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Dorsal Lateral Geniculate Nucleus
                &
     Parallel Processing

    GS Shrestha, M.Optom, FIACLE
               Lecturer
Introduction
•   The most significance
    – Number of optic nerve fibres project to the
      Lateral Geniculate Nucleus (LGN) in the
      Thalamus
     • Relay to the form vision
    – From LGN, the visual pathway proceeds to
      the primary visual cortex, V1
     • Complex processing of visual signals
    – Visual processing and object recognition is
      enhanced by more than 30 extrastriate
      cortical areas
Targets of the retinal projection
               Retinal ganglion cell axons

Major                                                  Minor

                                   •Several small
                                   hypothalamic nuclei
                                      •Suprachiasmatic , supra
                                      optic, paraventricular
                                      nuclei

                                   •Accessory optic system
                                      •Nucleus of optic tract
                                      •Dorsal, medial and
                                      terminal nuclei
dLGN
90%    retinal ganglion cells project to
 dLGN
Is   Laminated and shows Retinotopic
 Organization
Each   layer receives input from a specific
 eye and class of ganglion cell
Superior Colliculus
A   midbrain structure conjunction with cortical frontal
  eye fields and the brain stem reticular formation
 Is laminated and retinotopically organized nucleus.
 Visually guided saccadic eye movements
 Retinal projection segregates with alternating
  columns of left and right eye terminals.
 10% of all retinal ganglion cells project to the SC
 Are small caliber originate from ganglion cells with
  small dendritic fields and do not project to other
  retinal targets
The Pretectum
A   group of small midbrain nuceui is just rostral to the
  SC
 Receives    signals from a group of small diamter
  retinal ganglion cells with large receptive fields
 Involve   with the control of the pupillary light
  reflex by means of a projection to the Edinger-
  Westphal nucleus of oculomotor complex.
 Show   consensual response
The Pulvinar nucleus
 Largest  nucleus mass
 Receive projections from the small caliber fibres
  from the optic nerve and the SC
 It projects to several visual cortical area
  including V1 and extrastriate, parietal areas
 Represents second pathway that can bypass
  the LGN to get the visual V1 and may plays a
  role in processing from vision
 Code importance of visual stimuli-silence or
  attention
  ◦ Eg, the eye hand co-ordination
Hypothalamic nucleus
Receives   direct sparse retinal
 projection that leave the dosal surface
 of the optic chiasma and has been
 implicated in the synchronization of
 circadian rhythms
The paraventricular and supraoptic
nuclei
Involve with the regulation of the light
 dark cycle for neuroendrocrine
 functions
The Accessory optic systems
The  lateral terminal nucleus
The medial terminal nucleus,
the dorsal terminal nucleus
NOT in the mid brain


Important   role in optokinetic
 nystagmus in viewing with prolong
 large field motion
Overview of dLGN
Key gateway to visual signals
 entering the cortex
Less agreement in role of vision
 ◦ Receptive field properties of dLGN cells=
   retinal ganglion cell input
Regulate  the flow and strength of
 visual signals sent to cortex
Structural organization
Layers   2,3,5 receives input from Ipsilateral eye
                                    Ipsi
Layers   1,4,6 receives input from Contralateral eye
                                    Contra
Dorsal    four layers-small neurons-P
                layers
 cells=Parvocellular layer (midget cells)
Ventral   two layers-Large neurons M
 cells=magnocellylar layers (parasol cells)
Between    P and M cells=very small bistratified cells-
 konio cells
Combination    of all these layers=Parallel Processing
K6


             K5

                  K4

                                                  Konio cells
                       K3

                            K2



                                 K1




Coronal section of dorsolateral nucleus of the monkey
Structural Organizations
 Superior    hemifield in retina=Lateral zone
 Inferior   hemifield= medial zone
 Central    (foveal)= posterior zone
 Peripheral-anterior    zone
 Each   layer receives monocular input
 contalateral    input is received from contralateral eye only
  (nasal fibres)
 Ipsilateral   input receives input from ipsilateral eye only
  (temporal fiblres)
Difference in M,P,K cells
Morphology  of dendrites
Calcium binding protein content
Physiologic properties
Axonal projection within visual cortex
Difference in cell structures
P   cells orients   • M cells complex      • K cells orients
  perpendicular to     radially branching     parallel to the
  the cell layers      dendrites              dLGN layers
 Maintain compact   • Sample more          • A few long
  profile              widely within M        dendrites
 Small receptive      layers               • Larger receptive
  field centres      • Large receptive        field
 Calcium binding      field                • Calcium binding
  protein-           • Calcium binding        protein- calbindin
  parvalbumin          protein-                D 28K
                       parvalbumin
Cell Classes
         Two principal cell classes

• Relay cells: send axon
        cells              • Interneurons whose

  to visual cortex           axons remais with in

• Glutamic acid -neuro       the dLGN

  trasmitter               • γ-aminobutyric acid-

• 4:1                        neurotransmitter
                           • 1:4
X cells and y cells

First evidence of parallel processing
 in the mammalian retina (Enroth-
 Cugell and Robson, 1966)-cat
 ganglion cells to spatial stimuli
 specifically sine wave gratings
X- and Y-cells
X-   cells linear cells
 ◦ For an X-cell a spatial gratings can be
   positioned within the cell’s receptive field such
   that no response is elicited.
 ◦ Excitation and inhibition are linearly summed
   and cancel each other. The excitation is equal to
   the inhibition.
Y-cells   nonlinear cells
 ◦ Y- cells doesn’t sum spatial information in a
   linear fashion.
Afferent axons
80%  input from midget ganglion cells
7-9% input from parasol ganglion cells
Retinal input for K cells?
Efferent axons
 In primates- efferent out put from LGN terminates
  within the primary visual cortex and the visual
  sector of the thalamic reticular nucleus
 A minor efferent projection from LGN terminate in
  several extrastriate ares-originates from K LGN
  cells
  ◦ Implicates as residual vision in Blind Sight (loss of
    primary visual cortex)
 Inconclusion, most K cells and all P and M cells
  send axons to primary visual cortex
Efferent Axons
P  cells send efferent axons to 4Cß of
 Primary Visual Cortex
M cells send efferent axons to 4Cά
 more sparesly to layer 6
K cels send their axons to cortical layer
 3B where they terminate in patches of
 cells and some k cells also send axons
 to cortical layer to 1
Receptive field properties
On  and OFF centre with opposing
 surrounds
K relay cells appear to have
 nonstandard visual receptive field
Wave length based
discrimination of P cells
Response Time
Parvo
  ◦ Sustained response when presented with a long duration
    stimulus
 ◦ Sustained neurons respond to a stimuli for a
   longer period of time they are better suited to
   code Low Temporal Frequency Stimuli
Magno
  ◦ Transient response to the same stimulus with only
     Brief burst at stimulus onset and offset (transient
      amacrine cells)
  ◦ Transient respond to rapid illumination changes
    give M-neurons the capability to resolve high
    temporal frequency stimuli
Receptive Fields
Parvo
 ◦ Smaller Receptive Fields
 ◦ Higher Spatial Frequency Resolution
 ◦ Parvo cells make up the great majority of
   retinal ganglion cells, both foveal and
   nonfoveal.
Magno
 ◦ Larger Receptive Fields
Conduction Velocity
Parvo
 ◦ Slower
Magno
 ◦ Faster
 ◦ Larger Diameter Axons transmit
   information (action potentials) faster
Retinal Concentration
Parvo
 ◦ Represents 90% of Foveal Ganglion Cells
Magno
 ◦ Concentration is constant outside the
   fovea
 ◦ Represents 10% of non-Foveal Ganglion
   Cells
Functions of the Pathways
Magno      System
 ◦   “Where” System
 ◦   Alerts us that a visual event has occurred
 ◦   Detects movement with rapid transmission
 ◦   Dorsal cortical processing stream
Parvo    System
 ◦ “What” System
 ◦ Details of the event are analyzed
 ◦ Ventral cortical processing stream
Characteristics of Parvo and Magno neurons

Characteristics         P Cell      M Cell      K cell

Some size               Medium      large       small

Receptive field         Centre      Centre      variable
organization            surround    surround
Dendrite field size     Small       Medium      large

Contrast sensitivity    Low/ weak   High but    Intermediat
                                    saturated   e

Cortical projection     4Cß         4Cά         3b and 1

Color coding            Color       Non color   Some blue
                        opponent    opponent    on

Speed of transmission   Slow        Fast
Characteristics of Parvo and Magno neurons
Characteristics           P Cell         M Cell         K cell

TMTFs                     low            high           variable

Preferred spatial         High           Low            Low
frequency
Speed of transmission     medium (4      Fast (2msec)   Low (5msec)
                          msec)
Spatial linearity         Linear         Linear or      -
                                         nonlinear

Color vision and contrast Poor at high   Poor low
sensitivity               spatial        frequency
                          frequency      contrast

Temporal                  Sustained      Transient      Both type
responsiveness
Thank you

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Dorso-Lateral Geniculate Nucleus and Parallel Processing

  • 1. Dorsal Lateral Geniculate Nucleus & Parallel Processing GS Shrestha, M.Optom, FIACLE Lecturer
  • 2. Introduction • The most significance – Number of optic nerve fibres project to the Lateral Geniculate Nucleus (LGN) in the Thalamus • Relay to the form vision – From LGN, the visual pathway proceeds to the primary visual cortex, V1 • Complex processing of visual signals – Visual processing and object recognition is enhanced by more than 30 extrastriate cortical areas
  • 3. Targets of the retinal projection Retinal ganglion cell axons Major Minor •Several small hypothalamic nuclei •Suprachiasmatic , supra optic, paraventricular nuclei •Accessory optic system •Nucleus of optic tract •Dorsal, medial and terminal nuclei
  • 4. dLGN 90% retinal ganglion cells project to dLGN Is Laminated and shows Retinotopic Organization Each layer receives input from a specific eye and class of ganglion cell
  • 5. Superior Colliculus A midbrain structure conjunction with cortical frontal eye fields and the brain stem reticular formation  Is laminated and retinotopically organized nucleus.  Visually guided saccadic eye movements  Retinal projection segregates with alternating columns of left and right eye terminals.  10% of all retinal ganglion cells project to the SC  Are small caliber originate from ganglion cells with small dendritic fields and do not project to other retinal targets
  • 6. The Pretectum A group of small midbrain nuceui is just rostral to the SC  Receives signals from a group of small diamter retinal ganglion cells with large receptive fields  Involve with the control of the pupillary light reflex by means of a projection to the Edinger- Westphal nucleus of oculomotor complex.  Show consensual response
  • 7. The Pulvinar nucleus  Largest nucleus mass  Receive projections from the small caliber fibres from the optic nerve and the SC  It projects to several visual cortical area including V1 and extrastriate, parietal areas  Represents second pathway that can bypass the LGN to get the visual V1 and may plays a role in processing from vision  Code importance of visual stimuli-silence or attention ◦ Eg, the eye hand co-ordination
  • 8. Hypothalamic nucleus Receives direct sparse retinal projection that leave the dosal surface of the optic chiasma and has been implicated in the synchronization of circadian rhythms
  • 9. The paraventricular and supraoptic nuclei Involve with the regulation of the light dark cycle for neuroendrocrine functions
  • 10. The Accessory optic systems The lateral terminal nucleus The medial terminal nucleus, the dorsal terminal nucleus NOT in the mid brain Important role in optokinetic nystagmus in viewing with prolong large field motion
  • 11. Overview of dLGN Key gateway to visual signals entering the cortex Less agreement in role of vision ◦ Receptive field properties of dLGN cells= retinal ganglion cell input Regulate the flow and strength of visual signals sent to cortex
  • 12. Structural organization Layers 2,3,5 receives input from Ipsilateral eye Ipsi Layers 1,4,6 receives input from Contralateral eye Contra Dorsal four layers-small neurons-P layers cells=Parvocellular layer (midget cells) Ventral two layers-Large neurons M cells=magnocellylar layers (parasol cells) Between P and M cells=very small bistratified cells- konio cells Combination of all these layers=Parallel Processing
  • 13. K6 K5 K4 Konio cells K3 K2 K1 Coronal section of dorsolateral nucleus of the monkey
  • 14. Structural Organizations  Superior hemifield in retina=Lateral zone  Inferior hemifield= medial zone  Central (foveal)= posterior zone  Peripheral-anterior zone  Each layer receives monocular input  contalateral input is received from contralateral eye only (nasal fibres)  Ipsilateral input receives input from ipsilateral eye only (temporal fiblres)
  • 15. Difference in M,P,K cells Morphology of dendrites Calcium binding protein content Physiologic properties Axonal projection within visual cortex
  • 16. Difference in cell structures P cells orients • M cells complex • K cells orients perpendicular to radially branching parallel to the the cell layers dendrites dLGN layers  Maintain compact • Sample more • A few long profile widely within M dendrites  Small receptive layers • Larger receptive field centres • Large receptive field  Calcium binding field • Calcium binding protein- • Calcium binding protein- calbindin parvalbumin protein- D 28K parvalbumin
  • 17. Cell Classes Two principal cell classes • Relay cells: send axon cells • Interneurons whose to visual cortex axons remais with in • Glutamic acid -neuro the dLGN trasmitter • γ-aminobutyric acid- • 4:1 neurotransmitter • 1:4
  • 18. X cells and y cells First evidence of parallel processing in the mammalian retina (Enroth- Cugell and Robson, 1966)-cat ganglion cells to spatial stimuli specifically sine wave gratings
  • 19.
  • 20. X- and Y-cells X- cells linear cells ◦ For an X-cell a spatial gratings can be positioned within the cell’s receptive field such that no response is elicited. ◦ Excitation and inhibition are linearly summed and cancel each other. The excitation is equal to the inhibition. Y-cells nonlinear cells ◦ Y- cells doesn’t sum spatial information in a linear fashion.
  • 21. Afferent axons 80% input from midget ganglion cells 7-9% input from parasol ganglion cells Retinal input for K cells?
  • 22. Efferent axons  In primates- efferent out put from LGN terminates within the primary visual cortex and the visual sector of the thalamic reticular nucleus  A minor efferent projection from LGN terminate in several extrastriate ares-originates from K LGN cells ◦ Implicates as residual vision in Blind Sight (loss of primary visual cortex)  Inconclusion, most K cells and all P and M cells send axons to primary visual cortex
  • 23.
  • 24. Efferent Axons P cells send efferent axons to 4Cß of Primary Visual Cortex M cells send efferent axons to 4Cά more sparesly to layer 6 K cels send their axons to cortical layer 3B where they terminate in patches of cells and some k cells also send axons to cortical layer to 1
  • 25. Receptive field properties On and OFF centre with opposing surrounds K relay cells appear to have nonstandard visual receptive field
  • 27.
  • 28. Response Time Parvo ◦ Sustained response when presented with a long duration stimulus ◦ Sustained neurons respond to a stimuli for a longer period of time they are better suited to code Low Temporal Frequency Stimuli Magno ◦ Transient response to the same stimulus with only  Brief burst at stimulus onset and offset (transient amacrine cells) ◦ Transient respond to rapid illumination changes give M-neurons the capability to resolve high temporal frequency stimuli
  • 29. Receptive Fields Parvo ◦ Smaller Receptive Fields ◦ Higher Spatial Frequency Resolution ◦ Parvo cells make up the great majority of retinal ganglion cells, both foveal and nonfoveal. Magno ◦ Larger Receptive Fields
  • 30. Conduction Velocity Parvo ◦ Slower Magno ◦ Faster ◦ Larger Diameter Axons transmit information (action potentials) faster
  • 31. Retinal Concentration Parvo ◦ Represents 90% of Foveal Ganglion Cells Magno ◦ Concentration is constant outside the fovea ◦ Represents 10% of non-Foveal Ganglion Cells
  • 32. Functions of the Pathways Magno System ◦ “Where” System ◦ Alerts us that a visual event has occurred ◦ Detects movement with rapid transmission ◦ Dorsal cortical processing stream Parvo System ◦ “What” System ◦ Details of the event are analyzed ◦ Ventral cortical processing stream
  • 33. Characteristics of Parvo and Magno neurons Characteristics P Cell M Cell K cell Some size Medium large small Receptive field Centre Centre variable organization surround surround Dendrite field size Small Medium large Contrast sensitivity Low/ weak High but Intermediat saturated e Cortical projection 4Cß 4Cά 3b and 1 Color coding Color Non color Some blue opponent opponent on Speed of transmission Slow Fast
  • 34. Characteristics of Parvo and Magno neurons Characteristics P Cell M Cell K cell TMTFs low high variable Preferred spatial High Low Low frequency Speed of transmission medium (4 Fast (2msec) Low (5msec) msec) Spatial linearity Linear Linear or - nonlinear Color vision and contrast Poor at high Poor low sensitivity spatial frequency frequency contrast Temporal Sustained Transient Both type responsiveness

Editor's Notes

  1. A striking features of the dlGN is its division into three distinct sections, each constituted of a different types of neuron. The two most ventral layers in Fig 13.1 consist of large neurons referred to as magno cells, and the dorsal four layers consist of smaller neurons referred to as parvo cells. In between these principal layers , in interlaminar regions are collections of yet smaller cells called konio cells.
  2. Retinotopic map= each point in visual space represented along a line perpendicular to the layers is precise with the each point in the retina
  3. Single receptive field centre of midget ganglion cells constituted single cone contributing highly developed visual acuity
  4. Color opponency- wave length based discrimination is good
  5. Color opponency- wave length based discrimination is good