Related Experiment Video
Updated: May 6, 2026

09:12
Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry
Published on: January 12, 2018
14.8K
Abnormal erythrocyte membrane protein pattern in severe megaloblastic anemia
The Journal of Clinical Investigation
|April 1, 1978
Summary
Severe megaloblastic anemia, caused by vitamin deficiencies, alters erythrocyte membrane proteins. Treatment with vitamins normalizes the protein pattern, indicating a reversible defect in red blood cell membranes.
Area of Science:
- Hematology
- Biochemistry
- Cell Biology
Background:
- Megaloblastic anemia results from deficiencies in vitamin B12 or folic acid.
- Erythrocyte membrane proteins are crucial for red blood cell structure and function.
- Previous studies have not fully elucidated the erythrocyte membrane protein alterations in megaloblastic anemia.
Purpose of the Study:
- To investigate the erythrocyte membrane protein pattern in patients with megaloblastic anemia.
- To determine if the observed abnormalities are reversible with vitamin replacement therapy.
- To explore the role of endogenous proteases in these membrane changes.
Main Methods:
- Polyacrylamide gel electrophoresis in sodium dodecyl sulfate (SDS-PAGE) was used to analyze erythrocyte membrane proteins.
- Patients with severe and mild megaloblastic anemia, as well as iron deficiency anemia, were studied.
- Membrane protein analysis was performed before and after vitamin replacement therapy.
Main Results:
- Severe megaloblastic anemia showed a grossly abnormal erythrocyte membrane protein pattern, lacking spectrin (bands 1, 2) and band 3.
- Mild megaloblastic anemia and severe iron deficiency anemia exhibited normal erythrocyte membrane protein patterns.
- Vitamin replacement therapy in severe megaloblastic anemia patients normalized the erythrocyte membrane protein pattern.
- No significant difference in protease activity was found between normal and abnormal erythrocyte membranes.
Conclusions:
- The erythrocyte membrane protein pattern is significantly altered in severe megaloblastic anemia.
- These alterations are reversible with adequate vitamin B12 or folic acid replacement.
- The observed abnormalities are not due to increased endogenous protease activity.
Related Concept Videos
Asymmetric Lipid Bilayer
8.1K
Biological membranes show uneven distribution of different types of lipids in the inner and outer layers, resulting in transverse asymmetric membranes. The treatment of the erythrocyte membrane with the enzyme phospholipase confirmed the asymmetric nature of the lipid bilayer. The enzyme hydrolyzes lipids into fatty acids and hydrophilic groups. The phospholipase acts only on the outer layer of the membrane, while the inner layer remains intact. The phospholipase treatment resulted in 80%...
8.1K
Membrane Carbohydrates
5.9K
The plasma membrane is a dynamic barrier composed of lipids, proteins, and carbohydrates. It is the epicenter of many cellular processes required for cell growth and survival. Carbohydrates have unique structural and chemical properties that help the plasma membrane to carry out its functions effectively.
Membrane carbohydrates do not have any hydrophobic region and are exclusively located on the cell's outer surface. The addition of sugar molecules or glycosylation of proteins happens in...
Membrane carbohydrates do not have any hydrophobic region and are exclusively located on the cell's outer surface. The addition of sugar molecules or glycosylation of proteins happens in...
5.9K
Structure and Function of Erythrocytes
9.5K
There are between 4.2 and 6 million erythrocytes, also known as red blood cells, in every microliter of blood. These cells are small, flattened biconcave discs with centers that are depressed.
The erythrocyte plasma membrane is associated with proteins such as spectrin, which forms a flexible cytoplasmic meshwork. This meshwork allows erythrocytes to twist, turn, become cup-shaped, and regain their biconcave shape as they pass through narrow capillaries. Additionally, erythrocytes can form...
The erythrocyte plasma membrane is associated with proteins such as spectrin, which forms a flexible cytoplasmic meshwork. This meshwork allows erythrocytes to twist, turn, become cup-shaped, and regain their biconcave shape as they pass through narrow capillaries. Additionally, erythrocytes can form...
9.5K
Disorders of Erythrocytes
2.7K
Disorders of erythrocytes, or red blood cells (RBCs), include a range of conditions affecting their number, shape, or function.
Erythrocyte disorders can be broadly categorized into two main types: anemic and polycythemic conditions.
A low oxygen-carrying capacity of the blood due to the loss, lower production, or destruction of erythrocytes is termed anemia. Hemorrhagic anemia, for example, occurs when bleeding from an external wound or internal ulcer reduces erythrocyte counts.
On the other...
Erythrocyte disorders can be broadly categorized into two main types: anemic and polycythemic conditions.
A low oxygen-carrying capacity of the blood due to the loss, lower production, or destruction of erythrocytes is termed anemia. Hemorrhagic anemia, for example, occurs when bleeding from an external wound or internal ulcer reduces erythrocyte counts.
On the other...
2.7K
Rh Blood Group
4.4K
The Rhesus (Rh) antigen is crucial in determining blood groups and ensuring compatibility during blood transfusions.
4.4K
Inborn Errors of Metabolism
1.1K
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
1.1K

