animals,
cellular
senescence
senotherapeutics,
role
immune
system
aging,
metabolic
changes
neuronal
health
biomarkers
for
measuring
process.
Speakers
shared
findings
involving
variety
ranging
commonly
used
species
such
mice,
rats,
worms,
yeast,
fruit
flies,
less-common
ones
like
naked
mole-rats,
painted
turtles,
rotifers.
continues
emphasize
importance
supporting
emerging
fostering
environment,
positioning
itself
leader
not
only
showcased
current
state
biology
research
but
also
highlighted
consortium’s
training
next
generation
scientists
dedicated
improving
healthspan
well-being
population.
Aging Cell,
Journal Year:
2023,
Volume and Issue:
22(4)
Published: Feb. 16, 2023
Abstract
Neural
communication
between
the
brain
and
adipose
tissues
regulates
energy
expenditure
metabolism
through
modulation
of
tissue
functions.
We
have
recently
demonstrated
that
under
pathophysiological
conditions
(obesity,
diabetes,
aging),
total
subcutaneous
white
(scWAT)
innervation
is
decreased
(‘adipose
neuropathy’).
With
advanced
age
in
C57BL/6J
mouse,
small
fiber
peripheral
nerve
endings
die
back,
resulting
reduced
contact
with
adipose‐resident
blood
vessels
other
cells.
This
vascular
neuropathy
parenchymal
together
likely
pose
a
physiological
challenge
for
function.
In
current
work,
we
used
genetically
diverse
HET3
mouse
model
to
investigate
incidence
dysregulation
across
several
ages
both
male
female
mice.
also
investigated
anti‐aging
treatment
rapamycin,
an
mTOR
inhibitor,
as
means
prevent
or
reduce
neuropathy.
found
mice
displayed
phenotype
compared
inbred
C56BL/6
J
mice,
indicating
genetic
contributions
this
aging
phenotype.
Compared
had
worse
neuropathic
phenotypes
by
62
weeks
age.
Female
appeared
increased
protection
from
until
(126
weeks),
after
reproductive
senescence.
rapamycin
overall
little
impact
on
measures,
actually
worsened
inflammation
fibrosis.
Despite
its
success
longevity
higher
doses
longer
delivery
paradigms
may
lead
disconnect
life
span
beneficial
health
outcomes.
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
203, P. 107140 - 107140
Published: March 19, 2024
The
understanding
of
the
function
perivascular
adipose
tissue
(PVAT)
in
vascular
aging
has
significantly
changed
due
to
increasing
amount
information
regarding
its
biology.
Adipose
surrounding
blood
vessels
is
increasingly
recognized
as
a
key
regulator
disorders.
It
significant
endocrine
and
paracrine
effects
on
vasculature
mediated
by
production
variety
bioactive
chemicals.
also
participates
number
pathological
regulatory
processes,
including
oxidative
stress,
immunological
inflammation,
lipid
metabolism,
vasoconstriction,
dilation.
Mechanisms
homeostasis
interactions
between
cells
at
local
level
tightly
regulate
secretory
repertoire
PVAT,
which
can
become
dysregulated
during
aging.
PVAT
secretion
group
changes
from
being
reducing
inflammation
lowering
cholesterol
response
systemic
or
insulin
resistance.
In
addition,
interaction
reciprocal,
biological
processes
are
directly
influenced
pertinent
indicators
architectural
traits
molecular
mechanism
crosstalk
aging,
clinical
correlation
age-related
disorders
all
summarized
this
review.
paper
aims
elucidate
evaluate
potential
benefits
therapeutically
targeting
context
mitigating
Furthermore,
it
will
discuss
latest
advancements
technology
used
for
PVAT.
Aging Cell,
Journal Year:
2023,
Volume and Issue:
22(11)
Published: Sept. 28, 2023
Abstract
Age‐induced
degeneration
of
the
neuromuscular
junction
(NMJ)
is
associated
with
motor
dysfunction
and
muscle
atrophy.
While
impact
aging
on
NMJ
presynapse
postsynapse
well‐documented,
little
known
about
changes
perisynaptic
Schwann
cells
(PSCs),
synaptic
glia
NMJ,
undergo
during
aging.
Here,
we
examined
PSCs
in
young,
middle‐aged,
old
mice
three
muscles
different
susceptibility
to
Using
light
electron
microscopy,
found
that
acquire
age‐associated
cellular
features
either
prior
or
at
same
time
as
onset
degeneration.
Notably,
aged
fail
completely
cap
even
though
they
are
more
abundant
compared
young
mice.
We
also
form
processes
intrude
into
cleft
guide
axonal
sprouts
innervate
other
NMJs.
next
profiled
transcriptome
(SCs)
identify
mechanisms
altered
PSCs.
This
analysis
revealed
a
transcriptional
pattern
previously
shown
promote
phagocytosis
absent
SCs.
It
showed
upregulate
unique
pro‐inflammatory
molecules
Interestingly,
neither
synaptogenesis
genes
nor
typically
upregulated
by
repair
SCs
were
induced
These
findings
provide
insights
molecular
could
be
targeted
stave
off
deleterious
effects
Physiological Reports,
Journal Year:
2025,
Volume and Issue:
13(2)
Published: Jan. 1, 2025
Abstract
The
use
of
genetically
diverse
mouse
models
offers
a
more
accurate
reflection
human
genetic
variability,
improving
the
translatability
findings
to
heterogeneous
populations.
This
approach
is
particularly
valuable
in
understanding
immune
responses
disease
by
environmental
exposures.
study
investigates
inflammatory
acute
exposures
mainstream
cigarette
smoke
(CS)
and
tobacco
(ETS)
two
strains,
CC002/UncJ
(UNC)
&
Diversity
Outbred
(J:DO).
UM‐HET3
(HET3)
strain,
typically
used
aging
intervention
studies,
has
also
been
evaluate
this
model
for
age‐associated
pathologies.
involves
comprehensive
approach,
including
BALF
cytokine
analysis,
evaluation
lung
tissue
architecture,
assessment
macrophages
its
associated
proteins
(MMP9
MMP12)
abundance.
Several
cytokines/chemokines
were
found
be
upregulated
across
three
strains.
Notably,
UNC
strain
exclusively
showed
upregulation
TNF‐α,
IL‐17A,
IL‐13,
whereas
J:DO
an
KC.
number
alveolar
lungs
mice
was
very
low
at
baseline
compared
other
strains
studied
study,
which
indicative
some
inherent
shift
pulmonary
profiles
these
inbred
mice.
In
contrast,
characterized
outbreeding,
much
robust
macrophage
response
comparable
C57BL/6J.
provide
insight
into
how
diversity
affects
CS/ETS
exposure,
with
implications
stressors
studying
pathophysiology.
Proteoglycan Research,
Journal Year:
2025,
Volume and Issue:
3(1)
Published: Jan. 1, 2025
ABSTRACT
Glycosaminoglycans
(GAGs)
are
abundant
negatively
charged
polysaccharides
ubiquitously
expressed
in
mammalian
organs,
having
essential
biological
functions
development
and
homeostasis.
It
has
been
scarcely
reported
that
GAG
structures
changed
aged
diseased
human
organs;
however,
an
overall
landscape
of
GAGs
individual
organs
animal
is
missing.
Here,
we
performed
in‐depth
analysis
disaccharide
composition
chondroitin/dermatan
sulfate
(CS/DS)
heparan
(HS)
from
24
young
mice.
Quantification
the
species
showed
CS/DS
dominates
almost
all
but
HS
five
organs.
As
expected,
sulfation
pattern
varied
different
which
likely
correlates
with
their
a
given
organ.
Nevertheless,
age‐dependent
alteration
more
prominent
disaccharides
CS/DS,
may
suggest
important
role
aging.
This
first
report
comprehensive
amount
structure
should
be
highly
relevant
understanding
how
affect
diseases