Lecture 24: Immune And Lymphatic Tissue II Flashcards

1
Q

Describe the basic histology of the thymus

A
  • See Slide 5
  • Most developed at puberty:
  • 10-15 grams at birth to 30-40 grams at puberty
  • Involutes during adolescence
  • No lymph follicles (nodules)
  • No afferent lymph vessels
  • No lymph sinuses
  • Capsule:
  • Blood vessels
  • Efferent lymphatics are present.
  • Afferent lymphatics are not present: Therefore, lymph does not circulate through thymus.
  • Extends trabeculae (septa) into the parenchyma
  • Trabeculae (Septa):
  • Delicate CT
  • Divide the thymus into incomplete lobules
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2
Q

Describe the lobules of the thymus

A
  • Each lobule is composed of an outer, darker staining cortex and an inner, lighter staining medulla.
  • Cortex: (dark staining):
  • Stained densely with basic dyes such as H&E
  • Cell population:
    • Epithelial reticular cells: Secrete thymosin
    • T cells in various stages of differentiation
  • Thymocytes migrate from cortical areas to medullary areas
  • Blood vessels surrounded by continuous epithelial barrier.
    • Allows thymus to maintain lymphopoiesis while segregated from antigens.
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3
Q

Describe the medulla (usually light stained)

A
  • Specialized to allow entry channel into blood stream of mature lymphocytes
  • Capillary beds are not sheathed by epithelial cells.
  • Hassall’s corpuscles:
  • Whorls of highly keratinized medullary epithelial cells:
    • Produce cytokine thymic stromal lymphopoietin: Stimulates thymic dendritic cells needed for the maturation of single positive T cells
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4
Q

Describe differentiation in T Cells

A
  • Double negative T cells:
  • Lack cell surface molecules typical of mature T cells
  • Enter cortex from blood vessels
  • Proliferate in subcapsular area
  • Double positive T cells move to outer cortex.
  • Confronted with epithelial cells with cell surface MHC classes I and II for clonal selection
  • Express both CD4 and CD8 coreceptors and TCR receptors.
  • Single positive T cells move to inner cortex:
  • Express TCR receptors and either CD4 or CD8 coreceptors
  • Clonal deletion is completed in medulla.
  • See Slide 10-13 and study the expression of Foxn1 and Aire genes and the expression of various keratins in the thymic epithelial cells that regulate differentiation of T-cells.
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5
Q

Describe what I think is the blood thymic barrier in the thymus

A
  • Blood-thymic barrier.
  • Located in thymic cortex
  • Prevents antigens in the blood from reaching developing T cells in thymic cortex
  • Leaky during fetal life to allow for development of immunologic tolerance to self-antigen.
  • Components:
  • Endothelium
  • Endothelial basal lamina
  • Perivascular space
  • Basal lamina of reticular cells
  • Reticular cells
  • Thymicparenchymal cells
  • See Slide 14
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6
Q

Describe the morphology of the spleen

A
  • 5.6 x 4 inches
  • No lymph sinuses
  • No afferent lymph vessels
  • Covered by peritoneum except at hilus
  • Mesothelium-lined CT capsule contains some smooth muscle fibers and sends trabeculae into parenchyma
  • Blood vessels enter and leave hilus
  • Divided into red pulp and white pulp
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7
Q

Describe the blood filtering functions of the spleen

A
  • Only lymphatic organ specialized to filter blood:
  • Stores and removes worn-out RBCs
  • Recycles iron
  • Converts hemoglobin to bilirubin
  • Blood formation in the fetus
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8
Q

Describe the immunologic functions of the spleen

A
  • Screens foreign material in the blood
  • Produces lymphocytes and plasma cells
  • Removal leads to overwhelming bacterial infections in infants, children, and young adults.
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9
Q

Describe the histology of white pulp

A
  • Elongated, branched strands always associated with arteries
  • Zones of diffuse lymphoid tissue and germinal centers
  • Site of clonal expansion of antigen-stimulated lymphocytes
  • B cell area contains secondary follicles in which central arteriole is off center.
  • T cells are found in the areas surrounding the central artery near the center of the white pulp.
  • Forms the periarterial lymphatic sheath (PALS)
  • Reticular fibers are associated with fixed macrophages and support splenic pulp
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10
Q

Describe the histology of the marginal zone

A
  • Forms sinusoidal interface between red pulp and white pulp
  • Has an abundance of antigen-presenting cells
  • Lymphocytes first encounter antigens here.
  • Activated T-helper cells activate B cells here.
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11
Q

Describe the histology of red pulp

A
  • Surrounds white pulp and makes up about 80% of the spleen. • Functions to filter blood
  • Contains large numbers of RBCs and other blood elements
  • Billroth cords form red pulp parenchyma:
  • Contain various blood cells, plasma cells, and antigen presenting cells
  • Terminal capillaries open directly into substance of cords (open circulation).
  • Macrophages destroy worn-out or defective red blood cells.
  • Venous sinusoids:
  • Endothelial-lined sinusoids with a discontinuous basement membrane
  • Storage sites for healthy red blood cells
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12
Q

Describe the histology of the arteries within the spleen

A

Arteries:

  • Splenic artery enters hilus
  • Trabecular arteries branch off
  • Central arteries:
  • Review Figure 10-23 for vascular pattern
  • Adventitia loosens and becomes mesh-like reticulum infiltrated with lymphocytes.
  • Enlarged areas are splenic nodules
  • After capillaries form, supplying white pulp, central arteries lose their white pulp investment and enter red pulp to form a penicillus.
  • Penicillus:
  • Composed of pulp arteriole, sheathed arteriole, and terminal capillary.
  • Terminal capillary:
  • Drains into: Intercellular spaces (open system) or
  • Venous sinuses lined with reticuloendothelial cells (closed system)
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13
Q

Describe the histology of veins in the spleen

A
  • Venous sinuses are lined with reticuloendothelial cells.
  • Drain into:
  • Pulp veins which unite with:
  • Trabecular veins, forming
  • Splenic vein which
  • Exits at hilus
  • See Slide 28-32
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