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RT-PCR
micro punch specific brain areas, can extract and analyze RNA or proteins. only one gene of interest at a time
RT-PCR studies show inflammatory cytokines in greatest amounts one day post injury
immunohistochemistry
using antibodies conjugated to a fluorescent marker that leads to a color change. used to identify specific cells and the proteins they express
lesions and electrophysiology studies
used to gather information about brain areas in live, intact animals to study behavior
pre limbic cortex (locate)
fear expression, risk-reward decisions, involved in anxiety-like behavior
dentate gyrus (locate)
part of hippocampus. Learning and memory, neurogenesis
reticular substantia nigra (locate)
movement control, dopamine neurons degenerate here in Parkinson’s disease
periaqueductal gray (locate)
descending pain modulation, autonomic function, motivated behavior
dorsal raphe nucleus (locate)
source of serotonin, descending modulation of pain
putamen (locate)
modulates upper motor neurons for descending motor control. degenerates in Huntington’s disease
ventral tegmental area (locate)
regulates dopamine— reward, motivation, addiction
nucleus accumbens (locate)
regulation of motivated behaviors, reward, pleasure, addiction
cryostat
used for sectioning brain tissue
superior
above
inferior
below
anterior
in front of
posterior
behind
dorsal
upper/back
ventral
lower/below
coronal
frontal (hamburger)
saggital
axial (hot dog)
subdivisions of the spinal cord (top to bottom)
cervical
thoracic
lumbar
sacral
coccygeal

frontal lobe

central sulcus

parietal lobe

occipital lobe

temporal lobe
frontal lobe brain regions
primary motor cortex, premotor cortex, prefrontal cortex, Broca’s area
parietal lobe brain regions
primary somatosensory cortex, wernicke’s area
occipital lobe brain regions
primary visual cortex, primary auditory cortex
midbrain
structures include substantia nigra and periaqueductal gray
pons
relay center
medulla
autonomic reflex center
cardiovascular center
respiratory centers
hypothalamus
ANS
sleep/wake
hunger and satiety, body temp
physical response to emotions

pons

medulla

thalamus

midbrain

hypothalamus

corpus callosum

lateral ventricle
thalamus
relay center, gateway to the cortex
lateral ventricle
stores CSF

hippocampus (learning and memory)
corpus callosum
white matter tract that divides the left and right hemispheres
white matter
axons
gray matter
cell bodies

corpus callosum

amygdala

thalamus

lateral ventricle
blood brain barrier function
facilitates what enters the brain— drugs, pathogens, bacteria, viruses
disruptions to the blood brain barrier
can be caused by head trauma, disease, toxins, infection, and stress
result of the blood brain barrier being compromised
infection, inflammation of the brain. unique brain environment would be disrupted, brain factors entering periphery
CSF functions
shock absorption, nourishment, protection, waste removal, brain buoyancy
ventricular system
distributes CSF throughout the brain

dura mater

arachnoid mater

pia mater

chloroid plexus of lateral ventricle
neuronal development (concepts/processes)
cell proliferation, cell migration, cell differentiation, process outgrowth
gastrulation
local invagination of a subset of cells in the very early embryo. once complete, the embryo consists of 3 layers of cells called germ layers (ectoderm, mesoderm, endoderm).
gastrulation defines: midline, anterior-posterior axes, dorsal-ventral axes
notochord
transient structure that forms at the midline of the gastrulating embryo; central event for nervous system development
sends inductive signals to the overlying ectoderm to cause a subset of cells to differentiate into neuralectodermal precursor cells
neurulation
formation of neuralectodermal cells.
neural plate forms as a result of the thickening of neural ectoderm
neural tube later forms as result of neuronal plate infolding— gives rise to brain, spinal cord, and most of PNS
neural plate
forms on the ectoderm above the notochord, develops into neural tube
neural crest
after 20 days, begins to form within the neural plate/tube. after 22 days, cells of neural crest are separate from complete neural tube
neural tube
develops in later stages of neurulation. its roofplate and floorplate send location-dependent signals
neuroectodermal precursor cells/neural stem cells
undifferentiated cells with the capacity to divide to produce more precursor cells, or differentiate into any type of cells found in nervous tissue (i.e. astrocytes, microglia, neurons, etc.)
transient structures in neurulation
notochord, floorplate, roofplate. provide signals to developing neural tube, and disappear once initial nervous system development is complete
neural crest cells
arise from the lateral edges of the neural plate as the neural tube forms, migrate away from neural tube and give rise to a variety of progeny (not CNS; portions of the PNS)
structures derived from neural crest cells
neurons and glia of the sensory and autonomic ganglia (outside CNS)
neurosecretory cells of the adrenal gland
neurons of the enteric nervous system (GI tract)
non-neuronal structures: pigment cells beneath epidermis, cartilage, and bone (particularly face and skull) to support and protect brain
populations of neural crest cells
different migratory patterns
i. cranial
ii. vagal
iii. trunk
iv. sacral
cranial neural crest cells
cranial sensory ganglion, non-neural cells that become the cranial skeleton, thyroid gland, and teeth
vagal neural crest cells
enteric nervous sytem. Vagus nerve connects brain & gut
trunk neural crest cells
dorsal root ganglion
sacral neural crest cells
additional neurons of the enteric nervous system and posterior ganglion of the sympathetic chain
neural stem cell
gives rise to more stem cells, or full range of differentiated cell types in CNS & PNS
neural progenitor cell
can proliferate, but can only generate one class of differentiated progeny.
ES cells
embryonic stem cells, derived from pre-gastrula embryos. Can give rise to all tissues and cell types, proliferate more than neural stem cells and neural progenitor cells
IPSCs
induced pleuripotential stem cells. inducing differentiation of somatic cells with stem cells via transcription factors. regenerative potential for tissue repair
why experiments where neural stem cells are transplanted into the adult brain are unsuccessful
transplanted neural stem cells lack signals for differentiation and migration
formation of major brain subdivision
following formation of the neural tube, beginnings of major brain regions start to appear with bending, folding, and constriction of the neural tube
initial subdivisions of the neural tube into primitive brain regions
prosencephalon— forebrain
mesencephalon— midbrain
rhombencephalon— hindbrain
prosencephalon
telencephalon — cerebral cortex, hippocampus, and basal ganglia
diencephalon— thalamus and hypothalamus; optic cups — retina
mesencephalon
superior and inferior colliculi and midbrain tegmentum (ventral portion, substantia nigra)
rhombencephalon
metencephalon— cerebellum and pons
myelencephalon— medulla
inductive signaling
Molecular signals are secreted by one embryonic cell class and tissue and then diffuse and act on adjacent cell class or tissue (i.e. roofplate, floorplate). graded effects (based on distance from source of signal) and more specific effects
neural induction
gene expression, shape, and motility are changed in target cells after inductive signals bind to their receptors
major inductive signaling pathways in vertebrate embryos
turns on transcription factors for genes in the nucleus. signals can act on intracellular or extracellular receptors to cause a signaling cascade that activates transcription factors
ventricular zone
precursor cells located at the innermost cell layer surrounding the lumen of the neural tube. neural precursor cells undergo mitosis within ventricles, then migrate to cortex.
symmetrical divisions in ventricular zone
generates two neural stem cells
asymmetrical divisions in ventricular zone
generates a neuroblast (becomes a differentiated neuron) and a progenitor
neurogenesis
begins after initial patterning of brain is complete, occurs before birth (precursors disappear after birth, no way to replace lost neurons)
molecular and cellular mechanisms that guide neuronal and glial differentiation
excitatory signals induce cell differentiation
migrating neurons
guided by radial glia
reelin
neurotransmitter that guides radial glial migration. mutation leads to decreased brain tissue, enlarged ventricles from degeneration due to improper migration
lisencephaly (DCX)
enlarged ventricles, smooth brain (less surface area)
developmental disorders
spina bifida, anencephaly. from neural tube defects resulting from folic acid deficiency
retinoic acid
signaling molecule, alters gene expression of SHH leading to birth defects
medullablastoma
neurodevelopment disorder associated with SHH mutation. keeps some cells as precursors while others divide uncontrollably due to lack of SHH-mediated regulation of the Gli1 transcription factor
cell proliferation
stem cells into progenitors or more stem cells