Lecture 13/14: Support and defence system Flashcards

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1
Q

What are the various lines of defence? what type of defence are they?

A

Nonspecific defence (inniate immune system):

  • First line: nonspecific physical and chemical surface barriers
  • Second line: Nonspecifc internal cellular and chemical defense

Specific defence:
Third line: immune response

NOTE: if pathogen penetrates first defence then goes to second and if survives second goes to third

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2
Q

What are examples of the first line of defence?

A
  • tears: proects against substances in eyes
  • skin: physical barrier to outside
  • Large intestine: normal bacterial inhabitants prevents invaders
  • Saliva: washes awa microbes
  • Respiratory tract: mucus traps organisms
  • Stomach: acid skills organisms
  • Bladder: urine washes microbes from urea
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3
Q

What are examples of second line of defence?

A
  • identify foreign matter but isnt specific, doesn’t develop memory
  • defensive cells, protein,s inflammation and fever
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4
Q

Explain protein based defence

A
  • called lysis
  • mainly in liver, released in inactive form
  • deactivated by native proteins
  • become activated by: polysaccharides on bacteria surface or antigen/antibody complexes (adaptive immune response)
  • acts in digestive way, creates holes and fluid rushes in causing invader to burst
  • in brain has similar system made from glial cells
  • complement attacks the plaque and neurofibrillary tangles (common for alzheimers and neurodegradation)
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5
Q

How does inflammation workq

A
  • foreign object found
  • histamine is released
  • capillaries opened, inc blood flow carrying defence cells and chemicals causing redness
  • heat due to inc in metabolic rate
  • swelling due to fluid containing defensive chemicals
  • pain prevents movement allowing it to heal
  • can also occur as response to tissue damage, stress, arthritis, obesity
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6
Q

How does a fever work?

A
  • infection or toxins cause release of monocytes/macrophages then **pyrogenic cytokines
  • gets into hypothalamus and resets thermoregulatory point
  • why you get hot
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7
Q

How does the support and defence system defend against more than just invading microbes

A
  • part of CNN, SDS always on doing multiple things and is “watching” for invaders
  • protects against local tissue damage not due to infection
  • normal tissue turnover (cell death, regeneration during wound healing
  • appearance of transformed cell populations (cancer)
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8
Q

How does the support and defence system relate to obesity?

A
  • adipocytes increase number (hyperplasia) but also in size HYPERTROPHY
  • cell gets too big for capillaries and oxygen cant get to it
  • lead to reduced blood flow/hypoxia and cell death
  • Macrophages infiltrate these areas, recruited by kind of stress signal (MCP-1)
  • macrophages release inflammatory peptides such as TNF, IL-6 that cause insulin resistance in surrounding tissues such as muscle
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9
Q

How can insulin resistance in small amounts be beneficial for SDS and obesity

A
  • insulin promotes glucose uptake
  • dont want tissues to take away energy, want tissues to get it
  • if it becomes chonic and constant macrophages can lead to diabetes
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10
Q

Where do macrophages infiltrate?

A
  • areas of reduced blood flow/hypoxia
  • adipocytes
    skeletal muscle (in obese individuals)
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11
Q

What are parenchymal cells

A
  • think “parent”
  • functional cell, are the critical functional portion of the tissue (gland/organ)
    ex: liver, skeletal muscle, heart, brain, adipose tissue, pancreas
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12
Q

What are stromal Cells

A
  • non parenchymal cells
  • framework and support for parenchymal cells
    form support and defence system
    ex: neurons, astrocytes, fibroblasts, stem cells, gap junctions
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13
Q

What stromal changes occur during the development of pancreatic cancer

A

increase in sensory and SNS nerve fibers, macrophage infiltration, capillary density

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14
Q

What is MHC

A

major histocompatibility complex

- like a flag pole, holds an antogen that is either self or non self

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15
Q

What is an antigen

A

a molecule often on surface of a pathogen that the immune system recognizes as a specific foe

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16
Q

How does memory in the support and defence system work?

A

1) invader enters body
2) macrophage encounters, engulfs and digests the invader
- macrophage places a piece of invader (antigen) on its surface with the MHC marker
3) Alert: macrophage presents the antigen to a helper T cell and secrets a chemical that activates the T cell
4) alarm: activate T cell (effector helper T cell)
- activates into either naive cytotoxic T cell or a naive B cell

** slide21 of lec 13/14

17
Q

How can T cells detect a foreign antigen

A
  • cannot detect if circulating freely in the body
  • must be displayed on a MHC.
  • ability to trigger a T and B cell response to foreign antigens requires macrophages
18
Q

What happens to the Helper T cell once it is activated?

A
  • turns into effector helper T cell (means activates) it can either
    1) turn into Naive B cell
  • building specific defences, cell divides
  • plasma cell secretes antibodies targeting pathogens or toxins outside of cells
  • like missile response, is not direct
    2) turns into naive cytotoxic cell
  • builds specific defences and turns into effector cytotoxic cell
  • targets cells infected with intracellular pathogen (cancer cells/cells of organ transplants)
  • finds cells displays foreign antigen, kill by chemical means (perforins punching holes in target cell membrane like compliment)
  • engages directly
19
Q

How does memory play a role in subsequent encounters with pathogins

A
  • memory B cells and memory cytotoxic cells are created
  • first exposure to antigen will often get sick
  • second exposure has a much stronger response to antigen because of memory cells
20
Q

How is negative feedback involved with T cells

A
  • T suppressor cells suppress activation of immune system, particularly production of T helper cells
  • Too little T suppressor response: association with autoimmune disease, allergies, graft rejection, inflammatory bowel disease
  • too much T suppressor response: possible connection to cancer and increased incidence of infectious diseases
21
Q

How are glial cells used for protein based defence?

A
  • glial cells in brain recognize neurofibrillary tangles and plaque (brains form on compliment)
  • tangles and plaque are characteristic of alhziemer’s disease leading to neurodegredation
22
Q

What are neutrophils

A
  • type of phagocyte
  • first on scene and consume bacteria
  • method of cell based defence
23
Q

What are macrophages

A
  • phagocytes
  • consume almost anything
  • method of cell based defence
24
Q

What are Eosinophils

A
  • discharge enzymes that digest

- non phagocytes

25
Q

What are NK cells

A
  • constantly circulate and patrol for non-self, prime targets are cancer cells. Release perforin and proteases to destroy cells
  • non phagocytes