Retinal OFF Ganglion Cells Allow Detection of Quantal Shadows at Starlight

Summary: A small group of retinal cells, known as OFF ganglion cells, can detect small dips in light levels and appear to be responsible for shadow detection.

Source: Aalto University

Mice use a specific neural pathway to detect shadows, and it can detect just about the dimmest shadows possible, according to new research from Aalto University and the University of Helsinki. The human eye has the same neural circuit, which researchers think could be used to probe visual diseases at unprecedented resolution.

To test shadow detection, the researchers put mice in a maze with nearly no light. The exit was marked by a black spot, just barely distinct from the surrounding darkness.

By tracking how the mice moved through the maze and measuring the activity of neurons at the back of the eye—the retina—the team showed that a group of retinal cells known as OFF ganglion cells detected the extremely small dip in light levels.

“Our goal is to go from molecules all the way up to behavior,” says Professor Petri Ala-Laurila, who holds a joint appointment at Aalto and the University of Helsinki. This study builds on earlier work from his group which showed that ON ganglion cells are used to detect a very faint patch of light in darkness.

“The opposite task would be detecting the dimmest shadows, where just a few photons are missing. Our hypothesis was that that’s what the most sensitive OFF cells do in starlight, because they increase their firing rate in response to shadows,” says Ala-Laurila.

The team also calculated the fundamental limit of shadow detection based on the physical properties of the light receptors and neural pathways. After accounting for unavoidable losses—for example, not every photon that hits a receptor gets absorbed—they found that the behavior and the retinal activity of the mice came very close to a perfect response.

“Our tightly constrained modeling highlights that both visually-guided behavior and the most sensitive OFF ganglion cells are almost perfect shadow detectors,” says Dr. Johan Westö, one of the joint first authors of the study.

The research had to be done in nearly complete darkness in order to detect these differences. Nataliia Martyniuk, the study’s other first author, says that “the exquisite sensitivity of the visual system to the dimmest shadows sets high technical demands for the experiments that we carried out at these extremely low light levels.”

At higher light levels, many more retinal circuits become activated, which would have made the analysis prohibitively challenging.

“Insanely dim shadows can be detected. Even just a couple of photons missing from a few thousand rod receptors is enough for the animals to detect a shadow,” says Ala-Laurila.

“That probably relates to the huge evolutionary need to detect shadows because mice and other animals have evolved to avoid predators at really low light levels.” 

These findings show how the process of making sense of incoming light—turning it into a mental picture—is distributed across different cell types that carry out different computational tasks in the retina. Within the eye, input from thousands of receptors cascades up to ON and OFF ganglion cells, which act as modules to specifically detect light and shadows, respectively.

This shows a mouse
A night-vision image of a mouse swimming in darkness in the Ala-Laurila lab. Credit: Aarni Seppänen & Tuomas Turunen (Ala-Laurila Lab) / Aalto University

“That pushes a lot of computation onto the retina, and doing this detection early on simplifies the task for downstream processes in the brain,” says Ala-Laurila.

“We can demonstrate this principle in the eye at very low light levels. My guess is that it also applies at higher light levels and in other senses and other areas of neurobiology.”

The retinal circuit responsible for conveying information to ON and OFF ganglion cells is nearly identical in humans. Ala-Laurila explains that the ability to test the function of retinal cell-types specifically in starlight could also have clinical implications.

Many visual diseases are specific to particular cell-types in the retina. By carrying out tests at very low light levels, it might be possible to detect such diseases earlier and with greater precision, since at those light levels every photon counts.

“In my lifetime, I want to see revolutionary techniques for detecting visual diseases using very low light levels as a tool,” he says.

About this visual neuroscience research news

Author: Press Office
Source: Aalto University
Contact: Press Office – Aalto University
Image: The image is in the public domain

Original Research: Open access.
Retinal OFF ganglion cells allow detection of quantal shadows at starlight” by Johan Westö et al. Current Biology


Retinal OFF ganglion cells allow detection of quantal shadows at starlight


  • Mice can see quantal shadows elicited by a few missing photons in thousands of rods
  • Behavior guided by shadows relies on the most sensitive retinal OFF ganglion cells
  • The limit for detecting quantal shadows is set by retinal losses and neural noise


Perception of light in darkness requires no more than a handful of photons, and this remarkable behavioral performance can be directly linked to a particular retinal circuit—the retinal ON pathway. However, the neural limits of shadow detection in very dim light have remained unresolved.

Here, we unravel the neural mechanisms that determine the sensitivity of mice (CBA/CaJ) to light decrements at the lowest light levels by measuring signals from the most sensitive ON and OFF retinal ganglion cell types and by correlating their signals with visually guided behavior.

We show that mice can detect shadows when only a few photon absorptions are missing among thousands of rods. Behavioral detection of such “quantal” shadows relies on the retinal OFF pathway and is limited by noise and loss of single-photon signals in retinal processing.

Thus, in the dim-light regime, light increments and decrements are encoded separately via the ON and OFF retinal pathways, respectively.

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