Human iron metabolism: Difference between revisions
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| author = Ganz T, Nemeth E | | author = Ganz T, Nemeth E | ||
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===Erythropoetin=== | |||
Besides its role in erythropoesis, erythropoetin decreases DMT1 and increases ferroportin, thus reducing iron retention in macrophages, at least in rat models. <ref>{{citation | |||
| journal =J Cell Biochem | |||
| date = 2008 May 15 | volume = 104 | issue = 2 | pages = 629-41. | |||
| title = Decreased DMT1 and increased ferroportin 1 expression is the mechanisms of reduced iron retention in macrophages by erythropoietin in rats | |||
| author = Kong WN, ''et al.'' | |||
| url = http://www.ncbi.nlm.nih.gov/pubmed/18189270}}</ref> | |||
==Requirements== | ==Requirements== | ||
The actual requirement for iron in food is quite low, as the body conserves iron stores. Erythropoiesis requires 20-30 mg/day, so, with efficient conservation, only 1-2 mg/day of dietary iron is needed. <ref name=Munoz2009 /> | The actual requirement for iron in food is quite low, as the body conserves iron stores. Erythropoiesis requires 20-30 mg/day, so, with efficient conservation, only 1-2 mg/day of dietary iron is needed. <ref name=Munoz2009 /> | ||
Revision as of 02:30, 3 January 2010
Iron is an essential nutrient for human beings, although it can also be toxic. The most important role is in the heme protein of hemoglobin and cytochrome P-450, and secondarily for myoglobin, which transports oxygen into muscle cells. Iron also is a component of a number of enzymes. The greatest demand for iron is from erythropoesis: hemoglobin for the production of new erythrocytes (i.e., red blood cells). [1]
Regulation and homeostasis
Control mechanisms for iron metabolism are not fully understood, but two models, which may coexist, form current thinking: crypt programming and hepcidin.
Crypt programming
The principle of this model is that that enterocytes, in the crypt cells of the duodenum, take up iron from plasma via transferrin receptors 1 and 2 (TfR1 and TfR2). The more iron these cells take up from the plasma, the less they accept from the digestive tract.
Hepcidin
A peptide hormone produced in the liver, hepcidin, has received the most attention as the control mechanism. It also affects enterocytes, but also macrophages and the liver. Originally thought to be an antibacterial substance, [2] it is now believed to be an inhibitor of iron intake into the body. [3]
Erythropoetin
Besides its role in erythropoesis, erythropoetin decreases DMT1 and increases ferroportin, thus reducing iron retention in macrophages, at least in rat models. [4]
Requirements
The actual requirement for iron in food is quite low, as the body conserves iron stores. Erythropoiesis requires 20-30 mg/day, so, with efficient conservation, only 1-2 mg/day of dietary iron is needed. [1]
Digestion
Iron, in food, is processed differently depending if it is in the form of heme (e.g., in meats) or in other molecules. As food breaks down in the stomach, ferric (Fe+3) iron is reduced to ferrous (Fe+2) iron by the enzyme ferric reductase. Ascorbic acid and other reducing agents stimulates the reduction, and thus stimulates absorption.
Non-heme iron, however, may not be available to the digestive processes. While spinach is legendary as an iron source, the iron in raw spinach is bound into a non-absorbable oxalate. Cooking the spinach does make the iron bioavailable; the cartoon character Popeye the Sailor Man was correct in eating his spinach from a can.
Most actual absorption takes place in the duodenum. Heme is absorbed via the heme transporter protein. Non-heme iron enters the apical surface of the enterocytes lining the duodenum via divalent metal transporter 1 (DMT1)[5], carrying iron into the interstitial fluid by a protein called ferroportin (FP). [6]
Hepcidin binds to ferroportin, inhibiting its action. [3]
Distribution
Transferrin moves iron through the plasma; ferritin stores it.
Ferrous iron, in plasma, is reconverted to ferric, and bound to a carrier protein, ferritin.
Ferritin in plasma stays in equilibrium with ferritin in bone marrow, and plasma ferritin is indicative of actual iron stores in the marrow.
Marrow erythroblasts and liver hepatocytes store iron, primarily as ferritin complex but, to a lesser extent, as the breakdown product, hemosiderin. Hemosiderin is primarily present in macrophages.
Excretion
Disorders of iron metabolism
Not all anemia is due to disorders of iron metabolism, but iron deficiency anemia is a syndrome commonly seen, with many causes. Iron in excess through a metabolic error is less common, and called hemochromatosis. Among children in the U.S., iron supplements are the most common source of serious accidental poisoning.
Iron loading increases hepcidin synthesis (i.e., reducing iron intake), while hypoxia and anemia decrease its production. [3]
Hepcidin is markedly induced during inflammation, through the effect of interleukin-6 (IL-6). Increased hepcidin traps iron in macrophages, decreases plasma iron concentrations, and is a mechanism of anemia of chronic disease. [7]
References
- ↑ 1.0 1.1 Munoz M, Villar I, Garcia-Erce JA (2009), "An update on iron physiology", World J Gastroenterol 15 (37): 4617–4626., DOI:10.3748/wjg.15.4617.
- ↑ Park CH et al. (2001), "Hepcidin, a Urinary Antimicrobial Peptide Synthesized in the Liver", Journal of Biological Chemistry 276: 7806-7810, DOI:10.1074/jbc.M008922200
- ↑ 3.0 3.1 3.2 Ganz T, Nemeth E (2005), "Iron imports. IV. Hepcidin and regulation of body iron metabolism", Am J Physiol Gastrointest Liver Physiol 290: G199–G203, DOI:10.1152/ajpgi.00412.2005
- ↑ Kong WN, et al. (2008 May 15), "Decreased DMT1 and increased ferroportin 1 expression is the mechanisms of reduced iron retention in macrophages by erythropoietin in rats", J Cell Biochem 104 (2): 629-41.
- ↑ Chong WS et al. (Advance Access originally published online on August 25, 2005), "Expression of divalent metal transporter 1 (DMT1) isoforms in first trimester human placenta and embryonic tissues", Human Reproduction 20 (12): 3532-3538, DOI:10.1093/humrep/dei246
- ↑ De Domenico, I et al. (2006), "Ferroportin-mediated mobilization of ferritin iron precedes ferritin degradation by the proteasome", EMBO Journal 25: 5396 - 5404, DOI:10.1038/sj.emboj.7601409
- ↑ Nemeth E et al (2004), "IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin", J Clin Invest 113 (9): 1271–1276., DOI:10.1172/JCI200420945.