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Blood functions
Transport of Materials:
Oxygen
Nutrients, hormones
Wastes
Defense
Immune system:
White blood cells
Antibodies
Regulation:
Temperature
Osmotic pressure
pH
Blood composition
Plasma: Liquid medium of the blood
Dissolved substances: proteins, solutes
Formed elements: Cells
Red Blood Cells
White Blood Cells
Platelets
Components of Blood Plasma
Water (91%) + proteins + solutes
Proteins:
Albumins: thicken the blood
Globulins: immunity (antibodies)
Fibrinogen: used for blood clotting
Prothrombin: used for blood clotting
Solutes:
Ions (sodium, potassium), nutrients, waste products, gases, hormones
Serum: Plasma with the clotting factors removed still contains antibodies
Formed Elements of Blood
Formed in the blood marrow; skeletonal system
Erythrocytes (red blood cells)
Transport Oxygen and CO2
Leukocytes (white blood cells)
Cells of your immune system
Thrombocytes (platelets)
Blood clotting
Types of WBC
Neutrophils:
1st responders to tissue injury
Phagocytes
Eosinophils:
Target parasite worms
Clean up inflammatory proteins
Basophils:
Allergy cells - release histamine to initiate inflammation
Lymphocytes:
Specific immunity
B cells secrete antibodies
T cells kill virally-infected cells and cancer cells
Monocytes:
Turn into macrophages
Phagocytosis in the tissues
Erythrocytes (red blood cells)
Tough, flexible plasma membrane deforms easily
Allows RBCs to pass through small diameter capillaries
Biconcave disk shape
Large cellular surface for diffusion of Oxygen
No nucleus or organelles
Provides more space for hemoglobin
~25 trillion RBCs in your body
How do RBCS carry oxygen
RBS contain the protein Hemoglobin (Hb):
Iron containing molecule
35% of total RBC content (250 million/per cell)
binds to and holds oxygen
binds to small amounts of CO2
binds very well to CO
Carbon dioxide transport
23% CO2 is transported by Hemoglobin
7% CO2 is dissolved in plasma
70% is transported as a bicarbonate ion (HCO3)
Enzyme: carbonic anhydrase
RBC production
Develop and mature in the bone marrow
Lifespan = 120 days
Constant need to repair RBCs
Hemoglobin from dead RBCs is recycled
Erythropoietin:
Hormone secreted by kidneys to induce RBC production
Secreted when oxygen levels are too low
Blood clotting
Platelets play essential role in blood coagulation (clotting)
Blood vessel damage causes platelets to become sticky and form a “platelet plug”
Accumulated platelets release additional clotting factors that enter into the clotting mechanism
Platelets ultimately become a part of the clot itself
Basic steps of blood clotting
Release of clotting factors from injured cells and platelets at the injury site (forms a platelet plug)
Series of chemical reactions result in the formation of thrombin
Formation of fibrin threads to trap red blood cells to form a clot
Red blood cells disorders: anemia
Nutritional anemia: dietary deficiency (iron)
Pernicious anemia: vitamin B12 deficiency - slows RBC production
Thalassemia: genetic condition, body does not produce enough hemoglobin
Hemolytic anemia: rupture of too many RBCs (sickle cell anemia)
Symptoms include fatigue, weakness, faintness, skin pallor, and headaches
Sickle cell anemia
2 mutated genes on each chromosome result in abnormal Hemoglobin proteins
Causes oxygen to crystallize under low oxygen conditions
Causes blood stasis, clotting and “crises” that may be fatal
WBC disorders: Infectious mononucleosis
Caused by Epstein-Barr virus in saliva
AKA kissing disease
Highest incidence is within 15-25 years of age
Symptoms include fever, severe fatigue, sore throat, rash, and enlargement of lymph nodes and spleen
Generally self-limited and resolves without complications in about 4-6 weeks
Blood clotting disorders
Hemophilia:
Most serious “bleeding disease” worldwide
X-linked inherited disorder
Comes from the inability to produce Factor VIII (a plasma protein)
Responsible for blood clotting, clots don’t form properly
Internal bleeding is common, bleeding can be life threatening
Characterized by easy bruising, deep muscle hemorrhage, blood in urine, and repeated episdoes of bleeding into joints causing pain and deformity
Called the “Royal Disease” due to inbreeding from royals
Blood typing
Antigen: A molecule that stimulates an immune response
Antibodies: They bind to antigens to neutralize them (toxins) or to clump cells together
RBC’s have protein “antigens” sticking out of their cellular membranes
ABO Blood typing is a classification of blood based on the presence or absence of antigens on the surface of RBC’s
Agglutination: clumping of RBCs when bound by an antibody
Blood type
Blood Type A:
RBC surface antigen: A
Antibodies in blood: Anti B
Blood Type B:
RBC surface antigen: B
Antibodies in blood: Anti A
Blood Type AB: Universal Receiver (takes both A and B blood)
RBC Surface Antigen: AB
Antibodies in blood: None
Blood Type O: Universal Doner (can be given to blood type A, B, AB because no surface antigen; O blood can only be given O blood because they already have both A and B antibodies)
RBC Surface Antigen: None
Antibodies in blood: BOTH ANTI A + ANTI B
Rh blood types
Rh-postive blood: Rh factor antigen is present on RBCs (also found on the Rhesus monkey RBCs)
Rh-negative blood: Rh factor antigen is NOT present on RBCs
No anti-Rh antibodies are present in plasma naturally
Anti-RH antibodies appear in the plasma of Rh-negative persons if Rh-positive RBCs have been introduced into their bodies
Can cause erythroblastosis fetalis in second Rh-incompatible pregnancy
Rh incompatibility
1st pregnancy (Rh- mother carrying Rh+ fetus):
Sensitization: Mother makes anti-Rh antibodies
Usually this pregnancy is fine
2nd pregnancy:
Mother’s antibodies attack fetus’ RBCs
Solution: RhoGAM (artifical antibody to Rh factor)
It clears out fetal RBCs before the mother can make an antibody against them