CKAMP44 modulates integration of visual inputs in the lateral geniculate nucleus

Autor: Kevin Allen, Jakob von Engelhardt, Muhammad Aslam, Xufeng Chen, Tim Gollisch
Jazyk: angličtina
Rok vydání: 2018
Předmět:
0301 basic medicine
cytology [Geniculate Bodies]
physiology [Retina]
General Physics and Astronomy
Gating
Synaptic Transmission
0302 clinical medicine
Desensitization (telecommunications)
metabolism [Geniculate Bodies]
physiology [Geniculate Bodies]
Receptor
lcsh:Science
genetics [Nerve Tissue Proteins]
Neurons
Mice
Knockout

Multidisciplinary
medicine.diagnostic_test
musculoskeletal
neural
and ocular physiology

Geniculate Bodies
physiology [Neurons]
cytology [Retina]
metabolism [Neurons]
Excitatory postsynaptic potential
Female
ddc:500
metabolism [Retina]
genetics [Synaptic Transmission]
physiology [Excitatory Postsynaptic Potentials]
Science
Nerve Tissue Proteins
AMPA receptor
Biology
Lateral geniculate nucleus
Retinal ganglion
Retina
Article
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
medicine
Electroretinography
Animals
Receptors
AMPA

metabolism [Nerve Tissue Proteins]
CKAMP44 protein
mouse

metabolism [Receptors
AMPA]

Excitatory Postsynaptic Potentials
General Chemistry
Mice
Inbred C57BL

030104 developmental biology
nervous system
physiology [Synaptic Transmission]
Synapses
lcsh:Q
physiology [Synapses]
Neuroscience
030217 neurology & neurosurgery
Photic Stimulation
Zdroj: Nature Communications 9(1), 261 (2018). doi:10.1038/s41467-017-02415-1
Nature Communications, Vol 9, Iss 1, Pp 1-13 (2018)
Nature Communications
DOI: 10.1038/s41467-017-02415-1
Popis: Relay neurons in the dorsal lateral geniculate nucleus (dLGN) receive excitatory inputs from retinal ganglion cells (RGCs). Retinogeniculate synapses are characterized by a prominent short-term depression of AMPA receptor (AMPAR)-mediated currents, but the underlying mechanisms and its function for visual integration are not known. Here we identify CKAMP44 as a crucial auxiliary subunit of AMPARs in dLGN relay neurons, where it increases AMPAR-mediated current amplitudes and modulates gating of AMPARs. Importantly, CKAMP44 is responsible for the distinctive short-term depression in retinogeniculate synapses by reducing the rate of recovery from desensitization of AMPARs. Genetic deletion of CKAMP44 strongly reduces synaptic short-term depression, which leads to increased spike probability of relay neurons when activated with high-frequency inputs from retinogeniculate synapses. Finally, in vivo recordings reveal augmented ON- and OFF-responses of dLGN neurons in CKAMP44 knockout (CKAMP44−/−) mice, demonstrating the importance of CKAMP44 for modulating synaptic short-term depression and visual input integration.
The function of receptor desensitization in vivo is not well understood. Here, the authors show that deletion of CKAMP44, an AMPAR auxiliary protein that modulates desensitization of AMPAR currents, affects synaptic facilitation at retinogeniculate synapses and visually-evoked firing in awake mice.
Databáze: OpenAIRE