Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P02794 (
ferritin
)
17,525
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
An immunohistochemical analysis of formalin-fixed, paraffin-embedded brain sections was performed with antisera against holoferritin and the light(L)-subunit of
ferritin
. Sections immunostained using anti-glial fibrillary acidic protein (GFAP), Ricinus communis agglutinin-1 (RCA-1) stain for microglia and iron stain (Berlin blue stain) were compared. The L-subunit of
ferritin
was purified from normal human spleen according to the modified scrapie-associated fibrils purification, and the anti-serum was raised in a rabbit. Both
ferritin
antisera positively stained resting and, more markedly, reactive microglia, both of which were also stained with RCA-1 but not with GFAP. Ferritin-positive resting microglia were seen more abundantly in cerebral and cerebellar cortices than in white matter. The advantages of
ferritin
antisera over RCA-1 are as follows. (1) RCA-1 heavily stains blood vessels, while anti-
ferritin
does not, hence the microglial cells are more readily visualized with
ferritin
immunohistochemistry. (2) Reactive microglia and macrophages are more strongly stained with anti-
ferritin
. (3) The staining intensity of
ferritin
is independent of the length of tissue fixation in formalin. However, anti-
ferritin
is inferior to RCA-1 in staining resting microglia with a scanty cytoplasm, especially in the white matter, probably because the former recognizes cytoplasmic components, while the latter recognizes cell membrane. Iron stain only gave a reaction to microglial cells in brains with
neurosyphilis
and to hemosiderin-laden macrophages. Thus, in addition to RCA-1,
ferritin
antisera are useful as a microglia marker in formalin-fixed, paraffin-embedded sections.
...
PMID:Ferritin immunohistochemistry as a marker for microglia. 259 62
Although iron accumulates in the brain in a number of pathological conditions, including Hallervorden-Spatz syndrome, Parkinson's disease, and
neurosyphilis
, studies of brain iron metabolism have been performed only rarely. Neuronal-enriched cultures were prepared from fetal mouse brain. After 18 days the cells were exposed to radiolabeled iron. Total iron uptake and incorporation into
ferritin
were rapid and linear over four hours. The addition of either methylamine or ammonium chloride, both known blockers of transferrin-iron release through their lysosomotropic properties, inhibited total iron uptake. Methylamine also inhibited the rate of
ferritin
-iron incorporation, most likely by interfering with transferrin-iron release. The data suggest that neuronal iron transport, much like that in other mammalian tissues, is transferrin mediated and that blockers of transferrin-iron release may be of value in conditions in which there is brain iron overload.
...
PMID:Iron uptake by mammalian cortical neurons. 646 62
Few cases of MRI in
neurosyphilis
have been reported. We examined the value of MRI in patients with general paresis; MRI was performed on four HIV-negative patients with parenchymatous
neurosyphilis
. It demonstrated frontal and temporal atrophy, subcortical gliosis and, in one patient, increased
ferritin
in the basal ganglia. The progression of the lesions on MRI correlated well with the neuropsychiatric disturbances. The MRI findings correlated with the well-known neuropathological findings. This combination of pathological findings in
neurosyphilis
has not been described before and we suggest that MRI is of prognostic value in patients with general paresis.
...
PMID:MRI in patients with general paresis. 869 19