Related Experiment Video
Updated: Jul 12, 2026

09:43
Measurement of Heme Synthesis Levels in Mammalian Cells
Published on: July 9, 2015
[Heme-iron in the human body]
József Balla1, György Balla, Béla Lakatos
1Debreceni Egyetem, Orvos- és Egészségtudományi Centrum I. Belgyógyászati Klinika, Szülészeti Klinika, Nefrológiai Tanszék, Neonatológiai Tanszék Debrecen.
Orvosi Hetilap
|September 4, 2007
Summary
Iron absorption is tightly regulated to maintain balance. This review summarizes how the body processes heme, a crucial iron source, from diet and its release during hemolysis.
Area of Science:
- Biochemistry
- Physiology
- Cell Biology
Context:
- Iron is vital for life but toxic in excess, necessitating strict absorption control.
- Heme iron from diet is a major source in some populations, absorbed by intestinal cells.
- Heme is also a component of essential proteins like hemoglobin.
Purpose:
- To review the metabolic pathways of heme in the human body.
- To elucidate heme absorption, degradation, and its role in iron homeostasis.
- To summarize heme's fate following dietary intake and intravascular hemolysis.
Summary:
- Dietary heme is absorbed by enterocytes, degraded by heme oxygenase, and released as transferrin-bound iron.
- Hemoglobin released during hemolysis binds haptoglobin, is internalized by macrophages, and heme is degraded.
- Oxidation of hemoglobin to methemoglobin promotes free heme release, which is cleared by hemopexin or lipoproteins, potentially causing cell damage.
Impact:
- Understanding heme metabolism is crucial for managing iron overload disorders.
- This review provides insights into cellular iron uptake and utilization mechanisms.
- Knowledge of heme's role in oxidative stress and cell damage informs therapeutic strategies.
Related Concept Videos
Hemoglobin
Hemoglobin is a globular protein made up of four subunits. Two of these subunits are alpha chains, and the other two are beta chains. Each subunit contains a molecule of heme, which has an iron atom and can bind to oxygen. When an oxygen molecule binds to one heme group, it changes the shape of hemoglobin, making it easier for the other heme groups to bind oxygen as well.
When all four heme groups are bound to oxygen, the resulting molecule is called oxyhemoglobin. As a result, arterial blood...
When all four heme groups are bound to oxygen, the resulting molecule is called oxyhemoglobin. As a result, arterial blood...
Lifecycle of Erythrocytes
Erythrocytes, also known as red blood cells, constantly move through blood capillaries. As a result, they damage their plasma membrane due to the continuous friction. Typically, after 100 to 120 days, erythrocytes become rigid and fragile as they wear out. As they pass through small vessels in the spleen and liver, they can get trapped and break apart into fragments.
The resident phagocytic macrophages deal with these damaged cells by engulfing them and separating their globin and heme groups.
The resident phagocytic macrophages deal with these damaged cells by engulfing them and separating their globin and heme groups.
The Early Endosome: Endocytosis of Transferrin
Essential proteins such as insulin or low-density lipoprotein (LDL) and micronutrients such as iron enter a eukaryotic cell through receptor-mediated endocytosis. Subsequently, the early endosomes fuse with the vesicles containing such receptor-ligand complexes and play a vital role in sorting the incoming ligands and receptors. While the ligands are either degraded inside the vesicle or released into the cytosol, their receptors are returned to the plasma membrane for further rounds of...
Oxygen Transport in the Blood
Hemoglobin (Hb) is a crucial molecule in the human body, consisting of four polypeptide chains, each bound to an iron-containing heme group. This unique structure enables hemoglobin to bind to oxygen, with each molecule capable of combining with four molecules of oxygen, leading to rapid and reversible oxygen loading. When fully loaded with oxygen, it is called oxyhemoglobin, while hemoglobin that has released oxygen is called reduced hemoglobin or deoxyhemoglobin. As hemoglobin binds oxygen,...
Overview of Hematopoiesis
Hematopoiesis, or blood cell production, is a vital biological process that begins early in embryonic development and continues throughout life. This process generates the various types of cells found in blood, including red blood cells, white blood cells, and platelets from hematopoietic stem cells (HSCs).
Developmental Phases of Hematopoiesis
Initially, HSCs are formed in the embryonic yolk sac, a critical site for early blood cell production. These stem cells subsequently migrate to other...
Developmental Phases of Hematopoiesis
Initially, HSCs are formed in the embryonic yolk sac, a critical site for early blood cell production. These stem cells subsequently migrate to other...
Erythropoiesis
Red blood cells (RBCs) transport oxygen to all body tissues. These cells survive only for 120 days and then need to be replenished. Erythropoiesis is the process of RBC production. In healthy individuals, erythropoiesis ensures all tissues are amply supplied with oxygen. In addition, blood loss due to injury leads to a drop in the physiological oxygen level that will cause erythropoiesis. Any defect in erythropoiesis leads to several physiological disorders, including thalassemia, anemia, and...

