Q: What are the functions of blood?
A:
Transport (gases, nutrients, waste, hormones)
Regulation of pH and osmosis
Temperature maintenance
Protection (immune response)
Clot formation
Q: What are the components of blood?
A:
Plasma (55%) – Liquid portion with proteins (albumin, globulins, fibrinogen)
Formed Elements (45%) – RBCs, WBCs, Platelets
Q: What is hematopoiesis, and where does it occur?
A:
Process of blood cell formation
In fetus: Liver, spleen, thymus, lymph nodes, red bone marrow
In adults: Red bone marrow
Q: What are erythrocytes (RBCs)?
A:
Function: Transport oxygen & carbon dioxide
Structure: Biconcave, no nucleus, flexible
Lifespan: ~120 days
Main protein: Hemoglobin
Q: What is hemoglobin and its function?
A:
Red-pigmented protein in RBCs
Carries oxygen (O₂) & carbon dioxide (CO₂)
Oxygen binds to iron (Fe) in the heme group
Q: How are old RBCs broken down?
A:
Macrophages in spleen & liver remove RBCs
Globin → amino acids
Iron → recycled for new hemoglobin
Heme → converted to bilirubin (excreted in bile)
Q: What are leukocytes (WBCs) and their function?
A:
Fight infections & remove dead cells
Larger than RBCs, contain a nucleus
Types: Granulocytes & Agranulocytes
Q: What are the types of granulocytes?
A:
Neutrophils – Most common, phagocytic, first responders
Eosinophils – Attack parasites, reduce inflammation
Basophils – Release histamine (allergic reactions)
Q: What are the types of agranulocytes?
A:
Monocytes – Develop into macrophages (big eaters)
Lymphocytes – Specific immunity (B cells, T cells, NK cells)
Q: What are platelets (thrombocytes)?
A:
Cell fragments from megakaryocytes
Function: Clot formation & prevent blood loss
Lifespan: 5–9 days
Q: What are the three steps of hemostasis (blood clotting)?
A:
Vascular spasm – Constriction of blood vessel
Platelet plug formation – Platelets stick to damaged vessel
Coagulation – Fibrin network forms a clot
Q: What are clotting factors, and where are they made?
A:
Proteins in plasma that activate clot formation
Made in the liver
Require Vitamin K
Q: What are blood types based on?
A:
Presence of A & B antigens on RBCs
Type A: A antigen, anti-B antibodies
Type B: B antigen, anti-A antibodies
Type AB: A & B antigens, no antibodies (universal recipient)
Type O: No antigens, both anti-A & anti-B antibodies (universal donor)
Q: What is the Rh factor, and why is it important?
A:
Rh-positive (Rh⁺): Has Rh antigen
Rh-negative (Rh⁻): No Rh antigen, can develop anti-Rh antibodies
Important in pregnancy: Rh⁻ mother with Rh⁺ baby → Hemolytic Disease of Newborn
Q: What is Hemolytic Disease of the Newborn (HDN)?
A:
Rh⁻ mother’s immune system attacks Rh⁺ baby’s RBCs
Prevented by RhoGAM injection
Q: What is sickle-cell anemia?
A:
Genetic disorder causing abnormally shaped RBCs
Autosomal recessive inheritance
Provides natural resistance to malaria
Q: What are common blood disorders?
A:
Leukopenia – Low WBC count (caused by chemotherapy, radiation, viruses)
Leukocytosis – High WBC count (caused by infections, leukemia)
Hemophilia – Genetic disorder, blood doesn’t clot properly
Q: What are diagnostic blood tests?
A:
Complete Blood Count (CBC) – Measures RBC, WBC, hemoglobin, hematocrit
Hematocrit (Hct) – % of blood volume made of RBCs
Prothrombin Time – Time for blood to clot