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Microglia in diffuse plaques in hereditary cerebral hemorrhage with amyloidosis (Dutch). An immunohistochemical study.
[hereditary cerebral hemorrhage with amyloidosis]
In
hereditary
cerebral
hemorrhage
with
amyloidosis
(
Dutch
)
(
HCHWA-D
)
beta
/
A
4
amyloid
deposition
is
found
in
meningocortical
blood
vessels
and
in
diffuse
plaques
in
the
cerebral
cortex
.
Diffuse
plaques
putatively
represent
early
stages
in
the
formation
of
senile
plaques
.
Microglia
are
intimately
associated
with
congophilic
plaques
in
Alzheimer
's
disease
(
AD
)
,
but
microglial
involvement
in
diffuse
plaque
formation
is
controversial
.
Therefore
,
we
studied
the
relationship
between
microglia
and
diffuse
plaques
in
the
cerebral
cortex
of
four
patients
with
HCHWA-D
using
a
panel
of
macrophage
/
microglia
markers
(
mAbs
LCA
,
LeuM
5
,
LeuM
3
,
LN
3
,
KP
1
,
OKIa
,
CLB
54
,
Mac
1
,
Ki-
M
6
,
AMC
30
and
the
lectin
RCA
-
1
)
.
Eight
AD
patients
,
one
demented
Down
's
syndrome
(
DS
)
patient
and
four
non-demented
controls
were
included
for
comparison
.
In
controls
and
HCHWA-D
patients
ramified
or
"
resting
"
microglia
formed
a
reticular
array
in
cortical
gray
and
subcortical
white
matter
.
Microglial
cells
in
or
near
HCHWA-D
diffuse
plaques
retained
their
normal
regular
spacing
and
ramified
morphology
.
In
AD
/
DS
gray
matter
more
microglial
cells
were
stained
than
in
controls
and
HCHWA-D
patients
.
Intensely
immunoreactive
microglia
with
enlarged
cell
bodies
and
short
,
thick
processes
clustered
in
congophilic
plaques
.
In
contrast
to
the
resting
microglia
,
these
"
activated
microglia
"
strongly
expressed
class
II
major
histocompatibility
complex
antigen
,
HLA-
DR
,
and
were
AMC
30
-
immunoreactive
.
These
findings
support
the
view
that
microglia
play
a
role
in
the
formation
of
congophilic
plaques
but
do
not
initiate
diffuse
plaque
formation
.
Another
finding
in
this
study
is
the
presence
of
strong
monocyte
/
macrophage
marker
immunoreactivity
in
the
wall
of
cortical
congophilic
blood
vessels
in
HCHWA-D
.
Diseases
Validation
Diseases presenting
"hla-dr"
symptom
hereditary cerebral hemorrhage with amyloidosis
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