Bipolar cell of the retina

Retinal bipolar cell
Retina. Bipolar cells are shown in red.
Details
Location	Retina (inner nuclear layer)
Morphology	bipolar
Function	Convey gradients between photoreceptor cells to retinal ganglion cells
Neurotransmitter	Glutamate
Presynaptic connections	Rods, cones and horizontal cells
Postsynaptic connections	Retinal ganglion cells and amacrine cells
Identifiers
NeuroLex ID	Retinal Bipolar Cell
Anatomical terminology []

As a part of the retina, bipolar cells exist between photoreceptors (rod cells and cone cells) and ganglion cells. They act, directly or indirectly, to transmit signals from the photoreceptors to the ganglion cells.

Bipolar cells are so-named as they have a central body from which two sets of processes arise. They can synapse with either rods or cones (rod/cone mixed input BCs have been found in teleost fish but not mammals), and they also accept synapses from horizontal cells. The bipolar cells then transmit the signals from the photoreceptors or the horizontal cells, and pass it on to the ganglion cells directly or indirectly (via amacrine cells). Unlike most neurons, bipolar cells communicate via graded potentials, rather than action potentials.

Bipolar cells receive synaptic input from either rods or cones, or both rods and cones, though they are generally designated rod bipolar or cone bipolar cells. There are roughly 10 distinct forms of cone bipolar cells, however, only one rod bipolar cell, due to the rod receptor arriving later in the evolutionary history than the cone receptor.

In the dark, a photoreceptor (rod/cone) cell will release glutamate, which inhibits (hyperpolarizes) the ON bipolar cells and excites (depolarizes) the OFF bipolar cells. In light, however, light strikes the photoreceptor which causes the photoreceptor to be inhibited (hyperpolarized) due to the activation of opsins which activate 11-trans-Retinal, giving energy to stimulate G-Protein coupled receptors to activate phosphodiesterase (PDE) which cleaves cGMP into GMP. In photoreceptor cells, there is an abundance of cGMP in dark conditions, keeping cGMP-gated Na channels open and so, activating PDE diminishes the supply of cGMP, reducing the number of open Na channels and thus hyperpolarizing the photoreceptor cell, causing less glutamate to be released. This causes the ON bipolar cell to lose its inhibition and become active (depolarized), while the OFF bipolar cell loses its excitation (becomes hyperpolarized) and becomes silent.

Rod bipolar cells do not synapse directly on to ganglion cells. Instead, rod bipolar cells synapse on to a Retina amacrine cell, which in turn excite cone ON bipolar cells (via gap junctions) and inhibit cone OFF bipolar cells (via glycine-mediated inhibitory synapses) thereby overtaking the cone pathway in order to send signals to ganglion cells at scotopic (low) ambient light conditions.