2 major nerve cell types
neurons and glia
neuron function
transmit information (electrical/chemical) over long distances
glia function
provide physical support to neurons, maintain CNS, environment, transmit information, and provide immune function
Nissil stain
stains Nissil bodies; general look of neuron; less detailed; tells if cell is alive or dead
Golgi stain
more detailed; stains entire neuron but not all neurons
T or F: you can study an unstained brain
false
T or F: Both Nissil and golgi stains are used for visualizing neuronal structures
true
Neuron doctrine
concept that the nervous system is made up of discrete individual cells
who coined the term neuron and came up with neuron doctrine?
Waldeyer-Hartz
was the neuron doctrine fully validated after being named by Waldeyer-Hartz in 1891?
no the neuron doctrine wasn’t fully validated until 1955 when the synapse was captured on electron microscope
cell body
most prominent part of the neuron
what does the cell body of a neuron contain?
nucleus (surrounded by nuclear membrane
Specialized structures called organelles
Other names for the cell body
soma, perikaryon
organelles to know
cell membrane
cytoplasm
mitochondrion
nucleus
ribosome
endoplasmic reticulum
golgi apparatus
cell membrane function
protects the cell
cytoplasm function
cell buffer
mitochondrion function
generates energy (ATP), involved in signaling, cellular differntiation, cell death, maintain control of cell cycle/cellular growth
nucleus function
contains genetic material
rough endoplasmic reticulum function
makes proteins
smooth endoplasmic reticulum function
makes lipids, folds proteins, regulates calcium
golgi apparatus function
modifies, packages, and transports lipids and proteins
which organelles are not present throughout the entire neuron?
nucleus and rough endoplasmic reticulum
T or F: mitochondria are found throughout the entire neuron
true
where are mitochondria concentrated?
in pre and post synaptic neuron
T or F: each neuron contains the same genetic code, but uses the genetic code differently to make different proteins
true
nucleotide
molecule consisting of a nitrogen-containing base, a phosphate group, and a sugar that forms the basic structural unit of a nucleic acid
genes
segment of DNA that codes for the manufacture of a specific protein
DNA
molecule that carries genetic instructions for the development and functioning of all organisms and some viruses
chromosomes
long strands of DNA
transcription steps
RNA polymerase, with the help of transcription factors, binds to a specific sequence within a gene (the promoter) and splits the two strands of DNA apart
One strand is the template strand that RNA polymerase moves down to synthesize mRNA
Once RNA polymerase reaches the end of the gene termination occurs. This is when the enzyme detaches from the gene and the DNA is returned to its original state.
mRNA leaves the nucleus of the cell and moves into the cytoplasm where it will find a free ribosome.
exons
coding regions on pre-mRNA
introns
noncoding regions on pre-mRNA; cut out of the RNA strand during splicing after transcription has occurred
T or F: introns are included in mRNA
false
T or F: 1 section of a gene can make a variety of different proteins by splicing exons together differently
true
different types of ribosomes
attached
detached
poly
steps of translation
mRNA codon (3 nucleotides) will pair with a specific transfer RNA (tRNA) anticodon
Each tRNA anticodon is linked to an amino acid
As the process continues down the mRNA, ribosomes link the amino acids together forming a polypeptide chain
Once completed the polypeptide chain folds into a protein and exits the ribosome (or the polypeptide chain can exit the ribosome and then fold into a protein)
T or F: Proteins can be made of one or more polypeptides
true
protein folding after translation
this process involves four stages (primary, secondary, tertiary and quaternary structure) that gives rise to various 3D protein structures
amino acid sequence accounts for diff conformations
T or F: Some neurological impairments arise as a result of protein production problems or protein misfolding
true
T or F: smooth ER is not found throughout all parts of the neuron
false
neurons contain _____ amounts of endoplasmic reticulum
large
where is rough ER found in neurons?
mostly cell body and dendrites (little to no amount in axons)
cytoskeleton function
gives a neuron its characteristic shape
what 3 structures make up the cytoskeleton (in order of size largest to smallest)
microtubules
neurofilaments
microfilaments
protein that makes up microtubules
tubulin
microtubule associated proteins (MAPs)
proteins that interact with tubulin and microtubules to regulate their function and transport cargo; anchor neurons to one another and other parts of the neuron
microtubules are involved in ______-range axoplasmic transport
long
T or F: microtubules are not static and can change (lengthen/shorten) as the neuron changes
true
MAP protein Tau
when Tau becomes misfolded this leads to Alzheimers disease. Misfolded Tau causes breakdown of microtubules and eventually axon/neuron death
neurofilament protein
intermediate filament
neurofilament function
important for structure, shape, space filling (fill axons which increases connections/communication between neurons. increased filling also increases axon diameter and this leads to faster signaling)
neurofilaments move _________ along microtubules
bidirectionally
another name for neurofilaments
intermediate filaments
T or F: neurotubules have tracks for transport
false
another name for microfilaments
actin filaments
microfilament protein
actin
T or F: microfilaments are not static and can change (lengthen/shorten) as the neuron changes
true
microfilaments are involved in ______-range axoplasmic transport
short
____ is one of the most abundant proteins in cells of all types and plays a role in changing ____ shape (usually muscle contraction)
Actin; cell
T or F: microtubules extend all the way to the axon terminal
false
dendrites
projections that receive chemical signals (neurotransmitters) from other nerve cells
axon
slender projection that conducts the action potential
how many axons are there per neuron? how long is an axon?
1; long
how many dendrites are there per neuron? how long is a dendrite?
many; short
2 types of neurites
dendrites
axons
axon hillock
portion of the axon adjacent to the cell body that generates the action potential
axon collaterals
axons that split into numerous branches (how signal travels to other neurons)
axon varicosities
swellings that release NT along length of an axon
axon terminal
small enlargement at the end of an axon that stores and releases neurotransmitter
T or F: axons and dendrites are continuous (connected)
false
Wallerian degeneration
an active process of degeneration that results when a nerve fiber is cut which causes death to an axon distal to the injury
what kind of axons did Wallerian damage
frog axons
retrograde degeneration
injury occurs close to the cell body; neuron dies because damage moves backwards from site on injury to the soma
anterograde regeneration
injury occurs close to the axon terminal; neuron can regenerate because damage moves forwards from site of injury away from the soma
which MAP is responsible for anterograde transport?
MAP Kinesin
which MAP is responsible for retrograde transport?
MAP Dynein
anterograde transport
newly synthesized proteins are packaged in the soma and transported toward the axon terminal
retrograde transport
vesicles, organelles, and signaling molecules are carried from the axon terminal to the cell body for recycling
what uses slow axoplasmic transport?
cytosolic and cytoskeletal proteins
T or F: slow axoplasmic transport gets its name because the speed/rate of transport is slower than fast axoplasmic transport
F: slow axoplasmic transport runs at the same speed/rate as fast axonal transport but it makes more stops
what uses fast axoplasmic transport?
synaptic vesicles, membranous organelles, and proteins
synapse (synaptic cleft)?
the space between two signaling cells (presynaptic and postsynaptic)
synaptic transmission is mediated _______
chemically
where do many drugs act?
at the synapse
malfunctions at the ________ are responsible for many mental disorders
synapse
unipolar
one nerve process that extends from the cell body (axon that extends into dendrites, sensory ganglia, and dorsal root ganglia)
bipolar
two structures extending from the cell body (ex: retina, olfactory bulb)
multipolar
many dendrites; single axon (most neurons are this type)
how can neurons be classified?
number of neurites (unipolar, bipolar, multipolar)
shape of dendritic tree
connectivity (sensory, motor, interneurons)
axon length (golgi type I and II)
neurotransmitters released
gene expression
shape of dendritic tree
pyramidal cells (all spiny); most cells are this
stellate cells (some spiny, some aspinous)
sensory neurons
gather information from the sensory receptors and carry that information to the brain
interneurons
small neurons that connect other neurons to each other CNS
motor neurons
receive information from the brain and carries signals to muscles
golgi type 1 (projection neurons)
long axons; extend between brain regions, mostly pyramidal cells
golgi type 2 (local circuit neurons)
short axons; connect to neurons in vicinity; mostly stellate cells
neurotransmitter types
acetylcholine
glutamate
GABA
serotonin
dopamine
opioids
peptides
gene expression to classify neurons
can use RNA sequencing to identify genes expressed in certain neuron populations; neurons have their own specific combo of genes
neuroglia function
support neuron functioning, have signaling capabilities, supports synapse formation, and some can function as stem cells
neuroglia types
astrocytes
oligodendrocytes
schwann cells
microglia
radial glia & ependymal cells
2 most abundant neuroglia
astrocytes and oligodendrocytes