Circulatory System: Blood And Vessels Flashcards

1
Q

What Are The Components of Blood?

A

Platelets (55%)

Erythrocytes (45%)

Leukocytes

Plasma

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2
Q

What Is Plasma?

A

A Transport Medium For Inorganic/Organic Substances

Consists Of:

  • 90% Water
  • Na+ and Cl–
  • Plasma proteins (Organic)
  • (Other Organic): Waste Products, Dissolved
    Gases + Hormones
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3
Q

What Are The Key Plasma Proteins?

A
  • Albumins
  • Globulins (Alpha, Beta, Gamma)
  • Fibrinogen
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4
Q

Describe Erythrocytes.

A

Red Blood Cells, Transport Oxygen in Blood Structure Contains Globin (Protein) and Haem (Non-Protein)

Lack Nucleus and Organelles
Mature Erythrocytes only contain few key non-renewable enzymes

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5
Q

Describe Haemoglobin.

A

A Tetramer Containing x2 Alpha and x2 Beta Subunits with Haem Groups

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6
Q

List Erythrocyte Development Stages.

A
  1. Pluripotent Stem Cell → Myeloid Stem Cell
  2. Myeloid Stem Cell → Erythroblast
  3. Erythroblast → Reticulocyte
  4. Reticulocyte → Erythrocyte
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7
Q

Describe:

Pluripotent Stem Cell → Myeloid Stem Cell

A
  1. Pluripotent Stem Cells Commit to Myeloid
    Lineage
  2. Commitment Regulated By Transcription
    Factors (PU.1 + GATA-2)
  3. Commitment Driven By Interleukin-3 and
    Stem Cell Factor (SCF)
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8
Q

Describe:

Myeloid Stem Cell → Erythroblast

A

Erythroid Lineage Commitment Established using:

GATA-1: Activates Erythroid-Specific Genes

KLF1: Drives Haemoglobin Synthesis + RBC Maturation

Erythropoietin:
Hormone binds → Erythroid Precursor Receptors

Survival, Proliferation + Differentiation into Proerythroblasts Promoted

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9
Q

Describe:

Erythroblast → Reticulocyte

A

Erythroblasts Maturation Through Various Stages

Key Stages:

  1. Hemoglobin synthesis: Iron (Delivered by
    Transferrin) Incorporated into Haem Groups
  2. Nuclear Condensation: Nucleus Shrinks and
    Is Enucleated In Bone Marrow with
    Macrophages
  3. Reticulocyte Formed
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10
Q

Describe:

Reticulocyte → Erythrocyte

A
  1. Reticulocytes enter Bloodstream, Mature
    Into Erythrocytes
  2. Residual organelles lost, Cell Membrane
    Remodeled into Biconcave Shape
  3. Haemoglobin packing Complete, Cell
    Becomes Fully Functional
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11
Q

What is The Role of The Bone marrow In Relation To Erythrocytes?

A

To Continuously replace Erythrocytes using Erythropoiesis, as they have a short life span

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12
Q

How Is Erythropoiesis Controlled?

A

Controlled By Kidneys

Mechanism:

  1. Kidneys Detect Low O2 Carrying Capacity of
    Blood
  2. Kidneys Secrete Erythropoietin Into Blood
  3. Erythropoietin Stimulates Erythropoiesis by
    Red Bone Marrow
  4. Additional Circulating Erythrocytes Increase
    O2 Carrying Capacity
  5. Increased O2 Carrying Capacity Relieves
    Initial Stimulus That Triggered Erythropoietin
    Secretion
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13
Q

What Are Reticulocytes?

A

Immature Erythrocytes

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14
Q

What Is Synthetic Erythropoietin Used For?

A

To Boost RBC Production In Individuals With Suppressed Erythropoietic Activity

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15
Q

What Is Polycythemia?

A

Excess Erythrocytes Circulating In Blood, Causes Elevated Hematocrit

Consists Of 2 Types:

  1. Primary
  2. Secondary
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16
Q

What Are The Different Blood Types?

A
  • Type A
  • Type B
  • Type AB
  • Type O
17
Q

What is Different Between The Blood Groups?

A

The Antigens Each Blood Type Contains

Type A: A Antigens

Type B: B Antigens

Type AB: A and B Antigens

Type O: (Doesn’t Have A or B)

18
Q

What Blood Groups Are Compatible?

A

Type O
Can Donate To: All Blood Types
Can Receive: Only Type O Blood

Type A
Can Donate To: A and AB
Can Receive: A and O

Type B
Can Donate To: B and AB
Can Receive: B and O

Type AB
Can Donate To: AB
Can Receive: All Blood Types

19
Q

How is Blood Rh Positive/Negative Established?

A

By Identifying Rh Factor

Rh Factor Present: Rh Positive
Rh Factor Absent: Rh Negative

20
Q

Which Antibodies Does Each Blood Group Contain:

A

Type A: Anti-B

Type B: Anti-B

Type AB: None

Type O: Anti A & B

21
Q

What Would Happen If Incompatible Blood is Transfused?

A

Donor RBCs Have Antigens that react with recipient’s plasma antibodies (anti-X antibodies)

Antibodies in Recipient’s Plasma Bind To Donor RBC antigens, forming Antigen-Antibody Complexes

  1. Complement Activation

Immune System Activates Complement proteins, which punch holes in Donor RBC membranes.

This triggers haemolysis, releasing hemoglobin into bloodstream.

  1. Hemoglobin Release & Kidney Damage

Free hemoglobin clogs kidney tubules, causes:

Acute Kidney Injury (Dark Urine Due To Hemoglobinuria)

Severe Pain In Lower Back/Loins

  1. Clotting Cascade Activation

Damaged RBCs Release Pro-Clotting Factors, Leads to:

Disseminated Intravascular Coagulation (DIC)**: Widespread clotting → depletion of clotting factors → uncontrolled bleeding.

  1. Systemic Effect

Massive Immune Response Causes: Fever, Chills, Nausea, Vomiting, Rapid Heart Rate, Hypotension (low blood pressure).

22
Q

What Are Leukocytes?

A

Mobile Units Of The Body’s Immune Defense System

23
Q

What Are The 5 Types Of Leukocytes?

A
  • Neutrophils
  • Eosinophils
  • Basophils
  • Monocytes
  • Lymphocytes
24
Q

Describe The Function Of Each Leukocyte?

A

Neutrophils: Engulf + Destroy Bacteria Intracellularly

Eosinophils: Associated With Allergic Conditions + Parasite infestations

Basophils: Synthesize + Store Histamine and Heparin

Monocytes: Perform Phagocytosis

Lymphocytes: Provide Specific Immune Defense

25
Describe Leukocyte Production.
Leukocyte Production (Leukopoiesis) Location: Bone marrow Makes most WBCs (Granulocytes, Monocytes, B cells, NK cells) Thymus: Matures T cells Lineages: Myeloid Lineage: For Innate immunity cells: Granulocytes (Neutrophils, Eosinophils, Basophils) Monocytes → Become Macrophages/Dendritic Cells Lymphoid Lineage: For Adaptive immunity cells: - B cells (Bone Marrow) - T-Cells (Thymus) - NK cells Key Hormones: G-CSF (Makes Neutrophils) M-CSF (Makes Monocytes), Interleukins (e.g., IL-5 for eosinophils).
26
What Is Leukemia?
The Uncontrolled proliferation of WBC, it is Cancerous
27