Lecture 2- Neurons and glia Flashcards

1
Q

What is the role of neurons?

A

• Neuron is a key cell • 10 to the 11 neurons in human central nervous system •Neurons responsible for all “interesting phenomena? • Consciousness, self awareness, memory, emotion,planning • Control skeletal muscle, viscera and glands • Provide sensory input

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2
Q

What do glia mainly do?

A

-support neurons

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3
Q

What are some ways in which we can classify neurons?

A
  • by function (excitatory vs inhibitory) - by neurotransmitter (gluatamate, GABA, cholinergic etc.) - by projection (projection neurons vs interneurons) -by shape (basket cells, chandelier cells) -by system (motor, sensory, autonomic) -all are valid approaches and there are many more ways of classifying neurons
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4
Q

What are the classes of neurons and the associated neurotransmitters?

A
  1. Cholinergic (Acetylcholine) 2. Glutamatergic etc. (Glutamate, GABA etc.) 3. Noradrenergic etc. (Noradrenaline, 5-HT etc.) 4. Peptidergic (Endorphins, SP, etc.) 5. Purinergic (ATP and adenosine)
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5
Q

What is neuronal morphology like?

A

-very variable -dendrites= inputs -axon= outputs -cell body is the energy powerhouse supplying the rest of the neuron -variety of standard shapes -morphologically highly specialised

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6
Q

What is a neuron?

A
  • a protein producing cell - uses specialised proteins for all sorts of things - larger nucleus than most other cells as their DNA is unwrapped and accessible (Nissl bodies= rough ER, and free ribosomoes= these are so big that they actually stain!) -proteins are required for ion channels, receptors and the cytoskeleton
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7
Q

What is the importance of the cell membrane in a neuron?

A

-neuronal cell membrane is specialised for electrical activity -all cells have some sort of e difference across their membranes but neurons put theirs to work -the membrane can carry graded potentials and action potentials -requires energy expenditure to set up and maintain potential differences (ATPases drive ion flux)

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8
Q

What is a graded potential?

A

-passive electrotonic spread of current = local signal

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9
Q

What is an action potential?

A

-propagates long distances and requires specialised voltage-sensitive ion channels

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10
Q

What are the characteristics of dendrites?

A

-increase surface area for synaptic input -up to 10 000 inputs on a large neuron -lack major organelles -they increase the surface area of the membrane, means of harvesting information = the more surface area= the more info it can receive -in brain lot of neurons will have 10s of inputs -they lack features, it is the membrane that is important

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11
Q

What are the characteristics of an axon?

A

-over a metre long -carries AP -AP can be generated in cell body (axon hillock) or at tip of axon (for sensory neurons= dorsal root ganglia)

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12
Q

What is the volume distribution of neural components in a neuron?

A

-high proportion of total cell volume is in axons and dendrites -random damage often involves axon not the cell body -20 um diameter of the cell body and 30cm axon

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13
Q

How are neurons packed in the CNS?

A

-incredibly tightly, like a pack of tangled spaghetti

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14
Q

What does the shape of a neuron depend on?

A
  • the complex shape depends on cytoskeleton
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15
Q

What are the 3 main components of the cytoskeleton?

A
  • actin - intermediate filaments - microtubules - same classes of components as in any cell but neurons made it a crucial and specific part of the cell
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16
Q

What are the characteristics of actin?

A

-dynamic assembly/ disassembly allows shape changes and movement (e.g. spines and growth cones) -actin forms filaments from globular subfilaments and can disassemble just as quickly -the little bump on left= spines= input (excitatory) -actin forms growth cone= the growth cone can go on its own, axons are pulled by it to grow -grows spines even in the space of hours

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17
Q

What are the characteristics of microtubules?

A

-dynamic (rapid assembly/disassembly) -made of protein tubulin -have microtubule associated proteins (MAPs) -used for shifting things, like a railway

18
Q

What are the characteristics of intermediate filaments?

A

-permanent (much more), not dynamic protein filaments -neurofilaments are the major type present in neurons -in all processes -play a crucial role in establishing the basic shape of the cell

19
Q

How does axon transport work?

A

-have a long axon that needs nutrients etc. from the cell body so need a way of transporting these -microtubules are basis for axoplasmic transport -transports material from cell body to axon and dendrites and vice versa -moves membrane bound components by fast transport (400mm (40cm)/day)) and soluble material by slow transport (4mm/day) -fast transport is microtubule dependent and uses kinesin

20
Q

What is the retrograde axonal transport?

A

-have to get the material back from the axon to the cell body fro recycling etc. -damaged organelles brought back to cell body for recycling by retrograde axonal transport -samples of the local environment also brought back -some viruses (herpes, chicken pox) and bacteria (tetanus) exploit the retrograde transport

21
Q

What are the characteristics of the axon terminal?

A

-the axon terminal is where a signal passes from neuron to the target cell -the point of transmission is a specialised structure, the synapse -the information that the cell body is generating can be passed on= this is happening at the end of the axons -when AP reaches the terminal it starts a mechanism by which the information is passed on -via the synapse

22
Q

What are the possible target cells for neurons?

A

-the target cell can be another neuron or an effector cell (muscle or secretory cell) -targets are a variety of cells -neuro-neuronal synapse/ neuromuscular synapse

23
Q

What does a synapse (EM view, axo-dendritic) look like?

A

-the synaptic cleft is about 20nm

24
Q

What are the characteristics of synaptic vesicles and the synaptic density?

A
  • vesicles contain neurotransmitter
  • the presynaptic density contains the elements necessary to dock and exocytose the vesicle
  • the postsynaptic density contains receptors that respond to the neurotransmitter
  • mainly supplied by axonal transport
  • the binding of the neurotransmitter to receptor gets the response
25
Q

How does initiation of neurotransmitter release happen?

A

-vesicle exocytosis is Ca2+ dependent -voltage gated Ca2+ channels in the terminal open when an AP invades -AP triggers a Ca2+ spike -the activity of a neuron is mostly electrical but at the synaptic cleft it is chemical

26
Q

How does the termination of neurotransmitter action happen?

A

-the signal as brief as possible= so do not have to wait until you can transmit again -can speed things up by having enzymes or by having a re-uptake system and recycle (so you are faster than diffusion) -neurotransmitter diffuses almost instantly to the post-synaptic membrane -the post-synaptic effect is limited by: the diffusion of transmitter out of the cleft; destruction of transmitter by specialised enzymes; re-uptake of the neurotransmitter by the axon, target cell or glial cell

27
Q

What is the neuronal energy budget?

A
  • energy budget for rat cerebral cortex:
  • dominated by information transfer processes, synapses most important
  • can differ between neurons
  • need energy constantly, that is why you get brain damage if you don’t breathe even for a few minutes
  • budget of a neural cell, housekeeping is only a 1/4 of the energy, which is less than in other cells
  • very demanding energetically
28
Q

What are the brain metabolic demands?

A

-brain is only 2% of total body mass and consumes 20% of oxygen and 25% of glucose -very sensitive to loss of blood flow (O2 and glucose) as few energy reserves -glucose obligatory brain energy substrate (newborn can use ketone bodies) -can burn lactate or pyruvate (and some other metabolic intermediates) but these don’t cross blood brain barrier well -brain can only use glucose but neurons are bad at metabolising glucose so the glial cells convert it into lactate and pyruvate which the neurons metabolise well

29
Q

What is meant by activity-dependent vasodilation in CNS?

A

-local activity in CNS leads to local increase in blood flow (increases glucose and O2 availability) = to support the active neuron/s -basis for fMRI and PET functional imaging -MRI detects changes in local oxyhaemoglobin seen as Blood Oxygen Level Dependant (BOLD) signal

30
Q

What are the 3 types of CNS glial cells and their general functions?

A
  1. Astrocytes: help neurons survive, provide structural and metabolic support, take up excess K+ 2. Oligodendrocytes: insulate axons (myelination) 3. Microglia: defence cells
31
Q

What are the 2 types of glial cells in the PNS?

A

-Schwann cells (myelination) and satellite cells (similar to astrocytes in their function)

32
Q

What are the characteristics of astrocytes?

A

-have many processes -some processes associated with blood vessels (astrocyte end feet), others with dendrites and synapses -individual astrocytes occupy non-overlapping territories, connected by gap junctions -aways around a blood vessels around the synapse the glial cells wrap around it -so synapse it a 3 part structure -it doesn’t work if astrocyte is not there -astrocytes have territories, 1-1 no overlap -fill out the brain -most of the brain is the astrocyte processes

33
Q

What are the roles of astrocytes?

A

-revolution in understanding their roles as of late -multiple roles in supporting neurons and synapses -involved in: -blood vessel dilation in areas of neuronal activity -neuronal energy supply -synaptic plasticity -neurotransmitter recycling - K+ homeostasis -water homeostasis - oxidative stress protection - injury response and recovery

34
Q

What is the role of astrocytes in blood vessel dilation?

A

-astrocytes link synaptic activity to increased blood flow -exact messenger is still controversial -caged calcium release in astrocytic end feet leads to vasodilation -EET (epieicosatrienic acid= arachadonic acid metabolite)

35
Q

What is the role of astrocytes in neuronal energy supply?

A

-neurons happy to metabolise lactate -astrocytes generate lactate from glucose via glycolytic pathway (glycolytic pathway surpressed in neurons) -lactate appears in extracellular space, stimulated by glutamate -neurons have a very low ability to metabolise glucose, the main energy supply of the brain

36
Q

What are the glial cells in the periphery?

A

-satellite cells support nerve cell bodies in peripheral ganglia (collections of neurons outside the CNS) -Schwann cells support axons in peripheral nerves

37
Q

What are nerves?

A

-axons bundle together to form nerves -nerves exist outside the CNS -contain Schwann cells as well as axons -wrapped in connective tissues

38
Q

What are the characteristics of myelination?

A

-oligodendrocytes and some Schwann cells are responsible for myelinating axons in CNS and PNS -speeds up conduction (as does axonal diameter) -one axon per Schwann cell, many axons per oligodendrocyte -AP velocity is proportional to axonal diameter -myelination is another way of increasing conduction velocity -myelination involves a glial cell -a glial cell (oligodendrocyte or Schwann cell) wraps around axon and lays down myelin in the glial cell membrane -the yellow is the wrapping -wrap in the cell membrane (oligo or Schwann cell layer)

39
Q

What are the Nodes of Ranvier?

A

-oligodendrocytes or Schwann cells myelinate successive lengths of an axon -leave a gap= Node of Ranvier

40
Q

What are the characteristics of the Microglia?

A

-CNS is immune privileged -microglia are local defence cells from bone marrow -5-20% of cells in mouse brains -resemble macrophages (phagocytic) -activated by inflammation, injury= upregulate cytokines/growth factors -may play a role in development and disease (lack of microglia alters mouse behaviour)

41
Q

What is the cerebrospinal fluid?

A

-extracellular fluid of brain different to body -CSF low in K+, Ca2+, little protein

42
Q

What is the blood brain barrier?

A

-brain and spinal cord walled off from rest of body by blood brain barrier -BBB at level of capillaries -prevent free diffusion of most blood-born substance into brain -lipophilic substances penetrate easily by diffusion (etoh, nicotine, heroin) -most other entry by active transport