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Chapter 17: Blood – Structure, Function, and Clinical Aspects

스터디 가이드 - 스마트 노트

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Blood: Composition, Structure, and Function

Plasma Composition and Plasma Proteins

Blood plasma is the liquid matrix of blood, making up about 55% of total blood volume. It serves as a transport medium for nutrients, hormones, and waste products.

  • Major Components: Water (about 90%), plasma proteins, electrolytes, nutrients, gases, and waste products.

  • Major Plasma Proteins:

    • Albumin: Maintains osmotic pressure; produced by the liver.

    • Globulins: Include antibodies (immunoglobulins) and transport proteins; produced by the liver and immune cells.

    • Fibrinogen: Essential for blood clotting; produced by the liver.

Formed Elements of Blood

The formed elements include erythrocytes (RBCs), leukocytes (WBCs), and thrombocytes (platelets).

  • Erythrocytes (Red Blood Cells): Biconcave, anucleate cells specialized for oxygen transport.

  • Leukocytes (White Blood Cells): Five types, each with distinct morphology and function.

  • Thrombocytes (Platelets): Small, anucleate cell fragments involved in clotting.

Morphological Features of Blood Cells

  • Erythrocytes: Biconcave discs, lack nuclei and organelles, uniform appearance.

  • Leukocytes:

    • Granulocytes: Neutrophils (multi-lobed nucleus, pale granules), Eosinophils (bilobed nucleus, red-orange granules), Basophils (bilobed or S-shaped nucleus, dark blue granules).

    • Agranulocytes: Lymphocytes (large, round nucleus, scant cytoplasm), Monocytes (kidney-shaped nucleus, abundant cytoplasm).

  • Platelets: Small, irregularly shaped cell fragments, no nucleus.

Normal Ranges for Blood Cell Counts

  • Erythrocyte Count: Males: 4.7–6.1 million/μL; Females: 4.2–5.4 million/μL

  • Hematocrit: Males: 42–52%; Females: 37–47%

  • Total Leukocyte Count: 4,800–10,800/μL

  • Platelet Count: 150,000–400,000/μL

Leukocyte Types and Classification

The five types of leukocytes, in order of prevalence, and their classification:

Leukocyte

Prevalence (%)

Classification

Neutrophils

50–70

Granulocyte

Lymphocytes

20–40

Agranulocyte

Monocytes

3–8

Agranulocyte

Eosinophils

2–4

Granulocyte

Basophils

0.5–1

Granulocyte

Structural Differences: Platelets vs. Other Formed Elements

  • Platelets: Cell fragments derived from megakaryocytes; lack nuclei; contain granules with clotting factors.

  • Other Formed Elements: RBCs are whole cells without nuclei; WBCs are complete cells with nuclei and organelles.

Hematopoiesis: Location and Overview

  • Location: Occurs primarily in red bone marrow (e.g., flat bones, proximal epiphyses of long bones).

  • Process: All formed elements arise from hematopoietic stem cells (hemocytoblasts).

Erythropoiesis and Regulation

  • Erythropoiesis: The production of erythrocytes from stem cells in the bone marrow.

  • Regulation: Controlled by the hormone erythropoietin (EPO), produced by the kidneys in response to hypoxia (low oxygen levels).

Equation:

Megakaryocytes and Platelet Formation

  • Megakaryocytes: Large bone marrow cells that fragment to release platelets into the bloodstream.

Functions of Blood Cells

  • Red Blood Cells: Transport oxygen (via hemoglobin) and carbon dioxide.

  • Leukocytes: Immune defense (see table below).

  • Platelets: Initiate blood clotting (hemostasis).

Hemoglobin: Structure, Function, and Breakdown

  • Structure: Protein with four polypeptide chains, each containing a heme group with iron.

  • Function: Binds and transports oxygen; also carries some carbon dioxide.

  • Breakdown: In the spleen and liver, hemoglobin is broken down into heme (converted to bilirubin) and globin (broken into amino acids).

Functions of the Five Major Leukocytes

Leukocyte

Main Function

Neutrophils

Phagocytosis of bacteria

Lymphocytes

Adaptive immunity (B and T cells)

Monocytes

Phagocytosis; become macrophages in tissues

Eosinophils

Combat parasitic infections; modulate allergic responses

Basophils

Release histamine; mediate inflammatory responses

Hemostasis vs. Coagulation

  • Hemostasis: The overall process of stopping bleeding, involving vascular spasm, platelet plug formation, and coagulation.

  • Coagulation: The specific process of blood clot formation via a cascade of clotting factors.

Process of Hemostasis

  1. Vascular spasm (vasoconstriction)

  2. Platelet plug formation

  3. Coagulation (formation of fibrin mesh)

Hemostatic Disorders

Disorder

Cause

Thrombus

Clot forms in an unbroken vessel

Embolus

Clot or debris travels in bloodstream and lodges elsewhere

Hemophilia

Genetic deficiency of clotting factors

Disseminated Intravascular Coagulation (DIC)

Widespread clotting and bleeding due to overactivation of clotting cascade

Blood Groups: Surface Antigens and Antibodies

  • Surface Antigens: Glycoproteins on RBC membranes determine blood group (ABO and Rh systems).

  • ABO System: Type A (A antigen), Type B (B antigen), Type AB (both), Type O (neither).

  • Antibodies: Plasma contains antibodies against antigens not present on one's own RBCs.

Blood Type

Antigen(s)

Antibody(ies)

A

A

Anti-B

B

B

Anti-A

AB

A and B

None

O

None

Anti-A and Anti-B

Rh Factor

  • Rh Antigen (D): Presence = Rh positive; absence = Rh negative.

  • Anti-Rh Antibodies: Only develop after exposure to Rh-positive blood (e.g., transfusion or pregnancy).

  • Anti-A and Anti-B Antibodies: Present naturally without prior exposure.

Blood Transfusion Compatibility

  • Compatible Types: Determined by matching antigens and avoiding antibodies that would attack donor RBCs.

  • Transfusion Reaction: Occurs when incompatible blood is transfused, leading to agglutination and hemolysis.

  • Universal Donor: Type O negative (no A, B, or Rh antigens).

  • Universal Recipient: Type AB positive (has all antigens, no anti-A, anti-B, or anti-Rh antibodies).

Anemia: Types and Definitions

  • Anemia: Condition of reduced oxygen-carrying capacity of blood due to low RBC count or hemoglobin.

  • Types:

    • Iron-deficiency anemia: Due to insufficient iron for hemoglobin synthesis.

    • Pernicious anemia: Due to vitamin B12 deficiency.

    • Hemolytic anemia: Due to excessive RBC destruction.

    • Aplastic anemia: Due to bone marrow failure.

    • Sickle cell anemia: Due to abnormal hemoglobin S.

Other Blood Disorders

  • Polycythemia: Excessive RBC production, increasing blood viscosity.

  • Thrombocytopenia: Low platelet count, leading to bleeding risk.

  • Leukemia: Cancer of white blood cells, leading to abnormal proliferation of immature WBCs.

  • Erythroblastosis Fetalis: Hemolytic disease of the newborn due to Rh incompatibility between mother and fetus.

Additional info: Some details (e.g., specific anemia types and their mechanisms) were inferred based on standard Anatomy & Physiology curriculum.

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