Cargando…
Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements
Motor learning involves neural circuit modifications in the cerebellar cortex, likely through re-weighting of parallel fiber inputs onto Purkinje cells (PCs). Climbing fibers instruct these synaptic modifications when they excite PCs in conjunction with parallel fiber activity, a pairing that enhanc...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120752/ https://www.ncbi.nlm.nih.gov/pubmed/30117806 http://dx.doi.org/10.7554/eLife.36246 |
_version_ | 1783352325064097792 |
---|---|
author | Gaffield, Michael A Rowan, Matthew J M Amat, Samantha B Hirai, Hirokazu Christie, Jason M |
author_facet | Gaffield, Michael A Rowan, Matthew J M Amat, Samantha B Hirai, Hirokazu Christie, Jason M |
author_sort | Gaffield, Michael A |
collection | PubMed |
description | Motor learning involves neural circuit modifications in the cerebellar cortex, likely through re-weighting of parallel fiber inputs onto Purkinje cells (PCs). Climbing fibers instruct these synaptic modifications when they excite PCs in conjunction with parallel fiber activity, a pairing that enhances climbing fiber-evoked Ca(2+) signaling in PC dendrites. In vivo, climbing fibers spike continuously, including during movements when parallel fibers are simultaneously conveying sensorimotor information to PCs. Whether parallel fiber activity enhances climbing fiber Ca(2+) signaling during motor behaviors is unknown. In mice, we found that inhibitory molecular layer interneurons (MLIs), activated by parallel fibers during practiced movements, suppressed parallel fiber enhancement of climbing fiber Ca(2+) signaling in PCs. Similar results were obtained in acute slices for brief parallel fiber stimuli. Interestingly, more prolonged parallel fiber excitation revealed latent supralinear Ca(2+) signaling. Therefore, the balance of parallel fiber and MLI input onto PCs regulates concomitant climbing fiber Ca(2+) signaling. |
format | Online Article Text |
id | pubmed-6120752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61207522018-09-06 Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements Gaffield, Michael A Rowan, Matthew J M Amat, Samantha B Hirai, Hirokazu Christie, Jason M eLife Neuroscience Motor learning involves neural circuit modifications in the cerebellar cortex, likely through re-weighting of parallel fiber inputs onto Purkinje cells (PCs). Climbing fibers instruct these synaptic modifications when they excite PCs in conjunction with parallel fiber activity, a pairing that enhances climbing fiber-evoked Ca(2+) signaling in PC dendrites. In vivo, climbing fibers spike continuously, including during movements when parallel fibers are simultaneously conveying sensorimotor information to PCs. Whether parallel fiber activity enhances climbing fiber Ca(2+) signaling during motor behaviors is unknown. In mice, we found that inhibitory molecular layer interneurons (MLIs), activated by parallel fibers during practiced movements, suppressed parallel fiber enhancement of climbing fiber Ca(2+) signaling in PCs. Similar results were obtained in acute slices for brief parallel fiber stimuli. Interestingly, more prolonged parallel fiber excitation revealed latent supralinear Ca(2+) signaling. Therefore, the balance of parallel fiber and MLI input onto PCs regulates concomitant climbing fiber Ca(2+) signaling. eLife Sciences Publications, Ltd 2018-08-17 /pmc/articles/PMC6120752/ /pubmed/30117806 http://dx.doi.org/10.7554/eLife.36246 Text en © 2018, Gaffield et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Gaffield, Michael A Rowan, Matthew J M Amat, Samantha B Hirai, Hirokazu Christie, Jason M Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements |
title | Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements |
title_full | Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements |
title_fullStr | Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements |
title_full_unstemmed | Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements |
title_short | Inhibition gates supralinear Ca(2+) signaling in Purkinje cell dendrites during practiced movements |
title_sort | inhibition gates supralinear ca(2+) signaling in purkinje cell dendrites during practiced movements |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120752/ https://www.ncbi.nlm.nih.gov/pubmed/30117806 http://dx.doi.org/10.7554/eLife.36246 |
work_keys_str_mv | AT gaffieldmichaela inhibitiongatessupralinearca2signalinginpurkinjecelldendritesduringpracticedmovements AT rowanmatthewjm inhibitiongatessupralinearca2signalinginpurkinjecelldendritesduringpracticedmovements AT amatsamanthab inhibitiongatessupralinearca2signalinginpurkinjecelldendritesduringpracticedmovements AT hiraihirokazu inhibitiongatessupralinearca2signalinginpurkinjecelldendritesduringpracticedmovements AT christiejasonm inhibitiongatessupralinearca2signalinginpurkinjecelldendritesduringpracticedmovements |