CH7 Development of T lymphocytes

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17 Terms

1

T-cells are not thymus-dependent lymphocytes (T/F)

False (Development requires migration to the thymus)

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2

Thymocytes

immature T cells

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3

Thymic stroma

network of epithelial cells in the thymus

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4

Thymic anlage

The tissue formed from cell movements that will develop into the mature thymus

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5

Hassall’s corpuscles are often seen in thymus medulla. (T/F)

True

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6

Macrophages and dendritic cells-

-are responsible for removal of defective thymocytes.

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7

CD34

  • In all hematopoietic progenitor cells.

    – This protein is removed from thymocytes in the thymus

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8

CD2

  • adhesion molecule for retention in thymuS

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9

CD127

  • (= IL-7 receptor)

  • cytokine receptor for signals to T-cells

    – IL-7 (interleukin 7) is a cytokine produced by thymic stromal cells

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10

double-negative (or DN) thymocytes

  • immature thymocytes do not produce CD4 or CD8 proteins during early development

  • TCR receptor genes (for a and b proteins, or g and d proteins) begin to undergo genetic recombination

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11

double-positive (or Dt) thymocytes

Gene rearrangements to form TCRs; cells have both CD4 and CD8

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12
  • Notch 1 proteins

thymocytes act as a gene regulatory proteins to control production of appropriate thymocyte proteins

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13

IF functional proteins are produced (either y:d proteins, or beta proteins), the cells will not

then express CD4 and CD8 proteins. (T/F)

False

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14

If successful production of a beta chain protein inactivates the delta chain, this commits the thymocyte to producing alpha:beta T-cell receptor (T/F)

True

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15

positive selection for T cells

  • The T-cell receptor proteins are screened for binding to MHC receptor proteins on thymic epithelial cells

  • (~2%) survival rate for T cells.

  • occurs in the cortex

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16

Cells that bind tightly to self-antigens-

-are signaled for apoptosis. Moderate binding, antigen lives

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17

autoimmune regulator (AIRE

transcription factor that activates gene expression and protein synthesis for MHC I antigens

derived from these self proteins (e.g. insulin) – this

allows for immunotolerance of antigens from

phagocytized cells.

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