Skip to main content
뒤로

Study Guide: The Circulatory System – Blood

스터디 가이드 - 스마트 노트

자료에 맞춘 맞춤형 노트, 핵심 정의, 예시, 맥락을 확장해 제공합니다.

The Circulatory System: Blood

Introduction

The circulatory system is essential for transporting substances throughout the body, maintaining homeostasis, and defending against disease. Blood, as a key component, serves multiple functions and is composed of plasma and formed elements.

Functions of the Circulatory System

The circulatory system consists of the heart, blood vessels, and blood. Its primary functions include:

  • Transport: Delivers oxygen, nutrients, hormones, and removes waste products.

  • Protection: Defends against pathogens and prevents blood loss through clotting.

  • Regulation: Maintains pH, temperature, and fluid balance.

Components and General Properties of Blood

Blood is a liquid connective tissue composed of plasma and formed elements. It has unique physical and chemical properties:

  • Volume: 4-6 liters in adults

  • Body weight: ~8%

  • Temperature: 38°C

  • Viscosity: 5 times more viscous than water

    • Prevents blood from leaking; if too thin, it will not clot, bp will lower

    • if too thick, dehydrated, heart works harder sto pump blood

  • pH: 7.35 - 7.45 (acidosis < 7.35, alkalosis > 7.45)

Blood sample centrifugation showing plasma, buffy coat, and erythrocytes

Blood Composition

Blood consists of approximately 55% plasma and 45% formed elements. The formed elements include erythrocytes (red blood cells), leukocytes (white blood cells), and platelets.

  • Plasma: The liquid portion, mostly water, proteins, and solutes.

  • Formed Elements: Cellular components including RBCs, WBCs, and platelets.

Blood composition: plasma, buffy coat, and red blood cells

Blood Plasma

Plasma is a mixture of water (92%), proteins (7%), and other solutes (1%). Plasma proteins are the most abundant solute and play critical roles in clotting, immune defense, and transport.

  • Albumin: Smallest and most abundant; maintains viscosity and osmolarity.

    • contributes to thickness and allows blood to pass through

  • Globulins: Involved in immune defense and transport

  • Fibrinogen: Essential for blood clotting.

  • Liver supplies most proteins

Production of Blood (Hematopoiesis)

Blood cells are continuously produced through hematopoiesis. Daily production includes billions of platelets, RBCs, and WBCs. All formed elements originate from hematopoietic stem cells.

  • Erythropoiesis: Production of red blood cells.

  • Leukopoiesis: Production of white blood cells.

  • Thrombopoiesis: Production of platelets.

Erythrocyte developmental pathway

Erythrocytes (Red Blood Cells)

Quantity and Structure

Erythrocytes are the most abundant formed element and are critical for oxygen transport. Their bi-concave disc shape increases surface area for gas exchange. They lack a nucleus and most organelles, which allows more room for hemoglobin but prevents self-repair.

  • Hematocrit: Clinical measurement of RBC percentage in blood.

  • Shape: Bi-concave disc, 7.5 μm diameter, 2.0-2.5 μm thick, no nucleus

Erythrocyte structure: bi-concave disc

Hemoglobin

Hemoglobin is a red, iron-containing protein responsible for oxygen transport. Each iron atom binds one oxygen molecule. RBCs lack mitochondria and rely on anaerobic fermentation for ATP production.

  • Structure: Four globin chains, each with a heme group.

  • Function: Oxygen and carbon dioxide transport.

Hemoglobin structure and heme group

Life Cycle of Erythrocytes

RBCs live for about 120 days. Erythropoiesis takes 3-4 days, starting from hematopoietic stem cells. Old RBCs rupture (hemolysis) and their components are recycled.

  • Birth: Erythropoiesis in bone marrow.

  • Death: Hemolysis in capillaries.

Erythrocyte life cycle: hemolysis and recycling

Sickle-Cell Anemia

Sickle-cell anemia is caused by a genetic mutation in hemoglobin, resulting in sickle-shaped RBCs. This affects oxygen transport and can cause blockages in blood vessels.

  • Genetics: Two copies of the HbS gene cause the disease.

  • Treatments: Focus on symptom management and prevention of complications.

Sickled erythrocyte and hemoglobin mutation

Leukocytes (White Blood Cells)

Structure and Function

Leukocytes are the body's defense cells, residing mainly in connective tissues but traveling via the bloodstream. They are classified as granulocytes or agranulocytes based on the presence of granules.

  • Granulocytes: Neutrophils, eosinophils, basophils.

  • Agranulocytes: Monocytes, lymphocytes.

Types of granulocytes and agranulocytes

Leukocyte Life Cycle

Leukopoiesis is the process of WBC production, starting from hematopoietic stem cells. Leukocytes have varied lifespans and functions depending on their type.

Leukocyte developmental pathway

Leukocyte Disorders

Disorders include leukemias (overproduction of abnormal WBCs) and infectious mononucleosis (viral disease causing excess lymphocytes).

  • Leukemia: Cancerous proliferation of abnormal WBCs.

  • Infectious mononucleosis: Caused by Epstein-Barr virus, results in excess lymphocytes.

Platelets and Control of Bleeding

Platelet Structure and Function

Platelets are small fragments of megakaryocytes and play a crucial role in blood clotting. They are the second most abundant formed element after RBCs.

  • Origin: Megakaryocytes in bone marrow.

  • Function: Initiate clotting and repair damaged vessels.

Platelet developmental pathway

Control of Bleeding (Hemostasis)

Hemostasis is the process of stopping bleeding, involving three stages: vascular spasm, platelet plug formation, and coagulation.

  1. Vascular spasm: Smooth muscle contracts to reduce blood flow.

  2. Platelet plug: Platelets adhere to exposed collagen fibers.

  3. Coagulation: Fibrin forms a mesh that traps blood cells.

Stages of hemostasis

Agglutination vs. Coagulation

Both involve cells sticking together, but mechanisms differ:

  • Coagulation: Formed elements stuck by fibrin.

  • Agglutination: RBCs stuck by antibodies.

Agglutination reaction

Blood Types and Transfusion

Blood Typing

Blood types are determined by antigens (cell surface markers) and antibodies. Agglutination occurs when antibodies bind to antigens on RBCs, causing them to stick together.

  • Antigens: Identify self vs. foreign cells.

  • Antibodies: Recognize and bind to antigens.

Antigen-antibody interaction

ABO Blood Types

The ABO system classifies blood based on the presence of A and B antigens:

Type

Antigens

Antibodies

A

A

B

B

B

A

AB

A and B

None

O

None

A and B

ABO blood types and agglutination

Universal Donor and Recipient

Type O is the universal donor (no antigens), and type AB is the universal recipient (no antibodies). Only RBCs are transfused, not plasma.

Rh Blood Typing

The Rh system is based on the presence or absence of the Rh antigen. Blood types are denoted as positive or negative (e.g., A+, A-). Rh incompatibility can cause problems in pregnancy.

  • Rh positive: Rh antigen present.

  • Rh negative: Rh antigen absent; antibodies produced only if exposed.

Rh blood typing

Summary Table: Blood Components

Component

Percentage

Main Function

Plasma

~55%

Transport, regulation

Red Blood Cells (Erythrocytes)

~45%

Oxygen transport

White Blood Cells (Leukocytes)

<1%

Immune defense

Platelets

<1%

Clotting

Blood composition: plasma, buffy coat, and red blood cellsAdditional info: Academic context was added to clarify the functions, structure, and clinical relevance of blood components, as well as the mechanisms of hemostasis and blood typing.

Pearson Logo

스터디 프렙