Lecture 2 – CELLULAR ORGANISATION OF THE NERVOUS SYSTEM Flashcards

1
Q

Golgi and the Reticular Theory

A
  • Reduced silver strain that was invented which allowed the staining of entire neurons
  • Golgi believed that neurites were fused together to form a network which we now know is not the case, although this was the beginning of the idea that the brain was linked to a collection of cells
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2
Q

Cajal and the Neuron Doctrine

A
  • Each neuron is a discrete cell known as the neuron doctrine
  • Cajal argued that neurons are not fused together but are distinct cells which communicate by contact
  • Principle of dynamic polarisation – neurons have a preferred direction in which they transmit information
  • Principle of connectional specificity – contact only certain other neurons and even then, only specialised structures on that neuron
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3
Q

The development of the electron microscope

A
  • Human eye resolution: 0.1mm
  • Light microscope resolution: 0.1μm
  • Electron microscope resolution: 0.1nm
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4
Q

cell ultrastructure

A
  • shows how things work

- Confirmed the existence of synapses which was done by EM and gave more details about cells structure

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5
Q

Disadvantages of electron microscopy

A

cells must be fixed/ dead so cannot see any movement and its very difficult to see individual molecules

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6
Q

development of fluorescence labelling methods

A
  • determines protein distribution in cell as it absorbs one light and emits enough due to ligand tags
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7
Q

disadvantages of fluorescence labelling methods

A
  • limited by range of antibodies available as very specific to protein of interest
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8
Q

Development of confocal microscopes

A
  • include lasers, high sensitivity cameras and imaging software which can examine live cells and the physiology
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9
Q

disadvantages of confocal microscopes

A
  • modest resolution of 0.1μm
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10
Q

Neurons

A
  • neuron stained with MAP-2 and is red and is an individual cell
  • nervous system has not internal connect tissue for support
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11
Q

Glia

A
  • Outnumber neurons in some brain regions
  • 17:1 in the thalamus – predominant cell type in some areas of the brain
  • 1:1 in the cerebral cortex
  • may mediate some signalling in the brain
  • primary role is to support neurons – physically and physiologically important
  • can divide which neurons can’t do
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12
Q

Glia – astrocytes

A
  • majority of glia
  • star-shaped cells
  • fill space between neurons – need tissue for support of neurons
  • regulate composition of extracellular fluid – contains ions
  • new research shows that astrocytes can play an important role in directing the proliferation and differentiation of neural stem cells
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13
Q

Oligodendrocytes/ Schwann Cells

A
  1. myelinated axons of neurons
  2. Oligodendrocytes is the CNS with many axons
  3. Schwann cells are in the PNS with a single axon and form a sheath to insulate it (both) and if removed will not be able to function properly
  4. Diagram in black in white is myelinated optic nerve fibres
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14
Q

Microglia

A
  • act as the brain scavengers:
    1. Phagocytic/ immune function
    2. They can migrate and are very diverse
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15
Q

Ependymal cells

A
  1. Line ventricles – fluid filled spaces
  2. Direct migration during the development of the brain
  3. Type of glia
  4. Have cilia and structure looks a bit like epithelial cells
    Important role in production of CSF
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16
Q

The Prototypical Neuron

A
  • beginnings of polarity in epithelial cells which have specialised functions
  • Cilia are specialised so only need to be on one end of the cell
  • Neurons have several specialised structures: cell body, dendrites and axons
17
Q

Neuronal Structure:

A
  1. Common with all cells:
    - Cell body with cytosol and organelles including a nucleus
    - Cell membrane (plasma lemma)
  2. Unique to neuronal cells:
    - Cannot reproduce
    - Can trigger action potentials
  3. Cytosolic organelles: stay in cytoplasm
    - Peroxisomes
    - Mitochondria
    - Ribosomes
    - Vacuolar apparatus (secretory pathway/ endocytic pathway) which includes the ER, secretory vesicles, Golgi complex, endosomes, lysosomes
  4. Division at axon hillock includes the synaptic vesicles, mitochondria and smooth ER
18
Q

dendrites

A
  • Ca 2+ channels
  • Ligand-gated ion channels (Glutamate receptors)
  • G-Protein coupled receptors
  • MAP2 staining makes nuclei blue and the dendrites green
19
Q

Axon

A
  • G-Protein coupled receptors (terminals)
  • Ca2+ channel terminals
  • Na+ and K+ channels (axon shafts)
  • MAP2 staining makes the axon terminals orange
20
Q

How does the polar structure of neurons arise?

A
  1. Targeting of components to axons or dendrites
  2. Neuronal cytoskeleton
    - Structural support – shape and calibre of axons and dendrites
    - Transport cargo to and from axons and dendrites
    - Tethering of components at membrane surface
21
Q

Microtubules

A
  • Run along longitudinally down axons and dendrites
  • Big, 20nm wide and tubulin polymers
  • Polymerisation/depolymerisation changing the shape
  • Microtubule associated proteins (MAP2 and Tau)
  • Role: structural and transport
  • Kinesin (motor protein) that moves cargo enclosed in vesicles down the microtubule towards the axon terminal and Dynein which moves stuff back from the terminal to the cell body
22
Q

Neuro-filaments

A
  • 10nm wide
  • Filamentous protein threads
  • Role: Mechanical strength
23
Q

Microfilaments

A
  • 5nm wide
  • Actin polymers
  • Tethered to membrane
  • Role: mediate shape change
24
Q

distinct populations of neurons with different shapes

A

UNIPOLAR, BIPOLAR AND MULTIPOLAR

25
Q

neuronal classification

A
  • Sensory (afferent; somatic or visceral) neurons originate from sensory receptors to the processor
  • Motor (efferent; somatic and visceral) neurons conduct signals that originated in the CNS
  • Interneurons are between sensory and motor neurons
  • Can also be divided by a functional level – diversity of neurons in hippocampus
26
Q

Alzheimer’s

A

green is viable/ live cells, red are dead cells

27
Q

SUMMARY

A
  1. Golgi and Cajal together revealed neuronal structures
  2. Glia are the non-excitable cells of the CNS and the support neurons
  3. Neurons are very polarised and their structure reflects this
    The cytoskeleton is made of different structural elements – problems can lead to disease