4.3 Cells N Tissues Adapt Immunity Flashcards

1
Q

All blood cells are derived from?

A

bone marrow stem cells

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2
Q

bone marrow stem cells undergo what processes to become mature cell lineages?

A

activation
proliferation
differentiation

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3
Q

Specific cytokines are required for?

A
  1. activation
  2. proliferation
  3. differentiation
  4. development of T lymphocytes
  5. other cytokines for B lymphocytes
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4
Q

The Immune system is divided into _____ and ______ lymphoid structures

A

primary and secondary

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5
Q

Primary lymphoid organs are sites where lymphocytes? Ex

A

develop without the presence of antigen, (develop, mature and replace old with new)
Ex: Bone marrow and thymus

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6
Q

Secondary lymphoid organs are sites where lymphocytes? Ex?

A

respond and develop further in response to antigen

Ex: Lymph nodes and spleen

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7
Q

When cells leave the primary lymphoid

organs they are mature but?

A

naive

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8
Q

What does it mean to be a ‘naive’ immune cell?

A

have never encountered antigen

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9
Q

When cells develop and oftentimes leave the secondary lymphoid organs they are considered?

A

effector or memory cells

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10
Q

what is the thymus?

A
  • a lymphoepithelial primary lymphoid organ
  • found underneath the sternum positioned above the heart
  • composed of T lymphocyte lineage cells, epithelial cells, and macrophage lineage cells
  • site of developement and leasning self from non-self
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11
Q

Thymus is a primary lymphoid structure for development of?

A

mature T cells

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12
Q

What is the site that pre-T cells from the bone marrow migrate

A

thymus

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13
Q

Explain thymus cortex, medulla and capsule?

A

1) Cortex contain immature pre-T cells (a lot of them)
2) Medulla contains mature T cells (learning place for self and non-self and storage)
3) Capsule= outermost layer

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14
Q

the medulla of the thymus acts as?

A

1) learning place for self and non-self

2) storage place for t-cells

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15
Q

In the Cortex all preT cells

A

express TCR, CD3, CD4, and CD8 at the cell membrane

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16
Q

PreT cells that are incapable of reactivity to Self MHC on thymic epithelial cells?

A

will die through apoptosis

17
Q

apoptosis

A

a form of programmed

cell death

18
Q

All pre T cells capable of reactivity to self MHC on thymic epithelial cells do what?

A

1) survive
2) proliferate
3) move on for potential future maturation

19
Q

What are CDs?

A

cluster of differentiation

*CDs are molecules on the surface of the cell

20
Q

B cells death is all dependent on?

A

MHC

21
Q

In the Medulla, all T cells express?

A

TCR, CD3, CD4, or CD8- aka single positive (SP) T cells

22
Q

T cells near the medulla that are strongly reactive (high affinity) Self MHC on thymic epithelial or dendritic cells will?

A

die through apoptosis

23
Q

T cells in the medulla that are capable of weak (low/intermediate) reactivity to self MHC will?

A

1) survive
2) proliferate
3) complete maturation,
4) eventually exit to general circulation

24
Q

Where are death domains found?

A

cytoplasm of cell

25
Q

In order for apoptosis to happen, you must have?

A

1) interaction with TCR

2) FasL (a ligand) interact with Fas on cell

26
Q

the ligation of FasL and Fas causes

A

Fas to trimerise which ACTIVATED the death domain in Fas (which then interacts with the death domain in FADD)

27
Q

Procaspase binds to? This does what

A

binds to FADD,which creates caspase 3 which ULTIMATELY leads to apoptosis of the Fas-expressing cell

28
Q

death domains initiate the development of?

A

caspase 3

29
Q

caspase 3 is?

A

a key element that leads to an event for DNA fragmentation for programmed cell death

30
Q

is the medulla or cortex of thymus darker?

A

cortex

31
Q

the medulla has a lot of?

*responsible for?

A

cell death

*responsible for adaptive immunity in long run

32
Q

Cells stick around for how long in medulla before they die and are replaced?

A

21 days

33
Q

T cells-site of maturation is in the?

A

thymus

34
Q

two major T cell subsets are?

A

CD4+ and CD8+

35
Q

What are the 5 subsets of CD4+ are

A
  • T helper 1 (Th1)
  • T helper 2 (Th2)
  • T helper 17 (Th17)
  • T follicular helper (Tfh)
  • T regulatory (Treg)