The Cells of the Immune System (Week 2) Flashcards

1
Q
A
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2
Q

Stem Cells have…

A
  1. the ability to regenerate or “self-renew”
  2. the ability to differentiate from young, immature cells into diverse and mature cell types with specialized function
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3
Q

Embryonic stem cells

A
  • Pluripotent
  • give rise to all cell types in the body
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4
Q

Adult stem cells

A
  • multipotent
  • give rise to tissue-specific cell types
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5
Q

Hematopoietic stem cell (HSC)

A

the stem cell that all of our immune cells originate from

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6
Q

Hematopoiesis

A

maturation of HSC into immune cells

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7
Q

Where is the primary site of development for adult immune cells?

A

primary lymphoid organs
- bone marrow
- thymus

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8
Q

Stromal cells

A

specialized cells that maintain
the niche for immune cell development in these lymphoid organs

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9
Q

Thymus

A
  • primary lymphoid tissue
  • One specific immune cell precursor
    leaves the bone marrow and develops
    to a mature immune cell in the thymus
  • site of immune cell development
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10
Q

Leukocytes (white blood cells) arise from…

A

2 progenitor cells:
1. myeloid progenitor = myeloid cells
2. lymphoid progenitor = lymphocytes

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11
Q

Myeloid progenitors give rise to…

A
  • Leukocytes in the innate immune system
  • Red Blood Cells (RBCs)
  • Megakaryocytes and Platelets for clotting
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12
Q

Granulocytes (Polymorphonuclear Cells)

A
  • First responders to infection
  • Multi-lobed nuclei
  • Cytoplasmic granules
  • Intracellular membrane-bound vesicles
  • Release contents during infection =
    Degranulation
  • Contain proteins to harm pathogens, recruit immune cells or remodel tissue
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13
Q

Neutrophils

A
  • granulocytes
  • short-lived
  • Highly mobile
  • Infection -> Leukocytosis = temporary increase in neutrophil development
  • Phagocytes
  • granules have anti-microbial properties and help remodel tissue
  • undergo NETosis
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14
Q

Eosinophils

A
  • granulocyte
  • Mobile
  • Important for parasite infections
  • Granules damage parasite membranes
  • Secrete cytokines regulating immune
    responses
  • Contribute to allergies and asthma where parasites are not common
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15
Q

Basophils

A
  • granulocyte
  • Non phagocytic
  • Important for parasite infections
  • Granules contain histamine: Increases immune cell recruitment/tissue remodeling
  • Secrete cytokines regulating immune responses
  • Contribute to allergies and asthma where parasites are not common
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16
Q

Mast cells

A
  • granulocyte
  • non phagocytic
  • similar to basophils
  • Important for parasite infections
  • Granules contain histamine: Increases immune cell recruitment/tissue remodeling
  • Contribute to allergies and asthma where parasites are not common
17
Q

Monocytes

A
  • Migrate and differentiate into tissue resident phagocytes
  • 2 types: inflammatory and patrolling
18
Q

Inflammatory monocytes

A

enter issues upon infection
- differentiate into macrophages

19
Q

Patrolling monocytes

A

crawl along and monitor blood vessel repair

20
Q

How do immature dendritic cells (DCs) capture antigen?

A

through phagocytosis, endocytosis or pinocytosis (intake of extracellular fluid) and get activated

21
Q

Lymphoid progenitors give rise to…

A
  • Lymphocytes in the adaptive immune system
  • Innate Lymphoid Cells (ILCs)
22
Q

What are the different lymphocytes?

A
  1. ILCs (innate lymphoid cells): part of innate immunity
  2. T cells: differentiate into helper or cytotoxic (killer) T cells
  3. B cells: differentiate into plasma cells to secrete antibodies
    - and dendritic cells
23
Q

B Lymphocytes

A
  • Every B cell (B lymphocyte) has
    a unique B cell receptor (BCR)
  • BCR is membrane-bound,
    surface version of an antibody
  • Naïve, mature B cells are
    activated by antigen
  • BCRs recognize antigen in any
    form (soluble and particulate)
    triggering activation of the B cell
  • Activated B cells are pAPCs
24
Q

Plasma cells

A
  • Some activated B cells differentiate into Plasma cells
  • Plasma cells have no surface, membrane-bound BCR
  • Secrete 100s-1000s of antibody per second
  • Some are short-lived and some are long-lived
25
Q

T lymphocytes

A
  • develop in the Thymus
  • T cells have a T Cell Receptor (TCR)
  • TCRs recognize peptides attached to MHC molecules of APCs (MHC I) and pAPCs (MHC II)
  • either helpers or cytotoxic, distinguished by a specific molecule
26
Q

Helper T lymphocytes (CD4)

A
  • recognize pAPCs
  • get activated by pAPCs and
    also activate the pAPC
  • subtypes are specific to the
    type of pathogen (based on cytokines)
  • environment in which they get
    activated influences this
  • Named for the cytokines they secrete
  • Regulatory T cells (Treg) are inhibitory to control inflammation
27
Q

Cytotoxic T lymphocytes (CD8)

A
  • recognize all the cells in our body
  • monitor our cells for infection
  • Eliminate cells presenting non-self antigens
  • Differentiate into Cytotoxic T lymphocyte (CTL) upon recognition of non-self antigen on cells
  • CTLs release cytotoxins that poke holes in cell membrane and cause apoptosis
28
Q

Innate Lymphoid Cells (ILCs)

A
  • No antigen-specific receptors
  • 3 groups: ILC1, ILC2, ILC3 (based on cytokines)
29
Q

Natural Killer (NK) cells

A
  • ILCs
  • Cytotoxic cells that attack
    abnormal cells
  • Recognize a lack of MHC
    molecules and release cytotoxic
    granules to kill the cell
31
Q

Antigen receptors (B cells vs T cells)

A
  • B cell receptors (BCR) can recognize antigen in any form, particulate or soluble
  • T cell receptors (TCR) can only recognize antigen as a peptide
    presented on an MHC molecule (require antigen presentation)
32
Q

Antigen presentation

A
  • displaying peptides of antigen/pathogen
  • Peptides are presented on Major Histocompatibility Complex (MHC) Molecules
  • All cells have surface MHC I
  • Professional antigen presenting cells (pAPCs) have surface MHC II
  • pAPCs get activated, phagocytose pathogens, digest proteins into peptides, load them onto MHC II