Lecture 1 Flashcards
What is Hematology
What are the main components of blood?
What is hematocrit
What is the hematocrit value for males and what about females?
What is the least dense component of blood
What is the percentage of whole blood plasma?
What about the percentage of whole blood Buffy coat?
What does the Buffy coat contain?
What percentage of whole blood are erythrocytes
What is Hematology?”,”The study of blood and its components, including its formation and diseases.”
“What are the main components of blood?”,”Plasma and formed elements (erythrocytes (red blood cells), leukocytes (white blood cells), and platelets.)
“What is hematocrit?
the percentage of blood volume that is RBCs. Visualize a tube with plasma and RBCS settled at the bottom. The proportion or percentage of the tube that is filled with the RBCS is the hematocrit. It refers to the height of the tube filled with RBCS. In a hematocrit test, a sample of blood is placed into a thin, capillary tube and then centrifuged. During centrifugation, the components of blood separate based on their densities.
2. Measurement: After centrifugation, the red blood cells (RBCs) settle to the bottom of the tube, forming a packed layer. The height of this layer is then measured.
hematocrit is not merely against the volume within the tube itself but is interpreted as an indication of the percentage of red blood cells in the entire blood volume of the body.
What is it’s value in males?”,”47% ± 5%”
“What is the percentage of blood volume that is RBCs in females?”,”42% ± 5%”
“What is the least dense component of blood?”,”Plasma”
“What percentage of whole blood is plasma?”,”55%”
“What percentage of whole blood is the buffy coat?”,”<1%”. It is located between the plasma and the erythrocytes
“What does the buffy coat contain?”,”Leukocytes and platelets”
“What percentage of whole blood are erythrocytes?”,”45%”
Erythrocytes are the most dense part of whole blood
State 11 components of plasma
What is the difference between plasma and serum and how are both obtained?
Which of the two have a longer shelf life?
Plasma contains water, salts, enzymes, antibodies, proteins (albumin,globulins,fibrinogen), coagulation factors (e.g fibronogen, Factor VIII, etc ), electrolytes, amino acids,nitrogenous waste,nutrients,gases,
Plasma has clotting factors. You obtain it by centrifuging blood with anticoagulant. It also contains fibrinogen. It is easy and quicker to separate from blood sample and is used for tests that require you to detect clotting factors. Is the main medium for excretory product transportation
Serum- liquid that remains after blood clots. That’s why it doesn’t have clotting factors. Cuz they’ve already been used to make the blood to clot. It also has water, proteins, minerals,etc
Can be obtained by centrifuging coagulated blood.
You won’t add anticoagulant.
Has a longer shelf life (about 10 years) cuz there aren’t any clotting factors.
What is the ph of blood?
What’s the temperature of blood?(not temperature of body)
Blood constitutes what percentage of body weight?
What is the average blood volume for males?(in liters)
What is the average blood volume for females?(in liters)
Why do males have a higher blood volume than females
What are the physical characteristics of blood?”,”Sticky, opaque fluid, color ranges from scarlet to dark red, pH 7.35-7.45, temperature 38°C, ~8% of body weight.”
What is the average blood volume for females?”,”4-5 liters”
“What is the average blood volume for males?”,”5-6 liters
Males have more blood than females cuz they have larger muscle or body mass hence more blood vessels that have to perfuse the extra muscle mass or body mass.
Also,females lose blood every month when they menstruate so they’re blood is lower than males
State 8 functions of blood (3 distributive,3 regulatory,2 protective)
1.Distribution of:
•O2 and nutrients to body cells
•Metabolic wastes to the lungs and kidneys for elimination
•Hormones from endocrine organs to target organs
Regulation of:
•Body temperature by absorbing and distributing heat-Blood comes closer to skin surface for heat to leave the body hence regulating body temperature
•Normal pH using buffers-Able to resist changes in ph that’s why it’s a very good buffer.
•Adequate fluid volume in the circulatory system
Protection against:
•Blood loss-
•Plasma proteins and platelets initiate clot formation
•Infection-
•Antibodies
•Complement proteins
•WBCs defend against foreign invaders
Blood produced immunoglobulins to fight infections
Has complement proteins to coat or make the foreign body look appetizing to be eaten or phagocytosed(this process is opsonization)
How do you get blood from a person?
90% of plasma is comprised of what?
Which proteins are found in the plasma
State them in order of the most abundant
Here are three multiple-choice questions based on the provided percentages of blood plasma proteins:
-
What percentage of plasma proteins is represented by albumin?
- A) 36%
- B) 60%
- C) 4%
- D) 40%
-
Which of the following plasma proteins constitutes 4% of the total plasma proteins?
- A) Albumin
- B) Globulins
- C) Fibrinogen
- D) Enzymes
-
If the total plasma protein concentration is 100%, what percentage is represented by globulins?
- A) 60%
- B) 36%
- C) 4%
- D) 40%
Using syringe
Using vacutainer
90% water
•Proteins are mostly produced by the liver(mnemonic-Agcm. A is albumin and g is globulin so definitely the third and final is fibrinogen )
Here are three multiple-choice questions based on the provided percentages of blood plasma proteins:
-
What percentage of plasma proteins is represented by albumin?
- A) 36%
- B) 60%
- C) 4%
- D) 40%
- Answer: B) 60%
-
Which of the following plasma proteins constitutes 4% of the total plasma proteins?
- A) Albumin
- B) Globulins
- C) Fibrinogen
- D) Enzymes
- Answer: C) Fibrinogen
-
If the total plasma protein concentration is 100%, what percentage is represented by globulins?
- A) 60%
- B) 36%
- C) 4%
- D) 40%
- Answer: B) 36%
•60% albumin
•36% globulins
•4% fibrinogen
The following are components of plasma, state two examples each:
Nitrogenous by products of metabolism,nutrients,electrolytes,respiratory gases
Nitrogenous by-products of metabolism—lactic acid, urea, creatinine
•Nutrients—glucose, carbohydrates, amino acids
•Electrolytes—Na+, K+, Ca2+, Cl–, HCO3–
•Respiratory gases—O2 and CO2
•Hormones
Which plasma protein is the main contributor of osmotic pressure? Where is it produced?
What is the function of globulins and where are they produced?
Which molecules do they usually bind to?
Choose the odd one out;
Albumin
Alpha globulin
Beta globulin
Gamma globulin
Fibrinogen
Why is gamma globulin different from both alpha and beta globulins?
Where is fibrinogen produced and what is its function?
What is the function of electrolytes in the plasma?
Name two molecules whose hormones are carried by plasma proteins?
Plasma proteins are the most
abundant of the general plasma solutes. True or false
Albumin is the main contributor of osmotic pressure and is produced by liver.
Globulins is also produced in liver and are transport proteins. They bind with lipids and fat soluble vitamins(ADEK)
Especially alpha and beta globulins.
Gamma globulin is different from alpha and beta globulins.
How?
Gamma globulins are not produced by the liver but are antibodies that are released by plasma cells.
Fibrinogen is also produced by liver and forms fibrin thread during blood clots.
Choose the odd one out;
Albumin
Alpha globulin
Beta globulin
Gamma globulin
Fibrinogen
Answer is gamma globulin
Electrolytes in the plasma Maintain plasma osmotic pressure and normal blood ph
Steroid and thyroid hormones are carried by plasma proteins.
Plasma proteins are the most Makes up 80% by weight of plasma volume.
Hormones aren’t produced by liver.
Plasma proteins aren’t taken up to be used as fuel for metabolic nutrients by the cells the way other plasma solutes such as carbs,amino acids,are taken up to be used as fuel.
Yes, you’re right that albumin also plays a role in transporting substances, but it primarily binds to water-insoluble molecules like fatty acids, hormones, bilirubin, and drugs, rather than specifically fat-soluble vitamins.
- Albumin: It mainly transports free fatty acids, hormones, and drugs in the bloodstream, and it helps maintain osmotic pressure.
- Globulins: While albumin is more of a general transporter, globulins (alpha and beta) are involved in transporting specific molecules like lipids and fat-soluble vitamins (A, D, E, K). These globulins have specialized binding roles that help transport these substances more efficiently.
So, both albumin and globulins contribute to transporting fat-soluble substances, but globulins have more specialized roles in carrying specific vitamins and lipids.
Serum = plasma -fibrinogen
Which of the formed elements in blood are complete cells?
Which don’t have nuclei or organelles?
What are platelets
Where do blood cells originate from?
Only WBCs are complete cells
•RBCs have no nuclei or organelles
•Platelets are cell fragments
•Most formed elements survive in the bloodstream for only a few days
•Most blood cells originate in bone marrow and do not divide
most blood cells originate in the bone marrow through a process called hematopoiesis, but once they are fully matured and released into the bloodstream, they do not divide.
blood cells originate in the bone marrow, once they enter circulation, they do not divide, with the exception of lymphocytes that can proliferate during immune responses.
Buffy coat in plasma is found between blood plasma and formed elements(RBS or erythrocytes,WBCS or leukocytes ,platelets or thrombocytes )
True or false?
How will you identify the formed elements in blood under microscope?
Formed elements:
RBCS are anucleated(don’t have nuclei) and are more numerous.
Central pallor which is found in the the RBCS shows the type of anemia an individual has during microscopy.
Monocytes has a kidney or B shape.
Lymphocytes don’t have kidney or B shape
Neutrophils have numerous lobes of nuclei. Hence, they are referred to as polymorphonuclear
Name and identify the types of formed elements:
The absence of What structure in erythrocytes help them to easily change shape?
How do RBCS contribute to blood viscosity as a major contributor?
Erythrocytes can easy change shape or meander their way through blood vessels due to the fact that they don’t have a nucleus and they don’t have the typical cytoskeleton that cells usually have.
They contribute to blood viscosity(whether blood will appear thick or thin). So blood viscosity depends on the amount of RBCS you have in your blood
What happens in polycythemia Vera concerning reduced oxygen and what medications are given for it?
Polycythemia Vera (excess production of red blood cells than normal)- symptom is blood is highly viscous. So blood movement becomes reduced due to how thick the blood has become. Hence less oxygen gets to target organs. Blood thinners are given to thin the blood so it can be less thick and move more freely.
State five characteristics of RBCS
Biconcave discs, anucleate, essentially no organelles
•Filled with hemoglobin (Hb) for gas transport
•Contain the plasma membrane protein spectrin and other proteins this Provides flexibility to change shape as necessary
•Are the major factor contributing to blood viscosity
How does the structural characteristics of RBCS contribute to blood transport
Structural characteristics contribute to gas transport
•Biconcave shape—huge surface area relative to volume
•>97% hemoglobin (not counting water)
•No mitochondria; ATP production is anaerobic; no O2 is used in generation of ATP
Since there is no Mitochondria in RBCS then it produces ATP without oxygen(anaerobically).
RBCS has a huge surface area to carry more hemoglobin.
Oxyhaemoglobin- when haemoglobin binds to oxygen.
Hemoglobin binds irreversibly to oxygen true or false?
What is the structure of hemoglobin?
How many oxygen molecules can the iron atom in each gene bind to?
How many oxygen molecules can each haemoglobin carry?
False
RBCs are dedicated to respiratory gas transport
•Hemoglobin binds reversibly with oxygen
Hemoglobin structure
•Protein globin: two alpha and two beta chains
•Heme pigment bonded to each globin chain
•Iron atom in each heme can bind to one O2 molecule
•Each Hb molecule can transport four O2
Hemoglobin binds irreversibly to oxygen true or false?
What is the structure of hemoglobin?
How many oxygen molecules can the iron atom in each gene bind to?
How many oxygen molecules can each haemoglobin carry?
False
RBCs are dedicated to respiratory gas transport
•Hemoglobin binds reversibly with oxygen
Hemoglobin structure
•Protein globin: two alpha and two beta chains
•Heme pigment bonded to each globin chain
•Iron atom in each heme can bind to one O2 molecule
•Each Hb molecule can transport four O2
Oxygen loading into the lungs produces what type of haemoglobin? What is the color of this type of blood containing this type of haemoglobin?
CO2 loading into the tissues produces what type of haemoglobin?
Oxygen unloading into the tissues produces what type of haemoglobin? What is the color of this type of blood containing this type of haemoglobin?
O2 loading in the lungs
•Produces oxyhemoglobin (ruby red). In the lungs, oxygen binds to hemoglobin molecules in red blood cells, forming oxyhemoglobin.
•O2 unloading in the tissues
•Produces deoxyhemoglobin or reduced hemoglobin (dark red). As blood circulates to body tissues, oxyhemoglobin releases oxygen to cells where it is needed. This process converts oxyhemoglobin back to deoxyhemoglobin or reduced hemoglobin, which appears darker in color.
•CO2 loading in the tissues
•Produces carbaminohemoglobin (carries 20% of CO2 in the blood). In the tissues, carbon dioxide produced by cellular metabolism diffuses into red blood cells. Some of this carbon dioxide binds to hemoglobin, forming carbaminohemoglobin. This compound carries about 20% of carbon dioxide in the blood.
What is haematopoiesis
Name four areas it can occur
In the embryonic yolk sac, exaplin how haematopoiesis occurs
Hematopoiesis (hemopoiesis): blood cell formation
•Occurs in red bone marrow of axial skeleton, girdles and proximal epiphyses of humerus and femur
Embryonic yolk sac: transient site of haemopoiesis → embryonic red cells. Starts around 3rd week of embroyonic develpment
Which cells give rise to formed elements?
State two factors that push the above tote of cell toward the soecifc pathway of blood cell development
What is the difference between haematopoiesis and erytrhopoiesis
Hemocytoblasts (hematopoietic stem cells)
•Give rise to all formed elements
•Hormones and growth factors push the cell toward a specific pathway of blood cell development
•New blood cells enter blood sinusoids
Haematopoiesis is the formation of new blood cells while erythropoiesis is the formation of red blood cells specifically
Blasts- cells that form
Hemocytoblasts- so blood cells that are now forming.
Stem cells give rise to other cells.
The whole process occurs in red bone marrow
Haemeopoiesis is the formation of all cells or components in blood
Erythropoiesis is the formation of all red blood cells
State the types of stem cells?
What type of stem cells are hemacytoblasts and why?
Types of stem cells:
Totipotent
Pluripotent
Multipotent
Hemocytoblasts are pluripotent and multipotent.
Why?
Sure, here’s a simplified explanation of the differences between totipotent, pluripotent, and multipotent stem cells, with examples:
- Potential: Can become any type of cell in the body and extra-embryonic tissues (like the placenta).
- Example: The fertilized egg (zygote).
- Potential: Can become almost any type of cell in the body, but not extra-embryonic tissues.
-
Examples:
- Embryonic stem cells (from early embryos).
- Induced pluripotent stem cells (regular cells reprogrammed to be like embryonic stem cells).
- Potential: Can become multiple types of cells, but only within a related group.
-
Examples:
- Hematopoietic stem cells (can become different types of blood cells).
- Mesenchymal stem cells (can become bone, cartilage, and fat cells).
- Totipotent: Any cell type + extra-embryonic tissues.
- Pluripotent: Any cell type, but no extra-embryonic tissues.
- Multipotent: Limited to related cell types within a specific tissue or organ.
Explain the process of erythropoiesis and state three key factors important in this process
Hemocytoblasts—myeloid stem cell(Myeloids stem cells or progenitor cells give rise to RBCS,granulocytes,monocytes(macrophages and dendritic cells. Dendritic cells capture and present antigens to activate T cells in the immune response),platelets ) —-proerythroblast—early erythroblast—late erythroblast—normoblast or orthochromatic erythroblast (nucleated RBC with organelles such as mitochondria)—retuculocyte(young erythrocyte)—mature erythrocyte Erythropoiesis is the process of producing red blood cells (erythrocytes).
Here’s a summary of the steps involved:
-
Stem Cell Stage:
- Starts with hematopoietic stem cells (HSCs) in the bone marrow.
-
Progenitor Cell Stage:
- HSCs differentiate into common myeloid progenitor (CMP) cells.
- CMP cells further differentiate into erythroid progenitor cells.
-
Precursor Cell Stage:
- Erythroid progenitor cells develop into proerythroblasts.
- Proerythroblasts undergo several stages, transforming into basophilic erythroblasts, polychromatic erythroblasts, and orthochromatic erythroblasts.
-
Immature Red Blood Cell Stage:
- Orthochromatic erythroblasts expel their nucleus, becoming reticulocytes.
- Reticulocytes enter the bloodstream and mature into erythrocytes.
-
Mature Red Blood Cell Stage:
- Reticulocytes lose their remaining organelles, becoming fully mature erythrocytes (red blood cells).
- Erythropoietin (EPO): A hormone produced by the kidneys that stimulates erythropoiesis.
- Iron: Essential for hemoglobin synthesis.
- Vitamins: Vitamin B12 and folic acid are crucial for DNA synthesis and cell division.
Erythropoiesis is the production of red blood cells starting from hematopoietic stem cells in the bone marrow, progressing through several stages of differentiation, and culminating in the release of mature erythrocytes into the bloodstream.
During third trimester in babies, all bones takes over in haematopoiesis.
State the Dominant sites of haemopoiesis at different stages of development;
1. Fetus 2.infants 3.adults
During third trimester in babies, all bones takes over in haematopoiesis.
Fetus
0-2 months (yolk sac)
2-7 months (liver, spleen)
5-9 months (bone marrow)
Infants-
After birth in the tenth month, primary part is the tibia then as child ages, primary sites are vertebral and plexus,sternum,ribs and femur
Bone marrow (practically all bones); dwindling post-parturition contribution from liver/spleen that ceases in the first few months of life
Adults
Vertebrae, ribs, sternum, skull, sacrum and pelvis, proximal ends of femur
After birth, the bone marrow is the exclusive site for haemopoiesis.
What is the exception to this?
Exception: T lymphocytes maturation occur in the thymus in adults.
Explain Medullary (Bone marrow) and extramedullary haemopoiesis and where the haematopoiesis occurs in both sides
- Definition: Hemopoiesis (the formation of blood cells) that occurs in the bone marrow.
- Location: Primarily in the bone marrow of the pelvis, ribs, vertebrae, and sternum in adults.
- Process: Includes the production of red blood cells (erythropoiesis), white blood cells (leukopoiesis), and platelets (thrombopoiesis).
- Normal Function: Medullary hemopoiesis is the standard process for producing blood cells in healthy individuals.
- Definition: Hemopoiesis occurring outside the bone marrow.
- Location: Usually in organs like the liver, spleen, and lymph nodes.
-
Triggers: Often occurs when the bone marrow cannot meet the body’s blood cell production needs due to:
- Bone marrow diseases (e.g., myelofibrosis, leukemia).
- Severe chronic anemias (e.g., thalassemia).
- Increased demand for blood cells (e.g., during fetal development or in certain pathological conditions).
- Significance: Acts as a compensatory mechanism to maintain adequate blood cell levels when bone marrow function is impaired or insufficient.
-
Medullary Hemopoiesis:
- Normal, primary site of blood cell production.
- Located in the bone marrow.
- Occurs throughout life.
-
Extramedullary Hemopoiesis:
- Secondary, compensatory mechanism.
- Located outside the bone marrow (e.g., liver, spleen).
- Activated under specific conditions or diseases.
Medullary hemopoiesis is the regular production of blood cells in the bone marrow, essential for maintaining healthy blood cell levels. Extramedullary hemopoiesis occurs outside the bone marrow and typically acts as a backup system when the bone marrow cannot produce enough blood cells due to disease or increased physiological demand.
Sure, let’s incorporate the specified terms into the explanation of medullary and extramedullary hematopoiesis:
- Definition: Hematopoiesis (the formation of blood cells) that occurs in the bone marrow.
- Location: Primarily in the bone marrow of the pelvis, ribs, vertebrae, and sternum in adults.
- Process: Includes the production of red blood cells (erythropoiesis), white blood cells (leukopoiesis), and platelets (thrombopoiesis).
- Normal Function: This is the standard process for producing blood cells in healthy individuals.
- Term: Often referred to as bone marrow medullary hematopoiesis.
- Definition: Hematopoiesis occurring outside the bone marrow.
- Location: Usually in organs like the liver, spleen, and lymph nodes.
-
Types:
- Fetal Extramedullary Hematopoiesis: During fetal development, blood cell production occurs in the liver and spleen. This is a normal part of fetal development as the bone marrow is not yet fully functional.
-
Post-Natal Extramedullary Hematopoiesis: After birth, extramedullary hematopoiesis typically occurs as a compensatory mechanism when the bone marrow cannot meet the body’s blood cell production needs. This can be due to:
- Bone marrow diseases (e.g., myelofibrosis, leukemia).
- Severe chronic anemias (e.g., thalassemia).
- Increased demand for blood cells.
-
Medullary Hematopoiesis:
- Normal Function: Regular production of blood cells in the bone marrow.
- Location: Bone marrow.
- Lifespan: Occurs throughout life under normal conditions.
-
Extramedullary Hematopoiesis:
- Fetal Stage: Normal and essential during fetal development in organs like the liver and spleen.
- Post-Natal Stage: Acts as a secondary mechanism when bone marrow function is impaired or insufficient, occurring in organs like the liver, spleen, and lymph nodes.
-
Organ Enlargement and Dysfunction:
- Hepatomegaly: Liver enlargement and potential dysfunction.
- Splenomegaly: Spleen enlargement, leading to hypersplenism and cytopenias.
- Lymphadenopathy: Enlarged lymph nodes.
-
Compression Effects:
- Abdominal Discomfort: Due to enlarged organs.
- Neurological Symptoms: Rarely, spinal cord compression due to hematopoietic tissue in paraspinal areas.
-
Hematological Consequences:
- Anemia: Inadequate red cell production despite increased hematopoiesis.
- Thrombocytopenia and Leukopenia: Due to hypersplenism.
-
Other Clinical Manifestations:
- Pulmonary Issues: Rarely, respiratory symptoms from pulmonary EMH.
- Bone Pain: Related to primary bone marrow disease.
-
Diagnostic and Treatment Challenges:
- Difficulty in Diagnosis: EMH can mimic other conditions.
- Treatment Complications: Managing the underlying disease and considering interventions like splenectomy.
Bone marrow medullary hematopoiesis is the standard, ongoing production of blood cells in the bone marrow. Fetal extramedullary hematopoiesis is a normal process in fetal development, occurring in the liver and spleen. Post-natal extramedullary hematopoiesis occurs outside the bone marrow in response to disease or increased blood cell demand, leading to various clinical consequences and diagnostic challenges.
What is emigration and homing in haematopoiesis
- Definition: Homing refers to the process by which hematopoietic stem cells (HSCs) and progenitor cells migrate to and lodge in the bone marrow or other specific tissues where they can proliferate and differentiate.
-
Process:
- Circulation: HSCs circulate in the bloodstream after being released from the bone marrow.
- Chemotaxis: Specific signals, such as chemokines (e.g., SDF-1/CXCL12), guide HSCs to their target sites. HSCs originate in the bone marrow, where they reside and proliferate. When needed, they can exit the bone marrow and enter the bloodstream through a process called mobilization.
- Migration and Function: Once in the bloodstream, HSCs can migrate to other parts of the body, such as the thymus gland or peripheral lymphoid tissues, where they differentiate and mature into various types of blood cells, including T cells (in the thymus) or B cells (in lymphoid tissues).
- Return to Bone Marrow: After completing their tasks in peripheral tissues, some HSCs migrate back to the bone marrow where they divide into other cells which leads to formation of RBCS,wbcs and platelets
- Adhesion: HSCs adhere to the bone marrow endothelium via adhesion molecules (e.g., integrins).
- Transmigration: HSCs move across the blood vessel wall into the bone marrow.
- Lodging: HSCs lodge within the bone marrow niches, where they receive signals to proliferate and differentiate into various blood cells.
- Importance: Ensures that HSCs are properly localized in the bone marrow to maintain steady-state hematopoiesis and respond to hematopoietic demands.
- Definition: Emigration refers to the process by which hematopoietic stem cells and other mature blood cells exit the bone marrow or their primary sites and enter the circulation to reach peripheral tissues.
-
Process:
- Mobilization: HSCs and progenitor cells are mobilized from the bone marrow into the bloodstream. This can be induced by certain cytokines (e.g., G-CSF) or other factors.
- Circulation: These cells travel through the bloodstream to reach other tissues.
- Extravasation: Cells exit the bloodstream and enter peripheral tissues through the endothelium.
- Targeting: Mature blood cells reach their target tissues to perform their specific functions, such as immune response, oxygen transport, or clotting.
- Importance: Allows for the replenishment of blood cells in peripheral tissues, supports immune surveillance, and facilitates tissue repair and response to injury or infection.
-
Homing:
- Direction: Movement towards the bone marrow or specific niches.
- Purpose: Localization of HSCs for proliferation and differentiation.
- Key Factors: Chemokines (e.g., SDF-1/CXCL12), adhesion molecules (e.g., integrins).
-
Emigration:
- Direction: Movement away from the bone marrow into the bloodstream and then to peripheral tissues.
- Purpose: Distribution of mature blood cells to perform their functions in the body.
- Key Factors: Cytokines (e.g., G-CSF), mobilization signals.
-
Homing Example:
- Bone Marrow Transplantation: HSCs are infused into a patient and must home to the bone marrow to re-establish hematopoiesis.
-
Emigration Example:
- Immune Response: Mature lymphocytes migrate from the bone marrow or lymphoid organs into the bloodstream and then to sites of infection or inflammation.
Understanding these processes is crucial for effective therapies in regenerative medicine, hematopoietic stem cell transplantation, and treatments for blood disorders.