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Substitutions at codon 22 of Alzheimer's abeta peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells.
[hereditary cerebral hemorrhage with amyloidosis]
Cerebral
amyloid
angiopathy
is
commonly
associated
with
normal
aging
and
Alzheimer
's
disease
and
it
is
also
the
principal
feature
of
hereditary
cerebral
hemorrhage
with
amyloidosis
Dutch
type
,
a
familial
condition
associated
to
a
point
mutation
G
to
C
at
codon
693
of
the
amyloid
beta
(
Abeta
)
precursor
protein
gene
resulting
in
a
Glu
to
Gln
substitution
at
position
22
of
the
Abeta
(
E
22
Q
)
.
The
patients
carrying
the
AbetaE
22
Q
variant
usually
present
with
lobar
cerebral
hemorrhages
before
50
years
of
age
.
A
different
mutation
described
in
several
members
of
three
Italian
kindred
who
presented
with
recurrent
hemorrhagic
strokes
late
in
life
,
between
60
and
70
years
of
age
,
also
associated
with
extensive
cerebrovascular
amyloid
deposition
has
been
found
at
the
same
position
22
,
this
time
resulting
in
a
Glu
to
Lys
substitution
(
E
22
K
)
.
We
have
compared
the
secondary
structure
,
aggregation
,
and
fibrillization
properties
of
the
two
Abeta
40
variants
and
the
wild
type
peptide
.
Using
flow
cytometry
analysis
after
staining
with
propidium
iodide
and
annexin
V
,
we
also
evaluated
the
cytotoxic
effects
of
the
peptides
on
human
cerebral
endothelial
cells
in
culture
.
Under
the
conditions
tested
,
the
E
22
Q
peptide
exhibited
the
highest
content
of
beta
-sheet
conformation
and
the
fastest
aggregation
/
fibrillization
properties
.
The
Dutch
variant
also
induced
apoptosis
of
cerebral
endothelial
cells
at
a
concentration
of
25
micrometer
,
whereas
the
wild
type
Abeta
and
the
E
22
K
mutant
had
no
effect
.
The
data
suggest
that
different
amino
acids
at
position
22
confer
distinct
structural
properties
to
the
peptides
that
appear
to
influence
the
onset
and
aggressiveness
of
the
disease
rather
than
the
phenotype
.
Diseases
Validation
Diseases presenting
"also induced apoptosis"
symptom
hereditary cerebral hemorrhage with amyloidosis
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