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Motion anticipation in the retina

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Submitted on 15 Oct 2019

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Motion anticipation in the retina

Bruno Cessac, Selma Souihel

To cite this version:

Bruno Cessac, Selma Souihel. Motion anticipation in the retina. NeuroSTIC 2019 - 7e édition des journées NeuroSTIC, Oct 2019, Sophia-Antipolis, France. �hal-02316888�

(2)

Motion anticipation in the retina

Bruno Cessac, Selma Souihel

(3)

Motion anticipation in the retina

Bruno Cessac, Selma Souihel

(4)

Motion anticipation in the retina

Bruno Cessac, Selma Souihel

In collaboration with :

Frédéric Chavane

Olivier Marre

Matteo Di Volo

(5)

4

The visual flow

(6)
(7)

6

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

(8)

The visual flow

(9)

8

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion • Sensitive to « surprise » in a visual

scene

(10)

The visual flow

Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion

(11)

10

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion • Sensitive to « surprise » in a visual

scene

(12)

The visual flow

Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion

(13)

12

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion • Sensitive to « surprise » in a visual

scene

(14)

The visual flow

Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion

(15)

14

Visual Anticipation

(16)

Visual Anticipation

(17)

16

Visual Anticipation

Source : Berry et al. 1999

(18)

Visual Anticipation

What are the respective mechanisms underlying retinal

and cortical anticipation?

Trajectory

(19)

18

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

The retina is NOT a camera

• High transduction rate : 1 photon can

trigger a membrane voltage variation of ~1 mV

• Able to detect approaching motion • Able to detect differential motion • Sensitive to « surprise » in a visual

scene

(20)

The visual flow

(21)

20

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

« Analogic computing » No spikes (except in GCs)

Low energy consumption Dedicated circuits Small number of neurons

(22)

The visual flow

(23)

22

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

(24)

The visual flow

Encoding motion

(25)

24

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

Horizontal cells Amacrine cells

(26)

The visual flow

(27)

26

The visual flow

Source : Wikipedia

Decoding spike trains Encoding motion

(28)

The visual flow

Encoding motion

« Analogic computing » No spikes (except in GCs)

Low energy consumption Dedicated circuits Small number of neurons

(29)

28

Which generic computational paradigms are at

work in the retina ?

(30)
(31)

30

Visual Anticipation

(32)

Visual Anticipation

(33)

32

Visual Anticipation

(34)

Visual Anticipation

(35)

34

Visual Anticipation

(36)

Visual Anticipation

(37)

36

Visual Anticipation

Developping a retino-cortical model of anticipation so

as to

understand / propose

possible generic mechanisms for anticipation in the

retina and in the cortex.

(38)
(39)

38

The Hubel-Wiesel view of vision

Ganglion cells

Nobel prize 1981

Ganglion cells response is the convolution of the stimulus with a spatio-temporal

receptive field followed by a non linearity

Ganglion cells are independent encoders

(40)

The Hubel-Wiesel view of vision

Ganglion cells

(41)

40

Gain control (Berry et al, 1999, Chen et al. 2013)

Building a 2D retina model for motion

anticipation

(42)

Building a 2D retina model for motion

anticipation

(43)

42

Building a 2D retina model for motion

anticipation

(44)

Building a 2D retina model for motion

anticipation

(45)

44

1D results : smooth motion anticipation

with gain control

Bipolar layer Ganglion

(46)

1D results : smooth motion anticipation

with gain control

Anticipation variability with stimulus parameters

(47)

46

Building a 2D retina model for motion

anticipation

Ganglion cells are independent encoders

(48)

Building a 2D retina model for motion

anticipation

Ganglion cells are not

independent encoders

(49)

48

Building a 2D retina model for motion

anticipation

(50)

Building a 2D retina model for motion

anticipation

(51)

50

Building a 2D retina model for motion

anticipation

(52)

Building a 2D retina model for motion

anticipation

(53)

52

Smooth motion anticipation with gap

junctions

(54)

6

Smooth motion anticipation with gap

junctions

(55)

54 6

Low gap junction conductance High gap junction conductance

Smooth motion anticipation with gap

junctions

(56)

6

Smooth motion anticipation with gap

junctions

(57)

56

Anticipation variability with stimulus parameters

Smooth motion anticipation with gap

junctions

(58)

Building a 2D retina model for motion

anticipation

(59)

58

Building a 2D retina model for motion

anticipation

Ganglion cells are not

independent encoders

(60)

Amacrine cells connectivity

Building a 2D retina model for motion

anticipation

(61)

60

Amacrine cells connectivity

Building a 2D retina model for motion

anticipation

(62)

Amacrine cells connectivity

Building a 2D retina model for motion

anticipation

(63)

62

Amacrine cells connectivity

Building a 2D retina model for motion

anticipation

(64)

Amacrine cells connectivity

Building a 2D retina model for motion

anticipation

(65)

64

Amacrine cells connectivity

Diffusive wave of activity ahead of the bar

Building a 2D retina model for motion

anticipation

(66)

Building a 2D retina model for motion

anticipation

(67)

66

Building a 2D retina model for motion

anticipation

(68)

Building a 2D retina model for motion

anticipation

(69)

68

Building a 2D retina model for motion

anticipation

(70)

Building a 2D retina model for motion

anticipation

(71)

70

Building a 2D retina model for motion

anticipation

Spatial profiles w=3

(72)

Building a 2D retina model for motion

anticipation

(73)

72

Building a 2D retina model for motion

anticipation

(74)

1D results : smooth motion anticipation

with amacrine connectivity

(75)

74

1D results : smooth motion anticipation

with amacrine connectivity

Anticipation variability with stimulus parameters

(76)
(77)

76

Suggesting new experiments : 2D results

1) Angular anticipation

Stimulus t = 0 ms 100 200 ms 300 ms 400 ms 500 ms 600 ms 700 ms Bipolar linear response Bipolar gain response Ganglion linear response Ganglion gain response A) B) C)

(78)

Suggesting new experiments : 2D results

(79)

Conclusions

The retina is able to encode complex visual scene features, fast and reliably, with a

(80)

Conclusions

The retina is able to encode complex visual scene features, fast and reliably, with a

very low energy consumption, without spikes, except at the ganglion cells level.

(81)

Conclusions

The retina is able to encode complex visual scene features, fast and reliably, with a

very low energy consumption, without spikes, except at the ganglion cells level.

A large part of the « computation » is made by synapses.

Starting from the retina architecture one can extract circuits solving « tasks » such as

(82)

Conclusions

The retina is able to encode complex visual scene features, fast and reliably, with a

very low energy consumption, without spikes, except at the ganglion cells level.

A large part of the « computation » is made by synapses.

Starting from the retina architecture one can extract circuits solving « tasks » such as

motion anticipation.

The role of gain control and local synaptic balance between excitation-inhibition has

been experimentally shown to play a central rôle in anticipation

(Berry et al, 1999 ; Chen at al, 2013 ; Johnston-Lagando, 2015)

.

(83)

Conclusions

The retina is able to encode complex visual scene features, fast and reliably, with a

very low energy consumption, without spikes, except at the ganglion cells level.

A large part of the « computation » is made by synapses.

Starting from the retina architecture one can extract circuits solving « tasks » such as

motion anticipation.

The role of gain control and local synaptic balance between excitation-inhibition has

been experimentally shown to play a central rôle in anticipation

(Berry et al, 1999 ; Chen at al, 2013 ; Johnston-Lagando, 2015)

.

Here we propose that lateral connectivity also plays a role in motion anticipation

(84)

Conclusions

The retina is able to encode complex visual scene features, fast and reliably, with a

very low energy consumption, without spikes, except at the ganglion cells level.

A large part of the « computation » is made by synapses.

Starting from the retina architecture one can extract circuits solving « tasks » such as

motion anticipation.

The role of gain control and local synaptic balance between excitation-inhibition has

been experimentally shown to play a central rôle in anticipation

(Berry et al, 1999 ; Chen at al, 2013 ; Johnston-Lagando, 2015)

.

(85)

84

Anticipation in V1

(86)
(87)

86

A mean field model to reproduce VSDI

recordings

Zerlaut et al 2016

(88)

A mean field model to reproduce VSDI

recordings

Zerlaut et al 2016

(89)

88

A mean field model to reproduce VSDI

recordings

Zerlaut et al 2016

Chemla et al 2018

(90)

A mean field model to reproduce VSDI

recordings

Zerlaut et al 2016

(91)

90

A mean field model to reproduce VSDI

recordings

Zerlaut et al 2016

(92)

A mean field model to reproduce VSDI

recordings

Zerlaut et al 2016

(93)

Response of the cortical model to a LN

retina drive

(94)

Response of the cortical model to a retina

drive with gain control

(95)

Anticipation in the cortex : VSDI data

analysis

(Data courtesy of F.

(96)

Comparing simulation results to VSDI

recordings

Cortex experimental recordings

(97)

Conclusions

We developped a 2D retina with three ganglion cell layers,

implementing gain control and connectivity.

We use the output of our model as an input to a mean field model of

(98)

Conclusions

How to improve object identification

1) exploring the model's parameters and

2) using connectivity ?

Is our model able to anticipate more complex trajectories, with

accelerations for instance ?

(99)

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