Hephaestin: Difference between revisions
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'''Hephaestin''' is a [[protein]] that in | == Hephaestin == | ||
[[File:TEST_Hephaestin_illustration.png|thumb|right|Illustration of Hephaestin]] | |||
'''Hephaestin''' is a [[protein]] that plays a crucial role in the [[metabolism]] of [[iron]] within the human body. It is primarily involved in the process of iron transport across the [[intestinal epithelium]], facilitating the conversion of iron from its ferrous (Fe__) to ferric (Fe__) state, which is essential for its incorporation into [[transferrin]], the main iron transport protein in the blood. | |||
== Function == | == Function == | ||
== | Hephaestin is a [[ferroxidase]], an enzyme that catalyzes the oxidation of iron. It is homologous to [[ceruloplasmin]], another copper-containing ferroxidase, and is encoded by the ''HEPH'' gene located on the [[X chromosome]]. Hephaestin is predominantly expressed in the [[duodenum]], the first section of the [[small intestine]], where it facilitates the export of iron from [[enterocytes]] into the bloodstream. | ||
== Mechanism of Action == | |||
Hephaestin works in conjunction with the iron exporter [[ferroportin]] to mediate the transfer of iron from the enterocytes to the plasma. Once iron is absorbed from the diet, it is stored temporarily in the enterocytes in its ferrous form. Hephaestin oxidizes this iron to the ferric form, enabling its binding to transferrin. This process is critical for maintaining systemic iron homeostasis and preventing iron deficiency or overload. | |||
== | == Clinical Significance == | ||
Mutations or deficiencies in hephaestin can lead to disorders of iron metabolism. For instance, a lack of functional hephaestin can result in [[iron deficiency anemia]], as the body is unable to efficiently transport iron into the bloodstream. Conversely, dysregulation of hephaestin activity may contribute to conditions of iron overload, such as [[hemochromatosis]]. | |||
== Related Proteins == | |||
Hephaestin is part of a family of multicopper oxidases, which includes ceruloplasmin and [[hephaestin-like protein 1]] (HEPHL1). These proteins share structural similarities and are involved in various copper-dependent enzymatic processes. | |||
== Research and Developments == | |||
Ongoing research is focused on understanding the precise molecular mechanisms of hephaestin and its interactions with other proteins involved in iron metabolism. Studies are also exploring potential therapeutic targets for treating iron-related disorders by modulating hephaestin activity. | |||
== Related Pages == | |||
* [[Iron metabolism]] | * [[Iron metabolism]] | ||
* [[Ferroportin]] | |||
* [[Ceruloplasmin]] | * [[Ceruloplasmin]] | ||
* [[Transferrin]] | * [[Transferrin]] | ||
* [[ | * [[Iron deficiency anemia]] | ||
* [[Hemochromatosis]] | * [[Hemochromatosis]] | ||
[[Category:Proteins]] | [[Category:Proteins]] | ||
[[Category:Iron metabolism]] | [[Category:Iron metabolism]] | ||
[[Category: | [[Category:Enzymes]] | ||
Latest revision as of 05:14, 16 February 2025
Hephaestin[edit]
Hephaestin is a protein that plays a crucial role in the metabolism of iron within the human body. It is primarily involved in the process of iron transport across the intestinal epithelium, facilitating the conversion of iron from its ferrous (Fe__) to ferric (Fe__) state, which is essential for its incorporation into transferrin, the main iron transport protein in the blood.
Function[edit]
Hephaestin is a ferroxidase, an enzyme that catalyzes the oxidation of iron. It is homologous to ceruloplasmin, another copper-containing ferroxidase, and is encoded by the HEPH gene located on the X chromosome. Hephaestin is predominantly expressed in the duodenum, the first section of the small intestine, where it facilitates the export of iron from enterocytes into the bloodstream.
Mechanism of Action[edit]
Hephaestin works in conjunction with the iron exporter ferroportin to mediate the transfer of iron from the enterocytes to the plasma. Once iron is absorbed from the diet, it is stored temporarily in the enterocytes in its ferrous form. Hephaestin oxidizes this iron to the ferric form, enabling its binding to transferrin. This process is critical for maintaining systemic iron homeostasis and preventing iron deficiency or overload.
Clinical Significance[edit]
Mutations or deficiencies in hephaestin can lead to disorders of iron metabolism. For instance, a lack of functional hephaestin can result in iron deficiency anemia, as the body is unable to efficiently transport iron into the bloodstream. Conversely, dysregulation of hephaestin activity may contribute to conditions of iron overload, such as hemochromatosis.
Related Proteins[edit]
Hephaestin is part of a family of multicopper oxidases, which includes ceruloplasmin and hephaestin-like protein 1 (HEPHL1). These proteins share structural similarities and are involved in various copper-dependent enzymatic processes.
Research and Developments[edit]
Ongoing research is focused on understanding the precise molecular mechanisms of hephaestin and its interactions with other proteins involved in iron metabolism. Studies are also exploring potential therapeutic targets for treating iron-related disorders by modulating hephaestin activity.
