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

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Blood: Characteristics and Functions

Physical Properties of Blood

Blood is a specialized connective tissue with unique physical and functional characteristics essential for homeostasis.

  • pH: Slightly alkaline, typically 7.35–7.45.

  • Temperature: About 100.4°F (38°C), slightly higher than body temperature.

  • Viscosity: Blood is more viscous than water due to cellular and protein content.

  • Color: Varies from bright red (oxygen-rich) to dark red (oxygen-poor).

  • Volume: 5–6 L in males; 4–5 L in females.

  • Functions:

    • Transport: Oxygen, carbon dioxide, nutrients, wastes, hormones.

    • Regulation: pH, temperature, fluid balance.

    • Protection: Immune response, clotting.

Major Components of Whole Blood

Blood consists of plasma and formed elements, each with distinct roles.

  • Plasma: The liquid matrix, comprising 55% of blood volume; contains water, proteins (albumin, globulins, fibrinogen), electrolytes, nutrients, and wastes.

  • Formed Elements:

    • Erythrocytes (RBCs): Transport gases.

    • Leukocytes (WBCs): Immune defense.

    • Platelets: Clotting.

Blood sample centrifugation showing plasma, buffy coat, and erythrocytes Blood cells: leukocytes, erythrocytes, platelets

Hematopoiesis and Blood Cell Formation

Hematopoiesis: The Formation of Blood Cells

Blood cells are produced in the red bone marrow from pluripotent hematopoietic stem cells (hemocytoblasts).

  • Myeloid Stem Cells: Give rise to RBCs, platelets, monocytes, neutrophils, eosinophils, basophils.

  • Lymphoid Stem Cells: Give rise to B and T lymphocytes.

  • Regulatory Factors:

    • Erythropoietin (EPO): Produced by kidneys; stimulates RBC production.

    • Thrombopoietin: Produced by liver; stimulates platelet production.

    • Colony Stimulating Factors & Interleukins: Regulate WBC formation.

Hematocrit

The hematocrit is the percentage of blood volume occupied by RBCs. Normal values: Males ~47%, Females ~42%.

Blood Cell Types

Blood contains several cell types, each with specialized functions.

  • RBCs: Biconcave, anucleate, filled with hemoglobin.

  • WBCs: Spherical, nucleated; include granulocytes and agranulocytes.

  • Platelets: Cytoplasmic fragments essential for clotting.

Microscopic view of blood cells: erythrocytes, platelets, leukocytes

Erythrocytes (Red Blood Cells)

Structure and Function

Erythrocytes are specialized for gas transport due to their shape and hemoglobin content.

  • Shape: Biconcave disc increases surface area for gas exchange.

  • Anucleate: Mature RBCs lack a nucleus, maximizing space for hemoglobin.

  • Hemoglobin: Protein responsible for oxygen and carbon dioxide transport.

Erythrocyte shape: side and top view Hemoglobin structure and heme group

Fate and Destruction of RBCs

RBCs have a lifespan of about 120 days. Old or damaged RBCs are removed by macrophages, primarily in the spleen and liver.

  • Iron: Stored as ferritin and hemosiderin; transported by transferrin.

  • Bilirubin: Waste product from heme breakdown; excreted in bile.

  • Jaundice: Accumulation of bilirubin causes yellowing of skin and eyes.

Fate and destruction of erythrocytes

Regulation of Erythropoiesis

Erythropoietin Mechanism

Erythropoiesis is regulated by erythropoietin (EPO), primarily in response to hypoxia (low oxygen levels).

  • Stimulus: Hypoxia due to decreased RBC count or O2 availability.

  • Response: Kidneys release EPO, stimulating red bone marrow to increase RBC production.

  • Homeostasis: Restored when blood O2 levels normalize.

Erythropoietin mechanism for erythropoiesis

Clinical Aspects of Blood

Complete Blood Count (CBC)

CBC is a common diagnostic test measuring RBCs, WBCs, platelets, hemoglobin, and hematocrit. Differential counts identify specific WBC types.

Differential WBC count and formed elements

Anemia

Anemia is a condition of reduced oxygen-carrying capacity of blood. Types include:

  • Hemorrhagic: Blood loss.

  • Pernicious: Vitamin B12 deficiency.

  • Renal: EPO deficiency.

  • Aplastic: Bone marrow failure.

  • Hemolytic: RBC destruction (e.g., sickle cell, thalassemia).

Leukocytes (White Blood Cells)

Types and Functions

Leukocytes are divided into granulocytes and agranulocytes, each with distinct roles in immunity.

  • Granulocytes:

    • Neutrophils: Phagocytize bacteria; most abundant.

    • Eosinophils: Kill parasitic worms; involved in allergy/asthma.

    • Basophils: Release histamine; contain heparin.

  • Agranulocytes:

    • Lymphocytes: Mount immune response; B and T cells.

    • Monocytes: Phagocytosis; develop into macrophages.

Blood cell types: erythrocytes, platelets, leukocytes Differential WBC count and formed elements

Platelets and Hemostasis

Formation of Platelets

Platelets are formed from megakaryocytes in the bone marrow and are essential for blood clotting.

Formation of platelets from stem cells

Hemostasis and Coagulation

Hemostasis is the process of stopping bleeding, involving three steps:

  1. Vascular Spasm: Vasoconstriction reduces blood flow.

  2. Platelet Plug Formation: Platelets adhere to exposed collagen and release chemicals to attract more platelets.

  3. Coagulation: Blood changes from liquid to gel, forming a fibrin mesh that stabilizes the clot.

Hemostasis: vascular spasm, platelet plug, coagulation

Coagulation Pathways

Coagulation involves intrinsic and extrinsic pathways leading to the formation of prothrombin activator, which converts prothrombin to thrombin, and then fibrinogen to fibrin.

  • Intrinsic Pathway: Initiated by damage inside the vessel.

  • Extrinsic Pathway: Initiated by external trauma.

  • Fibrin: Forms the meshwork of the clot.

Intrinsic and extrinsic pathways of blood clotting Hemostasis: vascular spasm, platelet plug, coagulation Microscopic view of blood clot (fibrin mesh)

Fibrinolysis

Fibrinolysis is the process of dissolving the clot after tissue repair, involving plasminogen activation to plasmin, which digests fibrin.

Blood Disorders

Thrombus and Embolus

A thrombus is a stationary blood clot; an embolus is a clot that travels through the bloodstream. Both can cause serious complications.

Bleeding Disorders

  • Thrombocytopenia: Low platelet count.

  • Liver Disease: Impaired production of clotting factors.

  • Hemophilia: Genetic deficiency of clotting factors.

  • DIC (Disseminated Intravascular Coagulation): Widespread clotting and bleeding.

Restoring Blood Volume

  • Volume Replacement: Isotonic solutions (normal saline, Ringer’s solution).

  • RBC Replacement: Packed RBCs or whole blood transfusions.

  • Shock: Results from >30% blood loss.

Blood Groups and Transfusion

ABO and Rh Blood Groups

Blood groups are determined by antigens (agglutinogens) on RBC membranes. The ABO and Rh systems are clinically significant.

  • ABO Groups:

    • Type A: A antigen, anti-B antibody.

    • Type B: B antigen, anti-A antibody.

    • Type AB: A and B antigens, no antibodies (universal recipient).

    • Type O: No antigens, anti-A and anti-B antibodies (universal donor).

  • Rh Group: Rh antigen (D); anti-Rh antibodies form only after sensitization.

ABO blood group antigens and antibodies ABO grouping and anti-Rh antibodies

Hemolytic Disease of the Newborn (Erythroblastosis Fetalis)

Occurs when an Rh-negative mother carries an Rh-positive fetus, leading to antibody formation and fetal RBC destruction in subsequent pregnancies.

Hemolytic disease of the newborn mechanism

Clinical Applications and Review Questions

Blood Transfusion and Testing

  • Transfusion: Type and crossmatch blood to prevent reactions.

  • Tests: CBC, blood typing, antibody screening.

Review Questions

  • James is told he has type A blood. Which ABO antibody/antibodies does he have in his plasma? Which antigens are on his RBCs? Could he donate blood to an AB recipient? Could he receive blood from an AB donor?

  • Sketch a RBC. Label any antigens present if the blood type is B+. Also write the AB(s) present in the plasma.

  • A 17 year-old female is brought to the ER with a fever, headache, and stiff neck. You suspect bacterial meningitis. How would you expect her CBC with differential to be abnormal?

  • Mr. Stars, a 40 year-old teacher from New York, is visiting Colorado to study astronomy. He drives high on a mountain to get a clearer view of the night sky. After a couple of days, he notices he struggles to catch his breath after minimal activity and gets tired quickly. One month later, his symptoms have resolved but he goes to an appointment with his doctor anyway because he is due for an annual physical exam. Would you expect any abnormalities with his CBC? Explain.

  • Hemoglobin vs. Hematocrit

  • A young female presents to the ER with severe vaginal bleeding. She is 3 months pregnant. The doctor is concerned with the amount of blood loss. What type of transfusion is most likely to be given to this patient? What blood tests should be ordered before starting the transfusion?

Key Terms and Concepts

  • Hemoglobin: Oxygen-carrying protein in RBCs.

  • Hematocrit: Percentage of RBCs in blood.

  • Plasma: Liquid component of blood.

  • Platelets: Cell fragments for clotting.

  • Leukocytes: White blood cells for immunity.

  • Antigen: Surface marker on RBCs.

  • Antibody: Protein in plasma targeting foreign antigens.

Important Equations

  • Hematocrit Calculation:

  • Oxygen Carrying Capacity:

Summary Table: ABO Blood Groups

Blood Group

RBC Antigens

Plasma Antibodies

Blood That Can Be Received

Universal Status

A

A

Anti-B

A, O

B

B

Anti-A

B, O

AB

A, B

None

A, B, AB, O

Universal recipient

O

None

Anti-A, Anti-B

O

Universal donor

Summary Table: Formed Elements of Blood

Cell Type

Description

Count (per µL)

Life Span

Function

Erythrocytes

Biconcave, anucleate

4–6 million

100–120 days

Transport O2 and CO2

Neutrophils

Multilobed nucleus

3000–7000

6 hours–few days

Phagocytize bacteria

Eosinophils

Bilobed nucleus, red granules

100–400

~5 days

Kill parasites, allergy/asthma

Basophils

Bilobed nucleus, purple granules

20–50

Few hours–days

Release histamine, heparin

Lymphocytes

Spherical nucleus

1500–3000

Hours–years

Immune response

Monocytes

U/kidney-shaped nucleus

100–700

Months

Phagocytosis, macrophages

Platelets

Discoid fragments

150,000–400,000

5–10 days

Clotting

Additional info: Academic context was added to clarify mechanisms, clinical relevance, and definitions for completeness and exam preparation.

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