AMS Exam 2 Short Hand Flashcards
Hypersensitivity Type 2
IgG and IgM
hemolytic reactions in newborns (2 people)
Anencephaly
Flat head, Brain possibly exposed
Neural tube fails to close at cranial end
Lethal
Neural Tube Defect (NTD)
Light chains
2 light chains on antibody
2 types
kappa and lamda
Achondroplasia
FGFR3
Short limbed dwarf
Innate
Fast
General
foreign bodies, pathogens, injury
immediate
Steroid
4 carbon fused rings
Cholesterol, sex hormones
everywhere except nervous tissue
Transplant rejection
T cells are responsible
APC and MHC on cell surface
activate CD8 T cells
CD8 T cells cause cell lysis of donor cells
CD4 cells are activated
these prodcue interleukin2
IL2 activates
Helper T cells (autocrine)
Cytotoxic T cells (paracrine)
THese attack donor cells with
Perforin
granzyme
Hypersensitivity Type 4
T cells
delayed reactions to antigens
Tuberculin reactions, chronic asthma, contact dermatitis
IgD
present on the surface of B cells
antibody production
Control points of Glycolysis & Glycogen
Glycolysis —– Glycogen
Hexokinase —– glucose 6 phosphate
phosphofructokinase —– fructose 1,6 bisphosphatase
pyruvate kinase —– PEP carboxykinase
glycogen synthase —– phosphorylase
Gastrulation
The making of 3 germ layers Trilaminar disc Ectoderm Mesoderm Endoderm forms primitve streak
Oligo-saccharides
condensation porduct of 3-10 monosaccharides
undigestible
soluble fibers that help bowel movement
Nodal
Left sidedness
Secreted by primitive node
Fat
Glycerol with 3 fatty acid tails
Stores energy
Neutrophils
Granulocyte 95% of leukocytes
multi lobe
First to arrive attracted to selectin bind via integrin diapedesis phagocytosis can alos release granules
Glycogen
Similar to amylopectin but more branched
Stored in Liver and muscle cells
Glycogen is broken down into glucose when needed
(glycogen phosphorylase)
3/4 is in muscle
source of glucose for glycolysis
glycogen in liver is used for maintaining BGL
Innate immunity types
Physical
Chemical
Mechanical
Microbiological
Systemic defense = complement syytem, phagocytes
Fetal circulation deoxygenated blood
blood retruns from the IVC and SVC right atria right ventricle pulmonary artery ductous arterious and into descending aorta
lungs are collapsed and resist much of blood flow
a small amount makes it and then returns to left atrium
here it mixes with O2 blood form placenta
Phospholipids
Glycerol with 2 fatty acid tails
plasma membrane
phosphate polar head (hydrophilic)
fatty acid nonpolar tails (hydrophobic)
Fats, steroids, phopholipids, are all?
insoluble in water
lots of hydrocarbon bonds H—C
Hydrophobic
Noggin, Nodal & follistatin
Growth factors
inhibit BMP
Glycogen broken down
Glycolysis
Trace complement Alternate pathway
Trace complement Alternate pathway
Micelle
Ball of lipid molecules wiht non polar ends facing in
used for transporting around the cell
Glycogen generation
Glycogenesis
Control points of Glycogen
Glucose 6 phosphate
Fructose 1,6 bisphosphatase
PEP carboxykinase
Phosphorylase
Bladder exstrophy
common with spina bifida
protrusion bladder from abdomen
Closure is most important
Neurulation
The process of creating the neural tube from the neural plate
28 days neulation is complete (tube closed)
Truncus arteriosus
becomes the heart
aorta
ventricles
Split foot
Lobster claw
Too much programmed cell death in AER
Complement functions
opsonization
MAC
inflammation
kill pathogens
Epiblast
Dorsal layer
Forms all of the embroyonic tissues and cells
Septum secundum
Sheet that coners the foreamne ovale and creates it
Transamination
amino acid metabolism
removing an amine group from one amino acid to from another
ie Pyruvate — alanine
Trophoblast
Comes from morula
Outer cells become trophoblast
Becomes placenta nad umbilical cord
Crouzon Syndrome
FGFR2
Wide set bulging eyes
Beaked nose
vision, dental, hearing, jaw issues
cleft lip / palate
Langerhans cells of skin
take up microbial antigens to become fully functioning APC’s
Conjoined twins
Over expression of Goosecoid
Di-saccharides
condensation product of two monosaccharides
sugar transport, energy storage
lactose,maltose, sucrose
link together to form starch
HCG
Syncytiotrophoblast
formerly a trophoblast
Amino Acid metabolism
2 types
transamination
deamination
Acetyl CoA
Arises from glycolysis
oxidized to CO2 and H2O via citric acid cycle
Precursor for synthesis of cholesterol and steroids
used in liver to from ketone bodies (fasting/starvation)
Neural crest cells
come from ectoderm
Form bones of face
form septa of heart
Facial and heart defects
Fetal circulation oxygenated blood
oxygenated blood from placenta enters right atria goes through foramen ovale mixes with unoxygenated blood goes to left ventricle aorta to body and brain
Unsaturated fat
Not all C have H has double bond C liquid at room temp oil plant fats
Spinal bifida
Neural tube fails to close at caudal end Not-Lethal Folic acid deficiency normal intelligence walking, GI, Gu issues
Neural Tube Defect (NTD)
MHC
MHC I
MHC II
MHC I is found on all cells
MHC II is found on specialized APC’s
spiral septum
comes down truncus arterious and splits it
forms pulmonary artery
and aorta
Chordin
Growth factor from goosecoid
Primitive streak
Caudal end (tail) Shallow groove
Shows right and left and head and tail
Ductous arterious
hole in pulmonary artery that goes to aorta by-passing pulmonary vessels and ventricles
in fetus
Classical complement pathway is triggered by
antigen/antibody complex on invading cells
IgG and IgM trigger it
Need 2 IgG but only 1 IgM
How deos neurulation happen
Notchcord forms fro mesoderm right after gastrulation
Notchcord signals an inward folding of the ectoderma t the neural plate
Ends of the neural plate fuse and disconnect to form neural tube
(AER) Apical ectodermal ridge
Important for limb growth
FGF’s are secreted by AER
fibroblast growth factors
Caudal cranial establishment
Signals from two regions
anterior visceral endoderm
Goosecoid
Trans fat
result of incomplete hydrogenation
Macrophages / monocytes
become moncytes in blood
no memory
innate
U shaped nucleus
pahgocytosis , anti tumor
APC for T helper cells
Basophils / Mast Cells
Basophil in blood
Mast cell in tissue
lobed
0.2% of leukocytes
immune respone, inflammation
hypersensitivty type 1 (allergies)
histamine release
Syndactyl
Webfoot
Not enough cell death in AER
Dendritic cells
no MHC II
present antigen to B cells
Sacrococcygeal teratoma
Sacral tumor
contains all 3 germ layers
Gastrulation went too long
PITX2
Left sidedness (main)
Carbohydrates
Sugars
contain C H O
Mono-saccharides Di-saccharides Oligo-saccharides Poly-saccharides Starch Glycogen Cellulose
Septum primum
Acts as flutter valve over foramen ovale
One way vlave for blood to flow from
Right atrium to left atrium but not back
naive B cell
After infection Naive be cells switch from expressing IgM and IgD
to expressing
IgA, IgE, IgG
Becomes either a memory cell or effector cell
B cells
from bone marrow
can recognize specific antigens
iGm IGD on surface prior to infection
After, it activates and you have IgA, IgE, IgG
2 types of cells
memory
effector
deamination
amino acid metabolism
removing an amine group and breaking down an amino acid
amine nitrogen is excreted via urea
FGF Fibroblast growth factor
left side limb growth
secreted by primitive node
Dorsal and ventral establishment
Unhibited BMP = Ventral
Inhibited BMP = Dorsal
Gastroschisis
Hole in stomach to right of umbilicus
Intestines protruding
18-22 year old mothers = 90%
Hypersensitivoity types
Type 1,2,3,4
Starch
insoluble polysaccharide
2 types of starch
amylose
amylopectin (plant) (more branches)
Septum Transversum
Starts at 4 weeks
One continuous body cavity begins to seperate
Forms the diaphragm
Forms connective tissue of liver
Alternative complement pathway is triggered by
triggered by LPS on pathogen surface
NKX2.5
Heart development (Main)
IgE
Bind to mast cells and basophils
allergic response
stop parasites
no antigen bound, on mast cells and in tissue
Lipoproteins
mad eof fats and proteins that carry cholesterol through the bloodstream
Chylomicrons
VLDL
LDL
HDL
Gluconeogenysis
pyruvate—
———- NZ ———-pryuvate carboxylase
oxaloacetate—
——————– to cytosol
malate—
oxaloacteate—
———- NZ ———-PEP carboxykinase
PEP—
fructose1,6, bisphosphate—
———- NZ ———-fructose1,6, bisphosphotase
fructose 6 phosphate—
glucose 6 phosphate—
———- NZ ———- glucose 6 phosphotase
free glucose
Lipid metabolism
source of long chain fatty acids
fatty acids may be oxidized to A-CoA
or
esterized to glycerol
TCR 1
Heterodimer of gamma and delta chains
less than 10% of t cells
BMP Bone morphognetic protein
Expresses Dorsal and ventral regions
Growth Factor
Hydrogentaion
adding hydrogen atoms to unsaturated fats to mae them solids
Reduction reaction
Catalyst required (unless at high temps)
Caudal dysgenesis
Mermaid syndrome
When gastrulation stops too soon
Diabetic mothers
AVE anterior Viscerla endoderm
Head forming genes
Cranial region
(ZPA) Zone of polarizing activity
Group of cells near AER
regulates patterning of limb (thumb to pinkie)
Secretion of sonic hedgehog creates a gradient
Macrophages
present antigens to T helper cells
Mono-saccharides
cannot be hydrolysed
Classified by number of carbons i.e Pentose
aldehydes and ketones
xylitol, sorbitol
Control points of Glycolysis
Hexokinase
phosphofructokinase
pyruvate kinase
glycogen synthase
Brachydactyl
Short digits
AER stops working
IgM
produced during primary immune response
enhances phagocytosis
best at activating complement system
immediate antibody produced
Larger, temporary, lasts few weeks
Apert syndrome
FGFR2
underdeveloped midface
Cleft pallate
alwyas includes fusion of middle 3 digits
Lipid transport
Micelles
Lipoproteins
Embryoblast
Comes from morula
inner cells become embryoblast
Becomes embryo
Trace complement classical pathway
Trace complement classical pathway
Pfeiffer syndrome
FGFR 1 or 2
Abnormal shaped head, face, hands, feet, thumbs, big toes
Normal inlligence
T cells
TCR1
TCR2
85-95% of circulating lymphoid cells
recognition of antigens
kill target cells
activate B cells and other immune responses
APC cells
antigen presenting cells
Langerhans cells in skin
Dendritic cells
Macrophages
B cells
Saturated fat
all carbons are bound to Hydrogens no double bond carbons solid at room temp butter animal fats
Parts of antibody
glycoproteins found on b cells or in plasma cells
2 light chains
2 heavy chains
1 fab portion
1 fc portion
disulfide bonds in between
Poly-saccharides
Condensation product of 10 or more monosaccharides
Starches and dextrins
Energy = Starch, glycogen Structural = Cellulose, Chitin
Cellulose
Structural component of plants
Straight long, unbranched chain
froms hydrogen bonds with adjacent chains
Heavy chains
2 heavy chains on antibody
5 types
alpha, gamm, delta, epsilon, mu
Fc portion
Effector portion
Adaptive
slow Specific pathogens take over when innate fails complex response must first be recognized includes memory fro future
IgM vs IgG
IgG = long term, smaller, tighter bond, last longer, always in body
IgM = Larger, temporary, few weeks, replaced by IgG, produced quickly, immediatley
IgA
causes aggregation
first defense for mucaosal surfaces
no antigen bound, in milk, tears and gut
TCR 2
90-95% of t cells
heterodimer of alpha and beta chains
MHC dependant recognition
2 types
CD4 = recognize MHC II
CD8 = recognise MHC I
WNT
Inhibit BMP
Aid in heart development
Thalidomide induced limbe defects
disruption of AER
Polydactyl
Brachydactyl
Split foot
Syndactyl
Amniotic band Syndrome
Amniotic bands wrap around limbs or digits
cause amputations
Node of primitve streak
shallow depression at cranial end of streak
contains transcription signals
Specifically goosecoid
Eosinophils
2-5% of leukocytes
bi lobed
parasytic worms
Polydactyl
Extra digits
Too much AER
HOX genes
development,
pharygeal arches
limb locations
Septum secundum
Becomes the foramen ovale
Hole between right and left atrium
Foramen ovale
prenatal hole in septum between right and left atria
septum secundum is the coverinf that forms the foramen ovale
Septum primum is the base sheet of septum in which the hole is formed,
Spetum primum is the flutter one way valve
Closes shortly after birth due to preaaure in ventricle
Septum primum
Septum in which the hole is actually formed
serves as a one way flutter valve for foramen ovale
Anitbodies
GAMED IgG IgA IgM IgE IgD
IgG
70-75%
involved with complement system
can cross placenta
found throughout body in fluids (blood,lymph)
binds more tightly
Fab portion
anitgen binding portion
Hypoblast
Ventral layer
Eventaully displaced
Cranial-caudal axis
signaling
Hypersensitivity Type 1
IgE
Allergies
Hay fever
quick allergen/inflammatory response
Goosecoid
Formation of head
transcription factor
Hypersensitivity Type 3
Serum sickness
Rheumatoid arthritis
antigen / antibody complexes settle on tissues or organs