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22 Cards in this Set
- Front
- Back
Key characteristics of neurons |
Morphology- - Axons and Dendrites - Connections - Synapses Electrical properties - Action Potential Post mitotic - Can't undergo cell division |
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Cytoskeleton Component's |
~ Micro filaments (Actin) ~ Intermediate Filaments ~ Microtubules (Tubulin |
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Function of Microfilaments |
Major cytoskeletal element @ synapses Involved in growth of axons and dendrites during NS development |
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Function of Intermediate Filaments - Neurofilaments |
Prominent in Axons - Structural role - No polarity - No motor proteins |
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Function of Microtubules |
Involved in Transport of molecules, Vesicles and Organelles ~ Unipolar in axons ~ Multipolar in dendrites |
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Cytoskeleton - Monomers |
Globular (G) Actin Tubulin (a/b) |
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Cytoskeleton - Polymers |
Actin Filaments (F-Actin) Microtubules Both dynamic compared to Intermediate Filaments |
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Microtubule Associated Proteins - MAP's |
Tau - Predominantly in Axons ~ binding regulated by phosphorylation - ~ Hyperphosphorylation = pathogenic role in Alzheimers Disease MAP2 - Only in Dendrites MAP4 |
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Motor proteins |
Transport cargo along Microtubules and actin filaments - Kinesis and Dyenins in microtubules - Myosin in Actin Filaments |
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Myosin role in Cytoskeleton |
Motor proteins in Actin filaments |
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Kinesins and Dyenins role in cytoskeleton |
Motor proteins in Microtubules |
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Dendritic Spine |
Knob-like protrusion from dendrites Major sites of synapse formation in many neurons |
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Neurites |
Axon/ Dendrite Grows from cell body Find targets in response to poitive/ negative guidance cues |
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Actin role in microfilaments |
Synaptic plasticity Dendritic outgrowth Axon Guidance |
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Molecules that guide axons and migrating cells during brain development |
Receptors- transmembrane Soluble and/or membrane bound ligand - produced by other neurons/ neuroglia Attractive and repulsive Signals Signals usually transmitted to actin or microtubule based cytoskeleton - actin via Rho family via GTPases |
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Defects in axon guidance |
Horizontal gaze palsy w/ Progressive scoliosis ~ V.rare autosomal recessive disorder caused by mutations in Robo3 axons in the pons and medulla ~ Abnormal decussation (midline disorder) of axons in pons and medulla Congenital fibrosis of the extraocular muscles (Type 1) ~ Caused by mutations in KIF21A - coding for a kinesin Microtubules motor proteins ~ Bilateral blepharoptosis (drooping eyelids) and strabismus, - - absence of fusion and binocular vision. - - The eyes look down at rest, and cannot be elevated - - Variable horizontal movement. |
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Horizontal gaze palsy w/ Progressive scoliosis |
Horizontal gaze palsy w/ Progressive scoliosis ~ V.rare autosomal recessive disorder caused by mutations in Robo3 axons in the pons and medulla ~ Abnormal decussation (midline disorder) of axons in pons and medulla |
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Congenital fibrosis of the extraocular muscles (Type 1) |
Congenital fibrosis of the extraocular muscles (Type 1) ~ Caused by mutations in KIF21A - coding for a kinesin Microtubules motor proteins ~ Bilateral blepharoptosis (drooping eyelids) and strabismus, - - absence of fusion and binocular vision. - - The eyes look down at rest, and cannot be elevated - - Variable horizontal movement. |
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ATPase powered pump |
Protein - Sodium Pottasium ATPase 3na+ out 2k+ in Generates gradient |
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Extracellukar/ intracellular ion concentrations |
Intra:Extra Potassium - 140 : 5 Sodium - 5/15 : 145 Chloride- 4/30 : 110 Calcium- .0001: 1-2 |
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Typical membrane resting potential |
-70mV |
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Action Potential |
Electrical impulse travels from cell body through to axon Caused by voltage sensitive Na+ and K+ channels opening and closing briefly |