Iron absorption Flashcards
HFE
mutation responsible for most common absorption problems hemochromatosis
chromosome 6
protein HFE
HJV
mutation responsible for jeuvanile absorption problems
protein Hemojeuvelin
chromosome 1
TFR2
mutation responsible for clinically similar features to HFE but rare
chromosome 7
protein Transferrin receptor 2
SLC40A1
chromosome 2
protein ferroportin
HAMP
hepcidin, an iron regulation hormone critical for absorption
chromosome 19
factors that INCREASE iron absorption
inadequate diet impaired absorption celiac disease GI bleeding hypoxia anemias decreased erythropoiesis
factors decreasing iron absorption
regular blood transfusions
high iron diet
iron loading vitamins
human hemochromatosis protein
HFE
functions to regulate circulating iron uptake by regulating the interaction of the TFR 1/2 with transferrin
Hepcidin
key regulator of the entry of iron into circulation
transferrin
iron binding blood plasma glycoprotein that controls the level of free iron in biological fluids
TFR1
a protein required for iron imort from transferrin into cells by endocytosis
TFR2
protein involved in uptake of transferrin bound iron into cells by endocytosis, although role is minor compared to TFR1
Ferroportin
transmembrane protein that transports iron from the inside of the cell to the outside of the cell. inhabited by hepcidin, results in the retention of iron
Low iron and Hepcidin
low iron decreases hepcidin, which causes ferroportin to ne expressed in order to allow iron to be absorbed by the duodenum
High iron and hepcidin
high iron causes hepcidin to be high, which causes ferroportin to be prevented from bringing more iron in from the duodenum and gut