2.1.6 development of T-lymphocytes Flashcards

1
Q

______ stem cells can differentiate into all possible cell types

A

Totipotent

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2
Q

______ stem cells have the ability to differentiate into almost all cell types, but lack the capacity to contribute extraembryonic tissue

A

Pluripotent

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3
Q

____ stem cells have the potential to give rise to cells from multiple, but a limited number of lineages. an example of this is a mesenchymal stem cell or a _____

A

Multipotent, Hematopoietic stem cell

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4
Q

The ____ is a primary lymphoid organ that plays a role in maturation of thymocytes into ______

A

thymus
T-lymphocytes

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5
Q

The _____ is where B-cells mature

A

bone marrow

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6
Q

Precursor T-cells are derived from the ______ stem cell in the _____ and travel to the _____

A

Hematopoetic stem cell
Bone marrow
thymus

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7
Q

if a cell stays in the bone marrow to mature it becomes a _______

A

B-cell

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8
Q

In the ______ area of the thymus, thymocytes are tightly packed and have a large cell turnover

A

Cortical

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9
Q

As thymocytes mature in the thymus, they migrate to the ____ portion

A

medullary

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10
Q

Progenitor lymphocyte cells enter the thymus around the ______ and then go up into the ______

A

Medullary cortical region
cortex

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11
Q

what are the two types of cells in the cortex we need to know? Where do they originate?

A
  1. cortical epithelial cell
    - thymus
  2. thymocyte
    - bone marrow
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12
Q

what are the two types of cells in the medulla we need to know? Where do they originate?

A
  1. Dendritic cell
    - bone marrow
  2. macrophage
    - bone marrow
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13
Q

_______ can be found in both the cortex and medullary region

A

thymocytes

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14
Q

When is the thymus fully developed?

A

birth, after this it experiences Involution and degenerates

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15
Q

the thymus is replaced by what kind of material during involution?

A

Fatty material

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16
Q

which of these thymus would you expect to belong to an infant? which would belong to an elderly person?

A

A- infant, not very involuted
B- elderly, very degenerated

17
Q

when the uncommitted progenitor cell from the bone marrow comes in contact with the thymic epithelium it gives rise to ________. what does this mean?

A

Double negatives
- it is CD4/CD8 negative

18
Q

______ is the marker of immaturity/ an uncommitted progenitor

A

CD34

19
Q

when does a cell lose the CD34 expression?

A

when it becomes committed to become a T-cell

20
Q

what do double negative T-cells express?

A

CD2

21
Q

Thymocyte expresses a receptor called ______ which is activated when it interacts with the ____ ligand on the thymic epithelium

A

Notch1
Notch ligand

22
Q

what does the Notch 1 receptor do once activated?

A

drives T cell towards T cell development

23
Q

How does an uncommitted progenitor give rise to alpha/beta and gamma/delta cells?

A
  1. Uncommitted progenitor → committed double negative T-cell progenitor
  2. T-cell progenitor now goes through Beta or Gamma/Delta rearrangements
  3. Gamma/delta cells leave thymus
  4. Uncommitted double-positive thymocyte with Beta (has CD8 and CD4) goes through another set of rearrangements: either alpha OR gamma delta
  5. gamma/delta cell will leave and go to thymus
  6. now theres also a committed alpha/beta cell (majority)
24
Q

which rearrangement do most cells go through? Beta or delta/gamma?

A

Beta, its easier to just rearrange one

25
Q

the majority of T-cells are _____

A

alpha/beta

26
Q

Both alpha/beta and delta/gamma express ______

A

CD3

27
Q

When can an antibody to CD3 be used?

A

in suppressing and removing T cells in a patient who is undergoing a graft rejection

28
Q

Where are gamma/delta t-cells found?

A

epithelium surfaces including mucosal surfaces

29
Q

where are the two TCR checkpoints?

A
  1. during the first rearrangement (if neither gamma/delta or Beta rearrange, the cell will die
  2. second rearrangement (if cant rearrange gamma/delta or alpha, cell will die)
30
Q

what do CD3 and CD2 function in?

A

signal transduction

31
Q

why is there significant cell death in the cortical area?

A

positive and negative selection

32
Q

______ selection is when the T-cell receptor is removed if it doesn’t recognize the appropriate MHC

A

Positive

33
Q

_______ selection is when self-recognizing t-cells are removed

A

negative

34
Q

how do T-cells become either CD4 or CD8 positive?

A

if the TCR interacts with MHC1, CD4 is lost (will be CD8)

if TCR interacts with MHC2, CD8 is lost (will be CD4)

35
Q

_____ tolerance is negative selection in the thymus, while _____ tolerance is negative selection in self-reacting cells that leave the thymus

A

Central

Peripheral

36
Q

what are the APCs for positive selection?

A

cortical epithelial cells (thymically derived)

37
Q

what are the APCs for negative selection?

A

dendrites, macrophages (bone marrow derived)