neuron migration and motility Flashcards
types of neuron migration
gliophilic migration
neurophilic migration
biphilic migration
radial migration
gliophilic migration
radiate away from centre where they were born
tangential migration
neurophilic migration
follow contours of cortex, and run parallel to them
ex of neurons using neurophillic migration
interneurons emerging from the medial ganglionic eminence
granule cells of the cerebellum - development
embryonic
- GCs originate at rhombic lip and migrate to proliferative zone
- frist vision of GC near suffice membrane
- become bipolar by extending horizontal processes along parallel fibres of other GCs (neurophilic migration)
postnatal
- bipolar neurophilic extension continues
- become bipolar and migrate inwards from PZ
- vertical process attaches onto shaft of Bergman glia (gliophilic migration)
- once vertical process sufficient length the nucleus migrates through its own nerve shaft
- successive generations guided by same BG
what mechanism allows granule cells to have neurophilic and gliophilic migration
certain populations of cell adhesion molecule (NCAM-PSA) binding to glia and neurite changing over time
Weaver mice
natural mutation - ataxia, uneven gait
abnormal granule cell migration - can’t bind to Bergman glia
radial units
groups cells in ventricular PZ, coupled by gap junctions
come from same area and use same radial glial cells to reach cortex
if environmental insult early one, some columns may die off
if environmental insult later time point, cells may be prevented from migrating
lissencephaly
early defects when proliferating units are forming proliferating zone (first 7 weeks gestation)
number columns greatly reduced, normal number of cells in each
polymicrogyria
much thinner cortex
normal number of columns but much less neurons in each
defect after number of units formed - after first 7 weeks gestations
defect in neuron migration
microtubules support bidirectional transport
2 organelles pass each other going opposite directions - separate tracks on single MT
kinesin supports anterograde forward movement
dynein mediates retrograde movement
these molecules can be on same track and pass each other
how is retrograde flow of actin driven
1) coupled to ATP
actin flow due to high energy phosphates. F actin depoolymersises and becomes G actin, has ADP attached which will be phosphorylated to ATP. Globular actin with ATP comes into contact with barbed end , phosphate is released
2) coupled ot myosin I
myosin molecules attaches to sub membranous structure, requiring ATP. ATP –> ADP and energy drives the power stroke up to left. Lots of myosin molecules doing this contributes to retrograde flow
forward movement of actin
actin filament driven backwards by myosin attached to submembranous matrix
talin bound to integrin, which binds to ECM substrate
actin binds to talin and is now stationary due to rigid mechanical interaction with external substrate via integrin/talin complex
myosin and sub membranous matrix must not move forward
“molecular clutch”