Bio Final Flashcards
Immune system
the bodies protection system
includes 2 subsections
-> Innate (non specific)
-> adaptive (specific and memory)
a complex collection of cells and organs that destroys or neutralized pathogens
Adaptive immune system
specific and memory
- humoral (antibodies)
- cellular (APCs - antigen presenting cell)
slow response -> 4-14 days
Innate immune system
non specific
- physical (barriers)
- cellular(agranulocytes and granulocytes)
- chemical (substance in secretions)
fast response -> 0-4 hours
Innate immune cells
- natural killer cell (large granular lymphocyte)
- basophil
- neutrophil
- eosinophil
- monocyte -> macrophage
adaptive immune cells
small lymphocyte
-> T lymphocyte
-> B lymphocyte -> plasma
cell
adaptive immunity
an acquired defense against foreign pathogens that is characterized by specificity and memory
first exposure to an antigen stimulates a primary response -> subsequent exposures stimulate a faster and stronger secondary response
a dual system involving humoral immunity and cellular immunity
antigen
aka immunogens
a foreign molecule that will trigger an immune response
molecules that activate adaptive immunity
a single antigen possesses smaller epitopes, which are each capable of inducing a specific adaptive immune response
its ability to stimulate an immune response depends on is molecular class, complexity, and size
humoral immunity
part of adaptive immunity
it is antibodies produced by B cells
cellular immunity
part of adaptive immunity
it is T cells that are directed against intracellular pathogens
T cells
attack infected cells
B cells
attack invaders outside the cells
epitopes
the part of the antigen that antibodies attaches to
major histocompatibility complex (MHC)
a collection of genes coding for glycoprotein molecules expressed of the surface of all nucleated cells
are essential for the presentation of normal “self” antigens
MHC I
cells that become infected by intracellular pathogens can present foreign antigens on MHC I -> marking the infected cell for destruction
MHC II
MHC II molecule are expressed only on the surface of antigen-presenting cells (macrophages, dendritic cells, and B cells)
antigen presentation with MHC II is essential for the activation of T cells
Antigen-presenting cells (APCs)
- macrophages
- dendritic cells
- B cells
ingest pathogens by phagocytosis, destroy them in the phagolysosomes, process the protein antigens, and select the most antigenic/immunodominant epitopes with MHC II for presentation to T cells
T cell maturation process
immature T lymphocytes are produced in red bone marrow -> travel to the thymus for maturation -> undergoes thymic selection which is a 3 step process of negative and positive selection that determines which T cells will mature and enter the peripheral bloodstream
thymus
located behind the sternum
different from the thyroid
Central tolerance
involves the negative selection of self-reactive T cells in the thymus
Peripheral tolerance
involves the anergy and regulatory T cells that prevent self-reactive immune responses and autoimmunity
Helper T cells
activation = APCs presenting antigens with MHC II
functions = orchestrate humoral and cellular immunity and are involved in the activation of macrophages and NK cells
CD4
Regulatory T cells
activation = APCs presenting antigens associated with MHC II
functions = involved in peripheral tolerance and prevention of autoimmune responses
CD4
Cytotoxic T cells
activation = APCs or infected nucleated cells presenting antigens associated with MHC I
function = destroy cells infected with intracellular pathogens
CD8
once activated they target and kill cells infected with intracellular pathogens
-> requires recognition of specific pathogen epitomes presented on cell surfaces using MHC I molecules
Killing is mediated by perforin and granzymes that induce apoptosis
T-Cell Receptor (TCR)
similar in structure to immunoglobulins, but less complex
millions of unique epitope- binding TRCs are encoded
Immunoglobulins
aka antibodies
are glycoproteins produced by plasma cells
are Y-shaped glycoproteins with two Fab sites (V part of the Y) for binding antigens and an Fc portion (I portion of the Y) involved in complement activation and opsonization (makes a foreign cell more susceptible to phagocytosis)
classes of T cells
can be divided into 3 classes
- helper T cells
- cytotoxic T cells
- regulatory T cells
based on their expression of CD4 or CD8, the MHC molecules they interact with for activation and their respective funcitons
CD4
a glycoprotein that serves as a co-receptor for the T cell receptor
lead the fight against infections
CD8
a transmembrane glycoprotein that serves as a co-receptor for the T cell receptor
can kill cancer cells and other invaders
Activated helper T cells
differentiate into TH1, TH2, TH17, or memory T cell subtypes
differentiation is directed by the specific cytokines to which they are exposed
TH1, TH2, TH17
perform different functions related to the stimulation of adaptive and innate immune defenses
TH1 = stimulates cytotoxic T cells and produce memory cytotoxic T cells, stimulates macrophages and neutrophils for more effective killing of pathogens, and stimulates NK cells to kill more effectively
TH2= stimulate B cell activation and differentiation into plasma cells and memory B cells, direct antibody class switching in B cells
TH17= stimulate immunity to specific infections such as chronic mucocutaneous infections
Memory T cells
are long lived cells that can respond quickly to secondary exposures
remember a specific pathogen and mount a strong, rapid, secondary response upon re-exposure
Perforin
responsible for pore formation in cell membranes of target cells -> punch holes into the target cell membrane
Granzymes
induce the the death of virus-infected and other potentially harmful cells
Apoptosis
a type of cell death in which a series of molecular steps in a cell lead to its death
the process of programmed cell death
B cell maturation process
B cells are produced in the bone marrow, where the initial stages of maturation occur -> move to the spleen for the final steps of maturation into naive mature B cells
B cells produce antibodies involved in humoral immunity
5 classes of antibody
- IgM = 10 antigen binding sites
- IgG = 2 antigen binding sites
- IgA = 4 antigen binding sites
- IgE = 2 antigen binding sites
- IgD = 2 antigen binding sites
each differs in size, arrangement, location within the body, and function
5 primary functions of antibodies
- neutralization
- opsonization
- agglutination
- complement activation
- antibody-dependent cell-mediated cytotoxicity (ADCC)
opsonization
makes a foreign cell more susceptible to phagocytosis
antibody-dependent cell-mediated cytotoxicity (ADCC)
A type of immune reaction in which a target cell or microbe is coated with antibodies and killed by certain types of white blood cells
B cell receptors (BCRs)
membrane-bound monomeric forms of IgD and IgM that bind to specific antigen epitopes with their Fab antigen binding regions
T-dependent antigens
protein antigens that can only activate B cells with the cooperation of helper T cells
involves processing and presentation of protein antigens to helper T cells, activation of the B cells by cytokines secreted from activated TH2 cells, and plasma cells that produce different classes of antibodies as a result of class switching
memory B cells are also produced
T-independent antigens
molecule classes that do not require T cell cooperation to active B cells
Cytokines
when TH2 cells are activated they secrete specific signalling molecules called cytokines-> they play a crucial roles in activating B cells
facilitate various nonspecific responses by innate immune cells
play a key role in the inflammatory response -> phase proteins, histamine, leukotrienes, prostaglandins, and bradykinin
class switching
aka isotype switching
B cells change the class of antibodies they produce while maintaining the same antigen specificity, this allows for the production of antibodies of different classes
secondary exposures to T-dependent antigens
results in a secondary antibody response initiated by memory B cells
develops more quickly and produces higher and more sustained levels of antibody with higher affinity for the specific antigen
lymphatic system
a system of vessels, cells, and organs that carries excess fluid to the bloodstream, and filters pathogens from the blood
blood pressure causes leakage of fluid from the capillaries -> interstitial space -> lymph
lymph
immune cells and dietary fats
lymph is forced through the lymphatic vessels by the movements of the body, contraction of skeletal muscles, and breathing
pathway of the cells of the immune system
cells of the immune system use lymphatic vessels to make their way from interstitial spaces back into the circulation
and use lymph nodes as major staging areas for the development of critical immune responses
lymph node
a small, bean-shaped organ located throughout the lymphatic system
found commonly near the groin, armpits neck, chest, and abdomen
lymphatic vessels
one way valves (semi-lunar) in the vessels keep lymph moving forward toward the heart
movement of lymph
interstitial pressure increases -> flaps open -> lymph -> lymphatic capillaries -> lymphatic vessels -> dumped into the circulatory system via the lymphatic ducts located at the junction of the jugular and subclavian veins in the neck
chyle
in the small intestine, dietary triglycerides combine with other lipids and proteins and enter the lacteals (the lymphatic vessels of the small intestine) to form a milky fluid called chyle
chyle travels through the lymphatic system and will eventually enter the bloodstream
essential for immune function as is transports immunoglobulins and T lymphocytes through the body
lymphatic ducts
superficial and deep lymphatics merge to form larger vessels called lymphatic trunks
What drains into the right lymphatic duct
the right sides of the head, thorax, and right upper limb drain lymph fluid into the right subclavian vein via the right lymphatic duct
what drains into the thoracic duct
the left side of the body drains into the larger thoracic duct, which then drains into the left subclavian vein
lymphoid organs
are where lymphocytes mature, proliferate, and are selected = attack pathogens without harming the cells of the body
primary lymphoid organs
- bone marrow
- thymus gland
secondary lymphoid organs
- lymph nodes (lymph filters)
- spleen (blood filter)
- lymphoid nodules
lymphoid nodules
occur most typically in the cortex of lymph nodes (outer layer), in the spleen, tonsils
physical barriers
- the skin
- endothelia
- cell junctions
- mucociliary escalator (transports mucus with any captured foreign particles in an upstream direction towards the upper airway away from the alveoli)
mechanical defences
microbes trapped are removed from the body by mechanical actions -> shedding skin cells, mucociliary sweeping, coughing, peristalsis, flushing of bodily fluids
microbiome
the resident microbiota provide a physical defense by occupying available cellular binding sites and competing with pathogens for available nutrients
nonspecific innate immune defenses
- physical barriers
- mechanical defences
- microbiome
- chemicals and enzymes in body fluids
- antimicrobial peptides (AMPs)
- plasma protein mediators
- cytokines
- inflammation-eliciting mediators
- granulocytes
- agranulocytes
chemical and enzymes in body fluids
chemical mediators like sebum, saliva, mucus, gastric and intestinal fluids, urine, tears, cerumen, and vaginal secretions are found in body fluids
antimicrobial peptides (AMPs)
AMPs found on the skin and in other areas of the body are largely produced in response to pathogens
plasma protein mediators
plasma contains various proteins that serve as chemical mediators -> acute-phase proteins, complement proteins, and cytokines
complement protein system
The complement system is made up of a large number of distinct plasma proteins that react with one another to opsonize pathogens and induce a series of inflammatory responses that help to fight infection
involves many precursor proteins that circulate in plasma
these proteins become activated in a cascading sequence in the presence of microbes -> results in the opsonization of pathogens, chemoattraction of leukocytes, induction of inflammation, and cytolysis (disruption of cells) through the formation of a membrane attack complex
membrane attack complex (MAC)
forms pores in the plasma membrane of pathogens or targeted cells, leading to osmolysis (rupture of cell)
Granulocytes
leukocytes characterized by a lobed nucleus and granules in the cytoplasm
include neutrophils, eosinophils, and basophils
neutrophils
leukocytes found in the largest numbers in the bloodstream
primarily fight bacterial infections
eosinophils and basophils
eosinophils target parasitic infections
eosinophils and basophils are involved in allergic reactions
both release histamine and other pro-inflammatory
agranulocytes
natural killer (NK) cells are lymphocytes that recognize and kill abnormal of infected cells by releasing proteins that trigger apoptosis (cell death by a series of molecular steps)
Fas ligand
a type II membrane protein that is involved in the regulation of cell death (apoptosis)
Monocytes
large, mononuclear leukocytes that circulate the bloodstream
may leave the the bloodstream and enter tissues where they differentiate and become tissue-specific macrophages and dendritic cells
inflammatory response
the hallmark of the innate immune response is inflammation
cardinal signs = pain, heat, redness, swelling, loss of function
brings fluid and cells to the site to destroy the pathogen and remove debris from the site, and isolates the site limiting the spread of the pathogen
Acute inflammation
short-term inflammatory response to an insult to the body
chronic inflammation
ongoing inflammation -> 2 months
4 parts of the inflammatory response
tissue injury -> the injured cells stimulate the release of mast cell granules and inflammatory mediators like histamine, leukotrienes, and prostaglandins
vasodilation -> increased blood flow allows for grater access of the blood to the site of inflammation, is responsible for the heat and redness of inflamed tissue
increased vascular permeability -> leakage of fluid into the interstitial space, results in swelling
recruitment of phagocytes -> leukotrienes attract neutrophils from the blood to the site of infection by chemotaxis, stimulating more macrophages to clean up the debris
effect of histamine
histamine released -> vasodilation -> increased blood flow -> plasma leaks out into interstitial fluid -> causes swelling
leukotrienes
attract neutrophils from the blood by chemotaxis and increase vascular permeability
prostaglandins
cause vasodilation by relaxing vascular smooth muscles and a major cause of pain associated with inflammation
2 divisions of the respiratory system
- the conducting zone
- the respiratory zone
conducting zone
consists of all of the structures that provide passageways for air to travel into and out of the lungs
the nasal cavity = the conchae and meatuses helps warm, filter, and humidify air
pharynx = the nasopharynx(by nose), oropharynx (by mouth), and laryngopharynx (this is in order going down toward the lungs)
trachea
bronci
conchae
projections of the ethmoid bones in the nose
curved shelf of bone
meatus
three spaces in the nasal cavity
respiratory zone
includes the structures of the lung that are directly involved in gas exchange
terminal bronchioles
alveoli
respiratory epithelium
pseudostratified ciliated columnar epithelium with goblet cells - trachea
mucus traps pathogens and debris, and cilia move the mucus superiorly toward the throat where it is swallowed
as the bronchioles become smaller and near the alveoli the epithelium thins and is simple squamous epithelium in the alveoli
respiratory membrane
the endothelium of surrounding capillaries and the alveolar epithelium = the respiratory membrane
this is a blood-air barrier through which gas exchange occurs by simple diffusion
lungs
the major organs of the respiratory system
responsible for performing gas exchange
paired and separated into lobes
right lung = 3 lobes
left lung = 2 lobed
parasympathetic and sympathetic control of the respiratory system
the lungs are controlled by the parasympathetic and sympathetic nervous systems -> bronchodilation and bronchoconstriction of airways
pleura membrane
the membrane that encloses the lungs
composed of visceral (closer to the lung) and parietal layers (closer to the chest wall), with the pleural cavity in between
the mesothelial cells of the pleural membrane create pleural fluid
pressure
Boyles law describes = as volume increases, pressure decreases
as volume decreases, pressure increases
pressure is influenced by resistance
direction of air flow
air flows from a space of higher pressure to a space of lower pressure
pulmonary ventilation
it is the process of breathing, driven by pressure differences between the lungs and the atmosphere
consists of the process of inspiration and expiration, air entering and leaving the lungs
atmospheric pressure
the force exerted by gases present in the atmosphere
intraalveolar (intrapulmonary) pressure
the force exerted by gases within the alveoli
760 mmHg
will equalize with atmospheric pressure
intrapleural pressure
the force exerted by gases in the pleural cavity
756 mmHg
transpulmonary pressure
intrapleural pressure is lower to intra-alveolar pressure, this difference is called transpulmonary pressure
760 mmHg - 756 mmHg = 4 mmHg