UNIT B: Human Body Systems - PowerPoint PPT Presentation

1 / 25
About This Presentation
Title:

UNIT B: Human Body Systems

Description:

mast cells: a type of immune cell found especially in the skin, lungs, and intestinal tract histamine: a chemical that binds to receptors present on endothelial cells ... – PowerPoint PPT presentation

Number of Views:119
Avg rating:3.0/5.0
Slides: 26
Provided by: MHE131
Category:

less

Transcript and Presenter's Notes

Title: UNIT B: Human Body Systems


1
(No Transcript)
2
UNIT B Human Body Systems
  • Chapter 8 Human Organization
  • Chapter 9 Digestive System
  • Chapter 10 Circulatory System and Lymphatic
    System Section 10.7
  • Chapter 11 Respiratory System
  • Chapter 12 Nervous System
  • Chapter 13 Urinary System
  • Chapter 14 Reproductive System

3
Chapter 10 Circulatory System and Lymphatic
System
UNIT B
Chapter 10 Circulatory System and Lymphatic
System
  • In this chapter, you will learn about the
    structure and function of the circulatory system
    and lymphatic system.

What is the composition of blood, including blood
cells? What organs and structures control the
flow of blood throughout the body?
In 2013, Lance Armstrong confessed to long-term
blood doping and the use of banned substances.
Blood doping involves artificially boosting the
bloods ability to bring more oxygen to muscles.
Aerobic capacity and endurance improve where
there are additional red blood cells available to
carry oxygen.
TO PREVIOUS SLIDE
4
10.7 Innate and Adaptive Immunity
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • The lymphatic system works with the immune system
    to protect the body from pathogens, toxins, and
    other invaders.
  • Immunity is a condition where the body is
    protected from various threats (pathogens,
    toxins, cancer cells). There are two main types
    of immunity.
  • Innate immunity Fully functional without
    previous exposure to substances
  • Adaptive immunity Initiated and amplified after
    specific recognition of substances

TO PREVIOUS SLIDE
5
Innate Immunity
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Mechanisms of innate immunity can be divided into
    at least four types
  • Physical and chemical barriers
  • Inflammatory response
  • Phagocytes and natural killer cells
  • Protective proteins

TO PREVIOUS SLIDE
6
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Physical and Chemical Barriers
  • Physical barriers
  • Skin and mucous membranes lining the respiratory,
    digestive, and urinary tracts are physical
    barriers to pathogens
  • Chemical barriers
  • Oil glands in the skin secrete chemicals that
    weaken or kill certain bacteria
  • The acidic pH of the stomach kills many types of
    bacteria or inhibits their growth
  • Bacteria that reside in the intestine and other
    areas remove nutrients and block binding sites
    that could be used by pathogens

TO PREVIOUS SLIDE
7
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Inflammatory Response
  • Inflammatory response
  • A series of events that is initiated when there
    is damage to tissues by physical trauma, chemical
    agents, or pathogens
  • Inflamed areas have four signs redness, heat,
    swelling, pain
  • Mostly due to capillary changes in the damaged
    area
  • At least three types of cells in the skin and
    connective tissue play a role in the inflammatory
    response
  • Mast cells
  • Macrophages
  • Dendritic cells

TO PREVIOUS SLIDE
8
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
Figure 10.23 Inflammatory response. Due to
capillary changes in a damaged area and the
release of chemical mediators, such as histamine
by mast cells, an inflamed area exhibits redness,
heat, swelling, and pain. The inflammatory
reaction can be accompanied by other reactions to
the injury. Macrophages and dendritic cells,
present in the tissues, phagocytize pathogens, as
do neutrophils, which squeeze through capillary
walls from the blood. Macrophages and dendritic
cells release cytokines, which stimulate the
inflammatory and other immune reactions. A blood
clot can form to seal a break in a blood vessel.
TO PREVIOUS SLIDE
9
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Inflammatory Response
  • Mast cells
  • Reside in the skin, lungs, and intestinal tract
  • Respond to damage by releasing histamine
  • Histamine causes capillaries in the area to
    dilate and become more permeable, allowing fluids
    to escape to tissues and cause swelling
  • Swollen area stimulates free nerve endings,
    causing pain
  • Increased blood flow causes skin to redden and
    warm

TO PREVIOUS SLIDE
10
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Inflammatory Response
  • Macrophages and Dendritic Cells
  • Both are phagocytic cells
  • Release various proinflammatory cytokines, which
    are chemical messengers that influence other
    immune cells
  • Interleukin-8 attracts other immune cells to the
    scene
  • Colony-stimulating factor causes bone marrow to
    produce more white blood cells

TO PREVIOUS SLIDE
11
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Phagocytes and Natural Killer Cells
  • Phagocytes
  • Engulf pathogens into an endocytic vesicle, which
    fuses with a lysosome in the cell pathogen is
    destroyed by compounds in the lysosome
  • Includes neutrophils and monocytes
  • Neutrophils the first white blood cells to enter
    an inflamed area may accumulate to form pus
  • Monocytes migrate from blood and differentiate
    into macrophages in tissues if inflammatory
    reaction continues

TO PREVIOUS SLIDE
12
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Phagocytes and Natural Killer Cells
  • Natural killer (NK) cells
  • Large, granular cells that kill some
    virus-infected and cancer cells by cell-to-cell
    contact
  • NK cells induce target cells to undergo apoptosis
  • Seek out and kill cells that lack a type of
    self molecule, called MHC-I (major
    histocompatibility class I), on their surface
  • Some virus-infected and cancer cells lack MHC-I,
    which makes them susceptible to destruction by NK
    cells

TO PREVIOUS SLIDE
13
Adaptive Immunity
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • Adaptive immunity is activated when innate
    defences fail to prevent an infection.
  • The adaptive immune system recognizes, responds
    to, and usually eliminates antigens from the
    body.
  • Antigens any molecules that stimulate an
    adaptive immune response
  • Adaptive defences take 5 to 7 days to become
    fully activated and last for many years

TO PREVIOUS SLIDE
14
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • The adaptive immune system depends on the
    activity of B cells and T cells.
  • Both cells recognize antigens because they have
    specific antigen receptors
  • Each lymphocyte has only one type of receptor
  • Large diversity of antigen receptors on B and T
    cells
  • There are specific B cells and/or T cells for
    almost any possible antigen

TO PREVIOUS SLIDE
15
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • B Cells and Antibody-Mediated Immunity
  • Defence by B cells (antibody-mediated immunity)
  • B cells are activated in a lymph node or the
    spleen, when their receptors bind to specific
    antigens
  • Cytokines secreted by T cells stimulate B cells
    to divide
  • Most cells become plasma cells, which secrete
    antibodies
  • Antibodies are the secreted form of the receptor
    of the B cell that was activated
  • Some cells become memory B cells, which allow for
    long-term immunity
  • If the same antigen enters again, memory B cells
    divide and give rise to more plasma cells that
    can produce the antibody against the antigen

TO PREVIOUS SLIDE
16
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • B Cells and Antibody-Mediated Immunity
  • Antibody Structure
  • Antibodies are also called immunoglobulins (Ig),
    which are Y-shaped molecules with two arms made
    of polypeptides
  • Heavy (long) polypeptide chain
  • Light (short) polypeptide chain
  • C (constant) region set sequence of amino acids
  • V (variable) region amino acid sequence varies
    between antibodies forms the antigen-binding site

TO PREVIOUS SLIDE
17
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
Figure 10.24 Structure of an antibody. a. An
antibody contains two heavy (long) polypeptide
chains and two light (short) chains arranged so
that there are two variable regions, where a
particular antigen is capable of binding with an
antibody (V variable region, C constant
region). The shape of the antigen fits the shape
of the binding site. b. Computer model of an
antibody molecule. The antigen combines with the
two side branches.
TO PREVIOUS SLIDE
18
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • B Cells and Antibody-Mediated Immunity
  • Antigens combine with an antibody at the
    antigen-binding site in a lock-and-key manner
  • Antigen-antibody reactions can result in immune
    complexes (antigens combined with antibodies)
  • Immune complexes may mark the antigens for
    destruction by a neutrophil or macrophage
  • Antibodies can neutralize toxins by preventing
    them from binding to cells

TO PREVIOUS SLIDE
19
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • T Cells and Cell-Mediated Immunity
  • Defence by T cells (cell-mediated immunity)
  • T cells have a unique T-cell receptor but cannot
    recognize antigens on their own
  • Require antigens be presented to the receptors
    by an MHC (major histocompatibility complex)
    protein on the surface of another cell
  • There are two types of T cells
  • Helper T cells (TH cells)
  • Cytotoxic T cells (TC cells or CTLs)

TO PREVIOUS SLIDE
20
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • T Cells and Cell-Mediated Immunity
  • Helper T cells (TH cells)
  • Only recognize antigens presented by specialized
    antigen-presenting cells (APCs) with MHC class II
    proteins on their surface
  • Cytotoxic T cells (TC cells or CTLs)
  • Only recognize antigens presented by various
    cells with MHC class I proteins on their surface
  • Some T cells become memory T cells
  • Live for many years and can quickly initiate
    immune response to an antigen previously present
    in the body

TO PREVIOUS SLIDE
21
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • T Cells and Cell-Mediated Immunity
  • Cell-mediated immunity by TC cells
  • Activated TC cells bound to a virus-infected or
    cancer cell release perforin, which forms pores
    in the plasma membranes of the abnormal cell
  • This allows enzymes called granzymes to enter the
    target cell and induce apoptosis

Figure 10.25 Cell-mediated immunity. a. How a TC
cell destroys a virus-infected cell or cancer
cell.
TO PREVIOUS SLIDE
22
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  • T Cells and Cell-Mediated Immunity
  • TC cells are capable of moving on to kill other
    target cells

Figure 10.25 Cell-mediated immunity. b. The
scanning electron micrograph shows cytotoxic T
cells attacking and destroying a cancer cell
(target cell).
TO PREVIOUS SLIDE
23
Check Your Progress
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
  1. Name one physical and one chemical barrier to
    infection.
  2. List the four cardinal signs of inflammation, and
    explain why each one occurs.
  3. Contrast the way that macrophages typically kill
    pathogens with the method used by natural killer
    cells.
  4. Compare the specific functions of helper T cells
    and cytotoxic T cells.

TO PREVIOUS SLIDE
24
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
TO PREVIOUS SLIDE
25
UNIT B
Section 10.7
Chapter 10 Circulatory System and Lymphatic
System
TO PREVIOUS SLIDE
Write a Comment
User Comments (0)
About PowerShow.com