Multiple pathways of inhibition shape bipolar cell responses in the retina

Erika D Eggers, Peter D. Lukasiewicz

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

Bipolar cells (BCs) are critical relay neurons in the retina that are organized into parallel signaling pathways. The three main signaling pathways in the mammalian retina are the rod, ON cone, and OFF cone BCs. Rod BCs mediate incrementing dim light signals from rods, and ON cone and OFF cone BCs mediate incrementing and decrementing brighter light signals from cones, respectively. The outputs of BCs are shaped by inhibitory inputs from GABAergic and glycinergic amacrine cells in the inner plexiform layer, mediated by three distinct types of inhibitory receptors: GABAA, GABAC, and glycine receptors. The three main BC pathways receive distinct forms of inhibition from these three receptors that shape their light-evoked inhibitory signals. Rod BC inhibition is dominated by slow GABAC receptor inhibition, while OFF cone BCs are dominated by glycinergic inhibition. The inhibitory inputs to BCs are also shaped by serial inhibitory connections between GABAergic amacrine cells that limit the spatial profile of BC inhibition. We discuss our recent studies on how inhibitory inputs to BCs are shaped by receptor expression, receptor properties, and neurotransmitter release properties and how these affect the output of BCs.

Original languageEnglish (US)
Pages (from-to)95-108
Number of pages14
JournalVisual Neuroscience
Volume28
Issue number1
DOIs
StatePublished - Jan 2011

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Cell Shape
Retina
Amacrine Cells
Vertebrate Photoreceptor Cells
Light
Glycine Receptors
Neurotransmitter Receptor
GABA-A Receptors

Keywords

  • GABA
  • Glycine
  • Light

ASJC Scopus subject areas

  • Sensory Systems
  • Physiology

Cite this

Multiple pathways of inhibition shape bipolar cell responses in the retina. / Eggers, Erika D; Lukasiewicz, Peter D.

In: Visual Neuroscience, Vol. 28, No. 1, 01.2011, p. 95-108.

Research output: Contribution to journalArticle

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