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Regulation of brain iron uptake by apo- and holo-transferrin is dependent on sex and delivery protein
by
Simpson, Ian A.
, Baringer, Stephanie L.
, Palsa, Kondaiah
, Connor, James R.
, Neely, Elizabeth B.
in
Alzheimer's disease
/ Analysis
/ Animals
/ Apoferritins
/ Biological Transport
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood–brain barrier
/ Brain
/ Brain - metabolism
/ Consciousness
/ Drug delivery
/ Drug delivery systems
/ Drugs
/ Estrogen
/ Female
/ Ferritin
/ H-ferritin
/ Hematology
/ Iron
/ Iron - metabolism
/ Laboratory animals
/ Male
/ Mice
/ Microvasculature
/ Nervous system diseases
/ Neurobiology
/ Neurological diseases
/ Neurosciences
/ Oophorectomy
/ Parenchyma
/ Proteins
/ Restless legs syndrome
/ Sex difference
/ Sex differences
/ Surgery
/ Sutures
/ Transferrin
/ Transferrin - metabolism
/ Transferrins
/ Vehicles
/ Ventricle
/ Ventricles (cerebral)
2022
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Regulation of brain iron uptake by apo- and holo-transferrin is dependent on sex and delivery protein
by
Simpson, Ian A.
, Baringer, Stephanie L.
, Palsa, Kondaiah
, Connor, James R.
, Neely, Elizabeth B.
in
Alzheimer's disease
/ Analysis
/ Animals
/ Apoferritins
/ Biological Transport
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood–brain barrier
/ Brain
/ Brain - metabolism
/ Consciousness
/ Drug delivery
/ Drug delivery systems
/ Drugs
/ Estrogen
/ Female
/ Ferritin
/ H-ferritin
/ Hematology
/ Iron
/ Iron - metabolism
/ Laboratory animals
/ Male
/ Mice
/ Microvasculature
/ Nervous system diseases
/ Neurobiology
/ Neurological diseases
/ Neurosciences
/ Oophorectomy
/ Parenchyma
/ Proteins
/ Restless legs syndrome
/ Sex difference
/ Sex differences
/ Surgery
/ Sutures
/ Transferrin
/ Transferrin - metabolism
/ Transferrins
/ Vehicles
/ Ventricle
/ Ventricles (cerebral)
2022
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Regulation of brain iron uptake by apo- and holo-transferrin is dependent on sex and delivery protein
by
Simpson, Ian A.
, Baringer, Stephanie L.
, Palsa, Kondaiah
, Connor, James R.
, Neely, Elizabeth B.
in
Alzheimer's disease
/ Analysis
/ Animals
/ Apoferritins
/ Biological Transport
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood–brain barrier
/ Brain
/ Brain - metabolism
/ Consciousness
/ Drug delivery
/ Drug delivery systems
/ Drugs
/ Estrogen
/ Female
/ Ferritin
/ H-ferritin
/ Hematology
/ Iron
/ Iron - metabolism
/ Laboratory animals
/ Male
/ Mice
/ Microvasculature
/ Nervous system diseases
/ Neurobiology
/ Neurological diseases
/ Neurosciences
/ Oophorectomy
/ Parenchyma
/ Proteins
/ Restless legs syndrome
/ Sex difference
/ Sex differences
/ Surgery
/ Sutures
/ Transferrin
/ Transferrin - metabolism
/ Transferrins
/ Vehicles
/ Ventricle
/ Ventricles (cerebral)
2022
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Regulation of brain iron uptake by apo- and holo-transferrin is dependent on sex and delivery protein
Journal Article
Regulation of brain iron uptake by apo- and holo-transferrin is dependent on sex and delivery protein
2022
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Overview
Background
The brain requires iron for a number of processes, including energy production. Inadequate or excessive amounts of iron can be detrimental and lead to a number of neurological disorders. As such, regulation of brain iron uptake is required for proper functioning. Understanding both the movement of iron into the brain and how this process is regulated is crucial to both address dysfunctions with brain iron uptake in disease and successfully use the transferrin receptor uptake system for drug delivery.
Methods
Using in vivo steady state infusions of apo- and holo-transferrin into the lateral ventricle, we demonstrate the regulatory effects of brain apo- and holo-transferrin ratios on the delivery of radioactive
55
Fe bound to transferrin or H-ferritin in male and female mice. In discovering sex differences in the response to apo- and holo-transferrin infusions, ovariectomies were performed on female mice to interrogate the influence of circulating estrogen on regulation of iron uptake.
Results
Our model reveals that apo- and holo-transferrin significantly regulate iron uptake into the microvasculature and subsequent release into the brain parenchyma and their ability to regulate iron uptake is significantly influenced by both sex and type of iron delivery protein. Furthermore, we show that cells of the microvasculature act as reservoirs of iron and release the iron in response to cues from the interstitial fluid of the brain.
Conclusions
These findings extend our previous work to demonstrate that the regulation of brain iron uptake is influenced by both the mode in which iron is delivered and sex. These findings further emphasize the role of the microvasculature in regulating brain iron uptake and the importance of cues regarding iron status in the extracellular fluid.
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