Composition of blood and their functions notes

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Composition of Blood and Their Functions

Blood is a specialized connective tissue that circulates through the cardiovascular system. In a healthy adult, total blood volume is approximately 5 liters. Blood consists of two major components: plasma (the liquid portion, ~55%) and formed elements (cells and cell fragments, ~45%).

Overview: Components of Blood

Component% of Blood VolumeKey Elements
Plasma~55%Water, proteins, electrolytes, nutrients, hormones
Formed Elements~45%RBCs, WBCs, Platelets
The percentage of blood occupied by red blood cells is called the hematocrit (normal: ~42-47% in females, ~45-52% in males).

1. PLASMA

Plasma is the straw-colored liquid matrix of blood. It is approximately 90% water, with the remaining 10% consisting of dissolved substances.

Composition of Plasma

SubstanceApproximate ContentFunctions
Water~90%Solvent; transports dissolved substances; regulates temperature
Plasma Proteins6-8 g/dLSee below
ElectrolytesNa+, K+, Ca2+, Cl-, HCO3-Osmotic balance, acid-base regulation, nerve/muscle function
NutrientsGlucose, amino acids, lipids, vitaminsEnergy source, tissue repair
Waste ProductsUrea, creatinine, bilirubinTransported to kidneys/liver for excretion
HormonesInsulin, cortisol, thyroid hormonesEndocrine signaling
Dissolved GasesO2, CO2, N2Respiratory exchange

Plasma Proteins

Plasma proteins are produced mainly by the liver and constitute the major solutes in plasma.
ProteinNormal ValueFunctions
Albumin~4.5 g/dL (largest fraction)Maintains colloid osmotic (oncotic) pressure; transports fatty acids, bilirubin, drugs, hormones
Globulins (alpha, beta)~2.5 g/dLTransport lipids (lipoproteins), metals (transferrin), fat-soluble vitamins; complement proteins
Gamma-globulins (immunoglobulins)Part of globulin fractionAntibodies - immune defense
Fibrinogen~0.3 g/dLPrecursor to fibrin; essential for blood clotting
Clotting FactorsTraceFactor V, VIII, IX, X, etc. - coagulation cascade
Serum = plasma with fibrinogen and clotting factors removed (i.e., what remains after blood clots).

2. FORMED ELEMENTS

A. Erythrocytes (Red Blood Cells - RBCs)

Normal human erythrocytes - SEM micrograph, dimensional diagram, and histology showing rouleau formation
Normal human erythrocytes. (a) Pseudocolored SEM showing the biconcave shape. (b) Diagram with dimensions. (c) Rouleau formation in small vessels. - Junqueira's Basic Histology, 17e
Morphology:
  • Biconcave discs, ~7.5 μm in diameter, 2.6 μm thick at the rim, 0.75 μm thick in the center
  • Anucleate (lack a nucleus) and lack organelles
  • Cytoplasm completely filled with hemoglobin
  • Membrane: ~40% lipid, 10% carbohydrate, 50% protein (includes Band 3 protein, glycophorin A - basis of ABO blood group)
  • Submembranous cytoskeleton: spectrin + actin + ankyrin network maintains shape and flexibility
Normal Count:
  • Women: 3.9-5.5 million/μL
  • Men: 4.1-6.0 million/μL
Life Span: ~120 days; removed by macrophages in the spleen, liver, and bone marrow
Functions:
  1. Oxygen transport - Hemoglobin binds O2 (as oxyhemoglobin) and delivers it to tissues
  2. Carbon dioxide transport - Hemoglobin binds CO2 (as carbaminohemoglobin) and returns it to the lungs
  3. Acid-base buffering - Hemoglobin acts as a buffer by binding/releasing H+ ions
  4. Internal size standard - Uniform dimensions allow estimation of other cell sizes in histology
Energy: Rely on anaerobic glycolysis (no mitochondria)
Clinical Note: Anemia = RBC count below normal range. Polycythemia = increased RBC count (e.g., high-altitude adaptation).

B. Leukocytes (White Blood Cells - WBCs)

Normal count: ~7,000 WBCs/μL (vs. 5 million RBCs/μL)
Leukocytes are the mobile units of the body's immune and defense system. Unlike RBCs, they leave the vasculature to function in tissues - entering via diapedesis (extravasation) through capillary walls.
Genesis:
Genesis of WBCs from myelocyte and lymphocyte lineages
Genesis of white blood cells showing the myelocytic lineage (neutrophils, eosinophils, basophils, monocytes) and lymphocytic lineage (T cells, B cells, plasma cells). - Guyton & Hall Textbook of Medical Physiology
WBCs are divided into Granulocytes and Agranulocytes:

GRANULOCYTES (have prominent cytoplasmic granules; multilobed nuclei)

1. Neutrophils
  • Most abundant WBC: 62% of total WBCs
  • Nucleus: multilobed (3-5 lobes, "polymorphonuclear")
  • Granules: azurophilic (primary - contain MPO, defensins, lysozyme) + specific/secondary (collagenase, lactoferrin)
  • Life span: 4-8 hours in blood, 1-4 days in tissues
  • Functions:
    • Primary defense against bacterial infections
    • Phagocytosis: engulf and destroy bacteria in phagolysosomes
    • Release superoxide radicals (O2-) and H2O2 (oxidative burst) for microbial killing
    • Lactoferrin binds iron, starving bacteria
    • Short-lived; dying neutrophils + bacteria + tissue fluid = pus
    • Release proresolving mediators and chemokines to recruit other immune cells
2. Eosinophils
  • 2.3% of total WBCs (1-4% range)
  • Nucleus: bilobed
  • Granules: large, acidophilic (pink/red); contain Major Basic Protein (MBP), eosinophilic peroxidase
  • Life span: similar to neutrophils; concentrated in gut mucosa and lung tissue
  • Functions:
    • Defense against parasitic infections (helminths)
    • Modulate allergic responses (asthma, hay fever) by releasing chemokines, cytokines, and proresolving lipid mediators
    • Phagocytose antigen-antibody complexes
    • Increased in helminthic infections and allergic diseases (eosinophilia)
3. Basophils
  • Least common: 0.4% of total WBCs
  • Nucleus: bilobed or irregular, obscured by granules
  • Granules: large, intensely basophilic (purple-blue); contain histamine and heparin
  • Functions:
    • Release histamine - triggers vasodilation and increased vascular permeability in allergic reactions
    • Release heparin - local anticoagulant, promotes blood flow at inflammatory sites
    • Role in immediate hypersensitivity (Type I) reactions
    • Analogous to tissue mast cells

AGRANULOCYTES (few or no visible granules; non-lobed nuclei)

4. Monocytes
  • 5.3% of total WBCs; largest WBC (12-20 μm diameter)
  • Nucleus: kidney-shaped, indented, or C-shaped; basophilic cytoplasm with fine azurophilic granules
  • Transit in blood: only 10-20 hours, then migrate to tissues
  • In tissues: differentiate into macrophages (swelling up to 60-80 μm, much more potent)
  • Functions:
    • Phagocytosis of bacteria, cellular debris, and foreign particles (as macrophages)
    • Antigen presentation to lymphocytes
    • Tissue macrophages: long-lived tissue defense (months)
    • Monocyte recruitment is key in both acute and chronic inflammation
5. Lymphocytes
  • 30% of total WBCs; second most abundant
  • Small cells (6-12 μm); large, round, dark nucleus occupying most of the cell
  • Produced in bone marrow; mature in thymus (T cells) or bone marrow/lymphoid tissue (B cells)
  • Circulate continuously: blood → lymph → tissues → lymph → blood
  • Life span: weeks to months depending on activation state
  • Functions:
    • T lymphocytes (T cells): Cell-mediated immunity - destroy virus-infected/tumor cells (cytotoxic T cells); regulate immune responses (helper T cells)
    • B lymphocytes (B cells): Humoral immunity - differentiate into plasma cells that produce antibodies (immunoglobulins)
    • Natural Killer (NK) cells: Innate immunity against tumor and virus-infected cells
6. Plasma Cells (derived from B cells)
  • Found mainly in tissues, rarely in blood
  • Produce large quantities of specific antibodies
  • Identified by "clock-face" chromatin pattern in nucleus

C. Platelets (Thrombocytes)

Morphology:
  • Tiny, non-nucleated cell fragments, only 2-4 μm in diameter
  • Derived by budding from megakaryocytes in bone marrow
  • Contain alpha-granules (fibrinogen, vWF, growth factors) and dense granules (ADP, serotonin, Ca2+)
  • Open canalicular system (OCS) for rapid granule secretion
Normal Count: 150,000-400,000/μL (average ~300,000/μL)
Life Span: ~10 days; ~150 billion platelets produced daily
Functions:
  1. Primary hemostasis - rapidly adhere to damaged vessel wall (collagen exposure) via vWF, aggregate to form a "platelet plug"
  2. Activate coagulation cascade - release ADP, thromboxane A2, and other factors that trigger secondary hemostasis (fibrin clot formation)
  3. Repair microvascular tears - plug minor leaks in capillaries and venules
  4. Wound healing - release growth factors (PDGF, VEGF) promoting tissue repair
Clinical notes:
  • Thrombocytopenia (< 150,000/μL) = increased bleeding risk
  • Thrombocytosis (> 400,000/μL) = increased clotting risk

Summary Table: Formed Elements

CellNormal CountLife SpanKey Function
Erythrocytes (RBCs)4-6 million/μL120 daysO2/CO2 transport, acid-base buffering
Neutrophils62% of WBCs4-8 h (blood); 1-4 days (tissue)Phagocytosis, bacterial defense
Eosinophils2.3% of WBCsSimilar to neutrophilsAnti-parasitic, allergic modulation
Basophils0.4% of WBCsSimilar to neutrophilsAllergic reactions (histamine, heparin)
Monocytes5.3% of WBCs10-20 h (blood); months (tissue as macrophages)Phagocytosis, antigen presentation
Lymphocytes30% of WBCsWeeks to monthsAdaptive immunity (T & B cell responses)
Platelets150,000-400,000/μL10 daysHemostasis, clot formation, vessel repair

Key Terminology

  • Hematocrit: % of blood volume occupied by RBCs (~45%)
  • Hemoglobin: Iron-containing protein in RBCs; each molecule carries 4 O2 molecules
  • Diapedesis: WBC migration through capillary walls into tissues
  • Chemotaxis: Directed WBC movement toward chemical signals at sites of infection/inflammation
  • Phagocytosis: Engulfment and destruction of pathogens/debris by neutrophils and macrophages
  • Serum: Plasma minus clotting factors (what remains after a clot forms)
  • Rouleau: Stacking of RBCs in low-flow conditions, like coins in a roll

Sources: Guyton & Hall Textbook of Medical Physiology; Junqueira's Basic Histology, 17e; Henry's Clinical Diagnosis and Management by Laboratory Methods
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