BackComprehensive Study Notes: Blood – Structure, Function, and Clinical Aspects
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Blood
Overview of Blood
Blood is the only fluid tissue in the human body and is classified as a connective tissue. It plays a vital role in transporting substances, regulating physiological parameters, and protecting the body against disease.
Components of Blood:
Living cells: Formed elements (erythrocytes, leukocytes, platelets)
Non-living matrix: Plasma
Blood Centrifugation:
Erythrocytes (red blood cells) sink to the bottom (about 45% of blood, known as the hematocrit)
Buffy coat (less than 1% of blood) contains leukocytes (white blood cells) and platelets
Plasma rises to the top (about 55% of blood)
Physical Characteristics of Blood
Blood has distinct physical properties that are important for its function and clinical assessment.
Color Range:
Oxygen-rich blood is scarlet red
Oxygen-poor blood is dull red
pH: Must remain between 7.35–7.45
Temperature: Slightly higher than body temperature (about 100.4°F)
Volume: In a healthy adult, about 5–6 liters (8% of body weight)
Blood Plasma
Composition and Function
Plasma is the non-living, straw-colored fluid matrix of blood, making up about 55% of its volume. It serves as a transport medium for nutrients, hormones, and waste products.
Water: Approximately 90% of plasma
Dissolved Substances:
Nutrients
Salts (electrolytes)
Respiratory gases
Hormones
Plasma proteins
Waste products
Plasma Proteins:
Albumin: Regulates osmotic pressure
Clotting proteins: Help stem blood loss when a vessel is injured
Antibodies: Protect the body from pathogens
Blood pH Imbalances
Acidosis: Blood becomes too acidic
Alkalosis: Blood becomes too basic
Both conditions are regulated by the respiratory system and kidneys to restore normal pH
Formed Elements of Blood
Erythrocytes (Red Blood Cells, RBCs)
Erythrocytes are specialized for oxygen transport and have unique structural features to optimize this function.
Main Function: Carry oxygen
Structure:
Biconcave disks
Essentially bags of hemoglobin
Anucleate (no nucleus)
Contain very few organelles
Hemoglobin:
Iron-containing protein
Binds strongly, but reversibly, to oxygen
Each hemoglobin molecule has four oxygen binding sites
Each erythrocyte contains about 250 million hemoglobin molecules
Homeostatic Imbalance of RBCs
Anemia: Decrease in the oxygen-carrying ability of blood
Sickle Cell Anemia (SCA): Results from abnormally shaped hemoglobin
Polycythemia: Excessive or abnormal increase in the number of erythrocytes
Leukocytes (White Blood Cells, WBCs)
Leukocytes are crucial for the body's defense against disease. They are complete cells with nuclei and organelles and can move in and out of blood vessels (diapedesis).
Functions:
Respond to chemicals released by damaged tissues
Move by amoeboid motion
Normal Count: 4,000 to 11,000 WBCs per cubic millimeter of blood
Abnormal Numbers:
Leukocytosis: WBC count above 11,000/mm3 (usually indicates infection)
Leukopenia: Abnormally low WBC level (commonly caused by drugs such as corticosteroids and anticancer agents)
Leukemia: Bone marrow becomes cancerous, producing excess WBCs
Types of Leukocytes
Granulocytes: Granules in cytoplasm can be stained; possess lobed nuclei
Neutrophils: Multilobed nucleus, fine granules, act as phagocytes at infection sites
Eosinophils: Large brick-red cytoplasmic granules, respond to allergies and parasitic worms
Basophils: Histamine-containing granules, initiate inflammation
Agranulocytes: Lack visible cytoplasmic granules; nuclei are spherical, oval, or kidney-shaped
Lymphocytes: Nucleus fills most of the cell, important in immune response
Monocytes: Largest WBCs, function as macrophages, important in fighting chronic infection
Mnemonic for WBC abundance: Never Let Monkeys Eat Bananas (Neutrophils, Lymphocytes, Monocytes, Eosinophils, Basophils)
Platelets
Platelets are cell fragments derived from ruptured multinucleate cells and are essential for blood clotting.
Normal Count: 300,000/mm3
Hematopoiesis
Blood Cell Formation
Hematopoiesis is the process of blood cell formation, occurring primarily in red bone marrow.
All blood cells are derived from a common stem cell (hemocytoblast)
Lymphoid stem cell produces lymphocytes
Myeloid stem cell produces all other formed elements
Formation of Erythrocytes
RBCs are unable to divide, grow, or synthesize proteins
Wear out in 100 to 120 days
Eliminated by phagocytes in the spleen or liver
Replaced by division of hemocytoblasts in red bone marrow
Control of Production:
Rate controlled by hormone erythropoietin
Kidneys produce most erythropoietin in response to reduced oxygen levels
Homeostasis maintained by negative feedback from blood oxygen levels
Formation of White Blood Cells and Platelets
Controlled by hormones
Colony stimulating factors (CSFs) and interleukins prompt bone marrow to generate leukocytes
Thrombopoietin stimulates production of platelets
Hemostasis
Mechanism of Blood Clotting
Hemostasis is the process of stopping bleeding resulting from a break in a blood vessel. It involves three phases:
Vascular Spasms: Vasoconstriction causes blood vessel to spasm, narrowing the vessel and decreasing blood loss
Platelet Plug Formation:
Platelets become "sticky" and cling to fibers
Anchored platelets release chemicals to attract more platelets
Platelets pile up to form a platelet plug
Coagulation (Blood Clotting):
Injured tissues release tissue factor (TF)
PF3 (a phospholipid) interacts with TF, blood protein clotting factors, and calcium ions to trigger a clotting cascade
Prothrombin activator converts prothrombin to thrombin (an enzyme)
Thrombin joins fibrinogen proteins into hair-like molecules of insoluble fibrin
Fibrin forms a meshwork (basis for a clot)
Blood usually clots within 3 to 6 minutes.
Undesirable Clotting
Thrombus: A clot in an unbroken blood vessel; can be deadly in areas like the heart
Embolus: A thrombus that breaks away and floats freely in the bloodstream; can clog vessels in critical areas such as the brain
Bleeding Disorders
Thrombocytopenia: Platelet deficiency; even normal movements can cause bleeding from small blood vessels
Hemophilia: Hereditary bleeding disorder; normal clotting factors are missing
Blood Groups and Transfusions
Transfusions
Transfusions are the only way to replace blood quickly. Transfused blood must be of the same blood group.
Loss of over 30% causes shock, which can be fatal
Human Blood Groups
Blood contains genetically determined proteins called antigens, which may be attacked by the immune system if recognized as foreign.
Antibodies: "Recognizers" that cause blood with certain proteins to clump (agglutination)
Over 30 common red blood cell antigens; most vigorous transfusion reactions are caused by ABO and Rh blood group antigens
ABO Blood Groups
Based on the presence or absence of two antigens: A and B.
Blood Type | Antigen(s) Present | Antibody Produced | Can Receive From |
|---|---|---|---|
A | A | Anti-B | A, O |
B | B | Anti-A | B, O |
AB | A and B | None | A, B, AB, O (Universal recipient) |
O | None | Anti-A and Anti-B | O (Universal donor) |
Blood Typing
Blood samples are mixed with anti-A and anti-B serum
Coagulation or no coagulation leads to determining blood type
Typing for ABO and Rh factors is done in the same manner
Rh Blood Groups
Named for the presence or absence of one of eight Rh antigens (agglutinogen D) originally defined in Rhesus monkeys.
Most Americans are Rh+ (Rh positive)
Problems can occur in mixing Rh+ blood into a body with Rh– (Rh negative) blood
Rh Dangers During Pregnancy
Danger occurs only when the mother is Rh– and the father is Rh+, and the child inherits the Rh factor
RhoGAM shot can prevent buildup of anti-Rh antibodies in mother’s blood
Mismatch of an Rh– mother carrying an Rh+ baby can cause problems for the unborn child
First pregnancy usually proceeds without problems
Immune system is sensitized after the first pregnancy
In second pregnancy, mother’s immune system produces antibodies to attack the Rh+ blood (hemolytic disease of the newborn)
Developmental Aspects of Blood
Sites of Blood Cell Formation
Fetal liver and spleen are early sites of blood cell formation
Bone marrow takes over hematopoiesis by the seventh month
Fetal Hemoglobin
Fetal hemoglobin differs from hemoglobin produced after birth
Physiologic jaundice results in infants whose liver cannot rid the body of hemoglobin breakdown products fast enough