What Shields Red Blood Cells’ Outsides?


📹 Sickle Cell Anemia

MEDICAL ANIMATION TRANSCRIPT: Sickle cell anemia is an inherited blood disease that affects your red blood cells. It’s one of …


What is the protective function of RBC?

Red blood cells are vital for maintaining body health by bringing oxygen to tissues and releasing carbon dioxide for exhalation. Common conditions that affect red blood cell count include anemia, blood loss, bone marrow disorders, and cancer. Anemia causes the body to feel cold, tired, and weak, while blood loss results in the body losing more blood cells than it can produce. Bone marrow disorders, such as leukemia and lymphoma, damage the bone marrow, causing red blood cell formation. Certain cancers and chemotherapy treatment can also affect the number of red blood cells produced.

What is the outer layer of the blood vessel called?
(Image Source: Pixabay.com)

What is the outer layer of the blood vessel called?

The artery wall consists of three layers: the tunica intima, tunica media, and tunica externa. The tunica intima is a simple squamous epithelium surrounded by a connective tissue basement membrane. The tunica media is the thickest layer, providing support and regulating blood flow and pressure. The tunica externa is the outermost layer, connecting the vessel to the surrounding tissue.

Capillaries, the smallest and most numerous blood vessels, form the connection between arteries and veins, facilitating material exchange between blood and tissue cells. The distribution of capillaries varies with the metabolic activity of body tissues. Tissues like skeletal muscle, liver, and kidney have extensive capillary networks due to their metabolic activity and abundant supply of oxygen and nutrients.

Connective tissue, like the epidermis of the skin and the lens and cornea of the eye, lacks a capillary network. About 5% of the total blood volume is in systemic capillaries at any given time, and another 10% is in the lungs.

What is the outer covering of blood?

The peripheral vascular system consists of three layers: the adventitia, tunica media, and tunic intima. The adventitia provides structural support and shape to blood vessels, while the tunica media is composed of elastic and muscular tissue that regulates the vessel’s internal diameter. The tunic intima, an inner layer with an endothelial lining, provides a frictionless blood movement pathway.

What surrounds red blood cells?
(Image Source: Pixabay.com)

What surrounds red blood cells?

The RBC membrane and membrane skeleton are crucial for the shape and reversible deformability of RBC, which allows them to survive in circulation. The plasma membrane is composed of a lipid bilayer with embedded transmembrane proteins that form multi-protein complexes. The bilayer consists of equal proportions of cholesterol and phospholipids. For structural integrity, the bilayer links to the membrane skeleton through two macroprotein complexes: the ankyrin complex and the junctional complex (also known as the 4. 1R complex).

The RBC skeleton is a protein meshwork consisting of spectrin, actin, actin-associated proteins, protein 4. 1R, and ankyrin. The membrane skeleton consists of spectrin tetramers that bind short actin filaments, forming a pseudohexagonal arrangement with six triangular spectrins binding one actin filament. Each arrangement has three junction complexes and three ankyrin complexes that facilitate membrane-cytoskeleton linkages.

There are over 50 types of transmembrane proteins embedded in the lipid bilayer involved in transport, adhesion, and structural integrity. Transmembrane transport is executed by several proteins such as band 3, aquaporin-1, glucose transporter 1 (GLUT1), Kidd antigen protein, RhAG, and various ion transporters. Proteins involved in adhesion or cell-cell interactions include ICAM-4 and Lu.

RBC are generally not considered adhesive cells, but in certain pathological and disease-associated circumstances, such as sickle cell disease (SCD), malaria, polycythemia vera, hereditary spherocytosis, retinal vein occlusion, and diabetes mellitus, RBC notably change their behavior and become stimulated and adhesive to each other, particularly to the endothelium. The composition of integral membrane proteins incorporated into a phospholipid bilayer plays a significant role in the RBC membrane’s structure.

What is the exterior of the red blood cell?
(Image Source: Pixabay.com)

What is the exterior of the red blood cell?

Red blood cells are deformable, flexible, and able to interface with immune cells. Their membrane plays a crucial role in their functions, which are highly dependent on its composition. The red blood cell membrane consists of three layers: the glycocalyx, a lipid bilayer containing transmembrane proteins, and the membrane skeleton. Half of the membrane mass in human and most mammalian red blood cells is proteins, while the other half is lipids, specifically phospholipids and cholesterol.

The lipid bilayer, similar to all human cells, is composed of cholesterol and phospholipids in equal proportions by weight. This composition defines physical properties such as membrane permeability and fluidity, and regulates the activity of many membrane proteins. The major phospholipids are asymmetrically disposed, unlike cholesterol, which is evenly distributed between the inner and outer leaflets.

What are the proteins on the outside of RBCs called?

The red blood cell membrane is responsible for storing blood group antigens, which are primarily single-pass proteins, multi-pass proteins, and glycosylphosphatidylinositol (GPI)-linked proteins. These antigens determine an individual’s blood group, with the main two being ABO (with blood types A, B, AB, and O) and Rh (with RhD-positive or Rh D-negative blood types). The functions of many blood group antigens are unknown, and if they are missing from the red blood cell membrane, there is no ill effect. This suggests that if blood group antigens used to have a function, such as making red blood cells more resistant to parasite invasion, they may no longer be relevant today.

What is the protection of cells?
(Image Source: Pixabay.com)

What is the protection of cells?

The plasma membrane, also known as the cell membrane, is a crucial part of a cell’s structure and function. It provides protection, a stable environment, and facilitates the transport of nutrients and toxic substances within and out of the cell. The cell membrane also contains proteins that interact with other cells, either glycoproteins or lipid proteins. These proteins, which stick outside the membrane, enable cell interaction. The cell membrane also provides structural support.

Different types of cells have different plasma membranes, with cholesterol being a common component. Plants and microbes, like bacteria and algae, have different protective mechanisms and cell walls, which are more durable and structurally sound than the plasma membrane. Overall, the plasma membrane plays a crucial role in maintaining a stable and functional cell environment.

What is blood cell protection?

Blood plays a crucial role in protecting the body from infections, with white blood cells acting as immune system warriors. These cells, like warriors, attack invaders like bacteria and viruses. To enter the body, infective organisms must first overcome physical barriers like skin, nose hairs, mucus, and stomach acid. The immune system, consisting of various types of white blood cells, plays a second line of defense against bacterial, viral, fungal, and parasitic infections. When they detect an infection, these cells move to the site of attack to destroy the pathogen and prevent illness.

Which vitamin protects red blood cells?
(Image Source: Pixabay.com)

Which vitamin protects red blood cells?

The study investigates the effects of Trolox® or mannitol, two different antioxidants, on oxidative changes in manually isolated red blood cells from citrate-phosphate-dextrose (CPD) preserved whole blood, followed by up to 20 days refrigerated storage. The researchers also investigate whether Trolox supplemented to blood bank-manufactured saline-adenine-glucose-mannitol (SAGM) preserved RBC units would offer better storage conditions compared to SAGM alone.

The study measured the percentage of hemolysis and extracellular activity of lactate dehydrogenase (LDH) to assess RBC membrane integrity, and quantified lipid peroxidation, reduced glutathione levels, and total antioxidant capacity.

What covers red blood cells?

Red blood cells are a type of blood cell that contain hemoglobin and a membrane made of proteins and lipids. They are unique biconcave cells with a flat, indented center, allowing them to pass through small blood vessels. Recent advancements in red blood cell research have improved the diagnosis and treatment of blood-related disorders. One major breakthrough is the development of CRISPR gene-editing technology, which has shown promise in treating sickle cell disease and beta-thalassemia by correcting genetic mutations at the source. Additionally, advancements in stem cell therapy enable the production of red blood cells in vitro, offering the potential for transfusions without donor dependence.

What is the outer covering of RBC?
(Image Source: Pixabay.com)

What is the outer covering of RBC?

The human red blood cell (RBC) is a two-dimensional structure that undergoes large elastic deformations when passing through narrow blood vessels. This flexibility is primarily due to the cell membrane, which is composed of a cytoskeleton and a lipid bilayer, tethered together. The lipid bilayer includes various types of phospholipids, sphingolipids, cholesterol, and integral membrane proteins, such as band-3 and glycophorin. The RBC membrane resists bending but cannot sustain in-plane static shear stress as the lipids and proteins diffuse within the lipid bilayer at equilibrium.

The cytoskeleton plays a major role in the integrity of the RBC membrane, as demonstrated in blood disorders where defects in membrane proteins lead to membrane loss and reduced mechanical robustness of the RBC. In hereditary spherocytosis (HS), the tethering of the cytoskeleton to the lipid bilayer is partially disrupted, resulting in membrane loss and subsequently in the spherical shape of the RBCs.

In hereditary elliptocytosis (HE), the cytoskeleton is disrupted at α-β spectrin linkages or at spectrin-actin-4. 1R junctional complexes, diminishing the ability of the RBC to recover its biconcave shape after undergoing large deformations.

Several approaches have been followed for mathematical description and modeling of the RBC membrane, including continuum membrane models based on elasticity theory and atomistic simulations mainly studying the behavior of lipids in the lipid bilayer. However, it is challenging for continuum models to account for the detailed structure and defects in the RBC cytoskeleton, as it is not feasible for atomistic methods to simulate a representative sample of the RBC membrane including lipids, membrane proteins, and the cytoskeleton.

Particle-based mesoscale models have been introduced to study the biomechanical behavior of the RBC membrane. These models fall into two main groups: one group, which is modeled as a 2D canonical hexagonal network of particles, and the other group, which is simulated by coarse-grained methods. The lipids are forced to assemble the bilayer by additional solvent particles, or by an additional potential, in the case of solvent-free models.

Drouffe et al. simulated biological membranes by introducing a one-particle-thick, solvent-free, coarse-grained model, in which the interparticle interaction is described by a Lennard-Jones (LJ) type pair potential depending on the distance between the particles and their directionality. Noguchi and Gompper developed a one-particle thick, solvent-free, lipid bilayer model by introducing a multibody potential that eliminated the need for the rotational degree of freedom. Yuan et al. introduced a similar approach, but instead of the LJ potential, a soft-core potential was used to better represent the particle self-diffusion.


📹 Sickle cell anemia – causes, symptoms, diagnosis, treatment & pathology

What is sickle cell anemia? Sickle cell anemia is an autosomal recessive genetic condition where the beta-globin protein subunit …


What Shields Red Blood Cells' Outsides
(Image Source: Pixabay.com)

Rafaela Priori Gutler

Hi, I’m Rafaela Priori Gutler, a passionate interior designer and DIY enthusiast. I love transforming spaces into beautiful, functional havens through creative decor and practical advice. Whether it’s a small DIY project or a full home makeover, I’m here to share my tips, tricks, and inspiration to help you design the space of your dreams. Let’s make your home as unique as you are!

Email: [email protected], [email protected]

About me

12 comments

Your email address will not be published. Required fields are marked *

  • 19 year old sickle cell warrior here! This article is very updated. I was diagnosed with sickle cell disease at the age of three. Drinking plenty of water, eating healthy, taking daily medications and the grace of God has kept me going. My mum started to know more about my disease when she had a Google phone. I was weak when growing up, but it’s much better now. My eyes have already been infected by the disease, I’m now on lens. I’m in Medical school now, hoping to help the future generation, so they will not suffer what I/we have already went through. Love ♥️ to all my fellow warriors….. We are strong!

  • I knew little about the disease until my own children were diagnosed with the disease, what I can comment is thanks for the information, every 19th June of every year is a world sickle cell awareness day yet little has been done by countries to eliminate the disease through awareness. I have two warriors one 19 yrs and another 10yrs but it is not a walk in the park. I always pray that one day this will end for the better for my children and others who have the same condition. thanks

  • I had this disease at the age of eight, my eyes were yellow, and I was feeling tired and painful. My disease was diagnosed and treatment began. Healthy eating played a major role in my recovery. The doctor advised me to stay away from some foods such as foods that contains sugar, tea, coffee, and sweets, and he advised me to eat vegetables, red meat, and liver and everything that contains proteins, and I take a lot of rest, and within a year in this way I started to feel better until I recovered, and now I am 37 years old, in good health.

  • Been having this sickness ever since I existed Edit: btw I had to extract the spleen when I was about 6-10 years old because it was absorbing the blood and inflating was this the right choice and is there any special things I have to do now I’m 18 yes I was doing better ever since it was extracted but I just wanna ask and see if there is anything I just don’t know

  • I am developing a mathematical hypothesis to explain the C, N, O and H element cycles in the body. I have a question which its answer can help me to validate and/or modify my hypothesis. How do we know that there is a Fe atom in the Hemoglobin, or what is the scientific method that detected/isolated the Fe from Hemoglobin? My calculations is pointing to the element Phosphorus.

  • My roommate had them she didn’t want anyone to know till her mom told me she didn’t like that the mother was talking about her sickness. On june 4th me and her were cooking she started asking me about stock and what share I buy, I told her I will write them down and give it to her 3 days went by I didn’t see her I slide the list under her door I’m thinking she is in the bathroom since the water was running but its 4 of us in the house, I left on the 11th morning went up to Massachusetts around 10:30pm I got a call my landlord was like your room or her room smells. I’m like ewwu I probably forgot the fish in there, he went on to say I figured it wasn’t yours cause we’ve seen u .ok. well it was her room she passed away. I was shocked .

  • This medical animation provides an overview of sickle cell anemia, an inherited blood disease that affects the shape and function of red blood cells. Red blood cells are important because they carry oxygen throughout the body. In sickle cell anemia, the hemoglobin protein within the red blood cells is abnormal due to a mutation in the beta-globin gene. This leads to the formation of rigid strands of hemoglobin within the cell, causing the red blood cells to take on a sickle shape. These sickle-shaped cells can block blood flow, causing pain and tissue damage. Sickle cells also have a shorter lifespan than normal red blood cells, which can result in anemia. Symptoms of sickle cell anemia can vary but may include pain, jaundice, and fatigue. Complications of the disease can include severe pain and damage to various organs. People with ancestors from certain regions, including sub-Saharan Africa and parts of South America and the Mediterranean, are at higher risk for sickle cell anemia. If you are concerned about sickle cell anemia, talk to your healthcare provider for more information.

  • I’m only here because one of my co-workers has sickle cell as well as one of my customers and I want to better service them. The man actually had jaundice and I had asked him if he was okay. He said he had sickle cell and outside of the fact that mostly black people and Native Americans get it I don’t know much about it.

  • I recently lost a good friend of mine because of sickle desease. She used to have treatment which helped her deal with this disease but she got vaccinated against COVID a few months ago and she started to have more frequent outbreaks. Really sad that she passed away so young, 34 years old. Seems the vaccine increased her risks due to this health condition. May she rest in peace. She was always smiling and happy despite all the pain this sickness caused her 😔

  • I think I just figured out the way to cure this. So since sickle cell is caused by a mutation in the Hemoglobin cell, we can actually find a type of medicine that takes pieces from immature blood cells and uses them to reconstruct mature ones. To make this we can piece together a modified blood cell, if we use this I want it to be green, and the thing we can do with that is make it behave as if it is like a blood cell surgeon, or so I said. Basically what it would do is take immature blood cells, take pieces of those cells, and use the sickle cell’s property of sticking to things to piece it back together. As for the defective Hemoglobin, we could inject new mature blood cells with non defective HGBN and basically program the green blood cell to take the good Hemoglobin and give it to a sickle cell. P.S: I AM 12 YEARS OLD AND I FIGURED IT OUT HOW DID NOBODY THINK OF THIS????

  • I have to get for blood transfusion post-op from internal hemorrhaging after getting an appendectomy. Hemoglobin levels just kept dropping and dropping all night. I had to have an emergency surgery and 4 blood transfusions to fill me back up with blood. Doctors were baffled that I wasn’t dead. They had to cut me open like an old-time discectomy to find the bleeding and vacuum out all the blood. I had a staple puncturing a small artery at the appendix removal site. Closest I’ve been to death. Good thing they chose to keep me overnight or I would have died if I was sent home.

  • I have sickle cell disease but i haven very sick since last year as am writing this am on a hospital bed and its been so bad my spleen got inflammated and its hurts really bad but what hurts most is that after a month of so much pain am treated like am a drug addicted,or I don’t want to go home,or I just want drugs, or to be here, and some times the discharge me so early am tired the pain is too much I wish they would understand that the pain is too much and i need help

Pin It on Pinterest

We use cookies in order to give you the best possible experience on our website. By continuing to use this site, you agree to our use of cookies.
Accept
Privacy Policy