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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

Cytoskeleton Component's

~ Micro filaments (Actin)


~ Intermediate Filaments


~ Microtubules (Tubulin

Function of Microfilaments

Major cytoskeletal element @ synapses


Involved in growth of axons and dendrites during NS development

Function of Intermediate Filaments - Neurofilaments

Prominent in Axons


- Structural role


- No polarity


- No motor proteins

Function of Microtubules

Involved in Transport of molecules, Vesicles and Organelles


~ Unipolar in axons


~ Multipolar in dendrites

Cytoskeleton - Monomers

Globular (G) Actin


Tubulin (a/b)

Cytoskeleton - Polymers

Actin Filaments (F-Actin)


Microtubules



Both dynamic compared to Intermediate Filaments

Microtubule Associated Proteins - MAP's

Tau - Predominantly in Axons


~ binding regulated by phosphorylation


- ~ Hyperphosphorylation = pathogenic role in Alzheimers Disease


MAP2 - Only in Dendrites


MAP4

Motor proteins

Transport cargo along Microtubules and actin filaments


- Kinesis and Dyenins in microtubules


- Myosin in Actin Filaments

Myosin role in Cytoskeleton

Motor proteins in Actin filaments

Kinesins and Dyenins role in cytoskeleton

Motor proteins in Microtubules

Dendritic Spine

Knob-like protrusion from dendrites


Major sites of synapse formation in many neurons

Neurites

Axon/ Dendrite


Grows from cell body



Find targets in response to poitive/ negative guidance cues

Actin role in microfilaments

Synaptic plasticity


Dendritic outgrowth


Axon Guidance

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

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.

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

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.

ATPase powered pump

Protein - Sodium Pottasium ATPase


3na+ out


2k+ in


Generates gradient

Extracellukar/ intracellular ion concentrations

Intra:Extra


Potassium - 140 : 5


Sodium - 5/15 : 145


Chloride- 4/30 : 110


Calcium- .0001: 1-2

Typical membrane resting potential

-70mV

Action Potential

Electrical impulse travels from cell body through to axon


Caused by voltage sensitive Na+ and K+ channels opening and closing briefly