Untitled Flashcards Set

🫀 Cardiovascular and Immune System Study Guide (Module 6)

1. Layers of the Heart Wall

  • Epicardium: Outer protective layer; contains blood vessels and nerves.

  • Myocardium: Thick, muscular middle layer; responsible for heart contraction.

  • Endocardium: Inner lining of the heart chambers and valves; smooth surface for blood flow.

2. Poiseuille’s Law and Blood Flow

Poiseuille’s Law:

Q = \frac{\pi \Delta P r^4}{8 \eta L}

Where:

  • Q = flow rate

  • \Delta P = pressure gradient

  • r = radius of vessel

  • \eta = viscosity

  • L = length of vessel

Clinical Relevance:

  • Small changes in radius = big changes in flow (radius to the 4th power).

  • Vasodilation increases blood flow, vasoconstriction decreases it.

  • Important in blood pressure regulation, shock, and exercise physiology.

3. Vein Valves and Retrograde Flow

  • Vein valves are semilunar in shape.

  • They prevent backflow of blood—especially in the legs—when muscles contract and relax.

  • Work with skeletal muscle pump to return blood to the heart against gravity.

4. Endothelial Cells: Dual Roles

Anticoagulant Role

:

  • Produce nitric oxide (vasodilation, anti-platelet)

  • Secrete prostacyclin (inhibits platelet aggregation)

  • Express thrombomodulin (activates protein C to degrade clotting factors)

Prothrombotic Role

:

  • When injured, endothelial cells release:

    • von Willebrand Factor (vWF) from Weibel-Palade bodies → activates platelets

    • Tissue Factor (TF) → initiates coagulation cascade

5. DVT (Deep Vein Thrombosis)

  • Blood clot in a deep vein (usually leg).

  • Biggest risk: Pulmonary Embolism (PE) → clot travels to lungs, blocking arteries.

  • Can be life-threatening; often occurs with immobility, surgery, cancer.

6. Lymphoid Tissue Types

Type

Location/Function

Primary

Bone marrow (B-cell development), Thymus (T-cell education)

Secondary

Lymph nodes, spleen, MALT → where mature lymphocytes activate

Tertiary

Formed at inflammation/tumor sites (not always present)

7. T-cell Selection (Positive & Negative)

Occurs in thymus to ensure self-tolerance and functionality.

Positive Selection

(in cortex):

  • T-cells must bind weakly to self-MHC on cortical thymic epithelial cells (cTECs).

  • Weak binding = survive.

  • No binding = apoptosis.

Negative Selection

(in medulla):

  • T-cells that bind too strongly to self-antigens are eliminated.

  • Mediated by medullary thymic epithelial cells (mTECs) expressing AIRE.

  • Prevents autoimmune T-cells.

8. T-cell Education Pathway

  1. Enter corticomedullary junction as double negative (CD4-/CD8-).

  2. In subcapsular zone, T-cells proliferate.

  3. Become double positive (CD4+/CD8+) in cortex.

  4. Undergo positive selection via cTECs.

  5. Migrate to medulla, encounter AIRE-expressing mTECs for negative selection.

  6. Exit as single positive CD4+ (helper) or CD8+ (cytotoxic) T-cells.

9. Germinal Center Reactions

Located in secondary lymphoid organs (e.g., lymph nodes, spleen).

Functions:

  • Affinity Maturation: B-cells mutate antibody genes → select for higher affinity.

  • Class Switching: IgM switches to IgG, IgA, or IgE based on cytokine signals → functional specialization.

  • Result: Stronger, more effective immune responses.

10. Splenic Venous Sinusoids

  • Sinusoids: Open, leaky capillaries in the red pulp of the spleen.

  • Healthy RBCs squeeze through endothelial slits.

  • Old/damaged RBCs get trapped and are phagocytosed by macrophages.

  • Helps maintain healthy blood cell population.

️ Summary of Major Pathways

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Cardiovascular Flow Regulation

  • Governed by Poiseuille’s Law: radius has biggest effect.

  • Endothelial cells control vasodilation (NO) and clotting (vWF, TF).

  • Vein valves and muscle pump prevent blood backflow.

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T-Cell Development Pathway

  1. Origin in bone marrow → migrate to thymus

  2. Double negative → double positive → single positive

  3. Positive selection: binds self-MHC = survives.

  4. Negative selection: binds self-antigen strongly = deleted.

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B-Cell Activation in Germinal Centers

  1. B-cells bind antigen and present it to helper T-cells.

  2. Enter germinal center:

    • Dark zone: Proliferation and mutation.

    • Light zone: Selection for high-affinity clones.

  3. Class switch recombination and exit as memory or plasma cells.