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phys exam 3

QuestionAnswer
recognition of what is self and what is not self immunity
two types of immunity adaptive and innate
4 components of the immune system cells/organs, cytokines, complement proteins, antibodies,
what cells are part of innate immunity polymorphonuclear granulocytes: neutrophils, basophils, eosinophils,
what cells are part of adaptive immunity B cells, T cells, NK cells
function of neutrophil releases chemicals involved in inflammation
where is the neutrophil produced bone marrow
what type of cell is neutrophil phagocyte
where is basophil produced bone marrow
function of basophil release factors involved in inflammation
where is eosinophil produced bone marrow
function of eosinophil destroys multicellular parasites, participates in immediate hypersensitivity reactions
where do the lymphocytes of adaptive immunity mature NK and B in bone marrow T cells in the thymus
what is the function of the lymphocytes in adaptive immunity recognition cells in specific/adaptive immune responses
where is monocyte produced bone marrow
what does a monocyte differentiate into macrophage (in tissues)
what is the function of a monocyte phagocytosis
derivative of B cells makes antibodies plasma cell
antigen presenting cell, presents antigen to T cells dendritic cells
cell found in connective tissues and the skin, helps in wound healing and inflammatory response mast cells
proteins that kill bacteria/viruses complement proteins
chemical messengers of the immune system cytokines
too few WBC's leukopenia
too many WBC's leukocytosis
high neutrophils would be a sign of bacterial infection
high lymphocytes would be a sing of viral infection
describe innate immunity general defense of invader
what do cells recognize in innate immunity proteins on invader
what do cells recognize in adaptive immunity antigens on invader cells
what are the phagocytes of the immune system neutrophils, macrophages, dendritic cells
steps of inflammation mast cells/damaged tissue cells release histamine - causes hyperemia, capillary permeability increase, chemotaxis- injured tissues release chemicals that draw phagocytes, diapedesis - neutrophils and phagocytes squeeze through endothelial cells to reach s
molecule that binds the bacterium and exposes it to phagocyte to eat it opsonin
what protein acts as an opsonin in innate inflammation response C3B
describe how C3b works to fight invaders it binds to a bacterium then binds to a C3B receptor on a phagocyte and brings it to it to eat
describe the MAC system membrane attack complex kills bacteria by creating holes in the membrane
describe the process of type 1 interferons when i cells is infected before it dies it releases interferons to other cells which binds to an interferon receptor, those cells then make antiviral proteins that block the replication of the virus
what do primary lymphoid tissues do produce lymphocyte precursors and provide secondary lymphoid organs with mature lymphocytes
what are two organs of primary lymphoid tissue bone marrow, thymus gland
what are secondary lymphocytes where lymphocytes and antigens meet, are activated and proliferate
examples of secondary lymph organs lymph nodes, spleen tonsils
what two types of T cells are split up in the thymus helper T cells and cytotoxic T cells
where are B and T cells activated in secondary lymphoid organs
where on the body does the lymph return blood right side of heart
what does the lymphatic system do collects al the materials leaking out from the blood
helper T cells produce cytokines that help in what processes the Killer T cells fight antigen bearing cells and helps B cells produce plasma cells
a group of lymphocytes that are specific to one antigen clone
describe what happens when a B cells comes across an antigen it produces with that antigen and will either create plasma cells or memory cells
regions on an antibody Fc stem, antigen binding sites, variable and constant regions
what does the Fc stem do on an antigen binds Fc receptors on cells
antibodies act as opsonin
two types of MHC proteins MHC I and II
where are MHC class I found surface of all body cells except RBC's
where are MHC class II found only present on antigen presenting cells
what type of TCR do MHC I have CD8+
what type of TCR do MHC II have CD4+
what types of cells are antigen presenting macrophages, B cells, and dendritic cells
describe the process of antigen presentation to helper T cells after phagocytosis a piece of microbe is broken down into peptide pieces and combined with MHC II and presentated on surface of APC. CD4+ T cells bind to the complex, APC secretes: cytokines, to further activate CD4+
what's a difference between MHC I and II MHC I happens inside the cell while II the antigen complex is presented outside of the cell
explain the process of MHC I infected cells have viral DNA that gets hydrolyzed and combined with the cell's class I MHC proteins in the ER, and then shuttled to the plasma membrane, a cytotoxic T cell (CD+) binds to the antigen. sometimes needs a costimulus (CD4)
what does the CD8 cell produce perforin and granzyme
what does perforin do pokes holes in viral membrane
what does granzyme do goes through the holes poked by perforin and kills a virus
describe what NK cells do they attach to the antibody and create a tight immunological synapse with the cell where they release perforin and granzyme to kill it
what is the second bind required in T cells costimulus
how is cardiac muscle similar to skeletal has sarcomeres, T-tubules, actin, myosin, troponin
does cardiac muscle undergo mitossi no
traits unique to Cardiac muscle intercalated discs, desmosomes, gap junctions, arranged in layers
vessel flow arteries, arterioles, capillaries, venules, veins
two loops in the cardiovascular system pulmonary and systemic
describe pulmonary circulation blood circulation to lungs - R ventricle to L A
describe systemic circulation body circulation starts at left ventricle ends at R Atrium
resting membrane potenital of the heart -90
excitation contraction coupling in cardiac muscle depolarization opens Na - rushed into cell, K channels open leave cell, calcium enters causes more calcium to be released from SR, cross bridge cycling, calcium returned and muscle relaxes
how is the action potential in the heart generated through pacemaker cells from SA node
cardiac cells are connected by gap junctions
gap junctions in cardiac cells cause the heart to have a coordinated contraction
difference in cardiac and skeletal action potentials cardiac plateughs while skeltel drops sharply, has no long refractory period like skeletal
conduction system flow SA node, AV node, bundle of His (AV bundle), R and L bundle branches, perkinje fibers
effects of the sympathetic nervous system on the heart norepinephrine and epinephrine, increases heart rate, increases force of contraction, increased conduction speed and increases cardiac output
effects of the parasympathetic nervous system on the hear acetylcholine, decreased heart rate, decreased conduction speed, minimal effect on contractility, promots energy conservation and recovery
lub sound in the heart closure of AV valves
dup sound in the heart closure of pulmonary and aortic valves
when does the lub sound happend at the beginning of systole when AV valves close
when does the dup sound happen at the beginning of diastole when the semilunar valves close
whistle valves dont close all the way
gurgle valves have backflow
lub gurgle dup insuf. AV valve
lub whistle dup stenotic semilunar
lub dup gurgle insuf. semilunar
lub dup whistle stenotic AV valve
systole is ventricular contraction blood ejected out of heart
diastole is ventricular relaxation blood filling heart
systole and diastole can be subdivided into two periods: isovolumetric ventricular contraction/relaxation and ventricular contraction/relaxation
describe isovolumetric ventricular contraction/relaxation RA - RV and LA- LV
describe ventricular contraction relaxation RV to lungs LV to aorta
the first part of systole is called isovolumetric contraction
what is happening during the first part of systole blood left atria, all valves closed
2nd part of systole ventricular ejection (contracton)
what is happening during the 2nd part of systole pressure builds and pulmonary and aortic valves open blood ejected out
diastole first part is called isovolumetric relaxation
what is happening during diastole isovolumetric relaxation no blood entering or leaving the ventricles, all valves closed, atria are filling
diastole second part is ventricular relaxation
what is happening during diastole ventricular relaxation the ventricles are filling AV valve open semilunar closed
why do valves open difference in pressures
when the pressure in the atria is greater than the ventricles the AV are open
when the ventricle pressure is greater than the pressure in the aorta or pulmonary artery the semilunar will open
the volume of blood each ventricle pumps per unit time (minute) cardiac output
heart rate x stroke volume is cardiac output
the volume of blood at each contraction stroke volume
what happens when stroke volume declines cardiac ouput can be maintained by increasing heart rate
what is the frank sterling mechanism ventricle contracts more forefully when more blood enters during diastole
what happens if the heart stretchs beyond a certain point it can lose ability to contract and fail
the end diastolic volume is the amount of blood that enters heart
the more venous blood entering the more exiting
how does the heart prevent pulmonary edema and body edema the left side of the heart will stretch to pump out the extra fluid so it doesnt accumulate in the tissues, and the right side will
the parasympathetic has an impact on heart rate
the sympathetic has an impact on heart rate and stroke volume
increased end diastolic has an impact on stroke volume
pressure in vessels is due to cardiac output and peripheral resistence
peripheral resistence depends on viscosity, dehydration RBC
high peripheral resistance causes increased BP
low peripheral resistance causes decreased BP
flow rate is volume of blood passing through a vessel per minute
which of the following would cause vasoconstriction in an arteriole epinephrine
Created by: fjakdfjlsajdf
 



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