the Golgi staining technique is also known as reduced silver stain
reticular theory focused on random individual cells in detail
the principle of the neuron doctrine is each neuron is a discrete cell
the principle of dynamic polarization in neurons is that they transmit information in a particular direction
connections between neurons are organized and not random
the development of the electron microscope confirmed canals theory of separate neurons
electron microscopes examine cells ultrastructure
the electron microscope confirmed the existence of synapses
cells have to be dead is being used for the electron microscope
immunofluorescence labelling is used to prepare selective antibodies for a drug tagged with a fluorescent label and add them to target specific proteins
confocal microscopy can be used on living cells
rainbow gene modification can be used to genetically modify an animal to produce fluorescent dyes
there are around 10 different colours that can be made by genetically modified animals
the glial cells come from the neural tube and neural crest
glial cells support the neurons
glial cells can divide
Ependymal cells, oligodendrocytes, satellite cells, astrocytes, microglia, Schwann cells are all glial cells
in the thalamus glial cells outnumber neurons
the most abundant glial cell in the brain is astrocytes
astrocytes main function is to fill the pace between neurons and to regulate extracellular fluid compositions
in neural stem cells, astrocytes direct the proliferation and differentiation
oligodendrocytes myelinate axons of neurons in the CNS
oligodendrocytes are found in the CNS and have many axons
Schwann cells myelinate axons in the PNS
Schwann cells are found in the PNS and have a single axon
microglia act as brain scavengers and remove dead cells
microglia and ependymal cells migrate
ependymal cells line ventricles and direct cell migration during brain development
ependymal cells produce CSF
HD is an autosomal dominant disorder caused by genetic abnormality in the Huntingtin gene
HD is caused by the huntingtin gene coding a repeated sequence of glutamine residues, with greater than 40 leading to certainty of developing HD.
symptoms of HD are jerky movements due to effect on the basal ganglia
the huntingtin gene is not broken down correctly leading to accumulation in neurons as inclusion bodies, eventually causing cell death
other cells effected by HD are Astrocytes and microglia, leading to neuroinflammation
Amyloid plaques and tau protein are the two main proteins involved in AD
when the tau protein becomes heavily phosphorylated in AD it clumps to form neurofibrillary tangles inside the neuron, disrupting normal movement of cargo and can cause neuron death
astrocytes and glial cell in AD become active and induce neuroinflammation